rs768620927 Rat Genome Database

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Variant: rs768620927 -  Homo sapiens

RGD ID: 152049820
RS ID: rs768620927
ClinVar ID: CV1602539
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BBS1  ZDHHC24  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 66,293,581
GRCh38 11 66,526,110
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001348571.2:c.*21+826G>A
NM_024649.5:c.1111-13C>T
NG_009093.1:g.20463C>T
NC_000011.10:g.66526110C>T
More... 		12/29/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ZDHHC24
Accession:XM_011544894
Location:3UTRS;INTRON

Gene Symbol:ZDHHC24
Accession:NM_001348571
Location:3UTRS;INTRON

Gene Symbol:ZDHHC24
Accession:XM_005273874
Location:3UTRS;INTRON

Gene Symbol:ZDHHC24
Accession:XM_011544893
Location:INTRON

Gene Symbol:BBS1
Accession:NM_024649
Location:INTRON

Gene Symbol:ZDHHC24
Accession:NM_207340
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_047426710
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_047426709
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XR_007062470
Location:INTRON;NON-CODING

Gene Symbol:ZDHHC24
Accession:XR_949860
Location:INTRON;NON-CODING

Gene Symbol:ZDHHC24
Accession:XR_007062471
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002117506 CLINVAR
dbSNP (RS) rs768620927 CLINVAR
MedGen C0752166 CLINVAR
NCBI Gene BBS1 CLINVAR
  ZDHHC24 CLINVAR
OMIM 209901 CLINVAR
SNOMED CT 5619004 CLINVAR