Primary Site >> Liver Cancer

Gene >> MCTP1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000515393
Start 94779111:94779111(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2609A>T
AA Mutation p.Lys870Met(p.K870M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000515393
Start 94940191:94940191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1066A>G
AA Mutation p.Thr356Ala(p.T356A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000515393
Start 94940187:94940187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777016909
CDS Mutation c.1070A>T
AA Mutation p.Asp357Val(p.D357V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000515393
Start 94894749:94894749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1739T>A
AA Mutation p.Leu580Gln(p.L580Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000515393
Start 95017426:95017426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.779T>A
AA Mutation p.Met260Lys(p.M260K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000515393
Start 94868376:94868376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2393G>A
AA Mutation p.Cys798Tyr(p.C798Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000515393
Start 94909346:94909346(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1557A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000515393
Start 94868375:94868375(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2394C>A
AA Mutation p.Cys798Ter(p.C798*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript