RGD:156132803 Rat Genome Database

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Variant: RGD:156132803 -  Homo sapiens

RGD ID: 156132803
ClinVar ID: CV1977118
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TTC21B  TTC21B-AS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 166,797,520
GRCh38 2 165,941,010
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024753.5:c.710+17T>C
NG_030345.1:g.17829T>C
NC_000002.12:g.165941010A>G
NC_000002.11:g.166797520A>G
 05/27/2022 intron variant likely benign Chondroectodermal dysplasia-like syndrome; Infantile thoracic dystrophy; Jeune syndrome; Jeune's syndrome; juvenile nephronophthisis; Nephronophthisis; Short-rib thoracic dysplasia; Thoracic pelvic phalangeal dystrophy
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:TTC21B
Accession:XM_047445870
Location:5UTRS;EXON

Gene Symbol:TTC21B
Accession:XM_011511871
Location:5UTRS;EXON

Gene Symbol:TTC21B
Accession:XM_011511872
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_017004967
Location:INTRON

Gene Symbol:TTC21B
Accession:NM_024753
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_006712761
Location:INTRON

Gene Symbol:TTC21B-AS1
Accession:NR_038983
Location:INTRON;NON-CODING

Gene Symbol:TTC21B-AS1
Accession:NR_038984
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002593557 CLINVAR
MedGen C0265275 CLINVAR
NCBI Gene TTC21B CLINVAR
  TTC21B-AS1 CLINVAR
OMIM 612014 CLINVAR
SNOMED CT 75049004 CLINVAR