Mutation

Primary Site >> Stomach Cancer

Gene >> GPR39

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417139:132417139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>G
AA Mutation	p.Leu33Val(p.L33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417721:132417721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417155:132417155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764371015
CDS Mutation	c.113T>C
AA Mutation	p.Leu38Pro(p.L38P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132645245:132645245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>G
AA Mutation	p.Tyr334Cys(p.Y334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417356:132417356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>A
AA Mutation	p.Thr105Asn(p.T105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417190:132417190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>A
AA Mutation	p.Ala50Thr(p.A50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417407:132417407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375756316
CDS Mutation	c.365C>T
AA Mutation	p.Thr122Met(p.T122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329321
Start	132417134:132417134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92T>C
AA Mutation	p.Ile31Thr(p.I31T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417420:132417420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329321
Start	132417648:132417648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329321
Start	132645238:132645238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.998delT
AA Mutation	p.Phe333SerfsTer78(p.F333Sfs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript