Variant #0000519981 (NC_000003.11:g.46939587C>T, NM_000316.2:c.448C>T (PTH1R))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46939587C>T
DNA change (hg38) g.46898097C>T
Published as PTH1R(NM_000316.2):c.448C>T (p.R150C, p.(Arg150Cys)), PTH1R(NM_000316.3):c.448C>T (p.R150C)
ISCN -
DB-ID PTH1R_000041 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00169 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTH1R NM_000316.2 ?/. - c.448C>T r.(?) p.(Arg150Cys)


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