Mutation

Primary Site >> Stomach Cancer

Gene >> ZAP70

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97734619:97734619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989T>C
AA Mutation	p.Leu330Pro(p.L330P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97725164:97725164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>A
AA Mutation	p.Glu159Lys(p.E159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737799:97737799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550812644
CDS Mutation	c.1525G>A
AA Mutation	p.Glu509Lys(p.E509K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97724049:97724049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>A
AA Mutation	p.Ala5Thr(p.A5T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97725156:97725156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467C>T
AA Mutation	p.Thr156Met(p.T156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97725231:97725231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542C>T
AA Mutation	p.Ala181Val(p.A181V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97739440:97739440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802C>T
AA Mutation	p.Ala601Val(p.A601V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97739410:97739410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772A>C
AA Mutation	p.Gln591Pro(p.Q591P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97734703:97734703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737790:97737790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516T>C
AA Mutation	p.Tyr506His(p.Y506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737830:97737830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201003454
CDS Mutation	c.1556G>A
AA Mutation	p.Arg519His(p.R519H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97732944:97732944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625T>C
AA Mutation	p.Tyr209His(p.Y209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97724146:97724146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110G>A
AA Mutation	p.Arg37His(p.R37H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97735424:97735424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773397000
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97724273:97724273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97735388:97735388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97735349:97735349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97737792:97737792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750794851
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97724328:97724328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264972
Start	97724306:97724306(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.273delC
AA Mutation	p.Asp92ThrfsTer77(p.D92Tfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264972
Start	97735249:97735249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript