Variant #0000260119 (NC_000016.9:g.89351049_89351053del, NM_013275.5:c.1903_1907del (ANKRD11))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89351049_89351053del
DNA change (hg38) g.89284641_89284645del
Published as ANKRD11(NM_001256182.1):c.1903_1907del (p.?), ANKRD11(NM_001256182.2):c.1903_1907delAAACA (p.K635Qfs*26), ANKRD11(NM_013275.6):c.1903_1907delAAACA ...
ISCN -
DB-ID ANKRD11_000004 See all 8 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD11 NM_013275.5 +/. - c.1903_1907del r.(?) p.(Lys635GlnfsTer26)


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