Variant #0000919619 (NC_000004.11:g.140272760_140272763del, NM_057175.3:c.1009_1012del (NAA15))

Chromosome 4
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.140272760_140272763del
DNA change (hg38) -
Published as -
ISCN -
DB-ID NAA15_000036 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1553996086
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-02-23 16:57:01 +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     
NAA15 NM_057175.3 +/. - c.1009_1012del r.(?) p.(Glu337ArgfsTer5)


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