Variant #0000519976 (NC_000003.11:g.46937272G>C, NM_000316.2:c.226G>C (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.46937272G>C
DNA change (hg38) g.46895782G>C
Published as PTH1R(NM_000316.2):c.226G>C (p.G76R), PTH1R(NM_000316.3):c.226G>C (p.G76R)
ISCN -
DB-ID PTH1R_000037 See all 2 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) 0.00042 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 2021-09-17 14:40:49 +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.226G>C r.(?) p.(Gly76Arg)


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