RGD:407496678 Rat Genome Database

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Variant: RGD:407496678 -  Homo sapiens

RGD ID: 407496678
ClinVar ID: CV3450185
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MRGPRD  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 68,748,214
GRCh38 11 68,980,745
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_198923.2:c.242C>A
NC_000011.10:g.68980745G>T
NC_000011.9:g.68748214G>T
NP_944605.2:p.Ser81Tyr
 06/10/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004643553 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MRGPRD CLINVAR
OMIM 607231 CLINVAR