Variant Results

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Results for "RASSF3"

Variant Events: 9

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
RASSF3	AU2072302	chr12: 65098628-65098628	C	A	intergenic		De novo					-	-	Yuen2017 G
RASSF3	1-1000-003	chr12: 65061103-65061122	TTTTCTTTCTTTCTTTCTTT	TTTTCTTTCTTTCTTT	intronic		De novo					-	-	Yuen2017 G
RASSF3	2-1184-003	chr12: 65006299-65006299	T	TA	intronic		De novo					-	-	Yuen2016 G
RASSF3	iHART1440	chr12: 65085248-65085248	A	G	splicing		Paternal	splicing				22.4	-	Ruzzo2019 G
RASSF3	2-1605-004	chr12: 65011691-65011691	T	C	intronic		De novo					-	-	Yuen2017 G
RASSF3	A17	chr12: 65051745-65051745	T	C	intronic		De novo					-	-	Wu2018 G
RASSF3	AU1725306	chr12: 65059299-65059299	C	G	intronic		De novo					-	-	Yuen2017 G
RASSF3	NDAR_INVWJ494BME_wes1	chr12: 65082212-65082215	CGTT	C	exonic		De novo	nonframeshift deletion	NM_178169	c.437_439del	p.146_147del	-	-	DeRubeis2014 E Fu2022 E Kosmicki2017 E Satterstrom2020 E
RASSF3	2-1164-003	chr12: 65006038-65006038	A	T	intronic		De novo					-	-	Yuen2016 G 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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