RGD:407457180 Rat Genome Database

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Variant: RGD:407457180 -  Homo sapiens

RGD ID: 407457180
ClinVar ID: CV3492045
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZDHHC1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 67,428,598
GRCh38 16 67,394,695
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001323627.2:c.1364G>T
NM_013304.3:c.1429G>T
NC_000016.10:g.67394695C>A
NC_000016.9:g.67428598C>A
More... 		05/30/2024 missense variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004686230 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ZDHHC1 CLINVAR