RGD:11630717 Rat Genome Database

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Variant: RGD:11630717 -  Homo sapiens

RGD ID: 11630717
RS ID: rs759086924
ClinVar ID: CV352187
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PHEX  PTCHD1-AS  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 22,266,458
GRCh38 X 22,248,341
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
NG_007563.2:g.220538A>G
NC_000023.11:g.22248341A>G
NC_000023.10:g.22266458A>G
NM_000444.4:c.*388A>G
More... 		01/13/2018 3 prime utr variant benign|likely benign childhood Hypophosphatemia, vitamin D-resistant rickets; Hypophosphatemic Rickets, X-Linked Dominant; HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; Vitamin D-resistant rickets, X-linked
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PHEX
Accession:NM_001282754
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:XM_011545536
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:NM_000444
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:XM_017029579
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:XM_024452390
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:XM_011545533
Location:3UTRS;EXON

Gene Symbol:PHEX
Accession:XM_047442159
Location:INTRON

Gene Symbol:PTCHD1-AS
Accession:NR_073010
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000356831 CLINVAR
dbSNP (RS) rs759086924 CLINVAR
MedGen C0733682 CLINVAR
NCBI Gene PHEX CLINVAR
  PTCHD1-AS CLINVAR
OMIM 300550 CLINVAR
  307800 CLINVAR
SNOMED CT 82236004 CLINVAR