Variant #0000912246 (NC_000005.9:g.140054717G>A, NM_012208.3:c.-16517G>A (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140054717G>A
DNA change (hg38) -
Published as HARS1(NM_001258041.3):c.1136C>T (p.A379V), HARS1(NM_002109.6):c.1196C>T (p.A399V)
ISCN -
DB-ID HARS_000026 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) 0.00103 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
HARS NM_002109.3 -/. - c.1196C>T r.(?) p.(Ala399Val)
HARS2 NM_012208.3 -/. - c.-16517G>A r.(?) p.(=)
WDR55 NM_017706.4 -/. - c.*5478G>A r.(=) p.(=)
DND1 NM_194249.2 -/. - c.-1590C>T r.(?) p.(=)


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