Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OR7C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799548:14799548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589G>A
AA Mutation	p.Val197Met(p.V197M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799379:14799379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758G>A
AA Mutation	p.Gly253Asp(p.G253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799773:14799773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766648649
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Cys(p.R122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799698:14799698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439G>T
AA Mutation	p.Gly147Trp(p.G147W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799910:14799910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Thr76Met(p.T76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248073
Start	14799849:14799849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248073
Start	14799521:14799521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767188018
CDS Mutation	c.616C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000248073
Start	14799602:14799602(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.535delT
AA Mutation	p.Cys179ValfsTer7(p.C179Vfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OR7C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799772:14799772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756541110
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799487:14799487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650C>A
AA Mutation	p.Ser217Tyr(p.S217Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799489:14799489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648C>A
AA Mutation	p.Phe216Leu(p.F216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799524:14799524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772802995
CDS Mutation	c.613G>A
AA Mutation	p.Val205Ile(p.V205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799886:14799886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251A>G
AA Mutation	p.Asn84Ser(p.N84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000248073
Start	14799864:14799864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>A
AA Mutation	p.Phe91Leu(p.F91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript