Colon Cancer: Gene >> TAAR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589199:132589199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488C>A
AA Mutation	p.Ala163Glu(p.A163E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589524:132589524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764714090
CDS Mutation	c.163G>A
AA Mutation	p.Val55Met(p.V55M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589646:132589646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530575584
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589097:132589097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590A>G
AA Mutation	p.Asn197Ser(p.N197S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132588750:132588750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374357879
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Trp(p.R313W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589365:132589365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557518982
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Cys(p.R108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589094:132589094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371543236
CDS Mutation	c.593A>C
AA Mutation	p.Lys198Thr(p.K198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589680:132589680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589487:132589487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200C>G
AA Mutation	p.Thr67Arg(p.T67R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258034
Start	132588901:132588901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258034
Start	132588961:132588961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258034
Start	132589360:132589360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258034
Start	132589645:132589645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761349006
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAAR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132589475:132589475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212T>C
AA Mutation	p.Phe71Ser(p.F71S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258034
Start	132588944:132588944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>T
AA Mutation	p.Arg248Ile(p.R248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript