Colon Cancer: Gene >> ACD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393919
Start	67659934:67659934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Val157Met(p.V157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393919
Start	67658041:67658041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781117606
CDS Mutation	c.1409C>T
AA Mutation	p.Pro470Leu(p.P470L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393919
Start	67658189:67658189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762262197
CDS Mutation	c.1261C>T
AA Mutation	p.Arg421Cys(p.R421C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393919
Start	67658045:67658045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747913250
CDS Mutation	c.1405C>T
AA Mutation	p.Arg469Trp(p.R469W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393919
Start	67658233:67658233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217G>A
AA Mutation	p.Cys406Tyr(p.C406Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393919
Start	67659749:67659749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACD

No Mutation Annotation!