Variant #0001045490 (NC_000013.10:g.101727009G>A, NM_052867.2:c.3959C>T (NALCN))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.101727009G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NALCN_000103
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2033130135
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-25 21:25:02 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NALCN NM_052867.2 +?/. - c.3959C>T r.(?) p.(Thr1320Met)


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