Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> APOB

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000233242
Start 21025124:21025124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2245G>T
AA Mutation p.Asp749Tyr(p.D749Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21005764:21005764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11104C>A
AA Mutation p.Leu3702Ile(p.L3702I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007391:21007391(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9477G>T
AA Mutation p.Lys3159Asn(p.K3159N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009898:21009898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6970C>A
AA Mutation p.Leu2324Ile(p.L2324I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012387:21012387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4481C>T
AA Mutation p.Ser1494Leu(p.S1494L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21028030:21028030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1865C>A
AA Mutation p.Ser622Tyr(p.S622Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21042470:21042470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.128C>T
AA Mutation p.Ala43Val(p.A43V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21011188:21011188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5680A>G
AA Mutation p.Asn1894Asp(p.N1894D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007104:21007104(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9764T>A
AA Mutation p.Val3255Asp(p.V3255D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000233242
Start 21015258:21015258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3511G>A
AA Mutation p.Glu1171Lys(p.E1171K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006808:21006808(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10060G>T
AA Mutation p.Ala3354Ser(p.A3354S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21005181:21005181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759708973
CDS Mutation c.11687C>T
AA Mutation p.Ala3896Val(p.A3896V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007562:21007562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9306C>A
AA Mutation p.Phe3102Leu(p.F3102L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012458:21012458(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4410T>G
AA Mutation p.His1470Gln(p.H1470Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21022925:21022925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761179789
CDS Mutation c.2722G>A
AA Mutation p.Glu908Lys(p.E908K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012618:21012618(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200321839
CDS Mutation c.4250C>T
AA Mutation p.Thr1417Met(p.T1417M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21010151:21010151(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6717C>A
AA Mutation p.Asn2239Lys(p.N2239K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21005307:21005307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11561C>T
AA Mutation p.Thr3854Ile(p.T3854I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21015197:21015197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3572C>T
AA Mutation p.Ser1191Phe(p.S1191F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21008955:21008955(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7913A>C
AA Mutation p.Asn2638Thr(p.N2638T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009174:21009174(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7694C>A
AA Mutation p.Ala2565Glu(p.A2565E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006678:21006678(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10190C>T
AA Mutation p.Thr3397Ile(p.T3397I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002749:21002749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12673G>A
AA Mutation p.Gly4225Arg(p.G4225R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007852:21007852(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9016G>T
AA Mutation p.Gly3006Cys(p.G3006C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21029993:21029993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1375G>T
AA Mutation p.Gly459Trp(p.G459W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21010326:21010326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6542T>G
AA Mutation p.Phe2181Cys(p.F2181C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012403:21012403(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4465C>A
AA Mutation p.Gln1489Lys(p.Q1489K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21004331:21004331(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140424976
CDS Mutation c.12025G>A
AA Mutation p.Val4009Met(p.V4009M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21008623:21008623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8245A>G
AA Mutation p.Thr2749Ala(p.T2749A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000233242
Start 21030014:21030014(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1354T>A
AA Mutation p.Tyr452Asn(p.Y452N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21013460:21013460(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3916T>C
AA Mutation p.Ser1306Pro(p.S1306P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21010731:21010731(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6137T>C
AA Mutation p.Val2046Ala(p.V2046A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002681:21002681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12741A>C
AA Mutation p.Gln4247His(p.Q4247H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012518:21012518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4350A>C
AA Mutation p.Lys1450Asn(p.K1450N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21016642:21016642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3129G>T
AA Mutation p.Lys1043Asn(p.K1043N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21010358:21010358(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6510A>C
AA Mutation p.Lys2170Asn(p.K2170N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006365:21006365(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10503G>T
AA Mutation p.Lys3501Asn(p.K3501N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012517:21012517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4351G>T
AA Mutation p.Gly1451Cys(p.G1451C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21015526:21015526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3352A>G
AA Mutation p.Arg1118Gly(p.R1118G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002268:21002268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533755016
CDS Mutation c.13154G>A
AA Mutation p.Arg4385His(p.R4385H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21003033:21003033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12389T>G
AA Mutation p.Phe4130Cys(p.F4130C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007807:21007807(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9061C>A
AA Mutation p.His3021Asn(p.H3021N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007462:21007462(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs72653102
CDS Mutation c.9406C>T
AA Mutation p.Arg3136Cys(p.R3136C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21011805:21011805(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5063G>T
AA Mutation p.Gly1688Val(p.G1688V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002457:21002457(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533551460
CDS Mutation c.12965T>G
AA Mutation p.Phe4322Cys(p.F4322C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002724:21002724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377125320
CDS Mutation c.12698C>T
AA Mutation p.Ser4233Leu(p.S4233L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002931:21002931(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12491T>C
AA Mutation p.Phe4164Ser(p.F4164S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006360:21006360(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375284245
CDS Mutation c.10508C>T
AA Mutation p.Ser3503Leu(p.S3503L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007385:21007385(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9483C>A
