Variant #0000255254 (NC_000009.11:g.114337125A>G, NC_000009.11(NM_001007169.2):c.722-1520A>G (ZNF483))

Chromosome 9
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.114337125A>G
DNA change (hg38) g.111574845A>G
Published as PTGR1(NM_001146108.2):c.652-3T>C
ISCN -
DB-ID PTGR1_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 17:47:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF483 NM_001007169.2 -?/. - c.722-1520A>G r.(=) p.(=)
PTGR1 NM_001146108.1 -?/. - c.652-3T>C r.spl? p.?


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