Primary Site >> Stomach Cancer

Gene >> SHC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264554
Start 434854:434854(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61745866
CDS Mutation c.965C>T
AA Mutation p.Pro322Leu(p.P322L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264554
Start 422256:422256(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1510G>A
AA Mutation p.Asp504Asn(p.D504N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000264554
Start 434721:434721(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369107402
CDS Mutation c.1098G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264554
Start 422188:422188(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367900777
CDS Mutation c.1578C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000264554
Start 425192:425192(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1214delG
AA Mutation p.Gly405AlafsTer39(p.G405Afs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript