Mutation

Primary Site >> Stomach Cancer

Gene >> GRIK3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36891088:36891088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124T>G
AA Mutation	p.Phe42Val(p.F42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36805040:36805040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2512G>A
AA Mutation	p.Val838Met(p.V838M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36841853:36841853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1413G>T
AA Mutation	p.Lys471Asn(p.K471N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36872213:36872213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707C>G
AA Mutation	p.Thr236Ser(p.T236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36850420:36850420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217G>T
AA Mutation	p.Gly406Val(p.G406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36853625:36853625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202G>A
AA Mutation	p.Gly401Asp(p.G401D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36859879:36859879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763214417
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Trp(p.R309W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36825697:36825697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200138348
CDS Mutation	c.1660G>A
AA Mutation	p.Val554Ile(p.V554I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	37034021:37034021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Cys(p.R30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36872348:36872348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572T>C
AA Mutation	p.Leu191Pro(p.L191P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36880736:36880736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780055449
CDS Mutation	c.448G>A
AA Mutation	p.Val150Met(p.V150M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36817113:36817113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038A>T
AA Mutation	p.Thr680Ser(p.T680S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36825613:36825613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>T
AA Mutation	p.Val582Phe(p.V582F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36891049:36891049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163G>A
AA Mutation	p.Ala55Thr(p.A55T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36805036:36805036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2516C>T
AA Mutation	p.Ala839Val(p.A839V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36859957:36859957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Trp(p.R283W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000373091
Start	36872226:36872226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143358361
CDS Mutation	c.694G>A
AA Mutation	p.Asp232Asn(p.D232N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373091
Start	36806123:36806123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369987280
CDS Mutation	c.2295C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373091
Start	36872227:36872227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748826480
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373091
Start	36880692:36880692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373091
Start	36853618:36853618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373091
Start	36825802:36825802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1555delC
AA Mutation	p.Leu519Ter(p.L519*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373091
Start	36819743:36819744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1865dupT
AA Mutation	p.Met622IlefsTer6(p.M622Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373091
Start	36880789:36880790(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.394dupC
AA Mutation	p.His132ProfsTer49(p.H132Pfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript