Variant #0000722593 (NC_000009.11:g.94991319dup, NM_002161.5:c.3377dup (IARS))

Chromosome 9
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.94991319dup
DNA change (hg38) -
Published as IARS(NM_002161.6):c.3377dup (p.(Asn1126Lysfs*9)), IARS1(NM_013417.4):c.3377dupA (p.N1126Kfs*9)
ISCN -
DB-ID IARS_000004 See all 4 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IARS NM_002161.5 +?/. - c.3377dup r.(?) p.(Asn1126LysfsTer9)


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