Colon Cancer: Gene >> YY1AP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155688934:155688934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760613801
CDS Mutation	c.43G>A
AA Mutation	p.Gly15Arg(p.G15R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155660394:155660394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1654G>A
AA Mutation	p.Ala552Thr(p.A552T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155660406:155660406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642T>G
AA Mutation	p.Leu548Val(p.L548V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155659764:155659764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284C>T
AA Mutation	p.Pro762Ser(p.P762S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155668688:155668688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151172022
CDS Mutation	c.956G>A
AA Mutation	p.Arg319His(p.R319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155659671:155659671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2377A>G
AA Mutation	p.Ser793Gly(p.S793G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155660718:155660718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201580131
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155661420:155661420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021T>C
AA Mutation	p.Tyr341His(p.Y341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155676607:155676607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463C>A
AA Mutation	p.His155Asn(p.H155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155659679:155659679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2369A>C
AA Mutation	p.Glu790Ala(p.E790A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295566
Start	155672662:155672662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> YY1AP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155660138:155660138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910C>A
AA Mutation	p.Ala637Asp(p.A637D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155676611:155676611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459A>T
AA Mutation	p.Glu153Asp(p.E153D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295566
Start	155679455:155679455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550862847
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Cys(p.R93C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295566
Start	155660881:155660881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295566
Start	155676701:155676701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000295566
Start	155660346:155660346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757070737
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Ter(p.R568*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript