Colon Cancer: Gene >> CHRM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239907986:239907986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535A>G
AA Mutation	p.Lys179Glu(p.K179E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239907828:239907828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776861962
CDS Mutation	c.377C>T
AA Mutation	p.Thr126Met(p.T126M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908917:239908917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466C>T
AA Mutation	p.Ala489Val(p.A489V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908767:239908767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316A>C
AA Mutation	p.Lys439Thr(p.K439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908232:239908232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239907651:239907651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200A>G
AA Mutation	p.Gln67Arg(p.Q67R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908080:239908080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>G
AA Mutation	p.Phe210Cys(p.F210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908415:239908415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964C>T
AA Mutation	p.Pro322Ser(p.P322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908355:239908355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200967479
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239907964:239907964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777700262
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239908348:239908348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147784522
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239907601:239907601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375211682
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239907484:239907484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239908333:239908333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255380
Start	239909144:239909144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754500041
CDS Mutation	c.1700delA
AA Mutation	p.Lys567ArgfsTer31(p.K567Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000255380
Start	239908078:239908078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627C>A
AA Mutation	p.Tyr209Ter(p.Y209*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CHRM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255380
Start	239908117:239908117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>A
AA Mutation	p.Phe222Leu(p.F222L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255380
Start	239907562:239907562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript