Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC35F5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245680
Start	113755187:113755187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251T>C
AA Mutation	p.Val84Ala(p.V84A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245680
Start	113743744:113743744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245680
Start	113755288:113755288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245680
Start	113719260:113719260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1390delT
AA Mutation	p.Ser464HisfsTer5(p.S464Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000245680
Start	113719220:113719220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430G>A
AA Mutation	p.Trp477Ter(p.W477*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC35F5

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000245680
Start	113743793:113743793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Ser161Asn(p.S161N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245680
Start	113755295:113755295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143T>C
AA Mutation	p.Val48Ala(p.V48A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245680
Start	113725461:113725461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245680
Start	113734663:113734663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000245680
Start	113756368:113756368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript