Primary Site >> Stomach Cancer

Gene >> KRT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52675342:52675342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1786G>A
AA Mutation p.Gly596Ser(p.G596S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52677398:52677398(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769968882
CDS Mutation c.1046G>A
AA Mutation p.Ser349Asn(p.S349N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52678548:52678548(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs60359468
CDS Mutation c.800G>A
AA Mutation p.Arg267Gln(p.R267Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52676410:52676410(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1340T>G
AA Mutation p.Leu447Arg(p.L447R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52675201:52675201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1927A>C
AA Mutation p.Thr643Pro(p.T643P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52677374:52677374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1070A>G
AA Mutation p.Gln357Arg(p.Q357R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000252244
Start 52677171:52677171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1142A>G
AA Mutation p.Gln381Arg(p.Q381R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000252244
Start 52675577:52675577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1551C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000252244
Start 52675346:52675346(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1782C>T
Mutation Classification Silent
Feature Type Transcript