Variant Results

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Results for "SMO"

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
SMO	P1229	chr7: 128851858-128851858	C	A	intronic		De novo					-	-	Hashimoto2016 E
SMO	AU4015302	chr7: 128829689-128829689	G	T	intronic		De novo					-	-	Yuen2017 G
SMO	SP0021718	chr7: 128846509-128846509	G	A	intronic		De novo					-	-	Fu2022 E
SMO	SP0011117	chr7: 128845997-128845997	T	G	exonic		De novo	nonsynonymous SNV	NM_005631	c.T927G	p.N309K	12.1	-	Fu2022 E
SMO	SP0077387	chr7: 128846000-128846000	G	T	exonic		De novo	nonsynonymous SNV	NM_005631	c.G930T	p.E310D	17.01	-	Fu2022 E
SMO	SP0033071	chr7: 128848778-128848778	G	A	intronic		De novo					-	-	Fu2022 E
SMO	SP0038373	chr7: 128828989-128828989	G	C	UTR5		De novo					-	-	Fu2022 E
SMO	SP0089039	chr7: 128845997-128845997	T	G	exonic		De novo	nonsynonymous SNV	NM_005631	c.T927G	p.N309K	12.1	-	Fu2022 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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