Variant #0000323668 (NC_000014.8:g.50092466_50092470del, NM_001083908.1:c.2163_2167del (DNAAF2))

Chromosome 14
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.50092466_50092470del
DNA change (hg38) g.49625748_49625752del
Published as DNAAF2(NM_001083908.1):c.2163_2167del (p.(Asn721LysfsTer7))
ISCN -
DB-ID DNAAF2_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAAF2 NM_001083908.1 +?/. - c.2163_2167del r.(?) p.(Asn721LysfsTer7)
MGAT2 NM_002408.3 +?/. - c.*3136_*3140del r.(=) p.(=)


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