Variant #0000568002 (NC_000019.9:g.50091849C>T, NM_020719.1:c.-3063C>T (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.50091849C>T
DNA change (hg38) g.49588592C>T
Published as PRRG2(NM_001316335.1):c.328C>T (p.R110C)
ISCN -
DB-ID PRR12_000009
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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.397C>T r.(?) p.(Arg133Cys)
PRR12 NM_020719.1 ?/. - c.-3063C>T r.(?) p.(=)


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