Primary Site >> Liver Cancer

Gene >> ERBB4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211657790:211657790(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1910C>A
AA Mutation p.Pro637Gln(p.P637Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211712148:211712148(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1026G>C
AA Mutation p.Leu342Phe(p.L342F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211386915:211386915(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3419G>T
AA Mutation p.Ser1140Ile(p.S1140I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211630529:211630529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2012T>C
AA Mutation p.Phe671Ser(p.F671S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211679127:211679127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1547G>T
AA Mutation p.Gly516Val(p.G516V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211679080:211679080(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1594T>C
AA Mutation p.Cys532Arg(p.C532R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211750659:211750659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.602C>A
AA Mutation p.Thr201Lys(p.T201K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000342788
Start 211947507:211947507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.344A>T
AA Mutation p.Tyr115Phe(p.Y115F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000342788
Start 211673239:211673239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1641G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000342788
Start 211619274:211619274(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2204delG
AA Mutation p.Gly735ValfsTer10(p.G735Vfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript