Colon Cancer: Gene >> DHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49089896:49089896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49091203:49091203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Cys(p.R164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49091158:49091158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774203455
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49091230:49091230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781595957
CDS Mutation	c.463G>A
AA Mutation	p.Asp155Asn(p.D155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49091197:49091197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750409317
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266991
Start	49094230:49094230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266991
Start	49094477:49094477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266991
Start	49091294:49091294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266991
Start	49091231:49091231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DHH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266991
Start	49094255:49094255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>A
Mutation Classification	Silent
Feature Type	Transcript