Variant #0000926377 (NC_000016.9:g.89371724G>A, NM_013275.5:c.116C>T (ANKRD11))

Chromosome 16
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.89371724G>A
DNA change (hg38) -
Published as ANKRD11(NM_001256182.2):c.116C>T (p.T39I), ANKRD11(NM_013275.6):c.116C>T (p.(Thr39Ile), p.T39I)
ISCN -
DB-ID ANKRD11_000249 See all 3 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) 0.00015 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.116C>T r.(?) p.(Thr39Ile)


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