Mutation

Primary Site >> Stomach Cancer

Gene >> GOLGA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128261706:128261706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758084594
CDS Mutation	c.1105A>G
AA Mutation	p.Met369Val(p.M369V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128260152:128260152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768763105
CDS Mutation	c.1715C>T
AA Mutation	p.Ser572Leu(p.S572L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128265863:128265863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>T
AA Mutation	p.Gly224Trp(p.G224W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128273920:128273920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142168936
CDS Mutation	c.137A>G
AA Mutation	p.Lys46Arg(p.K46R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128258144:128258144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761852586
CDS Mutation	c.2263C>T
AA Mutation	p.Arg755Cys(p.R755C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257458:128257458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2705G>A
AA Mutation	p.Arg902Lys(p.R902K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128265854:128265854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679G>A
AA Mutation	p.Val227Ile(p.V227I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128258083:128258083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185837255
CDS Mutation	c.2324C>T
AA Mutation	p.Ala775Val(p.A775V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257653:128257653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748293881
CDS Mutation	c.2585G>A
AA Mutation	p.Arg862Gln(p.R862Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257173:128257173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534286778
CDS Mutation	c.2903G>A
AA Mutation	p.Arg968His(p.R968H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128268133:128268133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340C>G
AA Mutation	p.Leu114Val(p.L114V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128261494:128261494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211G>T
AA Mutation	p.Ser404Ile(p.S404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128259078:128259078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021G>A
AA Mutation	p.Arg674His(p.R674H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128258530:128258530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2133G>T
AA Mutation	p.Glu711Asp(p.E711D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128260151:128260151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373870855
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128260096:128260096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128267512:128267512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199949002
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128265855:128265855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199686673
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128262581:128262581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421699
Start	128257111:128257111(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763679060
CDS Mutation	c.2965delT
AA Mutation	p.Tyr989ThrfsTer9(p.Y989Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421699
Start	128273902:128273902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.155delA
AA Mutation	p.Asn52MetfsTer105(p.N52Mfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000421699
Start	128257788:128257788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript