Colon Cancer: Gene >> DHODH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72023545:72023545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>A
AA Mutation	p.Ala349Thr(p.A349T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72023207:72023207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762591793
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72014642:72014642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72012218:72012218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190C>A
AA Mutation	p.Leu64Met(p.L64M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72014570:72014570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>A
AA Mutation	p.Gly111Asp(p.G111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72021199:72021199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>C
AA Mutation	p.Val198Ala(p.V198A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72012078:72012078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50T>C
AA Mutation	p.Leu17Pro(p.L17P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72023174:72023174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200677583
CDS Mutation	c.829G>A
AA Mutation	p.Asp277Asn(p.D277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72021201:72021201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267606769
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72022386:72022386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267606768
CDS Mutation	c.730C>T
AA Mutation	p.Arg244Trp(p.R244W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219240
Start	72021221:72021221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375309794
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219240
Start	72014601:72014601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219240
Start	72023209:72023209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219240
Start	72012079:72012079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.56delG
AA Mutation	p.Gly19GlufsTer10(p.G19Efs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000219240
Start	72023164:72023164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DHODH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219240
Start	72023536:72023536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201947120
CDS Mutation	c.1036C>T
AA Mutation	p.Arg346Trp(p.R346W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript