Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HSPG2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21857323:21857323(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766592389
CDS Mutation c.5356G>A
AA Mutation p.Gly1786Arg(p.G1786R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21847988:21847988(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142226974
CDS Mutation c.7843G>A
AA Mutation p.Val2615Ile(p.V2615I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21841569:21841569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9298G>A
AA Mutation p.Ala3100Thr(p.A3100T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21873961:21873961(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113652076
CDS Mutation c.3707C>T
AA Mutation p.Ala1236Val(p.A1236V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21874410:21874410(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778103999
CDS Mutation c.3652G>A
AA Mutation p.Gly1218Ser(p.G1218S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21885369:21885369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1161C>G
AA Mutation p.His387Gln(p.H387Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21853065:21853065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561417019
CDS Mutation c.6445G>A
AA Mutation p.Gly2149Ser(p.G2149S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21852098:21852098(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6860C>T
AA Mutation p.Ala2287Val(p.A2287V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21876245:21876245(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373895855
CDS Mutation c.2987G>A
AA Mutation p.Arg996His(p.R996H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21879016:21879016(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2449C>A
AA Mutation p.Pro817Thr(p.P817T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21838995:21838995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9980C>T
AA Mutation p.Pro3327Leu(p.P3327L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21852927:21852927(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566319401
CDS Mutation c.6583C>T
AA Mutation p.Arg2195Trp(p.R2195W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21876353:21876353(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768568677
CDS Mutation c.2879G>A
AA Mutation p.Ser960Asn(p.S960N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21834697:21834697(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115616224
CDS Mutation c.10702G>A
AA Mutation p.Val3568Ile(p.V3568I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21855529:21855529(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761763385
CDS Mutation c.5848G>A
AA Mutation p.Val1950Met(p.V1950M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21880727:21880727(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575688004
CDS Mutation c.1927C>T
AA Mutation p.Arg643Cys(p.R643C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21879007:21879007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2458G>A
AA Mutation p.Asp820Asn(p.D820N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21836953:21836953(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150666616
CDS Mutation c.10204G>A
AA Mutation p.Val3402Met(p.V3402M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21823712:21823712(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761987723
CDS Mutation c.12907C>T
AA Mutation p.Arg4303Cys(p.R4303C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21843344:21843344(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372570791
CDS Mutation c.8711C>T
AA Mutation p.Ala2904Val(p.A2904V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21829520:21829520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769541964
CDS Mutation c.11855G>A
AA Mutation p.Arg3952His(p.R3952H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21852760:21852760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6664G>T
AA Mutation p.Gly2222Cys(p.G2222C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21878586:21878586(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140392638
CDS Mutation c.2549G>A
AA Mutation p.Arg850His(p.R850H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21872208:21872208(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374895557
CDS Mutation c.4199C>T
AA Mutation p.Pro1400Leu(p.P1400L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21887489:21887489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.889T>C
AA Mutation p.Cys297Arg(p.C297R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21839005:21839005(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9970G>A
AA Mutation p.Gly3324Arg(p.G3324R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21884608:21884608(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1574G>A
AA Mutation p.Gly525Asp(p.G525D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21839049:21839049(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370638163
CDS Mutation c.9926C>T
AA Mutation p.Ser3309Leu(p.S3309L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21878655:21878655(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752992263
CDS Mutation c.2480A>T
AA Mutation p.Asp827Val(p.D827V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21830058:21830058(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375127656
CDS Mutation c.11705G>A
AA Mutation p.Arg3902Gln(p.R3902Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21854680:21854680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6219G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21862101:21862101(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142756395
CDS Mutation c.4755C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21874960:21874960(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754721291
CDS Mutation c.3345C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21841567:21841567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9300C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21876361:21876361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762979069
CDS Mutation c.2871C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21887327:21887327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374656693
CDS Mutation c.966G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21874426:21874426(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775949784
CDS Mutation c.3636C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21880434:21880434(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139220302
CDS Mutation c.2124C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21854722:21854722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200272505
CDS Mutation c.6177G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21887607:21887607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21838973:21838973(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145279304
CDS Mutation c.10002C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21852187:21852187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149569423
CDS Mutation c.6771C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21874703:21874703(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550724412
CDS Mutation c.3441G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21850439:21850439(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7218G>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21879047:21879047(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2418C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21844211:21844211(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772559776
CDS Mutation c.8553C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21851618:21851618(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139001173
CDS Mutation c.7086C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21852794:21852794(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6630G>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000374695
Start 21847425:21847431(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.8087_8093delGCCGGGC
AA Mutation p.Cys2696SerfsTer49(p.C2696Sfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000374695
Start 21841279:21841279(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.9335delC
AA Mutation p.Pro3112LeufsTer13(p.P3112Lfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000374695
Start 21841639:21841655(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.9212_9228delCCAATGGCTCCATCATC
AA Mutation p.Pro3071HisfsTer100(p.P3071Hfs*100)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000374695
Start 21852941:21852941(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6569delG
AA Mutation p.Gly2190AlafsTer19(p.G2190Afs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000374695
Start 21890686:21890686(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747493127
CDS Mutation c.253C>T
AA Mutation p.Arg85Ter(p.R85*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000374695
Start 21854640:21854640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6259C>T
AA Mutation p.Arg2087Ter(p.R2087*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000374695
Start 21885148:21885149(version: GRCh38)
Mutation Type INS
dbSNP_RS rs763945561
CDS Mutation c.1219dupC
AA Mutation p.Gln407ProfsTer62(p.Q407Pfs*62)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> HSPG2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21824725:21824725(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12644C>T
AA Mutation p.Pro4215Leu(p.P4215L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374695
Start 21873420:21873420(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779841547
CDS Mutation c.3748G>A
AA Mutation p.Ala1250Thr(p.A1250T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000374695
Start 21832503:21832503(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150968006
CDS Mutation c.11199C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000374695
Start 21876625:21876625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2713G>T
AA Mutation p.Glu905Ter(p.E905*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript