Primary Site >> Liver Cancer

Gene >> KCNQ3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000388996
Start 132180222:132180222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.712C>A
AA Mutation p.Leu238Met(p.L238M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000388996
Start 132480357:132480357(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.176C>A
AA Mutation p.Ala59Asp(p.A59D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000388996
Start 132141329:132141329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1265A>T
AA Mutation p.Gln422Leu(p.Q422L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000388996
Start 132141240:132141240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1354G>A
AA Mutation p.Ala452Thr(p.A452T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000388996
Start 132140158:132140158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1486A>G
AA Mutation p.Met496Val(p.M496V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000388996
Start 132141322:132141322(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1272G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000388996
Start 132129727:132129727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2154G>C
Mutation Classification Silent
Feature Type Transcript