Variant #0001025736 (NC_000010.10:g.27318285A>G, NM_014915.2:c.3808T>C (ANKRD26))

Chromosome 10
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.27318285A>G
DNA change (hg38) -
Published as ANKRD26(NM_014915.2):c.3808T>C (p.L1270=), ANKRD26(NM_014915.3):c.3808T>C (p.L1270=)
ISCN -
DB-ID ANKRD26_000040 See all 2 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 2025-02-07 18:57:27 +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     
ANKRD26 NM_014915.2 -?/. - c.3808T>C r.(?) p.(Leu1270=)


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