Variant Results

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Results for "ADSL"

Variant Events: 6

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
ADSL	Chen2021:1	chr22: 40760331-40760331	A	T	exonic		Both parents	nonsynonymous SNV	NM_000026 NM_001123378	c.A1153T c.A1153T	p.I385F p.I385F	29.2	-	Chen2021 GET
ADSL	2-1297-003	chr22: 40763592-40763592	C	T	intergenic		De novo					-	-	Trost2022 G Yuen2017 G
ADSL	SSC05755	chr22: 40760307-40760307	C	T	exonic		De novo	synonymous SNV	NM_000026 NM_001123378	c.C1129T c.C1129T	p.L377L p.L377L	-	-	Fu2022 E Lim2017 E Trost2022 G
ADSL	07C68684	chr22: 40750245-40750245	C	T	intronic		De novo					-	-	Fu2022 E Satterstrom2020 E Trost2022 G Zhou2022 GE
ADSL	12738.p1	chr22: 40760307-40760307	C	T	exonic		De novo	synonymous SNV	NM_000026 NM_001123378	c.C1129T c.C1129T	p.L377L p.L377L	-	-	Iossifov2014 E Kosmicki2017 E Krupp2017 E Satterstrom2020 E Zhou2022 GE
ADSL	2-0171-003	chr22: 40755284-40755284	G	A	exonic		De novo	nonsynonymous SNV	NM_000026 NM_001123378	c.G675A c.G675A	p.M225I p.M225I	14.41	-	Trost2022 G Yuen2015 G Yuen2017 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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