Variant #0000727382 (NC_000019.9:g.4229587A>G, NM_133475.1:c.*5085A>G (ANKRD24))

Chromosome 19
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.4229587A>G
DNA change (hg38) -
Published as EBI3(NM_005755.3):c.40A>G (p.S14G)
ISCN -
DB-ID ANKRD24_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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EBI3 NM_005755.2 -?/. - c.40A>G r.(?) p.(Ser14Gly)
ANKRD24 NM_133475.1 -?/. - c.*5085A>G r.(=) p.(=)


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