Variant #0000608742 (NC_000003.11:g.46937345G>A, NM_000316.2:c.299G>A (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.46937345G>A
DNA change (hg38) g.46895855G>A
Published as PTH1R(NM_000316.2):c.299G>A (p.G100D, p.(Gly100Asp)), PTH1R(NM_000316.3):c.299G>A (p.G100D)
ISCN -
DB-ID PTH1R_000038 See all 3 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) 0.00205 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTH1R NM_000316.2 ?/. - c.299G>A r.(?) p.(Gly100Asp)


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