Colon Cancer: Gene >> TAAR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538594:132538594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305A>T
AA Mutation	p.Asp102Val(p.D102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538809:132538809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117057501
CDS Mutation	c.520G>A
AA Mutation	p.Glu174Lys(p.E174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539161:132539161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872A>G
AA Mutation	p.Tyr291Cys(p.Y291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538372:132538372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83C>T
AA Mutation	p.Ser28Leu(p.S28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539151:132539151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862A>G
AA Mutation	p.Thr288Ala(p.T288A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539187:132539187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898G>T
AA Mutation	p.Val300Phe(p.V300F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538467:132538467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178T>G
AA Mutation	p.Phe60Val(p.F60V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539044:132539044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755G>C
AA Mutation	p.Arg252Thr(p.R252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538656:132538656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367T>G
AA Mutation	p.Leu123Val(p.L123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538504:132538504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199962808
CDS Mutation	c.215C>T
AA Mutation	p.Ala72Val(p.A72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434551
Start	132538652:132538652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434551
Start	132538718:132538718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAAR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539171:132539171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882G>T
AA Mutation	p.Glu294Asp(p.E294D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132539314:132539314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025C>A
AA Mutation	p.Ser342Tyr(p.S342Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434551
Start	132538720:132538720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>G
AA Mutation	p.Phe144Cys(p.F144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript