Colon Cancer: Gene >> FARP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241441478:241441478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369372470
CDS Mutation	c.1333C>T
AA Mutation	p.Arg445Cys(p.R445C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241468204:241468204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371446032
CDS Mutation	c.1958G>A
AA Mutation	p.Arg653His(p.R653H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241468251:241468251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749525881
CDS Mutation	c.2005G>A
AA Mutation	p.Val669Ile(p.V669I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241463440:241463440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763386574
CDS Mutation	c.1783C>T
AA Mutation	p.Arg595Cys(p.R595C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241407557:241407557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Cys(p.R118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241441460:241441460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315A>G
AA Mutation	p.Ser439Gly(p.S439G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241491079:241491079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2523G>T
AA Mutation	p.Glu841Asp(p.E841D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241431754:241431754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778378417
CDS Mutation	c.847A>G
AA Mutation	p.Lys283Glu(p.K283E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241493335:241493335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145708249
CDS Mutation	c.2938G>A
AA Mutation	p.Val980Met(p.V980M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264042
Start	241475894:241475894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2169A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264042
Start	241456757:241456757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375721515
CDS Mutation	c.1422G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264042
Start	241403836:241403836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766643383
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264042
Start	241441345:241441345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1200A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264042
Start	241434186:241434186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896T>A
AA Mutation	p.Leu299Ter(p.L299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264042
Start	241491060:241491060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2505-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FARP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264042
Start	241411101:241411101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555590124
CDS Mutation	c.479C>T
AA Mutation	p.Ala160Val(p.A160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264042
Start	241468175:241468175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929C>T
Mutation Classification	Silent
Feature Type	Transcript