Mutation

Primary Site >> Stomach Cancer

Gene >> PSAT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78328121:78328121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>A
AA Mutation	p.Asp314Asn(p.D314N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78329062:78329062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089A>T
AA Mutation	p.Lys363Asn(p.K363N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78300615:78300615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74T>C
AA Mutation	p.Ile25Thr(p.I25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78328097:78328097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113824905
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78304800:78304800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257T>A
AA Mutation	p.Val86Asp(p.V86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78308508:78308508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114496656
CDS Mutation	c.665G>A
AA Mutation	p.Arg222Gln(p.R222Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376588
Start	78304850:78304850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377282696
CDS Mutation	c.307G>A
AA Mutation	p.Val103Met(p.V103M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376588
Start	78317682:78317682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376588
Start	78328054:78328054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376588
Start	78329056:78329057(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1089dupA
AA Mutation	p.Phe364IlefsTer12(p.F364Ifs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376588
Start	78304734:78304734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript