Mutation

Primary Site >> Stomach Cancer

Gene >> SLC12A7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1063864:1063864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765374153
CDS Mutation	c.2719G>A
AA Mutation	p.Glu907Lys(p.E907K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1074652:1074652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528117289
CDS Mutation	c.1987G>A
AA Mutation	p.Asp663Asn(p.D663N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1083765:1083765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780126009
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1083865:1083865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140054338
CDS Mutation	c.1009G>A
AA Mutation	p.Ala337Thr(p.A337T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1076186:1076186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799C>A
AA Mutation	p.Thr600Asn(p.T600N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1076744:1076744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1698G>C
AA Mutation	p.Glu566Asp(p.E566D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1065447:1065447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2273C>T
AA Mutation	p.Thr758Ile(p.T758I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1074642:1074642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200716950
CDS Mutation	c.1997G>A
AA Mutation	p.Arg666His(p.R666H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1083811:1083811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063T>C
AA Mutation	p.Tyr355His(p.Y355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1089074:1089074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>A
AA Mutation	p.Leu133Met(p.L133M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1076157:1076157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771733188
CDS Mutation	c.1828C>T
AA Mutation	p.Arg610Cys(p.R610C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1065408:1065408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139369204
CDS Mutation	c.2312G>A
AA Mutation	p.Arg771Gln(p.R771Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1052386:1052386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145103734
CDS Mutation	c.3226C>T
AA Mutation	p.Arg1076Trp(p.R1076W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1081622:1081622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252G>A
AA Mutation	p.Ala418Thr(p.A418T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1076772:1076772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575027481
CDS Mutation	c.1670C>T
AA Mutation	p.Ala557Val(p.A557V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1083856:1083856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018G>T
AA Mutation	p.Gly340Cys(p.G340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1053453:1053453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3056C>T
AA Mutation	p.Thr1019Met(p.T1019M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1085454:1085454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763301093
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1065402:1065402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2318G>A
AA Mutation	p.Gly773Asp(p.G773D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1073718:1073718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156A>G
AA Mutation	p.Lys719Arg(p.K719R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000264930
Start	1053430:1053430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370375362
CDS Mutation	c.3079G>A
AA Mutation	p.Val1027Ile(p.V1027I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1078727:1078727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1081719:1081719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374050825
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1076777:1076777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368591973
CDS Mutation	c.1665G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1081650:1081650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1057611:1057611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375298951
CDS Mutation	c.2886C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1081644:1081644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1073768:1073768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2106G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264930
Start	1064137:1064137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147157876
CDS Mutation	c.2553C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264930
Start	1074583:1074583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs767964038
CDS Mutation	c.2056delC
AA Mutation	p.His686ThrfsTer11(p.H686Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264930
Start	1085240:1085241(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.908dupC
AA Mutation	p.Asp304GlyfsTer50(p.D304Gfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264930
Start	1074582:1074583(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2056dupC
AA Mutation	p.His686ProfsTer230(p.H686Pfs*230)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264930
Start	1075369:1075369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1967+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript