Variant #0000330182 (NC_000004.11:g.175443507_175443509dup, NC_000004.11(NM_000860.5):c.93+1_93+3dup (HPGD))

Chromosome 4
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.175443507_175443509dup
DNA change (hg38) g.174522356_174522358dup
Published as HPGD(NM_000860.5):c.93+1_93+3dup (p.?)
ISCN -
DB-ID HPGD_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPGD NM_000860.5 -?/. - c.93+1_93+3dup r.spl? p.?


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