RGD:407456170 Rat Genome Database

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Variant: RGD:407456170 -  Homo sapiens

RGD ID: 407456170
ClinVar ID: CV3422991
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CIAO2A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 64,365,168
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001289108.2:c.*2549C>T
NM_001014812.3:c.*86C>T
NM_032231.7:c.445C>T
NC_000015.10:g.64072969G>A
More... 		03/25/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004610620 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CIAO2A CLINVAR
OMIM 618382 CLINVAR