Variant #0000611203 (NC_000007.13:g.76241034_76241036dup, NC_000007.13(NM_012230.3):c.437+5_437+7dup (POMZP3))

Chromosome 7
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.76241034_76241036dup
DNA change (hg38) g.76611717_76611719dup
Published as POMZP3(NM_012230.3):c.437+7_437+8insGGA (p.(=))
ISCN -
DB-ID POMZP3_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 09:57:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMZP3 NM_012230.3 -?/. - c.437+5_437+7dup r.spl? p.?


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