Variant #0000260960 (NC_000004.11:g.114276906G>A, NM_001148.4:c.7132G>A (ANK2))

Chromosome 4
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.114276906G>A
DNA change (hg38) g.113355750G>A
Published as ANK2(NM_001148.4):c.7132G>A (p.E2378K), ANK2(NM_001148.6):c.7132G>A (p.E2378K)
ISCN -
DB-ID ANK2_000064 See all 6 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) 0.00229 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANK2 NM_001148.4 -?/. - c.7132G>A r.(?) p.(Glu2378Lys)


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