Variant #0001000392 (NC_000013.10:g.101710377G>A, NM_052867.2:c.4937C>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.101710377G>A
DNA change (hg38) -
Published as NALCN(NM_052867.2):c.4937C>T (p.(Thr1646Met)), NALCN(NM_052867.4):c.4937C>T (p.T1646M)
ISCN -
DB-ID NALCN_000085 See all 2 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NALCN NM_052867.2 -?/. - c.4937C>T r.(?) p.(Thr1646Met)
NALCN-AS1 NR_047687.1 -?/. - n.1585G>A r.(?) -


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