RGD:408380562 Rat Genome Database

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Variant: RGD:408380562 -  Homo sapiens

RGD ID: 408380562
ClinVar ID: CV3501200
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ISCU  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 108,961,474
GRCh38 12 108,567,698
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NR_135127.1:n.1715G>T
NM_014301.4:c.343+430G>T
NM_213595.4:c.418+430G>T
NM_001301141.1:c.419-222G>T
More... 		08/01/2024 intron variant likely benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004727289 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ISCU CLINVAR
OMIM 611911 CLINVAR