RGD:405223665 Rat Genome Database

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Variant: RGD:405223665 -  Homo sapiens

RGD ID: 405223665
ClinVar ID: CV3151124
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YME1L1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 27,420,799
GRCh38 10 27,131,870
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_139312.3:c.1018C>T
NM_001253866.2:c.748C>T
NM_014263.4:c.847C>T
NG_047122.1:g.28409C>T
More... 		07/20/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003847549 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene YME1L1 CLINVAR
OMIM 607472 CLINVAR