RGD:156406388 Rat Genome Database

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Variant: RGD:156406388 -  Homo sapiens

RGD ID: 156406388
ClinVar ID: CV1963603
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LETM1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 1,818,434
GRCh38 4 1,816,707
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012318.3:c.1931+20C>T
NG_013063.1:g.44541C>T
NC_000004.12:g.1816707G>A
NC_000004.11:g.1818434G>A
 09/13/2023 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LETM1
Accession:NM_012318
Location:INTRON

Gene Symbol:LETM1
Accession:XM_006713884
Location:INTRON

Gene Symbol:LETM1
Accession:XM_047415673
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002585893 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LETM1 CLINVAR
OMIM 604407 CLINVAR