Colon Cancer: Gene >> NCOA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46079417:46079417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755272201
CDS Mutation	c.8C>T
AA Mutation	p.Thr3Met(p.T3M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46063506:46063506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35315891
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335His(p.R335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46062862:46062862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46062673:46062673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367C>T
AA Mutation	p.Ala456Val(p.A456V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46067077:46067077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607A>G
AA Mutation	p.Ile203Val(p.I203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46070496:46070496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79G>A
AA Mutation	p.Asp27Asn(p.D27N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46065139:46065139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719A>G
AA Mutation	p.Gln240Arg(p.Q240R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46065183:46065183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>A
AA Mutation	p.Met225Ile(p.M225I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46067161:46067161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764153135
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Trp(p.R175W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46063392:46063392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118G>T
AA Mutation	p.Arg373Leu(p.R373L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290231
Start	46070245:46070245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747394313
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290231
Start	46062494:46062494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290231
Start	46070518:46070518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290231
Start	46062765:46062765(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1275delC
AA Mutation	p.Thr426ProfsTer19(p.T426Pfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000290231
Start	46070277:46070277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Ter(p.R100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000290231
Start	46079391:46079391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Ter(p.R12*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000290231
Start	46070511:46070511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64C>T
AA Mutation	p.Arg22Ter(p.R22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000290231
Start	46070481:46070481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Ter(p.R32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NCOA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290231
Start	46070337:46070337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776509008
CDS Mutation	c.238G>A
AA Mutation	p.Asp80Asn(p.D80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290231
Start	46063550:46063550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290231
Start	46063500:46063500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1010delG
AA Mutation	p.Gly337AlafsTer38(p.G337Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript