RGD:14739074 Rat Genome Database

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Variant: RGD:14739074 -  Homo sapiens

RGD ID: 14739074
RS ID: rs74434776
ClinVar ID: CV658408
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNA1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 175,622,992
GRCh38 2 174,758,264
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000079.4:c.235-589G>T
NM_001039523.3:c.235-244G>T
NG_008172.1:g.11209G>T
NC_000002.12:g.174758264C>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNA1
Accession:XM_017003257
Location:INTRON

Gene Symbol:CHRNA1
Accession:NM_000079
Location:INTRON

Gene Symbol:CHRNA1
Accession:XM_017003256
Location:INTRON

Gene Symbol:CHRNA1
Accession:NM_001039523
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000839700 CLINVAR
dbSNP (RS) rs74434776 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNA1 CLINVAR
OMIM 100690 CLINVAR