Variant #0000148367 (NC_000008.10:g.41571774T>G, NC_000008.10(NM_000037.3):c.1702-2A>C (ANK1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41571774T>G
DNA change (hg38) g.41714256T>G
Published as -
ISCN -
DB-ID ANK1_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MANSOUR-HENDILI
Database submission license No license selected
Created by MANSOUR-HENDILI
Date created 2016-12-08 13:53:38 +01:00 (CET)
Date last edited 2024-03-06 10:04:46 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANK1 NM_000037.3 +?/. - c.1702-2A>C r.spl p.?



Screenings

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