Variant #0000568008 (NC_000019.9:g.50104825C>A, NM_020719.1:c.4423C>A (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.50104825C>A
DNA change (hg38) g.49601568C>A
Published as PRR12(NM_020719.1):c.4423C>A (p.(Pro1475Thr)), PRR12(NM_020719.3):c.4423C>A (p.P1475T)
ISCN -
DB-ID PRR12_000004 See all 2 reported entries
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) 0.00492 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRR12 NM_020719.1 -?/. - c.4423C>A r.(?) p.(Pro1475Thr)


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