Variant #0000336124 (NC_000023.10:g.153200861C>T, NM_003491.3:c.-504G>A (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.153200861C>T
DNA change (hg38) g.153935408C>T
Published as RENBP(NM_002910.5):c.1166-4G>A (p.?)
ISCN -
DB-ID RENBP_000005
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) 0.00697 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-21 14:00:06 +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.1166-4G>A r.spl? p.?
NAA10 NM_003491.3 ?/. - c.-504G>A r.(?) p.(=)


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