Variant #0000950933 (NC_000017.10:g.44791279C>T, NM_006178.3:c.1688C>T (NSF))

Chromosome 17
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.44791279C>T
DNA change (hg38) -
Published as NSF(NM_006178.3):c.1688C>T (p.(Pro563Leu)), NSF(NM_006178.4):c.1688C>T (p.P563L)
ISCN -
DB-ID NSF_000005 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NSF NM_006178.3 +/. - c.1688C>T r.(?) p.(Pro563Leu)


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