Colon Cancer: Gene >> SLC24A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19585047:19585047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500C>T
AA Mutation	p.Ser167Leu(p.S167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19681895:19681895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767986780
CDS Mutation	c.805A>G
AA Mutation	p.Thr269Ala(p.T269A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19654097:19654097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648T>G
AA Mutation	p.Asp216Glu(p.D216E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19580019:19580019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761018781
CDS Mutation	c.368C>T
AA Mutation	p.Ala123Val(p.A123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19698672:19698672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143870319
CDS Mutation	c.1711G>A
AA Mutation	p.Gly571Arg(p.G571R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19684188:19684188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150240114
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19515542:19515542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144636987
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19693370:19693370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436C>T
AA Mutation	p.Thr479Met(p.T479M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19696833:19696833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148354103
CDS Mutation	c.1528G>A
AA Mutation	p.Val510Ile(p.V510I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19684320:19684320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046G>T
AA Mutation	p.Arg349Leu(p.R349L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19698583:19698583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622C>A
AA Mutation	p.Ala541Asp(p.A541D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19673613:19673613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.726A>C
AA Mutation	p.Leu242Phe(p.L242F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19721054:19721054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849C>A
AA Mutation	p.Leu617Met(p.L617M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19580044:19580044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393C>A
AA Mutation	p.Phe131Leu(p.F131L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19515522:19515522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748005995
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19585475:19585475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19684213:19684213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149435919
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19580068:19580068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19585445:19585445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328041
Start	19684289:19684289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1020delC
AA Mutation	p.Lys341ArgfsTer11(p.K341Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328041
Start	19281079:19281080(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.263_264insATCATTCACAG
AA Mutation	p.Glu89SerfsTer85(p.E89Sfs*85)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC24A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19665886:19665886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>T
AA Mutation	p.Ser237Phe(p.S237F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328041
Start	19684181:19684181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907T>G
AA Mutation	p.Phe303Val(p.F303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19685351:19685351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760024054
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19685135:19685135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370751183
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19693287:19693287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328041
Start	19685318:19685318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript