Primary Site >> Stomach Cancer

Gene >> XRCC3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000352127
Start 103699453:103699453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777604903
CDS Mutation c.685G>A
AA Mutation p.Ala229Thr(p.A229T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000352127
Start 103708647:103708647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748765569
CDS Mutation c.68C>T
AA Mutation p.Ser23Leu(p.S23L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000352127
Start 103699474:103699474(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.664G>C
AA Mutation p.Glu222Gln(p.E222Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000352127
Start 103698939:103698939(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.900G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000352127
Start 103708562:103708562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.153A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000352127
Start 103698864:103698864(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.975delC
AA Mutation p.Ser326ProfsTer43(p.S326Pfs*43)
Mutation Classification Frame_Shift_Del
Feature Type Transcript