Variant #0000262164 (NC_000001.10:g.33478900T>A, NM_001625.3:c.602A>T (AK2))

Chromosome 1
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.33478900T>A
DNA change (hg38) g.33013299T>A
Published as AK2(NM_001199199.1):c.578A>T (p.(Tyr193Phe)), AK2(NM_013411.3):c.602A>T (p.Y201F)
ISCN -
DB-ID AK2_000008 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AK2 NM_001625.3 -?/. - c.602A>T r.(?) p.(Tyr201Phe)


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