Variant #0000574466 (NC_000023.10:g.153199918A>C, NM_003491.3:c.32T>G (NAA10))

Chromosome X
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.153199918A>C
DNA change (hg38) g.153934465A>C
Published as NAA10(NM_003491.3):c.32T>G (p.L11R)
ISCN -
DB-ID RENBP_000011
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RENBP NM_002910.5 ?/. - c.*821T>G r.(=) p.(=)
NAA10 NM_003491.3 ?/. - c.32T>G r.(?) p.(Leu11Arg)


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