RGD:408370323 Rat Genome Database

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Variant: RGD:408370323 -  Homo sapiens

RGD ID: 408370323
ClinVar ID: CV3503025
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SHANK2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 70,336,428
GRCh38 11 70,490,323
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_042866.1:g.639474C>T
NG_042866.2:g.667905C>T
NC_000011.10:g.70490323G>A
NC_000011.9:g.70336428G>A
More... 		05/24/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004724146 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SHANK2 CLINVAR
OMIM 603290 CLINVAR