Primary Site >> Stomach Cancer

Gene >> XRCC4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338635
Start 83195776:83195776(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.322C>T
AA Mutation p.Leu108Phe(p.L108F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338635
Start 83104966:83104966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.47T>A
AA Mutation p.Ile16Lys(p.I16K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338635
Start 83195909:83195909(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455T>C
AA Mutation p.Leu152Pro(p.L152P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338635
Start 83195882:83195882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.428A>G
AA Mutation p.His143Arg(p.H143R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338635
Start 83258651:83258651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.867G>T
AA Mutation p.Gln289His(p.Q289H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000338635
Start 83104988:83104988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.69T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000338635
Start 83111167:83111167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279T>C
Mutation Classification Silent
Feature Type Transcript