Colon Cancer: Gene >> OR10H5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794440:15794440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368159341
CDS Mutation	c.392G>A
AA Mutation	p.Arg131His(p.R131H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794188:15794188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794161:15794161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372682146
CDS Mutation	c.113C>T
AA Mutation	p.Thr38Met(p.T38M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794887:15794887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750292924
CDS Mutation	c.839C>T
AA Mutation	p.Thr280Met(p.T280M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794201:15794201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>A
AA Mutation	p.Ser51Arg(p.S51R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794391:15794391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343C>A
AA Mutation	p.Leu115Ile(p.L115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794589:15794589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776618344
CDS Mutation	c.541G>A
AA Mutation	p.Val181Met(p.V181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794513:15794513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>A
AA Mutation	p.Met155Ile(p.M155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794448:15794448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746677353
CDS Mutation	c.400G>A
AA Mutation	p.Val134Met(p.V134M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308940
Start	15794450:15794450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308940
Start	15794252:15794252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308940
Start	15794978:15794978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308940
Start	15794408:15794408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772836837
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308940
Start	15794432:15794432(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.388delC
AA Mutation	p.Leu130CysfsTer7(p.L130Cfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OR10H5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794949:15794949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773950886
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794251:15794251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203T>C
AA Mutation	p.Ile68Thr(p.I68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308940
Start	15794950:15794950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902C>T
AA Mutation	p.Ala301Val(p.A301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript