Colon Cancer: Gene >> SLC9A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27154289:27154289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46T>A
AA Mutation	p.Phe16Ile(p.F16I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27100414:27100414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200843173
CDS Mutation	c.2341G>A
AA Mutation	p.Ala781Thr(p.A781T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27114164:27114164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538855887
CDS Mutation	c.475G>A
AA Mutation	p.Asp159Asn(p.D159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27101209:27101209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201478450
CDS Mutation	c.2104G>A
AA Mutation	p.Gly702Ser(p.G702S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27100413:27100413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556347900
CDS Mutation	c.2342C>T
AA Mutation	p.Ala781Val(p.A781V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27114131:27114131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508A>G
AA Mutation	p.Ile170Val(p.I170V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27107690:27107690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578200492
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Ile(p.V414I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27103240:27103240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558G>A
AA Mutation	p.Glu520Lys(p.E520K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27154078:27154078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257G>A
AA Mutation	p.Arg86His(p.R86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27101785:27101785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143101417
CDS Mutation	c.1977C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27107661:27107661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140748912
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263980
Start	27107718:27107718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755603773
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
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

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000263980
Start	27100549:27100549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2206G>T
AA Mutation	p.Glu736Ter(p.E736*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263980
Start	27154128:27154129(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.206dupC
AA Mutation	p.Glu70ArgfsTer6(p.E70Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC9A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27103240:27103240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558G>A
AA Mutation	p.Glu520Lys(p.E520K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27109645:27109645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755250713
CDS Mutation	c.946G>A
AA Mutation	p.Ala316Thr(p.A316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263980
Start	27102540:27102540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665G>T
AA Mutation	p.Lys555Asn(p.K555N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript