Variant #0000534789 (NC_000008.10:g.41573269_41573278del, NM_000037.3:c.1495_1504del (ANK1))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41573269_41573278del
DNA change (hg38) g.41715751_41715760del
Published as ANK1(NM_001142446.2):c.1594_1603delGCCACCACCG (p.A532Pfs*31)
ISCN -
DB-ID ANK1_000131
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +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     
ANK1 NM_000037.3 +/. - c.1495_1504del r.(?) p.(Ala499ProfsTer31)


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