Variant Results

or

or

Results for "MTHFS"

Variant Events: 3

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
MTHFS	SSC08266	chr15: 80137553-80137553	T	TA	exonic		De novo	stoploss	NM_001199758 NM_006441 NM_001199760	c.439dupT c.610dupT c.538dupT	p.X147delinsL p.X204delinsL p.X180delinsL	-	-	Fu2022 E Trost2022 G
MTHFS	13590.p1	Complex Event; expand row to view variants					De novo	stoploss	NM_001199758 NM_006441 NM_001199760 NM_001199758 NM_006441 NM_001199760	c.439dupT c.610dupT c.538dupT c.438dupT c.609dupT c.537dupT	p.X147delinsL p.X204delinsL p.X180delinsL p.X147delinsL p.X204delinsL p.X180delinsL	-	-	Dong2014 E Iossifov2012 E Iossifov2014 E Ji2016 E Kosmicki2017 E Satterstrom2020 E Wilfert2021 G Willsey2013 E Zhou2022 GE
MTHFS	1-0665-003	chr15: 80152891-80152891	C	T	intronic		De novo					-	-	Trost2022 G Yuen2017 G

Source Variant Information

, -

Source:

Paper alias:

No records found.

Paper Information

Title
Authors
Technology
Variant source
Cohorts
Design
URL
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.
Variant event count
Curation notes	View
	More