Primary Site >> Stomach Cancer

Gene >> SHC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368445
Start 154965964:154965964(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747330503
CDS Mutation c.1366C>T
AA Mutation p.Arg456Trp(p.R456W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368445
Start 154970172:154970172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355G>A
AA Mutation p.Gly119Arg(p.G119R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368445
Start 154968511:154968511(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.734C>A
AA Mutation p.Ala245Asp(p.A245D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368445
Start 154966020:154966020(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376945597
CDS Mutation c.1310G>A
AA Mutation p.Arg437Gln(p.R437Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368445
Start 154965578:154965578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1588C>T
AA Mutation p.Pro530Ser(p.P530S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000368445
Start 154970266:154970266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.261A>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000368445
Start 154965992:154965992(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1338delC
AA Mutation p.Asn447IlefsTer15(p.N447Ifs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript