Variant #0000852299 (NC_000009.11:g.712727C>A, NM_015158.3:c.1961C>A (KANK1))

Chromosome 9
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.712727C>A
DNA change (hg38) -
Published as KANK1(NM_015158.3):c.1961C>A (p.(Ala654Asp)), KANK1(NM_015158.4):c.1961C>A (p.A654D)
ISCN -
DB-ID KANK1_000076 See all 2 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) 0.00095 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 2022-05-09 15:40:45 +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     
KANK1 NM_015158.3 -?/. - c.1961C>A r.(?) p.(Ala654Asp)


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