Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BMP6

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000283147
Start 7862433:7862433(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs577694907
CDS Mutation c.1139G>A
AA Mutation p.Arg380His(p.R380H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000283147
Start 7880195:7880195(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1394T>C
AA Mutation p.Val465Ala(p.V465A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000283147
Start 7879096:7879096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1227A>C
AA Mutation p.Lys409Asn(p.K409N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000283147
Start 7880337:7880337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1536C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000283147
Start 7880083:7880083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138326174
CDS Mutation c.1374C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000283147
Start 7727564:7727564(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770466865
CDS Mutation c.609G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000283147
Start 7845231:7845231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754411823
CDS Mutation c.756G>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> BMP6

No Mutation Annotation!