rs13054870 Rat Genome Database

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Variant: rs13054870 -  Homo sapiens

RGD ID: 150531355
RS ID: rs13054870
ClinVar ID: CV1291155
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127895804  NEFH  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 29,877,375
GRCh38 22 29,481,386
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021076.4:c.883+241A>T
NC_000022.11:g.29481386A>T
NC_000022.10:g.29877375A>T
NG_008404.1:g.6195A>T
 04/11/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NEFH
Accession:NM_021076
Location:INTRON

Gene Symbol:NEFH
Accession:XM_011530200
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001733031 CLINVAR
dbSNP (RS) rs13054870 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEFH CLINVAR
OMIM 162230 CLINVAR