Primary Site >> Pancreatic Cancer

Gene >> COL18A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45512357:45512357(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573442861
CDS Mutation c.5224G>A
AA Mutation p.Val1742Met(p.V1742M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45473920:45473920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201095161
CDS Mutation c.1922G>A
AA Mutation p.Arg641His(p.R641H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45488427:45488427(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3151G>A
AA Mutation p.Gly1051Ser(p.G1051S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45491276:45491276(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375408962
CDS Mutation c.3364G>A
AA Mutation p.Gly1122Arg(p.G1122R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45505948:45505948(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4443C>A
AA Mutation p.Asn1481Lys(p.N1481K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359759
Start 45482807:45482807(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201476017
CDS Mutation c.2932G>A
AA Mutation p.Ala978Thr(p.A978T)
Mutation Classification Missense_Mutation
Feature Type Transcript