RGD:407467459 Rat Genome Database

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Variant: RGD:407467459 -  Homo sapiens

RGD ID: 407467459
ClinVar ID: CV3434158
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DHX36  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 153,994,547
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001114397.2:c.2788C>T
NM_020865.3:c.2830C>T
NC_000003.12:g.154276758G>A
NC_000003.11:g.153994547G>A
More... 		05/14/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004614219 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DHX36 CLINVAR
OMIM 612767 CLINVAR