Variant #0000803908 (NC_000009.11:g.133557026_133557028dup, NM_021619.2:c.1074_1076dup (PRDM12))

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.133557026_133557028dup
DNA change (hg38) -
Published as PRDM12(NM_021619.2):c.1074_1076dupCGC (p.A359dup), PRDM12(NM_021619.3):c.1074_1076dupCGC (p.A359dup)
ISCN -
DB-ID PRDM12_000012 See all 3 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) 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM12 NM_021619.2 -/. - c.1074_1076dup r.(?) p.(Ala359dup)


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