Colon Cancer: Gene >> SLC9A3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264938
Start	488318:488318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149018338
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	475578:475578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2234C>T
AA Mutation	p.Ala745Val(p.A745V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	524220:524220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	476617:476617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534671417
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Trp(p.R606W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	482567:482567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337T>G
AA Mutation	p.Phe446Cys(p.F446C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	491996:491996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287G>A
AA Mutation	p.Gly96Asp(p.G96D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	477384:477384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1708G>A
AA Mutation	p.Val570Met(p.V570M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	477437:477437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758544114
CDS Mutation	c.1655G>A
AA Mutation	p.Arg552His(p.R552H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	488341:488341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777074221
CDS Mutation	c.650C>T
AA Mutation	p.Ser217Leu(p.S217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	524148:524148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175G>A
AA Mutation	p.Ala59Thr(p.A59T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	479940:479940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543C>A
AA Mutation	p.Leu515Ile(p.L515I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	482103:482103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368029489
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Trp(p.R471W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	492044:492044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239G>A
AA Mutation	p.Ser80Asn(p.S80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	485200:485200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768564666
CDS Mutation	c.707C>T
AA Mutation	p.Ala236Val(p.A236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	481572:481572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1510A>G
AA Mutation	p.Arg504Gly(p.R504G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000264938
Start	474899:474899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2485C>A
AA Mutation	p.Pro829Thr(p.P829T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	476346:476346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139579128
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	482086:482086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202060130
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	483413:483413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528584160
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	491809:491809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548489759
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	482659:482659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143761751
CDS Mutation	c.1245C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	476334:476334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558562725
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	476045:476045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746091250
CDS Mutation	c.2115G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	524167:524167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	483332:483332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369816699
CDS Mutation	c.1083G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC9A3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264938
Start	492016:492016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376704791
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript