RGD:152069175 Rat Genome Database

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Variant: RGD:152069175 -  Homo sapiens

RGD ID: 152069175
RS ID: rs1042120764
ClinVar ID: CV1535331
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124904198  RPE65  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 68,897,068
GRCh38 1 68,431,385
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000329.3:c.1244-9A>G
NG_008472.2:g.23575A>G
NC_000001.11:g.68431385T>C
NC_000001.10:g.68897068T>C
 09/15/2021 intron variant likely benign AMAUROSIS CONGENITA OF LEBER II; Amaurosis congenita of Leber, type 2; Retinitis pigmentosa 20; RP 20; RPE65-Related Leber Congenital Amaurosis
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RPE65
Accession:NM_001406857
Location:INTRON

Gene Symbol:RPE65
Accession:NM_001406860
Location:INTRON

Gene Symbol:RPE65
Accession:NM_001406859
Location:INTRON

Gene Symbol:RPE65
Accession:NM_000329
Location:INTRON

Gene Symbol:RPE65
Accession:NM_001406856
Location:INTRON

Gene Symbol:RPE65
Accession:NM_001406853
Location:INTRON

Gene Symbol:LOC124904198
Accession:XR_007066164
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002091349 CLINVAR
dbSNP (RS) rs1042120764 CLINVAR
MedGen C1859844 CLINVAR
NCBI Gene RPE65 CLINVAR
OMIM 180069 CLINVAR
  204100 CLINVAR
  613794 CLINVAR