Variant #0000538603 (NC_000009.11:g.88611437A>G, NM_024635.3:c.1001A>G (NAA35))

Chromosome 9
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.88611437A>G
DNA change (hg38) g.85996522A>G
Published as NAA35(NM_001321882.1):c.1001A>G (p.D334G), NAA35(NM_024635.3):c.1001A>G (p.(Asp334Gly))
ISCN -
DB-ID NAA35_000001 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) 0.0005 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAA35 NM_024635.3 -?/. - c.1001A>G r.(?) p.(Asp334Gly)


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