Variant #0000655101 (NC_000004.11:g.140272692T>C, NM_057175.3:c.941T>C (NAA15))

Chromosome 4
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.140272692T>C
DNA change (hg38) g.139351538T>C
Published as NAA15(NM_057175.4):c.941T>C (p.L314P), NAA15(NM_057175.5):c.941T>C (p.L314P)
ISCN -
DB-ID NAA15_000020 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAA15 NM_057175.3 +?/. - c.941T>C r.(?) p.(Leu314Pro)


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