Variant Results

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Results for "SCUBE3"

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
SCUBE3	iHART2272	chr6: 35182282-35182282	T	G	splicing		Maternal	splicing				16.86	-	Ruzzo2019 G
SCUBE3	72-1397	chr6: 35210840-35210840	G	A	exonic		Inherited	nonsynonymous SNV	NM_001303136 NM_152753	c.G1733A c.G1736A	p.R578Q p.R579Q	13.58	5.025E-5	Patowary2019 E
SCUBE3	Cukier2014:17351	chr6: 35212504-35212504	G	A	exonic		Unknown	nonsynonymous SNV	NM_001303136 NM_152753	c.G2314A c.G2317A	p.D772N p.D773N	24.4	6.0E-4	Cukier2014 E
SCUBE3	AU2156303	chr6: 35206212-35206212	G	A	intronic		De novo					-	-	Yuen2017 G
SCUBE3	DEASD_0075_001	chr6: 35200730-35200730	C	A	exonic		De novo	synonymous SNV	NM_001303136 NM_152753	c.C570A c.C573A	p.T190T p.T191T	-	-	DeRubeis2014 E Fu2022 E Kosmicki2017 E Lim2017 E 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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