Variant Results

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Results for "HNRNPH2"

Variant Events: 5

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
HNRNPH2	Miyake2023:11210	chrX: 100667398-100667398	T	A	exonic		De novo	nonsynonymous SNV	NM_001032393 NM_019597	c.T422A c.T422A	p.M141K p.M141K	12.74	-	Miyake2023 E
HNRNPH2	AU030703	chrX: 100669280-100669280	T	C	downstream		De novo					-	-	Yuen2017 G
HNRNPH2	Mahjani2021:53	chrX: 100667559-100667559	T	C	exonic			nonsynonymous SNV	NM_001032393 NM_019597	c.T583C c.T583C	p.Y195H p.Y195H	15.11	-	Mahjani2021 E
HNRNPH2	JASD_Fam0188	chrX: 100667398-100667398	T	A	exonic		De novo	nonsynonymous SNV	NM_001032393 NM_019597	c.T422A c.T422A	p.M141K p.M141K	12.74	-	Takata2018 E
HNRNPH2	NP142	chrX: 100667398-100667398	T	A	exonic		De novo	nonsynonymous SNV	NM_001032393 NM_019597	c.T422A c.T422A	p.M141K p.M141K	12.74	-	Satterstrom2020 E Trost2022 G Zhou2022 GE

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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