RGD:152102132 Rat Genome Database

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Variant: RGD:152102132 -  Homo sapiens

RGD ID: 152102132
RS ID: rs2148534355
ClinVar ID: CV1605877
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAA10  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 153,196,304
GRCh38 X 153,930,851
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256119.2:c.342-4C>G
NM_001256120.2:c.369-4C>G
NM_003491.4:c.387-4C>G
NG_013220.1:g.411C>G
More... 		12/02/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NAA10
Accession:NM_003491
Location:INTRON

Gene Symbol:NAA10
Accession:NM_001256119
Location:INTRON

Gene Symbol:NAA10
Accession:NM_001256120
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002095671 CLINVAR
dbSNP (RS) rs2148534355 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NAA10 CLINVAR
OMIM 300013 CLINVAR