RGD:407513450 Rat Genome Database

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Variant: RGD:407513450 -  Homo sapiens

RGD ID: 407513450
ClinVar ID: CV3443739
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: H1-1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 26,017,638
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005325.4:c.323T>C
NC_000006.12:g.26017410A>G
NC_000006.11:g.26017638A>G
NM_005325.3:c.323T>C
More...
06/19/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004627229 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene H1-1 CLINVAR
OMIM 142709 CLINVAR