Colon Cancer: Gene >> FBXL20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39285493:39285493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479C>A
AA Mutation	p.Ser160Tyr(p.S160Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39299038:39299038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281G>A
AA Mutation	p.Arg94Gln(p.R94Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39303631:39303631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>T
AA Mutation	p.Ser38Phe(p.S38F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39261530:39261530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1241C>T
AA Mutation	p.Ala414Val(p.A414V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39401373:39401373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>T
AA Mutation	p.Lys10Asn(p.K10N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39264324:39264324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>A
AA Mutation	p.Ala352Thr(p.A352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264658
Start	39264177:39264177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201A>T
AA Mutation	p.Arg401Trp(p.R401W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39281456:39281456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629A>G
AA Mutation	p.Asp210Gly(p.D210G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39264215:39264215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163A>C
AA Mutation	p.Asp388Ala(p.D388A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39264362:39264362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016C>T
AA Mutation	p.Thr339Ile(p.T339I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264658
Start	39261541:39261541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143298147
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264658
Start	39264282:39264282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs118097792
CDS Mutation	c.1096C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264658
Start	39261512:39261512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1259delC
AA Mutation	p.Pro420HisfsTer3(p.P420Hfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264658
Start	39299057:39299057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262C>T
AA Mutation	p.Arg88Ter(p.R88*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264658
Start	39297126:39297126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781515315
CDS Mutation	c.398+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FBXL20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264658
Start	39285549:39285549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>A
AA Mutation	p.Phe141Leu(p.F141L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264658
Start	39261541:39261541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143298147
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript