Mutation

Primary Site >> Stomach Cancer

Gene >> CHRM2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015818:137015818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953A>G
AA Mutation	p.Glu318Gly(p.E318G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015839:137015839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.974T>C
AA Mutation	p.Ile325Thr(p.I325T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015143:137015143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>T
AA Mutation	p.Pro93Leu(p.P93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015304:137015304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015244:137015244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379A>G
AA Mutation	p.Lys127Glu(p.K127E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137014931:137014931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66A>T
AA Mutation	p.Glu22Asp(p.E22D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137016014:137016014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>T
AA Mutation	p.Lys383Asn(p.K383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137014972:137014972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107T>C
AA Mutation	p.Val36Ala(p.V36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015692:137015692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827A>G
AA Mutation	p.Gln276Arg(p.Q276R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015823:137015823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958T>A
AA Mutation	p.Ser320Thr(p.S320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015685:137015685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820T>A
AA Mutation	p.Cys274Ser(p.C274S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015674:137015674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809T>C
AA Mutation	p.Val270Ala(p.V270A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137016097:137016097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232C>T
AA Mutation	p.Thr411Ile(p.T411I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015590:137015590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779600445
CDS Mutation	c.725A>G
AA Mutation	p.Lys242Arg(p.K242R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015883:137015883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018A>G
AA Mutation	p.Thr340Ala(p.T340A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015841:137015841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976A>G
AA Mutation	p.Arg326Gly(p.R326G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000320658
Start	137015386:137015386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>T
AA Mutation	p.Gly174Val(p.G174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137016045:137016045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781736829
CDS Mutation	c.1180T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137015858:137015858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137015192:137015192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137015318:137015318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137016110:137016110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320658
Start	137015711:137015711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320658
Start	137015403:137015403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.544delT
AA Mutation	p.Ser182ProfsTer18(p.S182Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript