Colon Cancer: Gene >> CRHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398285
Start	45834639:45834639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749376023
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Trp(p.R404W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398285
Start	45816486:45816486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>A
AA Mutation	p.Asp49Asn(p.D49N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398285
Start	45816510:45816510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778136105
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Cys(p.R57C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398285
Start	45834682:45834682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253C>T
AA Mutation	p.Ala418Val(p.A418V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398285
Start	45829241:45829241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754362644
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398285
Start	45830443:45830443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398285
Start	45821401:45821401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781652857
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CRHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398285
Start	45834685:45834685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419Gln(p.R419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398285
Start	45807066:45807066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543785844
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript