Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> WDR76

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263795
Start	43839652:43839652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656G>A
AA Mutation	p.Arg219Gln(p.R219Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263795
Start	43851211:43851211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386His(p.R386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263795
Start	43844035:43844035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013A>T
AA Mutation	p.Gln338Leu(p.Q338L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263795
Start	43828228:43828228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774710841
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263795
Start	43844012:43844012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263795
Start	43866127:43866127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WDR76

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263795
Start	43828123:43828123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749775453
CDS Mutation	c.219G>T
AA Mutation	p.Lys73Asn(p.K73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263795
Start	43828341:43828341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>A
AA Mutation	p.Ser146Asn(p.S146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263795
Start	43866326:43866326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1815G>A
Mutation Classification	Silent
Feature Type	Transcript