RGD:150405464 Rat Genome Database

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Variant: RGD:150405464 -  Homo sapiens

RGD ID: 150405464
RS ID: rs71519636
ClinVar ID: CV1190763
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNA2  LOC127459017  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 27,320,236
GRCh38 8 27,462,719
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000742.4:c.1464+260G>A
NM_001347707.2:c.870+260G>A
NM_001347708.2:c.870+260G>A
NM_001282455.2:c.1419+260G>A
More... 		11/21/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNA2
Accession:XM_047421313
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_001347706
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_001347707
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_001282455
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_001347705
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_000742
Location:INTRON

Gene Symbol:CHRNA2
Accession:XM_047421311
Location:INTRON

Gene Symbol:CHRNA2
Accession:XM_047421312
Location:INTRON

Gene Symbol:CHRNA2
Accession:NM_001347708
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001564294 CLINVAR
dbSNP (RS) rs71519636 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNA2 CLINVAR
OMIM 118502 CLINVAR