Variant #0000304525 (NC_000009.11:g.127269524_127269527del, NC_000009.11(NM_004959.4):c.-16+3_-16+6del (NR5A1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.127269524_127269527del
DNA change (hg38) g.124507245_124507248del
Published as NR5A1(NM_004959.4):c.-16+3_-16+6delAAGT
ISCN -
DB-ID NR5A1_000020
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 2020-06-25 18:16:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR5A1 NM_004959.4 ?/. - c.-16+3_-16+6del r.spl? p.?


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