RGD:407506054 Rat Genome Database

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Variant: RGD:407506054 -  Homo sapiens

RGD ID: 407506054
ClinVar ID: CV3466182
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGEF34P  ARHGEF35-AS1  OR2A1-AS1  OR2A7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 143,956,487
GRCh38 7 144,259,394
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001005328.2:c.235C>T
NC_000007.14:g.144259394G>A
NC_000007.13:g.143956487G>A
NR_033942.1:n.3806C>T
More... 		03/30/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004646294 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ARHGEF35-AS1 CLINVAR
  OR2A1-AS1 CLINVAR
  OR2A7 CLINVAR