Mutation

Primary Site >> Stomach Cancer

Gene >> SIRT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000212015
Start	67888930:67888930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Gln(p.R199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000212015
Start	67909424:67909424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339C>T
AA Mutation	p.Pro447Ser(p.P447S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000212015
Start	67916354:67916354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005A>G
AA Mutation	p.Ser669Gly(p.S669G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000212015
Start	67909404:67909404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319G>A
AA Mutation	p.Gly440Glu(p.G440E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000212015
Start	67912868:67912868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000212015
Start	67887490:67887490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000212015
Start	67887430:67887430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773494159
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000212015
Start	67916279:67916279(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1934delT
AA Mutation	p.Leu645CysfsTer41(p.L645Cfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000212015
Start	67912662:67912662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Ter(p.R516*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript