RGD:13526170 Rat Genome Database

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Variant: RGD:13526170 -  Homo sapiens

RGD ID: 13526170
RS ID: rs6090387
ClinVar ID: CV507405
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AL121827.1  CHRNA4  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 61,992,547
GRCh38 20 63,361,195
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.5149C>A
NC_000020.10:g.61992547G>T
NM_000744.5:c.-30C>A
NC_000020.11:g.63361195G>T
More... 		12/04/2017 5 prime utr variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CHRNA4
Accession:NM_001256573
Location:5UTRS;EXON

Gene Symbol:CHRNA4
Accession:NM_000744
Location:5UTRS;EXON

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

Gene Symbol:AL121827.1
Accession:NR_110634
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000603765 CLINVAR
dbSNP (RS) rs6090387 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene 100130587 CLINVAR
  CHRNA4 CLINVAR
OMIM 118504 CLINVAR