Colon Cancer: Gene >> OR13C8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569496:104569496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329C>T
AA Mutation	p.Thr110Met(p.T110M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104570059:104570059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892C>A
AA Mutation	p.Leu298Met(p.L298M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569484:104569484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317C>T
AA Mutation	p.Ala106Val(p.A106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569489:104569489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>T
AA Mutation	p.Gly108Trp(p.G108W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569634:104569634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467C>T
AA Mutation	p.Ser156Leu(p.S156L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569547:104569547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380G>T
AA Mutation	p.Cys127Phe(p.C127F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569826:104569826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659T>G
AA Mutation	p.Phe220Cys(p.F220C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335040
Start	104569581:104569581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335040
Start	104569185:104569185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335040
Start	104569337:104569337(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.174delC
AA Mutation	p.Met59CysfsTer22(p.M59Cfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000335040
Start	104570062:104570062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201484830
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Ter(p.R299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OR13C8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104570093:104570093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926A>G
AA Mutation	p.Asn309Ser(p.N309S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569325:104569325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158C>A
AA Mutation	p.Ser53Tyr(p.S53Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335040
Start	104569495:104569495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328A>G
AA Mutation	p.Thr110Ala(p.T110A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript