RGD:407508114 Rat Genome Database

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Variant: RGD:407508114 -  Homo sapiens

RGD ID: 407508114
ClinVar ID: CV3458008
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MVD  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 88,721,718
GRCh38 16 88,655,310
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002461.3:c.786G>C
LRG_52:g.740G>C
NG_052674.1:g.12844G>C
NG_007291.1:g.740G>C
More... 		05/16/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004647022 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MVD CLINVAR
OMIM 603236 CLINVAR