RGD:597797210 Rat Genome Database

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Variant: RGD:597797210 -  Homo sapiens

RGD ID: 597797210
ClinVar ID: CV3700920
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLK7  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 51,480,820
GRCh38 19 50,977,564
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001207053.2:c.518T>C
NM_001243126.1:c.713T>C
NM_005046.4:c.734T>C
NM_139277.2:c.734T>C
More... 		10/04/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004935729 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene KLK7 CLINVAR
OMIM 604438 CLINVAR