Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FBXO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32485135:32485135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713A>T
AA Mutation	p.Tyr238Phe(p.Y238F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32487805:32487805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>A
AA Mutation	p.Ser283Tyr(p.S283Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32485074:32485074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376214763
CDS Mutation	c.652G>A
AA Mutation	p.Glu218Lys(p.E218K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32493255:32493255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373Lys(p.R373K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32484000:32484000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376455464
CDS Mutation	c.521C>T
AA Mutation	p.Ser174Leu(p.S174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32487780:32487780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823A>C
AA Mutation	p.Lys275Gln(p.K275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266087
Start	32484067:32484067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32498424:32498424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463T>C
AA Mutation	p.Leu488Pro(p.L488P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32479108:32479108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>C
AA Mutation	p.Ala84Pro(p.A84P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266087
Start	32485126:32485126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704A>C
AA Mutation	p.Lys235Thr(p.K235T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266087
Start	32479266:32479266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776288097
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266087
Start	32498293:32498293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755248108
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript