Variant #0000559898 (NC_000016.9:g.89351286_89351300del, NM_013275.5:c.1652_1666del (ANKRD11))

Chromosome 16
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.89351286_89351300del
DNA change (hg38) g.89284878_89284892del
Published as ANKRD11(NM_001256182.2):c.1652_1666delGGAAAACCATTTCTT (p.W551_S555del)
ISCN -
DB-ID ANKRD11_000237
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD11 NM_013275.5 ?/. - c.1652_1666del r.(?) p.(Trp551_Ser555del)


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