Colon Cancer: Gene >> HYOU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119055317:119055317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Thr96Met(p.T96M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119047805:119047805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2524A>T
AA Mutation	p.Ile842Phe(p.I842F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119055008:119055008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781789542
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Cys(p.R158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119052813:119052813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>T
AA Mutation	p.Gly271Trp(p.G271W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119048292:119048292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782654390
CDS Mutation	c.2332G>A
AA Mutation	p.Ala778Thr(p.A778T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119051911:119051911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782770261
CDS Mutation	c.1246G>A
AA Mutation	p.Ala416Thr(p.A416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119046789:119046789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609C>G
AA Mutation	p.Ala870Gly(p.A870G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119047999:119047999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782759376
CDS Mutation	c.2458G>A
AA Mutation	p.Glu820Lys(p.E820K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119049789:119049789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1714T>G
AA Mutation	p.Ser572Ala(p.S572A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119055764:119055764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171A>C
AA Mutation	p.Glu57Asp(p.E57D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617285
Start	119045602:119045602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573944250
CDS Mutation	c.2991C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617285
Start	119051053:119051053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201408509
CDS Mutation	c.1647C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617285
Start	119052655:119052655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376041557
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000617285
Start	119049058:119049058(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1952delA
AA Mutation	p.Lys651ArgfsTer46(p.K651Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HYOU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119052740:119052740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>T
AA Mutation	p.Arg295Ile(p.R295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119048859:119048859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2020C>A
AA Mutation	p.Pro674Thr(p.P674T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119048850:119048850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147081612
CDS Mutation	c.2029G>A
AA Mutation	p.Val677Ile(p.V677I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000617285
Start	119055284:119055284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320A>G
AA Mutation	p.Gln107Arg(p.Q107R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript