Variant #0000855660 (NC_000019.9:g.50098633C>T, NM_020719.1:c.1041C>T (PRR12))

Chromosome 19
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.50098633C>T
DNA change (hg38) -
Published as PRR12(NM_020719.2):c.1041C>T (p.S347=)
ISCN -
DB-ID PRR12_000059
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) Retrieve
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.*4987C>T r.(=) p.(=)
PRR12 NM_020719.1 -?/. - c.1041C>T r.(?) p.(Ser347=)


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