Colon Cancer: Gene >> SLC9A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49855495:49855495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199598441
CDS Mutation	c.627C>A
AA Mutation	p.Phe209Leu(p.F209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49862982:49862982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767C>T
AA Mutation	p.Thr256Ile(p.T256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49874783:49874783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037T>G
AA Mutation	p.Leu346Arg(p.L346R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49815073:49815073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144315631
CDS Mutation	c.92C>T
AA Mutation	p.Thr31Met(p.T31M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49887904:49887904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150389961
CDS Mutation	c.1714G>A
AA Mutation	p.Gly572Ser(p.G572S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49886841:49886841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49887849:49887849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49815071:49815071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573582561
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49815056:49815056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361573
Start	49874765:49874765(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1022delC
AA Mutation	p.Pro341GlnfsTer46(p.P341Qfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000361573
Start	49823134:49823136(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.284_286delCTT
AA Mutation	p.Ser95del(p.S95del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC9A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49886842:49886842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746946184
CDS Mutation	c.1582G>A
AA Mutation	p.Val528Met(p.V528M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361573
Start	49855550:49855550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>A
AA Mutation	p.Leu228Ile(p.L228I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49839590:49839590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773532739
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361573
Start	49849608:49849608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript