RGD:407522410 Rat Genome Database

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Variant: RGD:407522410 -  Homo sapiens

RGD ID: 407522410
ClinVar ID: CV3444770
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: INKA2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 112,269,838
GRCh38 1 111,727,216
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_198926.2:c.601C>G
NM_019099.5:c.646C>G
NC_000001.11:g.111727216G>C
NC_000001.10:g.112269838G>C
More... 		03/19/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004630682 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene INKA2 CLINVAR
OMIM 620403 CLINVAR