Variant #0000855661 (NC_000019.9:g.50098646A>C, NM_020719.1:c.1054A>C (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.50098646A>C
DNA change (hg38) -
Published as PRR12(NM_020719.2):c.1054A>C (p.S352R)
ISCN -
DB-ID PRR12_000060
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) 9.0E-5 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRRG2 NM_000951.2 ?/. - c.*5000A>C r.(=) p.(=)
PRR12 NM_020719.1 ?/. - c.1054A>C r.(?) p.(Ser352Arg)


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