Variant #0000568904 (NC_000019.9:g.860686C>A, NM_001972.2:c.*4522C>A (ELANE))

Chromosome 19
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.860686C>A
DNA change (hg38) g.860686C>A
Published as CFD(NM_001928.2):c.125C>A (p.S42*)
ISCN -
DB-ID CFD_000005 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFD NM_001928.2 +/. - c.125C>A r.(?) p.(Ser42Ter)
ELANE NM_001972.2 +/. - c.*4522C>A r.(=) p.(=)


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