Colon Cancer: Gene >> AR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67717495:67717495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852571
CDS Mutation	c.2191G>A
AA Mutation	p.Val731Met(p.V731M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545777:67545777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763968978
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67723701:67723701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852581
CDS Mutation	c.2623C>T
AA Mutation	p.His875Tyr(p.H875Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545567:67545567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421G>A
AA Mutation	p.Ala141Thr(p.A141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545936:67545936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Trp(p.R264W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67643312:67643312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1673A>G
AA Mutation	p.Lys558Arg(p.K558R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67711540:67711540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2024T>C
AA Mutation	p.Leu675Pro(p.L675P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545429:67545429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Gly95Ser(p.G95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545237:67545237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Cys(p.R31C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545482:67545482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336G>T
AA Mutation	p.Glu112Asp(p.E112D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545687:67545687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541C>A
AA Mutation	p.Leu181Ile(p.L181I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67546743:67546743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1597G>A
AA Mutation	p.Gly533Arg(p.G533R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722944:67722944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2567G>C
AA Mutation	p.Arg856Pro(p.R856P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67686030:67686030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852569
CDS Mutation	c.1789G>A
AA Mutation	p.Ala597Thr(p.A597T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545240:67545240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Glu32Lys(p.E32K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722946:67722946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2569T>G
AA Mutation	p.Phe857Val(p.F857V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67717619:67717619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2315A>G
AA Mutation	p.Asn772Ser(p.N772S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545425:67545425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279G>T
AA Mutation	p.Glu93Asp(p.E93D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67711621:67711621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105T>A
AA Mutation	p.Leu702His(p.L702H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545237:67545237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91C>A
AA Mutation	p.Arg31Ser(p.R31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67722945:67722945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2568C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546268:67546268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546661:67546661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67717611:67717611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2307G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67711529:67711529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67545191:67545191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144502467
CDS Mutation	c.45G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67643281:67643281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67545953:67545953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767555714
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67717536:67717536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2232G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546124:67546124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374690
Start	67711401:67711401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000374690
Start	67546515:67546553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749465311
CDS Mutation	c.1382_1420delGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG
AA Mutation	p.Gly461_Gly473del(p.G461_G473del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545734:67545734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588A>C
AA Mutation	p.Gln196His(p.Q196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545190:67545190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Pro15Leu(p.P15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722859:67722859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2482T>C
AA Mutation	p.Phe828Leu(p.F828L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67686088:67686088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754201976
CDS Mutation	c.1847G>A
AA Mutation	p.Arg616His(p.R616H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722858:67722858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200801099
CDS Mutation	c.2481C>A
AA Mutation	p.Phe827Leu(p.F827L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript