Mutation

Primary Site >> Stomach Cancer

Gene >> TRPM7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50561787:50561787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5489C>T
AA Mutation	p.Thr1830Met(p.T1830M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50609633:50609633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377252016
CDS Mutation	c.2528G>A
AA Mutation	p.Arg843Gln(p.R843Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50561692:50561692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753258420
CDS Mutation	c.5584C>T
AA Mutation	p.Arg1862Cys(p.R1862C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50586421:50586421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4457G>A
AA Mutation	p.Arg1486Lys(p.R1486K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50614157:50614157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601G>A
AA Mutation	p.Arg534Gln(p.R534Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50575090:50575090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4781T>C
AA Mutation	p.Ile1594Thr(p.I1594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50599190:50599190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3095T>G
AA Mutation	p.Leu1032Arg(p.L1032R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50643443:50643443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>T
AA Mutation	p.Gln144His(p.Q144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50594450:50594450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3454G>A
AA Mutation	p.Asp1152Asn(p.D1152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50609628:50609628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2533T>G
AA Mutation	p.Phe845Val(p.F845V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50639477:50639477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758746706
CDS Mutation	c.607G>A
AA Mutation	p.Gly203Arg(p.G203R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50609930:50609930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2312T>C
AA Mutation	p.Ile771Thr(p.I771T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50596267:50596267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3278T>C
AA Mutation	p.Ile1093Thr(p.I1093T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313478
Start	50574980:50574980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4891T>A
AA Mutation	p.Cys1631Ser(p.C1631S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313478
Start	50586426:50586426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4452T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313478
Start	50592509:50592509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3726G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313478
Start	50613722:50613722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313478
Start	50593667:50593667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3558T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313478
Start	50574314:50574314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114933907
CDS Mutation	c.5268C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313478
Start	50632943:50632943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1057delA
AA Mutation	p.Thr353HisfsTer16(p.T353Hfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313478
Start	50591998:50591998(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4237delA
AA Mutation	p.Ser1413AlafsTer29(p.S1413Afs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313478
Start	50639460:50639461(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.623dupG
AA Mutation	p.Val209SerfsTer3(p.V209Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript