RGD:150422953 Rat Genome Database

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Variant: RGD:150422953 -  Homo sapiens

RGD ID: 150422953
RS ID: rs41301323
ClinVar ID: CV1182073
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAA10  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 153,196,094
GRCh38 X 153,930,641
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.426+122C>T
NM_001256120.2:c.453+122C>T
NM_003491.4:c.471+122C>T
NG_013220.1:g.621C>T
More... 		10/20/2020 intron variant likely benign none provided

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

Gene Symbol:NAA10
Accession:NM_001256120
Location:INTRON

Gene Symbol:NAA10
Accession:NM_001256119
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001553350 CLINVAR
dbSNP (RS) rs41301323 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NAA10 CLINVAR
OMIM 300013 CLINVAR