RGD:407527145 Rat Genome Database

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Variant: RGD:407527145 -  Homo sapiens

RGD ID: 407527145
ClinVar ID: CV3482918
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMOD2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 52,073,337
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001142885.2:c.590C>T
NM_014548.4:c.590C>T
NC_000015.10:g.51781140C>T
NC_000015.9:g.52073337C>T
More... 		05/30/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004679896 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TMOD2 CLINVAR
OMIM 602928 CLINVAR