Variant Results

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Results for "KLHL17"

Variant Events: 7

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
KLHL17	DEASD_1049_001	chr1: 897739-897739	T	C	exonic		De novo	nonsynonymous SNV	NM_198317	c.T716C	p.L239P	15.16	-	Fu2022 E
KLHL17	14505.p1	chr1: 897349-897349	G	A	exonic		De novo	synonymous SNV	NM_198317	c.G633A	p.K211K	-	-	Iossifov2014 E Kosmicki2017 E Satterstrom2020 E Zhou2022 GE
KLHL17	GEA347	chr1: 898548-898548	C	T	exonic		De novo	nonsynonymous SNV	NM_198317	c.C1102T	p.R368C	21.3	2.758E-5	Fu2022 E
KLHL17	09C91113	chr1: 898240-898240	A	C	exonic		De novo	nonsynonymous SNV	NM_198317	c.A985C	p.T329P	12.94	5.557E-5	Fu2022 E
KLHL17	09C87513	chr1: 897739-897739	T	C	exonic		De novo	nonsynonymous SNV	NM_198317	c.T716C	p.L239P	15.16	-	DeRubeis2014 E Kosmicki2017 E Lim2017 E Satterstrom2020 E Trost2022 G Zhou2022 GE
KLHL17	SP0000180	chr1: 898753-898753	C	T	exonic		De novo	synonymous SNV	NM_198317	c.C1224T	p.S408S	-	-	Feliciano2019 E Fu2022 E Trost2022 G Zhou2022 GE
KLHL17	36218	chr1: 897349-897349	G	A	exonic		De novo	synonymous SNV	NM_198317	c.G633A	p.K211K	-	-	Fu2022 E Trost2022 G

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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