Variant #0000657226 (NC_000013.10:g.101710337G>A, NM_052867.2:c.4977C>T (NALCN))

Chromosome 13
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.101710337G>A
DNA change (hg38) g.101057985G>A
Published as NALCN(NM_001350748.1):c.5064C>T (p.D1688=)
ISCN -
DB-ID NALCN_000044
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) 0.00307 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.4977C>T r.(?) p.(Asp1659=)
NALCN-AS1 NR_047687.1 -?/. - n.1545G>A r.(?) -


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