Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GDF15

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252809
Start 18386194:18386194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5C>A
AA Mutation p.Pro2His(p.P2H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252809
Start 18386344:18386344(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.155G>T
AA Mutation p.Arg52Ile(p.R52I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000252809
Start 18388658:18388658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.650G>A
AA Mutation p.Arg217His(p.R217H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000252809
Start 18386458:18386458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs114827523
CDS Mutation c.269C>T
AA Mutation p.Thr90Met(p.T90M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000252809
Start 18388701:18388701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.693G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000252809
Start 18386438:18386438(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.249C>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> GDF15

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252809
Start 18386205:18386205(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.16C>A
AA Mutation p.Leu6Ile(p.L6I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000252809
Start 18386254:18386254(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.65C>A
AA Mutation p.Ser22Ter(p.S22*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript