Variant #0001030009 (NC_000008.10:g.41580711G>A, NM_000037.3:c.841C>T (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.41580711G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ANK1_000182
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1829712320
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-20 16:00:01 +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     
ANK1 NM_000037.3 +/. - c.841C>T r.(?) p.(Arg281Ter)


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