Variant Results

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Results for "TBC1D22B"

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
TBC1D22B	14458_p1	chr6: 37280756-37280756	G	A	exonic		De novo	nonsynonymous SNV	NM_017772	c.G1045A	p.A349T	35.0	-	Fu2022 E
TBC1D22B	14458.p1	chr6: 37280756-37280756	G	A	exonic		De novo	nonsynonymous SNV	NM_017772	c.G1045A	p.A349T	35.0	-	Iossifov2014 E Ji2016 E Kosmicki2017 E Krupp2017 E Lim2017 E Satterstrom2020 E Turner2017 G Wilfert2021 G
TBC1D22B	2-1131-003	chr6: 37312068-37312068	T	C	intergenic		De novo					-	-	Yuen2016 G Yuen2017 G
TBC1D22B	AU2140306	chr6: 37316762-37316762	A	G	intergenic		De novo					-	-	Yuen2017 G
TBC1D22B	SP0148202	chr6: 37247253-37247253	C	T	exonic		De novo	nonsynonymous SNV	NM_017772	c.C287T	p.T96I	24.0	-	Fu2022 E
TBC1D22B	AU012803	chr6: 37267377-37267377	C	T	intronic		De novo					-	-	Yuen2017 G
TBC1D22B	AU4235303	chr6: 37234981-37234981	G	A	intronic		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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