Colon Cancer: Gene >> FFAR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359038:35359038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200224629
CDS Mutation	c.148G>A
AA Mutation	p.Val50Met(p.V50M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359564:35359564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674G>A
AA Mutation	p.Gly225Glu(p.G225E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359215:35359215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325G>A
AA Mutation	p.Val109Met(p.V109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359722:35359722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832T>G
AA Mutation	p.Phe278Val(p.F278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359200:35359200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310C>A
AA Mutation	p.Leu104Ile(p.L104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359660:35359660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770G>T
AA Mutation	p.Trp257Leu(p.W257L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359444:35359444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138338117
CDS Mutation	c.554G>A
AA Mutation	p.Arg185Gln(p.R185Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359335:35359335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530606489
CDS Mutation	c.445G>A
AA Mutation	p.Val149Met(p.V149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359576:35359576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686C>A
AA Mutation	p.Ala229Asp(p.A229D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327809
Start	35359007:35359007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148149328
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327809
Start	35359478:35359478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754166709
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327809
Start	35359856:35359856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327809
Start	35359064:35359064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146184076
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327809
Start	35359271:35359271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327809
Start	35358977:35358977(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.91delC
AA Mutation	p.Leu31SerfsTer27(p.L31Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000327809
Start	35359350:35359350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>T
AA Mutation	p.Glu154Ter(p.E154*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FFAR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359664:35359664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>T
AA Mutation	p.Arg258Ser(p.R258S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35358944:35358944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>A
AA Mutation	p.Phe18Leu(p.F18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327809
Start	35359335:35359335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530606489
CDS Mutation	c.445G>A
AA Mutation	p.Val149Met(p.V149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript