Colon Cancer: Gene >> DRD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782280:9782280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251C>T
AA Mutation	p.Ala84Val(p.A84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783290:9783290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261G>A
AA Mutation	p.Gly421Ser(p.G421S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783238:9783238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1209C>A
AA Mutation	p.His403Gln(p.H403Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782644:9782644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615G>T
AA Mutation	p.Glu205Asp(p.E205D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782705:9782705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.676G>A
AA Mutation	p.Ala226Thr(p.A226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782954:9782954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925T>C
AA Mutation	p.Trp309Arg(p.W309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782366:9782366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337T>A
AA Mutation	p.Cys113Ser(p.C113S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783296:9783296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267C>T
AA Mutation	p.Arg423Trp(p.R423W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783071:9783071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755998605
CDS Mutation	c.1042G>A
AA Mutation	p.Gly348Ser(p.G348S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783282:9783282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253T>C
AA Mutation	p.Val418Ala(p.V418A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782478:9782478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449G>A
AA Mutation	p.Arg150His(p.R150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782663:9782663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>A
AA Mutation	p.Val212Met(p.V212M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782834:9782834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773943990
CDS Mutation	c.805G>A
AA Mutation	p.Ala269Thr(p.A269T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782388:9782388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359A>G
AA Mutation	p.Asp120Gly(p.D120G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782341:9782341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9783052:9783052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754203793
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782362:9782362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9783448:9783448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782719:9782719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782425:9782425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782059:9782059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755213948
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DRD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782387:9782387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Asp120Asn(p.D120N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782865:9782865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757838962
CDS Mutation	c.836C>T
AA Mutation	p.Ala279Val(p.A279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782522:9782522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493T>C
AA Mutation	p.Trp165Arg(p.W165R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782870:9782870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Asp281Asn(p.D281N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783278:9783278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>A
AA Mutation	p.Ala417Thr(p.A417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9782697:9782697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668G>A
AA Mutation	p.Arg223Gln(p.R223Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304374
Start	9783336:9783336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9782332:9782332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304374
Start	9783448:9783448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript