RGD:407494170 Rat Genome Database

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Variant: RGD:407494170 -  Homo sapiens

RGD ID: 407494170
ClinVar ID: CV3417321
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BAHD1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 40,751,172
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301132.2:c.509G>A
NM_001411044.1:c.509G>A
NM_014952.5:c.509G>A
NC_000015.10:g.40458973G>A
More... 		05/23/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004605527 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene BAHD1 CLINVAR
OMIM 613880 CLINVAR