RGD:150444099 Rat Genome Database

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Variant: RGD:150444099 -  Homo sapiens

RGD ID: 150444099
RS ID: rs10929352
ClinVar ID: CV1258469
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NBAS  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 15,372,731
GRCh38 2 15,232,607
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015909.4:c.6147-96A>C
NC_000002.11:g.15372731T>G
NC_000002.12:g.15232607T>G
NG_032964.1:g.333742A>C
 05/13/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NBAS
Accession:XM_011510360
Location:INTRON

Gene Symbol:NBAS
Accession:XM_047444735
Location:INTRON

Gene Symbol:NBAS
Accession:XM_017004317
Location:INTRON

Gene Symbol:NBAS
Accession:XM_047444733
Location:INTRON

Gene Symbol:NBAS
Accession:XM_011510358
Location:INTRON

Gene Symbol:NBAS
Accession:XM_011510361
Location:INTRON

Gene Symbol:NBAS
Accession:NM_015909
Location:INTRON

Gene Symbol:NBAS
Accession:XM_011510357
Location:INTRON

Gene Symbol:NBAS
Accession:XM_047444734
Location:INTRON

Gene Symbol:NBAS
Accession:NR_052013
Location:INTRON;NON-CODING

Gene Symbol:NBAS
Accession:XR_007076390
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001679667 CLINVAR
dbSNP (RS) rs10929352 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NBAS CLINVAR
OMIM 608025 CLINVAR