Colon Cancer: Gene >> NDST3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118224567:118224567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616A>G
AA Mutation	p.Asn539Ser(p.N539S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118114952:118114952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216T>A
AA Mutation	p.Phe406Ile(p.F406I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118138061:118138061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232G>A
AA Mutation	p.Gly411Asp(p.G411D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054873:118054873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963G>T
AA Mutation	p.Met321Ile(p.M321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054045:118054045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>T
AA Mutation	p.Glu45Asp(p.E45D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118138196:118138196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367A>C
AA Mutation	p.Lys456Thr(p.K456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118233077:118233077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1885A>C
AA Mutation	p.Lys629Gln(p.K629Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054242:118054242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118053936:118053936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26G>T
AA Mutation	p.Arg9Ile(p.R9I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118226943:118226943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Cys(p.R594C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118138103:118138103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274C>T
AA Mutation	p.Ser425Leu(p.S425L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118143566:118143566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421G>T
AA Mutation	p.Arg474Ile(p.R474I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118053947:118053947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140478292
CDS Mutation	c.37A>G
AA Mutation	p.Arg13Gly(p.R13G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296499
Start	118240693:118240693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2288A>G
AA Mutation	p.Gln763Arg(p.Q763R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296499
Start	118138107:118138107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767900257
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296499
Start	118054192:118054192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762740085
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296499
Start	118240682:118240682(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2282delC
AA Mutation	p.Pro761HisfsTer5(p.P761Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296499
Start	118143616:118143616(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1475delG
AA Mutation	p.Gly492ValfsTer27(p.G492Vfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000296499
Start	118143655:118143655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1510G>T
AA Mutation	p.Glu504Ter(p.E504*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000296499
Start	118143607:118143607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462G>T
AA Mutation	p.Glu488Ter(p.E488*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDST3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054791:118054791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>T
AA Mutation	p.Gly294Val(p.G294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054866:118054866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778628771
CDS Mutation	c.956C>T
AA Mutation	p.Thr319Ile(p.T319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054432:118054432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>A
AA Mutation	p.Ser174Arg(p.S174R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118226944:118226944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781G>A
AA Mutation	p.Arg594His(p.R594H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296499
Start	118054721:118054721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811C>T
AA Mutation	p.Leu271Phe(p.L271F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript