RGD:28884122 Rat Genome Database

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Variant: RGD:28884122 -  Homo sapiens

RGD ID: 28884122
RS ID: rs138510668
ClinVar ID: CV903291
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ELP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 111,659,331
GRCh38 9 108,897,051
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_251t1:c.2502-13C>T
NM_001330749.2:c.1455-13C>T
NM_001318360.2:c.2160-13C>T
NM_003640.5:c.2502-13C>T
More... 		09/12/2023 intron variant likely benign|uncertain significance FD; Hereditary sensory and autonomic neuropathy 3; Hereditary sensory neuropathy type 3; HSAN 3; HSAN III; HSN 3; NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; none provided; Riley Day syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ELP1
Accession:NM_001330749
Location:INTRON

Gene Symbol:ELP1
Accession:NM_001318360
Location:INTRON

Gene Symbol:ELP1
Accession:NM_003640
Location:INTRON

Gene Symbol:ELP1
Accession:XM_047423991
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001168405 CLINVAR
  RCV003769820 CLINVAR
dbSNP (RS) rs138510668 CLINVAR
MedGen C0013364 CLINVAR
  C3661900 CLINVAR
NCBI Gene ELP1 CLINVAR
OMIM 223900 CLINVAR
  603722 CLINVAR
SNOMED CT 29159009 CLINVAR