Colon Cancer: Gene >> WDR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358625
Start	134154511:134154511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.677G>T
AA Mutation	p.Gly226Val(p.G226V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358625
Start	134154523:134154523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689T>C
AA Mutation	p.Leu230Pro(p.L230P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358625
Start	134156563:134156563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874G>C
AA Mutation	p.Glu292Gln(p.E292Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358625
Start	134156571:134156571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358625
Start	134157948:134157948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358625
Start	134140720:134140720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358625
Start	134142641:134142641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541927663
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358625
Start	134154476:134154476(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.648delC
AA Mutation	p.Val217CysfsTer4(p.V217Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000358625
Start	134148286:134148286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WDR5

No Mutation Annotation!