Variant #0000574464 (NC_000023.10:g.153197573A>G, NC_000023.10(NM_003491.3):c.342-5T>C (NAA10))

Chromosome X
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.153197573A>G
DNA change (hg38) g.153932120A>G
Published as NAA10(NM_003491.3):c.342-5T>C
ISCN -
DB-ID RENBP_000009
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) 0.00011 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-21 13:59:21 +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.*3166T>C r.(=) p.(=)
NAA10 NM_003491.3 -?/. - c.342-5T>C r.spl? p.?


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