Variant #0000888655 (NC_000009.11:g.133557014_133557028del, NM_021619.2:c.1062_1076del (PRDM12))

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.133557014_133557028del
DNA change (hg38) -
Published as PRDM12(NM_021619.3):c.1062_1076delCGCCGCCGCCGCCGC (p.A355_A359del)
ISCN -
DB-ID PRDM12_000018
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM12 NM_021619.2 -?/. - c.1062_1076del r.(?) p.(Ala355_Ala359del)


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