Colon Cancer: Gene >> FBXL19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30928585:30928585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806C>A
AA Mutation	p.Ala269Asp(p.A269D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30930491:30930491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268C>A
AA Mutation	p.Pro423His(p.P423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30928522:30928522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743T>C
AA Mutation	p.Leu248Pro(p.L248P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30930083:30930083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781616493
CDS Mutation	c.860C>T
AA Mutation	p.Pro287Leu(p.P287L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380310
Start	30947052:30947052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1907G>A
AA Mutation	p.Gly636Asp(p.G636D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30946784:30946784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1742G>A
AA Mutation	p.Gly581Asp(p.G581D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30946775:30946775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733G>A
AA Mutation	p.Arg578His(p.R578H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380310
Start	30928511:30928511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376169841
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380310
Start	30927880:30927880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.606delG
AA Mutation	p.Pro205ArgfsTer26(p.P205Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FBXL19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380310
Start	30946903:30946903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1861C>T
AA Mutation	p.Pro621Ser(p.P621S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript