Mutation

Primary Site >> Stomach Cancer

Gene >> EXO1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241881959:241881959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2153A>T
AA Mutation	p.Gln718Leu(p.Q718L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241872140:241872140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376T>C
AA Mutation	p.Phe459Ser(p.F459S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241872155:241872155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391T>C
AA Mutation	p.Val464Ala(p.V464A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241878855:241878855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Glu541Lys(p.E541K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241857372:241857372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>A
AA Mutation	p.Leu145Ile(p.L145I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241857391:241857391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241872200:241872200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750940919
CDS Mutation	c.1436C>T
AA Mutation	p.Thr479Met(p.T479M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241882009:241882009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2203A>T
AA Mutation	p.Arg735Trp(p.R735W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000348581
Start	241879164:241879164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200876518
CDS Mutation	c.1930C>T
AA Mutation	p.Pro644Ser(p.P644S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241872105:241872105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241872093:241872093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241853424:241853424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348581
Start	241852355:241852355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141548668
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348581
Start	241881990:241881990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752940417
CDS Mutation	c.2190delA
AA Mutation	p.Asp731ThrfsTer4(p.D731Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348581
Start	241878966:241878967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1733_1734delCA
AA Mutation	p.Thr578SerfsTer5(p.T578Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348581
Start	241885457:241885457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2358delG
AA Mutation	p.Leu787TyrfsTer37(p.L787Yfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000348581
Start	241858551:241858551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Gln197Ter(p.Q197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000348581
Start	241857484:241857484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript