Variant #0000574463 (NC_000023.10:g.153197564G>A, NM_003491.3:c.346C>T (NAA10))

Chromosome X
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.153197564G>A
DNA change (hg38) g.153932111G>A
Published as NAA10(NM_003491.4):c.346C>T (p.R116W)
ISCN -
DB-ID NAA10_000002 See all 6 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RENBP NM_002910.5 +?/. - c.*3175C>T r.(=) p.(=)
NAA10 NM_003491.3 +?/. - c.346C>T r.(?) p.(Arg116Trp)


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