RGD:155939141 Rat Genome Database

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Variant: RGD:155939141 -  Homo sapiens

RGD ID: 155939141
ClinVar ID: CV2071755
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAA35  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 88,633,600
GRCh38 9 86,018,685
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321881.2:c.1915-14C>T
NM_001321882.2:c.1915-14C>T
NM_024635.4:c.1915-14C>T
NC_000009.12:g.86018685C>T
More... 		07/08/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FLJ21613
Accession:NM_024635
Location:INTRON

Gene Symbol:NAA35
Accession:XM_005252127
Location:INTRON

Gene Symbol:NAA35
Accession:NM_001321881
Location:INTRON

Gene Symbol:NAA35
Accession:XM_024447649
Location:INTRON

Gene Symbol:NAA35
Accession:NM_001321882
Location:INTRON

Gene Symbol:NAA35
Accession:XM_024447648
Location:INTRON

Gene Symbol:NAA35
Accession:XM_047423710
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002839288 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NAA35 CLINVAR
OMIM 619438 CLINVAR