Variant Results

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Results for "SUMF2"

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
SUMF2	3701_18au	chr7: 56147549-56147549	G	A	exonic		De novo	synonymous SNV	NM_001130069	c.G1062A	p.E354E	-	-	Fu2022 E
SUMF2	SP0009759	chr7: 56132149-56132149	G	T	intronic		De novo					-	-	Fu2022 E Trost2022 G Trost2022 G
SUMF2	13507.p1	chr7: 56144465-56144466	CT	C	intronic		De novo					-	-	Dong2014 E Kosmicki2017 E Satterstrom2020 E
SUMF2	SP0061155	chr7: 56132018-56132018	G	A	exonic		De novo	nonsynonymous SNV	NM_001042469 NM_001042470 NM_001130069 NM_015411	c.G71A c.G71A c.G71A c.G71A	p.G24E p.G24E p.G24E p.G24E	13.3	-	Fu2022 E Trost2022 G Trost2022 G Zhou2022 GE
SUMF2	SSC07951	chr7: 56144465-56144466	CT	C	intronic		De novo					-	-	Trost2022 G
SUMF2	REACH000288	chr7: 56146447-56146447	C	T	intronic		De novo					-	-	Trost2022 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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