Mutation

Primary Site >> Stomach Cancer

Gene >> MGAM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142021631:142021631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368879552
CDS Mutation	c.604G>A
AA Mutation	p.Val202Met(p.V202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142027718:142027718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371373847
CDS Mutation	c.1204G>A
AA Mutation	p.Ala402Thr(p.A402T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142005552:142005552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22A>C
AA Mutation	p.Lys8Gln(p.K8Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142055605:142055605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370241545
CDS Mutation	c.3362G>A
AA Mutation	p.Arg1121His(p.R1121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142063530:142063530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4289G>A
AA Mutation	p.Gly1430Glu(p.G1430E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000549489
Start	142094862:142094862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4769G>T
AA Mutation	p.Arg1590Met(p.R1590M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142105872:142105872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370916883
CDS Mutation	c.5555C>T
AA Mutation	p.Thr1852Met(p.T1852M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142025140:142025140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973A>G
AA Mutation	p.Asn325Asp(p.N325D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142103297:142103297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5354A>T
AA Mutation	p.Asn1785Ile(p.N1785I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142040166:142040166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2368G>A
AA Mutation	p.Glu790Lys(p.E790K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142052841:142052841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3016A>G
AA Mutation	p.Ser1006Gly(p.S1006G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142050808:142050808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2749C>T
AA Mutation	p.His917Tyr(p.H917Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000549489
Start	142036842:142036842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096T>C
AA Mutation	p.Phe699Ser(p.F699S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000549489
Start	142096413:142096413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750406655
CDS Mutation	c.5002C>T
AA Mutation	p.Arg1668Cys(p.R1668C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142047869:142047869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2583G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142008579:142008579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781996087
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142019219:142019219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142047860:142047860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142027696:142027696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142054837:142054837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3243A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142052897:142052897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375312122
CDS Mutation	c.3072C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142105834:142105834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5517T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142031769:142031769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000549489
Start	142027717:142027717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368738284
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000549489
Start	142036920:142036920(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2176delC
AA Mutation	p.Leu726SerfsTer52(p.L726Sfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000549489
Start	142100854:142100854(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765764785
CDS Mutation	c.5243delG
AA Mutation	p.Gly1748AlafsTer35(p.G1748Afs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000549489
Start	142034761:142034761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1879G>T
AA Mutation	p.Gly627Ter(p.G627*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000549489
Start	142095715:142095715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4919+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript