rs148117167 Rat Genome Database

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Variant: rs148117167 -  Homo sapiens

RGD ID: 28897508
RS ID: rs148117167
ClinVar ID: CV868345
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BBS1  ZDHHC24  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 66,299,695
GRCh38 11 66,532,224
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024649.5:c.*187C>T
NG_009093.1:g.26577C>T
NC_000011.10:g.66532224C>T
NC_000011.9:g.66299695C>T
More... 		01/13/2018 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:BBS1
Accession:NM_024649
Location:3UTRS;EXON

Gene Symbol:ZDHHC24
Accession:XM_011544893
Location:INTRON

Gene Symbol:ZDHHC24
Accession:NM_001348571
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_047426709
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_011544894
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_047426710
Location:INTRON

Gene Symbol:ZDHHC24
Accession:NM_207340
Location:INTRON

Gene Symbol:ZDHHC24
Accession:XM_005273874
Location:INTRON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001102624 CLINVAR
dbSNP (RS) rs148117167 CLINVAR
MedGen C2936862 CLINVAR
NCBI Gene BBS1 CLINVAR
  ZDHHC24 CLINVAR
OMIM 209900 CLINVAR
  209901 CLINVAR