Colon Cancer: Gene >> OR9Q2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58190822:58190822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332A>G
AA Mutation	p.Asp111Gly(p.D111G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58191368:58191368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Lys(p.R293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58190969:58190969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479C>T
AA Mutation	p.Thr160Met(p.T160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58190624:58190624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134T>C
AA Mutation	p.Met45Thr(p.M45T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58191316:58191316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>T
AA Mutation	p.Val276Leu(p.V276L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58191263:58191263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773T>C
AA Mutation	p.Met258Thr(p.M258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58191174:58191174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684C>G
AA Mutation	p.Ile228Met(p.I228M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58191295:58191295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>A
AA Mutation	p.Glu269Lys(p.E269K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58190755:58190755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142991971
CDS Mutation	c.265G>A
AA Mutation	p.Gly89Ser(p.G89S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311591
Start	58190966:58190966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762401748
CDS Mutation	c.476G>A
AA Mutation	p.Arg159Gln(p.R159Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000311591
Start	58191271:58191271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765098308
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Ter(p.R261*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OR9Q2

No Mutation Annotation!