Variant Results

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Results for "CDK9"

Variant Events: 6

Gene Gene symbol on which the variant is located	ID Subject Identifier from the original study	Location Genomic location of the reference allele	REF Reference allele	ALT Alternate allele	Context Variant functional categories	Variant validation performed by an orthogonal method and reported	Inheritance Reported inheritance status	Effects Variant effect on transcript per Annovar	Transcript Transcript used for the cDNA/Protein mutation	cDNA cDNA variant notation	Protein Protein variant notation	CADD-Phred v1.0 CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores	ExAC v0.3 ExAC population frequency (version 0.3)	Sources Source(s) where variants from this event are reported
CDK9	JASD_Fam0010	chr9: 130549061-130549061	G	C	exonic		De novo	synonymous SNV	NM_001261	c.G174C	p.G58G	-	-	Takata2018 E
CDK9	iHART2111	chr9: 130551566-130551566	C	T	exonic		De novo	nonsynonymous SNV	NM_001261	c.C863T	p.A288V	31.0	-	Ruzzo2019 G
CDK9	05HI4255A	chr9: 130549867-130549867	T	G	exonic		De novo	nonsynonymous SNV	NM_001261	c.T245G	p.I82S	15.25	-	Fu2022 E Satterstrom2020 E
CDK9	2-1112-003	chr9: 130556931-130556931	C	T	intergenic		De novo					-	-	Yuen2016 G Yuen2017 G
CDK9	SP0139811	chr9: 130550933-130550933	G	A	exonic		De novo	nonsynonymous SNV	NM_001261	c.G715A	p.A239T	11.82	-	Fu2022 E
CDK9	12046.p1	chr9: 130549918-130549918	C	T	intronic		De novo					-	8.261E-6	Satterstrom2020 E

Source Variant Information

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Paper Information

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Pubmed
Subject count	The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
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