Primary Site >> Stomach Cancer

Gene >> FGF9

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000382353
Start 21681042:21681042(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.278G>A
AA Mutation p.Gly93Asp(p.G93D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21672181:21672181(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.269G>T
AA Mutation p.Ser90Ile(p.S90I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21672120:21672120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.208A>G
AA Mutation p.Thr70Ala(p.T70A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21701228:21701228(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765041263
CDS Mutation c.420C>A
AA Mutation p.Phe140Leu(p.F140L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21681092:21681092(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774141078
CDS Mutation c.328G>A
AA Mutation p.Val110Met(p.V110M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21671998:21671998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.86G>A
AA Mutation p.Ser29Asn(p.S29N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21671953:21671953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.41A>G
AA Mutation p.Gln14Arg(p.Q14R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000382353
Start 21672151:21672151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.239G>A
AA Mutation p.Gly80Asp(p.G80D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000382353
Start 21701249:21701249(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764396440
CDS Mutation c.441G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000382353
Start 21701191:21701191(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.387delA
AA Mutation p.Lys129AsnfsTer2(p.K129Nfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000382353
Start 21672039:21672039(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.132delG
AA Mutation p.Leu45SerfsTer13(p.L45Sfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000382353
Start 21701289:21701289(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481C>T
AA Mutation p.Arg161Ter(p.R161*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript