Variant #0000326720 (NC_000019.9:g.50098268C>A, NM_020719.1:c.676C>A (PRR12))

Chromosome 19
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.50098268C>A
DNA change (hg38) g.49595011C>A
Published as PRR12(NM_020719.1):c.676C>A (p.(Pro226Thr))
ISCN -
DB-ID PRR12_000002
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) 0.0086 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRRG2 NM_000951.2 ?/. - c.*4622C>A r.(=) p.(=)
PRR12 NM_020719.1 ?/. - c.676C>A r.(?) p.(Pro226Thr)


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