Variant Results

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Results for "FAHD1"

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
FAHD1	74-0688	Complex Event; expand row to view variants					De novo					-	-	Michaelson2012 G Michaelson2012 G
FAHD1	P1325	chr16: 1877625-1877625	G	C	exonic		De novo	nonsynonymous SNV	NM_001018104 NM_001142398 NM_031208	c.G395C c.G395C c.G395C	p.S132T p.S132T p.S132T	26.1	-	Hashimoto2016 E
FAHD1	P1325	chr16: 1877669-1877669	A	C	exonic		De novo	nonsynonymous SNV	NM_001018104 NM_001142398 NM_031208	c.A439C c.A439C c.A439C	p.K147Q p.K147Q p.K147Q	12.94	-	Hashimoto2016 E
FAHD1	mAGRE4563	chr16: 1877234-1877234	G	T	exonic		Maternal	stopgain	NM_001018104 NM_001142398 NM_031208	c.G4T c.G4T c.G4T	p.G2X p.G2X p.G2X	29.1	2.616E-5	Cirnigliaro2023 G
FAHD1	mAGRE4562	chr16: 1877234-1877234	G	T	exonic		Maternal	stopgain	NM_001018104 NM_001142398 NM_031208	c.G4T c.G4T c.G4T	p.G2X p.G2X p.G2X	29.1	2.616E-5	Cirnigliaro2023 G
FAHD1	2-1357-003	chr16: 1886497-1886501	ACAGT	GCTCC	intronic		De novo					-	-	Trost2022 G
FAHD1	AU4033304	chr16: 1881819-1881819	C	T	intronic		De novo					-	-	Trost2022 G Yuen2017 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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