Variant #0000537983 (NC_000009.11:g.33524697G>A, NC_000009.11(NM_001244752.1):c.206+4G>A (ANKRD18B))

Chromosome 9
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.33524697G>A
DNA change (hg38) g.33524699G>A
Published as ANKRD18B(NM_001244752.1):c.206+4G>A (p.?)
ISCN -
DB-ID ANKRD18B_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 2020-06-25 13:07:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD18B NM_001244752.1 -?/. - c.206+4G>A r.spl? p.?


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