Mutation

Primary Site >> Stomach Cancer

Gene >> PLCG1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41163267:41163267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758702634
CDS Mutation	c.781T>C
AA Mutation	p.Tyr261His(p.Y261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41170264:41170264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2803G>A
AA Mutation	p.Ala935Thr(p.A935T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41159651:41159651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Gln(p.R88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41165702:41165702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Cys(p.R559C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41172607:41172607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3092G>A
AA Mutation	p.Cys1031Tyr(p.C1031Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41160143:41160143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774118487
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41163433:41163433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769806657
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41166220:41166220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747210988
CDS Mutation	c.1826G>A
AA Mutation	p.Arg609His(p.R609H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41170147:41170147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146143589
CDS Mutation	c.2686G>A
AA Mutation	p.Val896Ile(p.V896I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41163396:41163396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Cys(p.R270C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41170166:41170166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140033921
CDS Mutation	c.2705C>T
AA Mutation	p.Ala902Val(p.A902V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41160114:41160114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777319797
CDS Mutation	c.473G>A
AA Mutation	p.Arg158Gln(p.R158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41165034:41165034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319A>G
AA Mutation	p.Lys440Arg(p.K440R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41164099:41164099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759833563
CDS Mutation	c.1115C>T
AA Mutation	p.Pro372Leu(p.P372L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373271
Start	41162724:41162724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141297485
CDS Mutation	c.680C>T
AA Mutation	p.Thr227Met(p.T227M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41160135:41160135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494A>T
AA Mutation	p.Asp165Val(p.D165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41164109:41164109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>A
AA Mutation	p.Met375Ile(p.M375I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41166279:41166279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1885T>G
AA Mutation	p.Phe629Val(p.F629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41162654:41162654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756870964
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Cys(p.R204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000373271
Start	41166561:41166561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764393595
CDS Mutation	c.2086C>T
AA Mutation	p.Arg696Trp(p.R696W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41172198:41172198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2814T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41165518:41165518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41165068:41165068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1353A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41162713:41162713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41164166:41164166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373271
Start	41168799:41168799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2412C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000373271
Start	41166567:41166567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2092G>T
AA Mutation	p.Glu698Ter(p.E698*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000373271
Start	41172647:41172647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3130+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript