Genomic variant #0000162915

Individual ID 00100211
Chromosome 3
Allele Paternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.46944033C>G
DNA change (hg38) g.46902543C>G
Published as -
ISCN -
DB-ID PTH1R_000008 See all 3 reported entries
Variant remarks -
Reference PubMed: Bastepe et al. 2004
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Arrate Pereda




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     
PTH1R NM_000316.2 +/. 14 c.1229C>G - r.(?) p.(Thr410Arg) - - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000100615 DNA SEQ peripheral blood - PTH1R 1 Arrate Pereda