Primary Site >> Stomach Cancer

Gene >> PMS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 5987264:5987264(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs540287433
CDS Mutation c.1501G>A
AA Mutation p.Val501Met(p.V501M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 6002514:6002514(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.476T>C
AA Mutation p.Val159Ala(p.V159A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 5986825:5986825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1940A>C
AA Mutation p.Lys647Thr(p.K647T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 5987284:5987284(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587782602
CDS Mutation c.1481C>T
AA Mutation p.Ser494Leu(p.S494L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 5987522:5987522(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138387687
CDS Mutation c.1243G>A
AA Mutation p.Val415Met(p.V415M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265849
Start 5987312:5987312(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1453A>G
AA Mutation p.Thr485Ala(p.T485A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000265849
Start 5989951:5989951(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186577215
CDS Mutation c.993C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000265849
Start 5977690:5977690(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs786202531
CDS Mutation c.2343G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000265849
Start 5987268:5987268(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1497T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000265849
Start 5997406:5997406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.723T>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000265849
Start 6002539:6002539(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.451delC
AA Mutation p.Arg151AlafsTer50(p.R151Afs*50)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000265849
Start 5987526:5987526(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1239delA
AA Mutation p.Asp414ThrfsTer34(p.D414Tfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript