Primary Site >> Stomach Cancer

Gene >> CA4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300900
Start 60156596:60156596(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777463944
CDS Mutation c.149G>A
AA Mutation p.Arg50His(p.R50H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000300900
Start 60156560:60156560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.113T>C
AA Mutation p.Val38Ala(p.V38A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300900
Start 60156682:60156682(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531909330
CDS Mutation c.235C>A
AA Mutation p.Gln79Lys(p.Q79K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300900
Start 60158435:60158435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.733C>T
AA Mutation p.His245Tyr(p.H245Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300900
Start 60157462:60157462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.304G>A
AA Mutation p.Gly102Arg(p.G102R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000300900
Start 60158296:60158296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.594G>A
Mutation Classification Silent
Feature Type Transcript