Primary Site >> Liver Cancer

Gene >> COL1A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297268
Start 94427726:94427726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3367C>A
AA Mutation p.Arg1123Ser(p.R1123S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297268
Start 94427834:94427834(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3475C>G
AA Mutation p.Pro1159Ala(p.P1159A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297268
Start 94426476:94426476(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3051A>T
AA Mutation p.Arg1017Ser(p.R1017S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000297268
Start 94424416:94424416(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2646T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000297268
Start 94400240:94400240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000297268
Start 94410933:94410933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1242T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000297268
Start 94422978:94422978(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2429delC
AA Mutation p.Pro810LeufsTer25(p.P810Lfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript