Colon Cancer: Gene >> FBXL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15636602:15636602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658C>G
AA Mutation	p.Leu220Val(p.L220V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15625936:15625936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166A>T
AA Mutation	p.Asp389Val(p.D389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15644671:15644671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15628027:15628027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>A
AA Mutation	p.Ser300Tyr(p.S300Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15625945:15625945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144046392
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15612275:15612275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1990A>T
AA Mutation	p.Asn664Tyr(p.N664Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15638674:15638674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>T
AA Mutation	p.Met139Ile(p.M139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15638539:15638539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552T>A
AA Mutation	p.Phe184Leu(p.F184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341285
Start	15625764:15625764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341285
Start	15625758:15625758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759078175
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341285
Start	15636531:15636531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371090462
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341285
Start	15638689:15638689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.402delT
AA Mutation	p.Gln135SerfsTer4(p.Q135Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341285
Start	15625550:15625551(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1551_1552insAGAAGAT
AA Mutation	p.Ser518ArgfsTer7(p.S518Rfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341285
Start	15626872:15626872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FBXL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15627982:15627982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764719880
CDS Mutation	c.944G>A
AA Mutation	p.Arg315His(p.R315H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341285
Start	15636532:15636532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780034015
CDS Mutation	c.728C>T
AA Mutation	p.Ser243Leu(p.S243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript