Variant Results

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Results for "CLCC1"

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
CLCC1	A21	chr1: 109473268-109473268	T	C	UTR3		De novo					-	-	Wu2018 G
CLCC1	111299	chr1: 109482667-109482667	C	G	exonic			nonsynonymous SNV	NM_001278202 NM_001048210 NM_015127	c.G531C c.G894C c.G744C	p.K177N p.K298N p.K248N	25.5	8.275E-6	Woodbury-Smith2022 E
CLCC1	2-1508-003	chr1: 109484371-109484371	G	T	intronic		De novo					-	-	Trost2022 G Yuen2017 G
CLCC1	1-0402-003	chr1: 109510471-109510471	C	T	intergenic		De novo					-	-	Yuen2017 G
CLCC1	2-0273-003	chr1: 109495219-109495219	G	C	intronic		De novo					-	-	Trost2022 G Yuen2017 G
CLCC1	SSC07419	chr1: 109490271-109490271	A	G	exonic		De novo	synonymous SNV	NM_001278202 NM_001278203 NM_001048210 NM_015127	c.T301C c.T301C c.T301C c.T301C	p.L101L p.L101L p.L101L p.L101L	-	-	Fu2022 E Lim2017 E Trost2022 G
CLCC1	11838.p1	chr1: 109490271-109490271	A	G	exonic		De novo	synonymous SNV	NM_001278202 NM_001278203 NM_001048210 NM_015127	c.T301C c.T301C c.T301C c.T301C	p.L101L p.L101L p.L101L p.L101L	-	-	Krumm2015 E Satterstrom2020 E 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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