Variant #0000717445 (NC_000001.10:g.33502405C>T, NM_001625.3:c.25G>A (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.33502405C>T
DNA change (hg38) -
Published as AK2(NM_001199199.1):c.25G>A (p.(Glu9Lys)), AK2(NM_001319141.1):c.25G>A (p.E9K), AK2(NM_001625.4):c.25G>A (p.E9K)
ISCN -
DB-ID AK2_000025 See all 3 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) 0.00057 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AK2 NM_001625.3 -?/. - c.25G>A r.(?) p.(Glu9Lys)


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