Primary Site >> Liver Cancer

Gene >> CTNND2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11732215:11732215(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.95G>A
AA Mutation p.Ser32Asn(p.S32N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11098692:11098692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2520G>T
AA Mutation p.Met840Ile(p.M840I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11117550:11117550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2177G>T
AA Mutation p.Gly726Val(p.G726V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11384922:11384922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.920T>A
AA Mutation p.Leu307Gln(p.L307Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11082735:11082735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2749C>T
AA Mutation p.Arg917Trp(p.R917W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11384817:11384817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1025C>T
AA Mutation p.Ser342Phe(p.S342F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11384953:11384953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.889G>A
AA Mutation p.Gly297Ser(p.G297S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000304623
Start 11159604:11159604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2131G>A
AA Mutation p.Val711Met(p.V711M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000304623
Start 10992645:10992645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3117G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000304623
Start 11117519:11117519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2208T>A
AA Mutation p.Cys736Ter(p.C736*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript