Colon Cancer: Gene >> EPX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58199129:58199129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151055641
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Cys(p.R404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58194020:58194020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522G>T
AA Mutation	p.Glu174Asp(p.E174D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58200279:58200279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369774099
CDS Mutation	c.1592G>A
AA Mutation	p.Arg531His(p.R531H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58196958:58196958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748790405
CDS Mutation	c.821G>A
AA Mutation	p.Arg274His(p.R274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58197114:58197114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35832094
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58203234:58203234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1862A>G
AA Mutation	p.Glu621Gly(p.E621G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58197227:58197227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573827983
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Cys(p.R364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58197231:58197231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577707337
CDS Mutation	c.1094C>T
AA Mutation	p.Ser365Leu(p.S365L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58193764:58193764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58193462:58193462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>T
AA Mutation	p.Arg88Trp(p.R88W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58199645:58199645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1388C>T
AA Mutation	p.Ala463Val(p.A463V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58193388:58193388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772997855
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58203309:58203309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1937A>T
AA Mutation	p.Asp646Val(p.D646V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58199056:58199056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753243977
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58194017:58194017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536094300
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58204354:58204354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58197172:58197172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58197121:58197121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58204288:58204288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58195086:58195086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770078560
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225371
Start	58197181:58197181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000225371
Start	58204289:58204290(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2014_2015insAATGAGCAC
AA Mutation	p.Ser672delinsTer(p.S672delins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225371
Start	58195149:58195150(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.786dupC
AA Mutation	p.Cys263LeufsTer10(p.C263Lfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EPX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225371
Start	58193506:58193506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306G>T
AA Mutation	p.Glu102Asp(p.E102D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript