Variant #0000678833 (NC_000010.10:g.27328937C>G, NM_014915.2:c.2332G>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.27328937C>G
DNA change (hg38) -
Published as ANKRD26(NM_014915.2):c.2332G>C (p.E778Q, p.(Glu778Gln)), ANKRD26(NM_014915.3):c.2332G>C (p.E778Q)
ISCN -
DB-ID ANKRD26_000028 See all 4 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) 0.00225 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD26 NM_014915.2 -?/. - c.2332G>C r.(?) p.(Glu778Gln)


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