Variant #0000521526 (NC_000004.11:g.125593697_125593699del, NC_000004.11(NM_020337.2):c.743-6_743-4del (ANKRD50))

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.125593697_125593699del
DNA change (hg38) g.124672542_124672544del
Published as ANKRD50(NM_001167882.1):c.206-6_206-4del (p.?)
ISCN -
DB-ID ANKRD50_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 14:46:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD50 NM_020337.2 -?/. - c.743-6_743-4del r.spl? p.?


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