Primary Site >> Stomach Cancer

Gene >> KRT7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52243055:52243055(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.902T>C
AA Mutation p.Leu301Pro(p.L301P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52235321:52235321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376567055
CDS Mutation c.491C>T
AA Mutation p.Ala164Val(p.A164V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52235330:52235330(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370849999
CDS Mutation c.500G>A
AA Mutation p.Arg167Gln(p.R167Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52241604:52241604(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771955592
CDS Mutation c.826C>T
AA Mutation p.Arg276Trp(p.R276W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52233607:52233607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311C>G
AA Mutation p.Ser104Cys(p.S104C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000331817
Start 52245508:52245508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081C>A
AA Mutation p.Leu361Met(p.L361M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000331817
Start 52237521:52237521(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.549A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000331817
Start 52243068:52243068(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.915G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000331817
Start 52241480:52241480(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.702A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000331817
Start 52235235:52235235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.405C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence inframe_deletion
Transcription ID ENST00000331817
Start 52233608:52233610(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.313_315delTTC
AA Mutation p.Phe105del(p.F105del)
Mutation Classification In_Frame_Del
Feature Type Transcript