Colon Cancer: Gene >> HRH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397056
Start	11259506:11259506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>A
AA Mutation	p.Leu157Met(p.L157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397056
Start	11259263:11259263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370754604
CDS Mutation	c.226G>A
AA Mutation	p.Val76Met(p.V76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397056
Start	11260224:11260224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138501310
CDS Mutation	c.1187C>T
AA Mutation	p.Ser396Leu(p.S396L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397056
Start	11260264:11260264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770888159
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397056
Start	11260034:11260034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997A>G
AA Mutation	p.Thr333Ala(p.T333A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397056
Start	11259560:11259560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201947424
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397056
Start	11259376:11259376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201790628
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript