Variant #0000253828 (NC_000009.11:g.114341254del, NM_001007169.2:c.*2560del (ZNF483))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.114341254del
DNA change (hg38) g.111578974del
Published as PTGR1(NM_001146108.2):c.496-9delT
ISCN -
DB-ID PTGR1_000004
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF483 NM_001007169.2 -/. - c.*2560del r.(?) p.(=)
PTGR1 NM_001146108.1 -/. - c.496-9del r.(=) p.(=)


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