Mutation

Primary Site >> Stomach Cancer

Gene >> SLC9A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27109711:27109711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Gly294Ser(p.G294S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27102506:27102506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1699C>T
AA Mutation	p.Arg567Cys(p.R567C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27101804:27101804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958C>T
AA Mutation	p.Thr653Met(p.T653M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27109731:27109731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Gly287Asp(p.G287D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27102525:27102525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680G>C
AA Mutation	p.Lys560Asn(p.K560N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263980
Start	27106085:27106085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>C
AA Mutation	p.Val429Leu(p.V429L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27109693:27109693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527454172
CDS Mutation	c.898G>A
AA Mutation	p.Val300Met(p.V300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27100395:27100395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2360G>T
AA Mutation	p.Ser787Ile(p.S787I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263980
Start	27109527:27109527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064C>T
AA Mutation	p.Ala355Val(p.A355V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27102438:27102438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200162869
CDS Mutation	c.1767G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27102079:27102079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1872C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27100430:27100430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770127268
CDS Mutation	c.2325C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263980
Start	27100415:27100415(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2340delC
AA Mutation	p.Ala781ArgfsTer115(p.A781Rfs*115)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263980
Start	27114177:27114177(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.462delC
AA Mutation	p.Phe155SerfsTer36(p.F155Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263980
Start	27153981:27153981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript