Primary Site >> Stomach Cancer

Gene >> KRT76

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332411
Start 52776775:52776775(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752943841
CDS Mutation c.517G>A
AA Mutation p.Asp173Asn(p.D173N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332411
Start 52775467:52775467(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.736G>A
AA Mutation p.Asp246Asn(p.D246N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332411
Start 52775593:52775593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610C>A
AA Mutation p.Leu204Met(p.L204M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332411
Start 52776723:52776723(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.569T>G
AA Mutation p.Leu190Arg(p.L190R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000332411
Start 52775591:52775591(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.612G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000332411
Start 52777199:52777199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.93C>T
Mutation Classification Silent
Feature Type Transcript