Variant #0000576021 (NC_000023.10:g.43817823G>C, NM_000266.3:c.69C>G (NDP))

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.43817823G>C
DNA change (hg38) g.43958577G>C
Published as NDP(NM_000266.3):c.69C>G (p.(Asp23Glu)), NDP(NM_000266.4):c.69C>G (p.D23E)
ISCN -
DB-ID NDP_000047 See all 2 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) 0.00144 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDP NM_000266.3 -?/. - c.69C>G r.(?) p.(Asp23Glu)


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