Variant #0000910722 (NC_000001.10:g.10042688G>A, NM_022787.3:c.769G>A (NMNAT1))

Chromosome 1
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.10042688G>A
DNA change (hg38) -
Published as NMNAT1(NM_001297778.1):c.769G>A (p.E257K), NMNAT1(NM_022787.3):c.769G>A (p.E257K, p.(Glu257Lys))
ISCN -
DB-ID NMNAT1_000002 See all 108 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) 0.0007 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NMNAT1 NM_022787.3 +/. - c.769G>A r.(?) p.(Glu257Lys)


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