Mutation

Primary Site >> Stomach Cancer

Gene >> BIRC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350200:102350200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>G
AA Mutation	p.Leu116Val(p.L116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350281:102350281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427T>A
AA Mutation	p.Leu143Met(p.L143M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350722:102350722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868C>A
AA Mutation	p.Leu290Ile(p.L290I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102377702:102377702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573A>G
AA Mutation	p.Lys525Glu(p.K525E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102349895:102349895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531296011
CDS Mutation	c.41C>T
AA Mutation	p.Ser14Leu(p.S14L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000227758
Start	102350429:102350429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182528901
CDS Mutation	c.575A>G
AA Mutation	p.His192Arg(p.H192R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227758
Start	102378018:102378018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227758
Start	102349879:102349880(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.29dupT
AA Mutation	p.Gly12ArgfsTer8(p.G12Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript