Colon Cancer: Gene >> FBXO5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152972437:152972437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927T>G
AA Mutation	p.Phe309Leu(p.F309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152974948:152974948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777A>T
AA Mutation	p.Leu259Phe(p.L259F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152975110:152975110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615A>T
AA Mutation	p.Leu205Phe(p.L205F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152975396:152975396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329C>G
AA Mutation	p.Thr110Ser(p.T110S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152975396:152975396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>T
AA Mutation	p.Thr110Ile(p.T110I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152975066:152975066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766507735
CDS Mutation	c.659T>G
AA Mutation	p.Leu220Arg(p.L220R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152972291:152972291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358Gln(p.R358Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229758
Start	152971286:152971286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148568194
CDS Mutation	c.1221G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229758
Start	152972338:152972338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229758
Start	152972347:152972347(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1017delA
AA Mutation	p.Asp340MetfsTer30(p.D340Mfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229758
Start	152975105:152975105(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.620delA
AA Mutation	p.Lys207ArgfsTer9(p.K207Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000229758
Start	152975610:152975610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>T
AA Mutation	p.Glu39Ter(p.E39*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152972381:152972381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983T>C
AA Mutation	p.Val328Ala(p.V328A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229758
Start	152975384:152975384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148207003
CDS Mutation	c.341G>A
AA Mutation	p.Arg114His(p.R114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000229758
Start	152974971:152974971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Ter(p.R252*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript