RGD:407529707 Rat Genome Database

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Variant: RGD:407529707 -  Homo sapiens

RGD ID: 407529707
ClinVar ID: CV3493532
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: VIPR1  VIPR1-AS1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 42,572,998
GRCh38 3 42,531,506
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001251883.2:c.196G>T
NM_001251884.2:c.682G>T
NM_001251882.2:c.703G>T
NM_001251885.2:c.745G>T
More... 		03/28/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004681052 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene VIPR1 CLINVAR
  VIPR1-AS1 CLINVAR
OMIM 192321 CLINVAR