Colon Cancer: Gene >> DOHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250937
Start	3496673:3496673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771915905
CDS Mutation	c.142G>A
AA Mutation	p.Asp48Asn(p.D48N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250937
Start	3496807:3496807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200328323
CDS Mutation	c.8C>T
AA Mutation	p.Thr3Met(p.T3M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250937
Start	3496607:3496607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753023201
CDS Mutation	c.208G>A
AA Mutation	p.Ala70Thr(p.A70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250937
Start	3491747:3491747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250937
Start	3496578:3496578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250937
Start	3496662:3496662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376432012
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DOHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250937
Start	3496700:3496700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765301122
CDS Mutation	c.115G>A
AA Mutation	p.Ala39Thr(p.A39T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript