Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OR10H3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741552:15741552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769130878
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741589:15741589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197C>T
AA Mutation	p.Ala66Val(p.A66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741964:15741964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770494327
CDS Mutation	c.572G>A
AA Mutation	p.Gly191Glu(p.G191E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741633:15741633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Cys(p.R81C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305892
Start	15741470:15741470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305892
Start	15741965:15741965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305892
Start	15742145:15742145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OR10H3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741973:15741973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Thr194Ile(p.T194I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741954:15741954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562T>A
AA Mutation	p.Leu188Met(p.L188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15741804:15741804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412A>C
AA Mutation	p.Ser138Arg(p.S138R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305892
Start	15742144:15742144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752T>C
AA Mutation	p.Val251Ala(p.V251A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305892
Start	15741827:15741827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435T>C
Mutation Classification	Silent
Feature Type	Transcript