RGD:150458064 Rat Genome Database

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Variant: RGD:150458064 -  Homo sapiens

RGD ID: 150458064
RS ID: rs7928030
ClinVar ID: CV1237162
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PANX1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 93,886,838
GRCh38 11 94,153,672
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015368.4:c.321+42G>C
NG_027936.1:g.29745G>C
NC_000011.10:g.94153672G>C
NC_000011.9:g.93886838G>C
 06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PANX1
Accession:XM_047426702
Location:5UTRS;INTRON

Gene Symbol:PANX1
Accession:XM_011542734
Location:5UTRS;INTRON

Gene Symbol:PANX1
Accession:NM_015368
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001648841 CLINVAR
dbSNP (RS) rs7928030 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PANX1 CLINVAR
OMIM 608420 CLINVAR