Variant #0000965700 (NC_000010.10:g.27306492A>G, NM_014915.2:c.4445T>C (ANKRD26))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27306492A>G
DNA change (hg38) -
Published as ANKRD26(NM_001256053.1):c.4442T>C (p.(Ile1481Thr)), ANKRD26(NM_014915.2):c.4445T>C (p.I1482T), ANKRD26(NM_014915.3):c.4445T>C (p.I1482T)
ISCN -
DB-ID ANKRD26_000012 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) 0.00426 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD26 NM_014915.2 -/. - c.4445T>C r.(?) p.(Ile1482Thr)


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