Colon Cancer: Gene >> WDR48

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302313
Start	39063084:39063084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83A>G
AA Mutation	p.Tyr28Cys(p.Y28C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302313
Start	39063168:39063168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167T>C
AA Mutation	p.Ile56Thr(p.I56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302313
Start	39091657:39091657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1701C>A
AA Mutation	p.Phe567Leu(p.F567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302313
Start	39069740:39069740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576224342
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302313
Start	39084172:39084172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302313
Start	39069741:39069741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000302313
Start	39063089:39063089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Ter(p.R30*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000302313
Start	39084154:39084154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WDR48

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302313
Start	39078144:39078144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980A>C
AA Mutation	p.Lys327Thr(p.K327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript