Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209693992:209693992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1822A>G
AA Mutation p.Thr608Ala(p.T608A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694362:209694362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2192T>G
AA Mutation p.Ile731Ser(p.I731S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694550:209694550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2380G>T
AA Mutation p.Asp794Tyr(p.D794Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694979:209694979(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763603161
CDS Mutation c.2809G>A
AA Mutation p.Ala937Thr(p.A937T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694332:209694332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2162G>T
AA Mutation p.Gly721Val(p.G721V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695811:209695811(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3641C>A
AA Mutation p.Pro1214His(p.P1214H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694509:209694509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2339C>T
AA Mutation p.Thr780Ile(p.T780I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694133:209694133(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1963C>A
AA Mutation p.Pro655Thr(p.P655T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209693760:209693760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1590G>T
AA Mutation p.Lys530Asn(p.K530N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209693513:209693513(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1343C>A
AA Mutation p.Thr448Asn(p.T448N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694283:209694283(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2113C>T
AA Mutation p.Pro705Ser(p.P705S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694766:209694766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2596G>T
AA Mutation p.Asp866Tyr(p.D866Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209725778:209725778(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5143C>T
AA Mutation p.Arg1715Cys(p.R1715C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209693123:209693123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.953A>C
AA Mutation p.Gln318Pro(p.Q318P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209705715:209705715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758141796
CDS Mutation c.4720C>T
AA Mutation p.Arg1574Trp(p.R1574W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209653184:209653184(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148723167
CDS Mutation c.14G>A
AA Mutation p.Arg5Gln(p.R5Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695667:209695667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3497C>T
AA Mutation p.Ala1166Val(p.A1166V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209705610:209705610(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4615T>A
AA Mutation p.Ser1539Thr(p.S1539T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694701:209694701(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372993675
CDS Mutation c.2531G>A
AA Mutation p.Arg844His(p.R844H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209700331:209700331(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4577A>G
AA Mutation p.Lys1526Arg(p.K1526R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694779:209694779(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2609G>A
AA Mutation p.Cys870Tyr(p.C870Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209653303:209653303(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181207847
CDS Mutation c.133G>A
AA Mutation p.Ala45Thr(p.A45T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209710238:209710238(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5057A>G
AA Mutation p.Gln1686Arg(p.Q1686R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209730270:209730270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5357C>G
AA Mutation p.Ser1786Cys(p.S1786C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209696210:209696210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4040C>T
AA Mutation p.Ser1347Phe(p.S1347F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695841:209695841(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149194467
CDS Mutation c.3671C>T
AA Mutation p.Thr1224Met(p.T1224M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209709988:209709988(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4807C>T
AA Mutation p.Pro1603Ser(p.P1603S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209696336:209696336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4166G>T
AA Mutation p.Trp1389Leu(p.W1389L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694302:209694302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2132C>T
AA Mutation p.Ser711Phe(p.S711F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209710145:209710145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750357842
CDS Mutation c.4964C>T
AA Mutation p.Ala1655Val(p.A1655V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694747:209694747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2577A>C
AA Mutation p.Lys859Asn(p.K859N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360351
Start 209710252:209710252(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781736914
CDS Mutation c.5071C>A
AA Mutation p.Gln1691Lys(p.Q1691K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695915:209695915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3745C>T
AA Mutation p.Leu1249Phe(p.L1249F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209696625:209696625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4264C>T
AA Mutation p.Leu1422Phe(p.L1422F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209705721:209705721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4726A>G
AA Mutation p.Thr1576Ala(p.T1576A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209729859:209729859(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5165G>A
AA Mutation p.Arg1722His(p.R1722H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209696031:209696031(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772176261
CDS Mutation c.3861C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209694978:209694978(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570922955
CDS Mutation c.2808C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209678588:209678588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209694285:209694285(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376603789
CDS Mutation c.2115G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209695671:209695671(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3501C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209710164:209710164(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4983G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209729854:209729854(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780072425
CDS Mutation c.5160C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209692884:209692884(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.714A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209695845:209695845(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3675C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209695203:209695203(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3033C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209710113:209710113(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140691086
CDS Mutation c.4932C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209695140:209695140(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780188011
CDS Mutation c.2970C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209692749:209692749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.579A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209696322:209696322(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571107524
CDS Mutation c.4152C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000360351
Start 209696943:209696943(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4420delA
AA Mutation p.Thr1474GlnfsTer14(p.T1474Qfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 52
Mutation Consequence frameshift_variant
Transcription ID ENST00000360351
Start 209693218:209693218(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1053delA
AA Mutation p.Lys351AsnfsTer38(p.K351Nfs*38)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209653297:209653297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.127C>T
AA Mutation p.Arg43Ter(p.R43*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209694524:209694524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2354C>A
AA Mutation p.Ser785Ter(p.S785*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209694043:209694043(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1873G>T
AA Mutation p.Glu625Ter(p.E625*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209695255:209695255(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3085G>T
AA Mutation p.Glu1029Ter(p.E1029*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000360351
Start 209696942:209696943(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4420dupA
AA Mutation p.Thr1474AsnfsTer22(p.T1474Nfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> MAP2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694131:209694131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1961C>A
AA Mutation p.Ser654Tyr(p.S654Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209696099:209696099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3929G>A
AA Mutation p.Arg1310His(p.R1310H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694328:209694328(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2158C>T
AA Mutation p.Arg720Trp(p.R720W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209700317:209700317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4563A>T
AA Mutation p.Lys1521Asn(p.K1521N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209696172:209696172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4002A>C
AA Mutation p.Glu1334Asp(p.E1334D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209710112:209710112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4931T>C
AA Mutation p.Val1644Ala(p.V1644A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209710193:209710193(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5012A>G
AA Mutation p.Lys1671Arg(p.K1671R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695782:209695782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3612C>G
AA Mutation p.Ser1204Arg(p.S1204R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209678629:209678629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.320A>G
AA Mutation p.Lys107Arg(p.K107R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209692982:209692982(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs547929820
CDS Mutation c.812C>T
AA Mutation p.Thr271Met(p.T271M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209694145:209694145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1975A>G
AA Mutation p.Met659Val(p.M659V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360351
Start 209695623:209695623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3453G>T
AA Mutation p.Lys1151Asn(p.K1151N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209696202:209696202(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4032A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209695986:209695986(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3816C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000360351
Start 209697026:209697026(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4497C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209694524:209694524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2354C>A
AA Mutation p.Ser785Ter(p.S785*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000360351
Start 209696589:209696589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4228G>T
AA Mutation p.Glu1410Ter(p.E1410*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000360351
Start 209696942:209696943(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4420dupA
AA Mutation p.Thr1474AsnfsTer22(p.T1474Nfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript