Variant Results

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Results for "SOSTDC1"

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
SOSTDC1	SJD_34	chr7: 16502441-16502441	T	C	exonic		Maternal	nonsynonymous SNV	NM_015464	c.A353G	p.Y118C	16.22	-	Toma2013 E
SOSTDC1	AU006804	chr7: 16527704-16527704	G	T	intergenic		De novo					-	-	Yuen2017 G
SOSTDC1	AU2950302	chr7: 16532353-16532353	C	T	intergenic		De novo					-	-	Yuen2017 G
SOSTDC1	EGAN00001101086	chr7: 16502519-16502519	A	G	exonic		De novo	nonsynonymous SNV	NM_015464	c.T275C	p.I92T	13.45	-	Fu2022 E Satterstrom2020 E Trost2022 G Zhou2022 GE
SOSTDC1	12568.p1	chr7: 16540465-16540465	T	C	intergenic		De novo					-	-	Turner2016 G
SOSTDC1	2-0244-003	chr7: 16561614-16561614	G	A	intergenic		De novo					-	-	Yuen2017 G
SOSTDC1	AU4463303	chr7: 16531983-16531983	T	C	intergenic		De novo					-	-	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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