Mutation

Primary Site >> Stomach Cancer

Gene >> IFIT2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306426:89306426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773713688
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89307146:89307146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190A>C
AA Mutation	p.Glu397Ala(p.E397A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306501:89306501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>T
AA Mutation	p.Ser182Ile(p.S182I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306707:89306707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537050168
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306657:89306657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701A>G
AA Mutation	p.Lys234Arg(p.K234R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306293:89306293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769134303
CDS Mutation	c.337G>A
AA Mutation	p.Val113Ile(p.V113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89306989:89306989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>A
AA Mutation	p.Ala345Thr(p.A345T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371826
Start	89307074:89307074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118T>C
AA Mutation	p.Leu373Pro(p.L373P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371826
Start	89306946:89306946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990T>C
Mutation Classification	Silent
Feature Type	Transcript