Mutation

Primary Site >> Stomach Cancer

Gene >> A2M

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9069769:9069769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4239C>A
AA Mutation	p.Asn1413Lys(p.N1413K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9113488:9113488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142T>C
AA Mutation	p.Cys48Arg(p.C48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9079281:9079281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3082T>G
AA Mutation	p.Phe1028Val(p.F1028V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9093549:9093549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745894309
CDS Mutation	c.2156G>A
AA Mutation	p.Arg719His(p.R719H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9109394:9109394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685T>C
AA Mutation	p.Phe229Leu(p.F229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9068783:9068783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4323T>A
AA Mutation	p.Asp1441Glu(p.D1441E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9109949:9109949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>T
AA Mutation	p.Glu197Asp(p.E197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9101605:9101605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>A
AA Mutation	p.His446Asn(p.H446N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318602
Start	9109321:9109321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758T>C
AA Mutation	p.Leu253Pro(p.L253P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9074780:9074780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3536A>C
AA Mutation	p.Asn1179Thr(p.N1179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9093510:9093510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195G>A
AA Mutation	p.Arg732Gln(p.R732Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9089987:9089987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2633A>G
AA Mutation	p.Glu878Gly(p.E878G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9101460:9101460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481C>T
AA Mutation	p.Ser494Phe(p.S494F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9112388:9112388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>A
AA Mutation	p.Pro140Gln(p.P140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9074673:9074673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3643G>A
AA Mutation	p.Ala1215Thr(p.A1215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9093566:9093566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139G>A
AA Mutation	p.Met713Ile(p.M713I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9070528:9070528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4154T>C
AA Mutation	p.Met1385Thr(p.M1385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9079250:9079250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3113A>C
AA Mutation	p.Asn1038Thr(p.N1038T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9074656:9074656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3660G>T
AA Mutation	p.Gln1220His(p.Q1220H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9101644:9101644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576930283
CDS Mutation	c.1297G>A
AA Mutation	p.Gly433Ser(p.G433S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318602
Start	9091202:9091202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2468G>A
AA Mutation	p.Arg823Gln(p.R823Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9076866:9076866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3422G>A
AA Mutation	p.Gly1141Asp(p.G1141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000318602
Start	9115783:9115783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376129998
CDS Mutation	c.67G>A
AA Mutation	p.Ala23Thr(p.A23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9093542:9093542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2163G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9091306:9091306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2364C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9098676:9098676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9079282:9079282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3081C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9091204:9091204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2466C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9098712:9098712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754296966
CDS Mutation	c.1746C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9107581:9107581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202126909
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9077391:9077391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775982089
CDS Mutation	c.3306C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9112192:9112192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318602
Start	9101552:9101552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318602
Start	9109964:9109964(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.576delT
AA Mutation	p.Leu194SerfsTer40(p.L194Sfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000318602
Start	9112400:9112400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407C>A
AA Mutation	p.Ser136Ter(p.S136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000318602
Start	9079272:9079272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091C>T
AA Mutation	p.Arg1031Ter(p.R1031*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000318602
Start	9098757:9098757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript