Colon Cancer: Gene >> ANKH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284268
Start	14716757:14716757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>A
AA Mutation	p.Ala364Thr(p.A364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284268
Start	14751146:14751146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Cys(p.R204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284268
Start	14713655:14713655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154C>T
AA Mutation	p.Ala385Val(p.A385V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284268
Start	14712896:14712896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768077784
CDS Mutation	c.1343C>T
AA Mutation	p.Ala448Val(p.A448V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284268
Start	14745934:14745934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851C>A
AA Mutation	p.Pro284His(p.P284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANKH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284268
Start	14713654:14713654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146419748
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284268
Start	14749277:14749277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript