RGD:14717411 Rat Genome Database

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Variant: RGD:14717411 -  Homo sapiens

RGD ID: 14717411
RS ID: rs56146528
ClinVar ID: CV657079
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNB2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 154,544,662
GRCh38 1 154,572,186
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000748.3:c.1338+25G>A
NG_008027.1:g.9406G>A
NC_000001.11:g.154572186G>A
NC_000001.10:g.154544662G>A
More... 		06/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNB2
Accession:NM_000748
Location:INTRON

Gene Symbol:CHRNB2
Accession:XM_017000180
Location:INTRON

Gene Symbol:CHRNB2
Accession:XR_001736952
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000830053 CLINVAR
dbSNP (RS) rs56146528 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNB2 CLINVAR
OMIM 118507 CLINVAR