RGD:407453102 Rat Genome Database

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Variant: RGD:407453102 -  Homo sapiens

RGD ID: 407453102
ClinVar ID: CV3486274
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM123  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 102,272,803
GRCh38 11 102,402,072
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_052932.3:c.292A>G
NC_000011.10:g.102402072T>C
NC_000011.9:g.102272803T>C
NM_052932.2:c.292A>G
More... 		03/25/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004684389 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TMEM123 CLINVAR
OMIM 606356 CLINVAR