Variant #0000323461 (NC_000013.10:g.101707691_101707694dup, NM_052867.2:c.5173_5176dup (NALCN))

Chromosome 13
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.101707691_101707694dup
DNA change (hg38) g.101055339_101055342dup
Published as NALCN(NM_052867.2):c.5173_5176dupACTG (p.(Val1726AspfsTer10))
ISCN -
DB-ID NALCN_000007
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_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 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     
NALCN NM_052867.2 ?/. - c.5173_5176dup r.(?) p.(Val1726AspfsTer10)
NALCN-AS1 NR_047687.1 ?/. - n.663_666dup r.(?) -


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