Colon Cancer: Gene >> CYHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000438911
Start	144452548:144452548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Cys(p.R170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000438911
Start	144453402:144453402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Arg102Gln(p.R102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000438911
Start	144453265:144453265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000438911
Start	144450513:144450513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955C>G
AA Mutation	p.His319Asp(p.H319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000438911
Start	144450624:144450624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844A>G
AA Mutation	p.Thr282Ala(p.T282A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438911
Start	144453308:144453308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182495946
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438911
Start	144450631:144450631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYHR1

No Mutation Annotation!