Primary Site >> Stomach Cancer

Gene >> KRT4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52813646:52813646(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747520287
CDS Mutation c.413G>A
AA Mutation p.Arg138His(p.R138H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52813644:52813644(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758810156
CDS Mutation c.415G>A
AA Mutation p.Glu139Lys(p.E139K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52808786:52808786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767527715
CDS Mutation c.899G>A
AA Mutation p.Arg300His(p.R300H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52813613:52813613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.446C>T
AA Mutation p.Ala149Val(p.A149V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52808310:52808310(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1109A>G
AA Mutation p.Glu370Gly(p.E370G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52809435:52809435(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.782A>C
AA Mutation p.Lys261Thr(p.K261T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000551956
Start 52813895:52813895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.164T>C
AA Mutation p.Leu55Pro(p.L55P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000551956
Start 52813861:52813861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.198T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000551956
Start 52808842:52808842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.843C>A
Mutation Classification Silent
Feature Type Transcript