Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PHGDH

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369409
Start 119735340:119735340(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777155018
CDS Mutation c.689G>A
AA Mutation p.Arg230His(p.R230H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369409
Start 119741850:119741850(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1162G>A
AA Mutation p.Val388Met(p.V388M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000369409
Start 119712097:119712097(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752195785
CDS Mutation c.75T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369409
Start 119737230:119737230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762185673
CDS Mutation c.909C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000369409
Start 119735305:119735305(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.654delT
AA Mutation p.Asn218LysfsTer15(p.N218Kfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> PHGDH

No Mutation Annotation!