rs45600633 Rat Genome Database

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Variant: rs45600633 -  Homo sapiens

RGD ID: 153000736
RS ID: rs45600633
ClinVar ID: CV1685611
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARCN1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 118,460,957
GRCh38 11 118,590,242
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001655.5:c.819-99G>A
NG_051953.1:g.22856G>A
NM_001142281.2:c.555-99G>A
NC_000011.9:g.118460957G>A
More... 		12/05/2021 intron variant benign SHORT STATURE-MICROGNATHIA SYNDROME
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ARCN1
Accession:NM_001655
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001142281
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425076
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425073
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425078
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425077
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425074
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425079
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425075
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425081
Location:INTRON

Gene Symbol:ARCN1
Accession:NM_001425080
Location:INTRON

Gene Symbol:ARCN1
Accession:NR_189132
Location:INTRON;NON-CODING

Gene Symbol:ARCN1
Accession:NR_189131
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002260429 CLINVAR
dbSNP (RS) rs45600633 CLINVAR
MedGen C4310686 CLINVAR
NCBI Gene ARCN1 CLINVAR
OMIM 600820 CLINVAR
  617164 CLINVAR