Variant #0000617957 (NC_000019.9:g.860766G>A, NM_001972.2:c.*4602G>A (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.860766G>A
DNA change (hg38) g.860766G>A
Published as CFD(NM_001928.2):c.205G>A (p.(Glu69Lys))
ISCN -
DB-ID CFD_000002 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) 0.00541 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 2019-12-04 15:24:38 +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.205G>A r.(?) p.(Glu69Lys)
ELANE NM_001972.2 -?/. - c.*4602G>A r.(=) p.(=)


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