RGD:156030204 Rat Genome Database

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Variant: RGD:156030204 -  Homo sapiens

RGD ID: 156030204
ClinVar ID: CV2022623
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNA3  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 78,911,017
GRCh38 15 78,618,675
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000743.5:c.223-14A>G
NM_001166694.2:c.223-14A>G
NG_016143.1:g.7621A>G
NC_000015.10:g.78618675T>C
More... 		11/19/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNA3
Accession:NM_001166694
Location:INTRON

Gene Symbol:CHRNA3
Accession:NM_000743
Location:INTRON

Gene Symbol:CHRNA3
Accession:XM_006720382
Location:INTRON

Gene Symbol:CHRNA3
Accession:NR_046313
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002735777 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNA3 CLINVAR
OMIM 118503 CLINVAR