AA Mutation p.Phe3161Leu(p.F3161L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009808:21009808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7060A>C
AA Mutation p.Ile2354Leu(p.I2354L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012176:21012176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4692G>T
AA Mutation p.Glu1564Asp(p.E1564D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21038010:21038010(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.485C>A
AA Mutation p.Ser162Tyr(p.S162Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21027831:21027831(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774188993
CDS Mutation c.2064C>G
AA Mutation p.Ile688Met(p.I688M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21016458:21016458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375294575
CDS Mutation c.3313G>A
AA Mutation p.Ala1105Thr(p.A1105T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009111:21009111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7757C>T
AA Mutation p.Thr2586Ile(p.T2586I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006600:21006600(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761983757
CDS Mutation c.10268T>C
AA Mutation p.Val3423Ala(p.V3423A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 57
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21008571:21008571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8297C>A
AA Mutation p.Ser2766Tyr(p.S2766Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 58
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21011008:21011008(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5860C>A
AA Mutation p.Leu1954Ile(p.L1954I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 59
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21032422:21032422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284G>T
AA Mutation p.Glu428Asp(p.E428D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 60
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21010227:21010227(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6641A>G
AA Mutation p.Glu2214Gly(p.E2214G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 61
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21028483:21028483(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766083346
CDS Mutation c.1673G>A
AA Mutation p.Arg558Gln(p.R558Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002993:21002993(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12429G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21007397:21007397(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9471C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 64
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002624:21002624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12798C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 65
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21008405:21008405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8463G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 66
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21032374:21032374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1332G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 67
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21012617:21012617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs72653082
CDS Mutation c.4251G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 68
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21006359:21006359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769351301
CDS Mutation c.10509G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 69
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21038060:21038060(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576323709
CDS Mutation c.435G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 70
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21012206:21012206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4662C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 71
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21019062:21019062(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs558838327
CDS Mutation c.3051C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 72
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21010772:21010772(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768573736
CDS Mutation c.6096G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 73
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21011468:21011468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5400C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 74
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21029702:21029702(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1554G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 75
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21007352:21007352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9516T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 76
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21007808:21007808(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9060G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 77
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21005924:21005924(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370314131
CDS Mutation c.10944C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 78
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21010190:21010190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6678C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 79
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002546:21002546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12876C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 80
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002453:21002453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12969T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 81
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21005327:21005327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11541C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 82
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21011744:21011744(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5124A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 83
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21004566:21004566(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11898A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 84
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21019785:21019785(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145649470
CDS Mutation c.2937C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 85
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21009833:21009833(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368113811
CDS Mutation c.7035C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 86
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21003017:21003017(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12405T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 87
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002723:21002723(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs56675344
CDS Mutation c.12699G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 88
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21005261:21005261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11607C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 89
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21007142:21007142(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9726C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 90
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21011939:21011939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200623857
CDS Mutation c.4929G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 91
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21022971:21022971(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759072451
CDS Mutation c.2676G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 92
