Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VMP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59817725:59817725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.926T>C
AA Mutation p.Ile309Thr(p.I309T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59811686:59811686(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.812T>A
AA Mutation p.Phe271Tyr(p.F271Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262291
Start 59737455:59737455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.215T>C
AA Mutation p.Leu72Ser(p.L72S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59735392:59735392(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.131T>G
AA Mutation p.Ile44Ser(p.I44S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59773772:59773772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.601G>A
AA Mutation p.Gly201Arg(p.G201R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59838356:59838356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1036C>T
AA Mutation p.Arg346Trp(p.R346W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59839849:59839849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1159A>G
AA Mutation p.Met387Val(p.M387V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59731491:59731491(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45G>A
AA Mutation p.Met15Ile(p.M15I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59738864:59738864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.331C>A
AA Mutation p.Leu111Ile(p.L111I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262291
Start 59817723:59817723(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.924T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000262291
Start 59735342:59735342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.81C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000262291
Start 59839905:59839905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1215T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000262291
Start 59735411:59735411(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768887557
CDS Mutation c.150G>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> VMP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59735366:59735366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.105G>T
AA Mutation p.Arg35Ser(p.R35S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262291
Start 59731511:59731511(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.65G>A
AA Mutation p.Gly22Glu(p.G22E)
Mutation Classification Missense_Mutation
Feature Type Transcript