Colon Cancer: Gene >> FBXO31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87334162:87334162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87360303:87360303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404A>G
AA Mutation	p.Tyr135Cys(p.Y135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87360313:87360313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Trp(p.R132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87333965:87333965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318T>C
AA Mutation	p.Cys440Arg(p.C440R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87360342:87360342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311635
Start	87335364:87335364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371017127
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311635
Start	87336253:87336253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747440641
CDS Mutation	c.744G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311635
Start	87383442:87383442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000311635
Start	87360294:87360294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87335440:87335440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87343711:87343711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Val182Ile(p.V182I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311635
Start	87336257:87336257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740G>A
AA Mutation	p.Arg247Gln(p.R247Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311635
Start	87335424:87335424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766491669
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript