Variant #0000830989 (NC_000004.11:g.140258101_140258102del, NM_057175.3:c.239_240del (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.140258101_140258102del
DNA change (hg38) -
Published as -
ISCN -
DB-ID NAA15_000008 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs779009256
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-12-23 09:16:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAA15 NM_057175.3 +/. - c.239_240del r.(?) p.(His80ArgfsTer17)


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