Mutation

Primary Site >> Liver Cancer

Gene >> GRIA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157332871:157332871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777296512
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157335856:157335856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452G>A
AA Mutation	p.Met484Ile(p.M484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157336440:157336440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537T>A
AA Mutation	p.Ser513Thr(p.S513T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157360001:157360001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749173821
CDS Mutation	c.2149T>C
AA Mutation	p.Ser717Pro(p.S717P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157335785:157335785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381T>A
AA Mutation	p.Tyr461Asn(p.Y461N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157321579:157321579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147349807
CDS Mutation	c.862G>T
AA Mutation	p.Ala288Ser(p.A288S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157341346:157341346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927G>A
AA Mutation	p.Ala643Thr(p.A643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264426
Start	157341347:157341347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1928C>A
AA Mutation	p.Ala643Asp(p.A643D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264426
Start	157341423:157341423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004T>C
Mutation Classification	Silent
Feature Type	Transcript