Mutation

Primary Site >> Stomach Cancer

Gene >> ANGPTL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108479:127108479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253C>T
AA Mutation	p.His85Tyr(p.H85Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108277:127108277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770228069
CDS Mutation	c.455C>T
AA Mutation	p.Ala152Val(p.A152V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108140:127108140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780586834
CDS Mutation	c.592G>A
AA Mutation	p.Ala198Thr(p.A198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127088974:127088974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447A>G
AA Mutation	p.Met483Val(p.M483V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127108717:127108717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183125504
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127093769:127093769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127093775:127093775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127108279:127108279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377308519
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373425
Start	127108078:127108078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.654delC
AA Mutation	p.Ala219LeufsTer30(p.A219Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000373425
Start	127108137:127108137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>T
AA Mutation	p.Gln199Ter(p.Q199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript