Mutation

Primary Site >> Stomach Cancer

Gene >> VAV1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6825075:6825075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759730093
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6854021:6854021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2407C>A
AA Mutation	p.Leu803Ile(p.L803I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6833921:6833921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140267055
CDS Mutation	c.1745G>A
AA Mutation	p.Arg582His(p.R582H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6821661:6821661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6772974:6772974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167A>C
AA Mutation	p.Asn56Thr(p.N56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6772872:6772872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65G>T
AA Mutation	p.Arg22Leu(p.R22L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6833601:6833601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684C>T
AA Mutation	p.Pro562Ser(p.P562S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000602142
Start	6828164:6828164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016T>A
AA Mutation	p.Leu339His(p.L339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6821663:6821663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777740563
CDS Mutation	c.363C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6853048:6853048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760094090
CDS Mutation	c.2301G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6821657:6821657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373664582
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602142
Start	6833613:6833613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000602142
Start	6828648:6828649(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1121_1125dupAGCGA
AA Mutation	p.Asp376SerfsTer74(p.D376Sfs*74)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000602142
Start	6829787:6829788(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1268_1271dupATGC
AA Mutation	p.Phe425CysfsTer12(p.F425Cfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000602142
Start	6833734:6833734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1731+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript