Colon Cancer: Gene >> NDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686373:23686373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>C
AA Mutation	p.Val282Ala(p.V282A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686662:23686662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>T
AA Mutation	p.Pro186Ser(p.P186S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686610:23686610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686776:23686776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686305:23686305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Trp(p.R305W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686533:23686533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>T
AA Mutation	p.Gly229Trp(p.G229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23687204:23687204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14G>T
AA Mutation	p.Ser5Ile(p.S5I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686667:23686667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765248776
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686794:23686794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686524:23686524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Trp(p.R232W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686414:23686414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686909:23686909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752319081
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23687110:23687110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686609:23686609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686501:23686501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000331837
Start	23686553:23686553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665G>A
AA Mutation	p.Trp222Ter(p.W222*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000331837
Start	23686341:23686341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Ter(p.R293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23687157:23687157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61G>A
AA Mutation	p.Glu21Lys(p.E21K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686870:23686870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
AA Mutation	p.Lys116Asn(p.K116N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23686449:23686449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>A
AA Mutation	p.Glu257Lys(p.E257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331837
Start	23687132:23687132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200385262
CDS Mutation	c.86C>T
AA Mutation	p.Ser29Leu(p.S29L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686444:23686444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331837
Start	23686534:23686534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149718513
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript