Colon Cancer: Gene >> DNER

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229367097:229367097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1878C>A
AA Mutation	p.His626Gln(p.H626Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229447360:229447360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761933088
CDS Mutation	c.1442C>T
AA Mutation	p.Thr481Met(p.T481M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229591650:229591650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143332732
CDS Mutation	c.515C>T
AA Mutation	p.Thr172Met(p.T172M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229588424:229588424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146172282
CDS Mutation	c.650C>T
AA Mutation	p.Ser217Phe(p.S217F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229358620:229358620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134G>T
AA Mutation	p.Asp712Tyr(p.D712Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229366963:229366963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012G>A
AA Mutation	p.Gly671Asp(p.G671D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229366925:229366925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549129843
CDS Mutation	c.2050C>T
AA Mutation	p.Arg684Cys(p.R684C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229366979:229366979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749718515
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Cys(p.R666C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229447499:229447499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769511648
CDS Mutation	c.1303G>A
AA Mutation	p.Ala435Thr(p.A435T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229585882:229585882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777616075
CDS Mutation	c.823G>A
AA Mutation	p.Ala275Thr(p.A275T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229477154:229477154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247G>A
AA Mutation	p.Cys416Tyr(p.C416Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229447528:229447528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274C>A
AA Mutation	p.Ser425Tyr(p.S425Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229588413:229588413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>A
AA Mutation	p.Pro221Thr(p.P221T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229447489:229447489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150154624
CDS Mutation	c.1313C>T
AA Mutation	p.Pro438Leu(p.P438L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229512868:229512868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1062G>C
AA Mutation	p.Gln354His(p.Q354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229477239:229477239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749871660
CDS Mutation	c.1162C>T
AA Mutation	p.Leu388Phe(p.L388F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229591610:229591610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555A>T
AA Mutation	p.Lys185Asn(p.K185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229547049:229547049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229546959:229546959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375308811
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229585883:229585883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779156111
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229512844:229512844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556414531
CDS Mutation	c.1086G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229477153:229477153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DNER

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229591729:229591729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143360352
CDS Mutation	c.436G>A
AA Mutation	p.Glu146Lys(p.E146K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229547074:229547074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866T>C
AA Mutation	p.Val289Ala(p.V289A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229512918:229512918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012T>A
AA Mutation	p.Cys338Ser(p.C338S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341772
Start	229366988:229366988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987C>T
AA Mutation	p.Arg663Cys(p.R663C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229447533:229447533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267599244
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341772
Start	229591625:229591625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146704189
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000341772
Start	229591768:229591768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>T
AA Mutation	p.Glu133Ter(p.E133*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript