Variant Results

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Results for "STMN1"

Variant Events: 8

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
STMN1	SP0012361	chr1: 26227586-26227586	G	C	intronic		De novo					-	-	Fu2022 E Trost2022 G
STMN1	1-0541-003	chr1: 26213571-26213573	CCT	C	intronic		De novo					-	-	Trost2022 G Yuen2017 G
STMN1	A15	chr1: 26255995-26255995	C	T	intergenic		De novo					-	-	Wu2018 G
STMN1	14471.p1	chr1: 26228141-26228141	A	G	exonic		Mosaic	synonymous SNV	NM_001145454 NM_005563 NM_203399 NM_203401	c.T219C c.T219C c.T219C c.T219C	p.A73A p.A73A p.A73A p.A73A	-	-	Krupp2017 E
STMN1	MSSNG00049-003	chr1: 26224983-26224983	C	T	intronic		De novo					-	-	Trost2022 G
STMN1	12832.p1	chr1: 26234201-26234201	T	G	upstream		De novo					-	-	Wilfert2021 G
STMN1	SP0050016	chr1: 26231008-26231008	A	G	intronic		De novo					-	-	Fu2022 E
STMN1	5-0123-003	chr1: 26236733-26236733	C	T	intergenic		De novo					-	-	Yuen2017 G

Source Variant Information

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Paper Information

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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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