Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DLC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13085857:13085857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4541C>T
AA Mutation p.Ser1514Phe(p.S1514F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13090446:13090446(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747060194
CDS Mutation c.3880C>T
AA Mutation p.Arg1294Cys(p.R1294C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13091389:13091389(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3784G>T
AA Mutation p.Asp1262Tyr(p.D1262Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13099944:13099944(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755906883
CDS Mutation c.2393G>A
AA Mutation p.Arg798His(p.R798H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499915:13499915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>T
AA Mutation p.Asp53Tyr(p.D53Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499406:13499406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.666G>T
AA Mutation p.Glu222Asp(p.E222D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499569:13499569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.503G>A
AA Mutation p.Gly168Asp(p.G168D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13305280:13305280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1337A>G
AA Mutation p.Lys446Arg(p.K446R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000276297
Start 13095243:13095243(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3170C>T
AA Mutation p.Ala1057Val(p.A1057V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100037:13100037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2300C>T
AA Mutation p.Ala767Val(p.A767V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13102840:13102840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1516T>G
AA Mutation p.Leu506Val(p.L506V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499518:13499518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.554A>G
AA Mutation p.Asp185Gly(p.D185G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499636:13499636(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.436T>C
AA Mutation p.Ser146Pro(p.S146P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13086315:13086315(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4441A>G
AA Mutation p.Thr1481Ala(p.T1481A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13085863:13085863(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747768907
CDS Mutation c.4535G>A
AA Mutation p.Arg1512Gln(p.R1512Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100344:13100344(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1993C>T
AA Mutation p.Arg665Cys(p.R665C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13401594:13401594(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148727515
CDS Mutation c.1049C>T
AA Mutation p.Ala350Val(p.A350V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13393617:13393617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs73551600
CDS Mutation c.1250C>T
AA Mutation p.Thr417Ile(p.T417I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000276297
Start 13393554:13393554(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs545557528
CDS Mutation c.1313C>T
AA Mutation p.Thr438Met(p.T438M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13099635:13099635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2702A>G
AA Mutation p.Asp901Gly(p.D901G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499395:13499395(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.677T>G
AA Mutation p.Leu226Arg(p.L226R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13099923:13099923(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766262406
CDS Mutation c.2414C>T
AA Mutation p.Thr805Met(p.T805M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100185:13100185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2152G>A
AA Mutation p.Ala718Thr(p.A718T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13393638:13393638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377063736
CDS Mutation c.1229G>A
AA Mutation p.Arg410Gln(p.R410Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100424:13100424(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1913G>T
AA Mutation p.Gly638Val(p.G638V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100097:13100097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2240C>T
AA Mutation p.Ser747Leu(p.S747L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13095089:13095089(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775545560
CDS Mutation c.3324T>A
AA Mutation p.Asp1108Glu(p.D1108E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13102808:13102808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1548T>G
AA Mutation p.Ile516Met(p.I516M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13086308:13086308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4448T>C
AA Mutation p.Met1483Thr(p.M1483T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100517:13100517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1820C>T
AA Mutation p.Ala607Val(p.A607V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13088572:13088572(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760440807
CDS Mutation c.4207G>A
AA Mutation p.Glu1403Lys(p.E1403K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100281:13100281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2056G>T
AA Mutation p.Ala686Ser(p.A686S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13086431:13086431(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4325G>T
AA Mutation p.Cys1442Phe(p.C1442F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13088545:13088545(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4234T>G
AA Mutation p.Tyr1412Asp(p.Y1412D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499534:13499534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.538G>A
AA Mutation p.Glu180Lys(p.E180K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13092820:13092820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3532C>T
AA Mutation p.Pro1178Ser(p.P1178S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13092673:13092673(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201136617
CDS Mutation c.3679G>A
AA Mutation p.Val1227Met(p.V1227M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13100369:13100369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1968C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13099565:13099565(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761051677
CDS Mutation c.2772G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13100426:13100426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1911C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13099601:13099601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2736C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13499637:13499637(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750244627
CDS Mutation c.435C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13100621:13100621(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752727723
CDS Mutation c.1716G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13499979:13499979(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.93T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13401571:13401571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1072C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000276297
Start 13110772:13110772(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1472delT
AA Mutation p.Leu491TrpfsTer13(p.L491Wfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000276297
Start 13095127:13095127(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3286delC
AA Mutation p.Gln1096SerfsTer33(p.Q1096Sfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000276297
Start 13100488:13100488(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1849delC
AA Mutation p.Arg617GlyfsTer37(p.R617Gfs*37)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000276297
Start 13099850:13099850(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2487delC
AA Mutation p.Ser830ArgfsTer7(p.S830Rfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000276297
Start 13095115:13095115(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763428774
CDS Mutation c.3298C>T
AA Mutation p.Arg1100Ter(p.R1100*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000276297
Start 13499234:13499234(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.838C>T
AA Mutation p.Gln280Ter(p.Q280*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000276297
Start 13095124:13095124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3289C>T
AA Mutation p.Gln1097Ter(p.Q1097*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000276297
Start 13499216:13499217(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.855dupC
AA Mutation p.Asn286GlnfsTer6(p.N286Qfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> DLC1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13088629:13088629(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778397065
CDS Mutation c.4150C>T
AA Mutation p.Arg1384Cys(p.R1384C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499096:13499096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.976G>A
AA Mutation p.Ala326Thr(p.A326T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499554:13499554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.518C>A
AA Mutation p.Ala173Glu(p.A173E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13100368:13100368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1969G>A
AA Mutation p.Glu657Lys(p.E657K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13401578:13401578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1065G>A
AA Mutation p.Met355Ile(p.M355I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13499705:13499705(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.367G>A
AA Mutation p.Asp123Asn(p.D123N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13094938:13094938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3347C>T
AA Mutation p.Ser1116Leu(p.S1116L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000276297
Start 13305289:13305289(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1328T>G
AA Mutation p.Ile443Ser(p.I443S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13100000:13100000(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2337C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13100279:13100279(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372344109
CDS Mutation c.2058G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13099700:13099700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2637C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13499613:13499613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.459C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000276297
Start 13499175:13499175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.897T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000276297
Start 13393639:13393639(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752937229
CDS Mutation c.1228C>T
AA Mutation p.Arg410Ter(p.R410*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript