Variant #0000503797 (NC_000001.10:g.156214675C>T, NM_199173.4:c.*1722C>T (BGLAP))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156214675C>T
DNA change (hg38) g.156244884C>T
Published as PAQR6(NM_024897.3):c.319G>A (p.G107S)
ISCN -
DB-ID BGLAP_000004
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) 0.00032 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMF1-BGLAP NM_001199661.1 -?/. - c.*1801C>T r.(=) p.(=)
PMF1 NM_007221.3 -?/. - c.*5283C>T r.(=) p.(=)
SMG5 NM_015327.2 -?/. - c.*5703G>A r.(=) p.(=)
PAQR6 NM_024897.2 -?/. - c.319G>A r.(?) p.(Gly107Ser)
TMEM79 NM_032323.2 -?/. - c.-39566C>T r.(?) p.(=)
BGLAP NM_199173.4 -?/. - c.*1722C>T r.(=) p.(=)


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