Colon Cancer: Gene >> OXR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106702948:106702948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721A>C
AA Mutation	p.Met241Leu(p.M241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106739500:106739500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083G>A
AA Mutation	p.Val695Met(p.V695M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106740413:106740413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2237G>C
AA Mutation	p.Gly746Ala(p.G746A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106519074:106519074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158A>G
AA Mutation	p.Asn53Ser(p.N53S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106740433:106740433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2257T>G
AA Mutation	p.Tyr753Asp(p.Y753D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106713844:106713844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1818C>A
AA Mutation	p.Phe606Leu(p.F606L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106684348:106684348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>C
AA Mutation	p.Asp173His(p.D173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106683256:106683256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140427774
CDS Mutation	c.364G>A
AA Mutation	p.Glu122Lys(p.E122K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106706594:106706594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376088140
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359Gln(p.R359Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106706491:106706491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973A>C
AA Mutation	p.Ser325Arg(p.S325R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106706886:106706886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>T
AA Mutation	p.Glu456Asp(p.E456D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106692845:106692845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646A>G
AA Mutation	p.Lys216Glu(p.K216E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442977
Start	106740421:106740421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442977
Start	106683285:106683285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442977
Start	106710704:106710704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442977
Start	106750815:106750815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2499T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442977
Start	106707098:106707098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1584delA
AA Mutation	p.Glu529LysfsTer13(p.E529Kfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000442977
Start	106706917:106706917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399G>T
AA Mutation	p.Glu467Ter(p.E467*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OXR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106710655:106710655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761400977
CDS Mutation	c.1661G>A
AA Mutation	p.Arg554Gln(p.R554Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442977
Start	106742297:106742297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395A>G
AA Mutation	p.Thr799Ala(p.T799A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000442977
Start	106706383:106706383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>T
AA Mutation	p.Asp289Tyr(p.D289Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000442977
Start	106703053:106703053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>T
AA Mutation	p.Glu276Ter(p.E276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript