Mutation

Primary Site >> Stomach Cancer

Gene >> TAP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32838209:32838209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25T>C
AA Mutation	p.Trp9Arg(p.W9R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32829453:32829453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879G>A
AA Mutation	p.Val627Ile(p.V627I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32830302:32830302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600A>G
AA Mutation	p.Ile534Val(p.I534V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32830370:32830370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532C>T
AA Mutation	p.Thr511Ile(p.T511I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32835679:32835679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145890763
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Cys(p.R235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32832772:32832772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756271450
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32835723:32835723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550712305
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32832742:32832742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376467259
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343His(p.R343H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32835287:32835287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812T>G
AA Mutation	p.Leu271Arg(p.L271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32835237:32835237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774034040
CDS Mutation	c.862A>G
AA Mutation	p.Ile288Val(p.I288V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374897
Start	32837816:32837816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418A>G
AA Mutation	p.Arg140Gly(p.R140G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374897
Start	32838126:32838126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374897
Start	32838011:32838011(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.223delC
AA Mutation	p.Leu75Ter(p.L75*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript