RGD:407494909 Rat Genome Database

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Variant: RGD:407494909 -  Homo sapiens

RGD ID: 407494909
ClinVar ID: CV3456916
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MARVELD3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 71,663,278
GRCh38 16 71,629,375
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001271329.2:c.313C>T
NM_001017967.4:c.476C>T
NM_052858.6:c.476C>T
NC_000016.10:g.71629375C>T
More... 		06/10/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004643098 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MARVELD3 CLINVAR
OMIM 614094 CLINVAR