Primary Site >> Pancreatic Cancer

Gene >> COL6A3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237371861:237371861(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146092501
CDS Mutation c.4156G>A
AA Mutation p.Glu1386Lys(p.E1386K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237336473:237336473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367635298
CDS Mutation c.8627C>T
AA Mutation p.Pro2876Leu(p.P2876L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237340880:237340880(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749957183
CDS Mutation c.8036G>A
AA Mutation p.Ser2679Asn(p.S2679N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237344499:237344499(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7519C>A
AA Mutation p.Leu2507Ile(p.L2507I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237374496:237374496(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3595C>G
AA Mutation p.Gln1199Glu(p.Q1199E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295550
Start 237377068:237377068(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2774G>A
AA Mutation p.Arg925Lys(p.R925K)
Mutation Classification Missense_Mutation
Feature Type Transcript