Variant Results

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Results for "MPEG1"

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
MPEG1	2-1258-003	chr11: 59118832-59118832	A	T	intergenic		De novo					-	-	Yuen2017 G
MPEG1	iHART1532	chr11: 58979221-58979222	AT	A	exonic		Maternal	stopgain	NM_001039396	c.1117delA	p.M373X	-	7.452E-5	Ruzzo2019 G
MPEG1	2-1437-003	chr11: 59118832-59118832	A	T	intergenic		De novo					-	-	Yuen2017 G
MPEG1	mAGRE1532	chr11: 58979221-58979222	AT	A	exonic		Maternal	stopgain	NM_001039396	c.1117delA	p.M373X	-	7.452E-5	Cirnigliaro2023 G
MPEG1	mAGRE5593	chr11: 58978776-58978777	TC	T	exonic		Maternal	frameshift deletion	NM_001039396	c.1562delG	p.G521fs	-	2.0E-4	Cirnigliaro2023 G
MPEG1	13617.p1	chr11: 58979891-58979891	C	G	exonic		Mosaic, De novo	nonsynonymous SNV	NM_001039396	c.G448C	p.V150L	18.07	-	Dou2017 E Ji2016 E Krumm2015 E Krupp2017 E Zhou2022 GE
MPEG1	SP0111341	chr11: 58978998-58978998	G	A	exonic		De novo	synonymous SNV	NM_001039396	c.C1341T	p.T447T	-	4.143E-5	Fu2022 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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