RGD:407514850 Rat Genome Database

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Variant: RGD:407514850 -  Homo sapiens

RGD ID: 407514850
ClinVar ID: CV3484644
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC41A2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 105,199,035
GRCh38 12 104,805,257
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001387128.1:c.*124C>G
NM_001387129.1:c.*124C>G
NM_001387130.1:c.*124C>G
NM_001352169.2:c.1617C>G
More... 		05/01/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004674723 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SLC41A2 CLINVAR
OMIM 610802 CLINVAR