Variant Results

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Results for "FBXL6"

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
FBXL6	13874.p1	chr8: 145580668-145580668	C	T	exonic		De novo	synonymous SNV	NM_012162 NM_024555	c.G753A c.G735A	p.L251L p.L245L	-	8.336E-6	Satterstrom2020 E Turner2016 G
FBXL6	SP0023093	chr8: 145579317-145579317	C	G	exonic		Mosaic	synonymous SNV	NM_012162 NM_024555	c.G1494C c.G1476C	p.P498P p.P492P	-	8.757E-6	Feliciano2019 E
FBXL6	13874_p1	chr8: 145580668-145580668	C	T	exonic		De novo	synonymous SNV	NM_012162 NM_024555	c.G753A c.G735A	p.L251L p.L245L	-	8.336E-6	Fu2022 E
FBXL6	iHART1751	chr8: 145579627-145579627	C	T	splicing		Maternal	splicing				14.67	-	Ruzzo2019 G
FBXL6	1-0231-003	chr8: 145579963-145579963	G	C	exonic		De novo	nonsynonymous SNV	NM_012162 NM_024555	c.C1222G c.C1204G	p.R408G p.R402G	2.394	-	Yuen2015 G
FBXL6	SSC06654	chr8: 145580321-145580321	C	T	exonic		De novo	nonsynonymous SNV	NM_012162 NM_024555	c.G932A c.G914A	p.R311H p.R305H	2.288	1.667E-5	Fu2022 E Lim2017 E
FBXL6	SP0039239	chr8: 145580418-145580418	G	A	intronic		De novo					-	-	Fu2022 E
FBXL6	13063.p1	chr8: 145580321-145580321	C	T	exonic		De novo	nonsynonymous SNV	NM_012162 NM_024555	c.G932A c.G914A	p.R311H p.R305H	2.288	1.667E-5	Iossifov2014 E Kosmicki2017 E Krupp2017 E Satterstrom2020 E Wilfert2021 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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