Variant #0001027285 (NC_000019.9:g.856130C>T, NM_001972.2:c.770C>T (ELANE))

Chromosome 19
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.856130C>T
DNA change (hg38) -
Published as ELANE(NM_001972.2):c.770C>T (p.P257L, p.(Pro257Leu))
ISCN -
DB-ID ELANE_000006 See all 4 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) 0.00638 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFD NM_001928.2 -?/. - c.-3560C>T r.(?) p.(=)
ELANE NM_001972.2 -?/. - c.770C>T r.(?) p.(Pro257Leu)


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