Variant #0000973893 (NC_000001.10:g.33502381G>C, NM_001625.3:c.49C>G (AK2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.33502381G>C
DNA change (hg38) -
Published as AK2(NM_001319141.1):c.49C>G (p.R17G), AK2(NM_001625.4):c.49C>G (p.(Arg17Gly), p.R17G)
ISCN -
DB-ID AK2_000015 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) 0.00114 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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.49C>G r.(?) p.(Arg17Gly)


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