Variant #0000659168 (NC_000023.10:g.153197863G>A, NM_003491.3:c.247C>T (NAA10))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153197863G>A
DNA change (hg38) g.153932410G>A
Published as NAA10(NM_003491.3):c.247C>T (p.R83C), NAA10(NM_003491.4):c.247C>T (p.R83C)
ISCN -
DB-ID NAA10_000006 See all 15 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RENBP NM_002910.5 +/. - c.*2876C>T r.(=) p.(=)
NAA10 NM_003491.3 +/. - c.247C>T r.(?) p.(Arg83Cys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.