RGD:401926698 Rat Genome Database

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Variant: RGD:401926698 -  Homo sapiens

RGD ID: 401926698
ClinVar ID: CV2821467
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FTHL18P  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 37,061,390
GRCh38 X 37,043,317
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000023.11:g.37043317G>A
NC_000023.10:g.37061390G>A
NR_171164.1:n.476C>T
 01/01/2023 non-coding transcript variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FTHL18P
Accession:NR_171164
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003438051 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FAM47C CLINVAR
OMIM 301067 CLINVAR