Primary Site >> Esophagus Cancer

Gene >> KRT14

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000167586
Start 41583584:41583584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1020C>G
AA Mutation p.Asn340Lys(p.N340K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000167586
Start 41586459:41586459(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764842172
CDS Mutation c.376C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000167586
Start 41583901:41583913(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.774_786delTGCCCTGAGAGGC
AA Mutation p.Ala259ArgfsTer18(p.A259Rfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000167586
Start 41583800:41583806(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.881_887delTGGCAGA
AA Mutation p.Met294ArgfsTer18(p.M294Rfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript