RGD:151745251 Rat Genome Database

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Variant: RGD:151745251 -  Homo sapiens

RGD ID: 151745251
RS ID: rs1417977595
ClinVar ID: CV1469632
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127822741  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 118,955,413
GRCh38 11 119,084,703
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_1076:g.4827C>G
NG_008093.1:g.4827C>G
NC_000011.10:g.119084703C>G
NC_000011.9:g.118955413C>G
 04/06/2022 uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001912343 CLINVAR
dbSNP (RS) rs1417977595 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HMBS CLINVAR
OMIM 609806 CLINVAR