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21008074:21008074(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.8794delG
AA Mutation p.Ala2932ProfsTer19(p.A2932Pfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 93
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21001800:21001800(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.13622delA
AA Mutation p.Lys4541SerfsTer8(p.K4541Sfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 94
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21011106:21011106(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5762delG
AA Mutation p.Gly1921GlufsTer13(p.G1921Efs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 95
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21015204:21015204(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3565delA
AA Mutation p.Met1189Ter(p.M1189*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 96
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21007522:21007522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9346G>T
AA Mutation p.Gly3116Ter(p.G3116*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 97
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21001895:21001895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13527C>A
AA Mutation p.Tyr4509Ter(p.Y4509*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 98
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21010717:21010717(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6151G>T
AA Mutation p.Glu2051Ter(p.E2051*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 99
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21027844:21027844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2051C>A
AA Mutation p.Ser684Ter(p.S684*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 100
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21033432:21033432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.991G>T
AA Mutation p.Glu331Ter(p.E331*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 101
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21007510:21007510(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9358G>T
AA Mutation p.Glu3120Ter(p.E3120*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 102
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21010424:21010425(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.6443dupA
AA Mutation p.Tyr2149ValfsTer2(p.Y2149Vfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 103
Mutation Consequence frameshift_variant
Transcription ID ENST00000233242
Start 21005271:21005272(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.11596_11597insATTTCTTA
AA Mutation p.Ser3866TyrfsTer21(p.S3866Yfs*21)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 104
Mutation Consequence splice_donor_variant
Transcription ID ENST00000233242
Start 21024931:21024931(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2436+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> APOB

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21005956:21005956(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61744151
CDS Mutation c.10912C>T
AA Mutation p.Arg3638Trp(p.R3638W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009480:21009480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7388C>T
AA Mutation p.Ala2463Val(p.A2463V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21028401:21028401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1755G>T
AA Mutation p.Gln585His(p.Q585H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002068:21002068(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13354C>A
AA Mutation p.Leu4452Ile(p.L4452I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21004616:21004616(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11848G>T
AA Mutation p.Ala3950Ser(p.A3950S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009330:21009330(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554045156
CDS Mutation c.7538G>A
AA Mutation p.Arg2513Gln(p.R2513Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21012330:21012330(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780817600
CDS Mutation c.4538G>A
AA Mutation p.Arg1513Gln(p.R1513Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009706:21009706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7162G>T
AA Mutation p.Asp2388Tyr(p.D2388Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006196:21006196(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs12713559
CDS Mutation c.10672C>T
AA Mutation p.Arg3558Cys(p.R3558C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21008664:21008664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8204A>C
AA Mutation p.Asp2735Ala(p.D2735A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21006355:21006355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10513C>A
AA Mutation p.Leu3505Ile(p.L3505I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007761:21007761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9107C>A
AA Mutation p.Ser3036Tyr(p.S3036Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21015138:21015138(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3631C>A
AA Mutation p.Leu1211Ile(p.L1211I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21042470:21042470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.128C>T
AA Mutation p.Ala43Val(p.A43V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007858:21007858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9010G>T
AA Mutation p.Ala3004Ser(p.A3004S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21002833:21002833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12589C>A
AA Mutation p.Leu4197Met(p.L4197M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21003162:21003162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12260A>T
AA Mutation p.Lys4087Met(p.K4087M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21007423:21007423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9445G>T
AA Mutation p.Asp3149Tyr(p.D3149Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21009109:21009109(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375855688
CDS Mutation c.7759G>C
AA Mutation p.Val2587Leu(p.V2587L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21011001:21011001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5867C>A
AA Mutation p.Ser1956Tyr(p.S1956Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000233242
Start 21042446:21042446(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764776276
CDS Mutation c.152A>G
AA Mutation p.Lys51Arg(p.K51R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002723:21002723(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs56675344
CDS Mutation c.12699G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21029651:21029651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763856498
CDS Mutation c.1605G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21005390:21005390(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11478G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21010733:21010733(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6135C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21011252:21011252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5616C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21015464:21015464(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140456702
CDS Mutation c.3414C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21002300:21002300(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13122A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21011245:21011245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5623C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000233242
Start 21019077:21019077(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3036G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21013379:21013379(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121918383
CDS Mutation c.3997C>T
AA Mutation p.Arg1333Ter(p.R1333*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000233242
Start 21028484:21028484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1672C>T
AA Mutation p.Arg558Ter(p.R558*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript