Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC35B3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8414941:8414941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374587821
CDS Mutation	c.1022C>T
AA Mutation	p.Ser341Leu(p.S341L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8416965:8416965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143437815
CDS Mutation	c.904C>A
AA Mutation	p.Leu302Ile(p.L302I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8420795:8420795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608C>T
AA Mutation	p.Ala203Val(p.A203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379660
Start	8420779:8420779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC35B3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8430108:8430108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>A
AA Mutation	p.Thr18Asn(p.T18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8422551:8422551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>T
AA Mutation	p.Gly165Cys(p.G165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8416902:8416902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967G>A
AA Mutation	p.Ala323Thr(p.A323T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379660
Start	8414931:8414931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032C>A
AA Mutation	p.Phe344Leu(p.F344L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript