Colon Cancer: Gene >> CHRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910655:62910655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Ala149Val(p.A149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910950:62910950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151A>G
AA Mutation	p.Lys51Glu(p.K51E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910173:62910173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753639928
CDS Mutation	c.928G>A
AA Mutation	p.Glu310Lys(p.E310K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910142:62910142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773788891
CDS Mutation	c.959G>A
AA Mutation	p.Arg320Gln(p.R320Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62909741:62909741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376730515
CDS Mutation	c.1360C>T
AA Mutation	p.Arg454Cys(p.R454C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910766:62910766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335C>T
AA Mutation	p.Ser112Phe(p.S112F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306960
Start	62910071:62910071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030C>T
AA Mutation	p.Arg344Cys(p.R344C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306960
Start	62910414:62910414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306960
Start	62909952:62909952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306960
Start	62911005:62911005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373462832
CDS Mutation	c.96G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHRM1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306960
Start	62910774:62910774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript