RGD:405222592 Rat Genome Database

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Variant: RGD:405222592 -  Homo sapiens

RGD ID: 405222592
ClinVar ID: CV2891074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: A2ML1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 8,988,123
GRCh38 12 8,835,527
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.8835527T>A
NC_000012.11:g.8988123T>A
NP_653271.3:p.Ile168=
NM_144670.6:c.504T>A
More... 		05/14/2023 synonymous variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003554154 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene A2ML1 CLINVAR
OMIM 610627 CLINVAR