RGD:12845513 Rat Genome Database

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Variant: RGD:12845513 -  Homo sapiens

RGD ID: 12845513
RS ID: rs201097839
ClinVar ID: CV378341
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHRNA4  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 61,978,085
GRCh38 20 63,346,733
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011931.1:g.19611G>C
NC_000020.11:g.63346733C>G
NC_000020.10:g.61978085C>G
NM_000744.5:c.*5G>C
More... 		11/30/2015 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHRNA4
Accession:NM_000744
Location:3UTRS;EXON

Gene Symbol:CHRNA4
Accession:NM_001256573
Location:3UTRS;EXON

Gene Symbol:CHRNA4
Accession:NR_046317
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001712185 CLINVAR
dbSNP (RS) rs201097839 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHRNA4 CLINVAR
OMIM 118504 CLINVAR