Variant #0000963463 (NC_000005.9:g.140057501G>A, NM_012208.3:c.-13733G>A (HARS2))

Chromosome 5
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.140057501G>A
DNA change (hg38) -
Published as HARS1(NM_002109.6):c.622C>T (p.L208=)
ISCN -
DB-ID DND1_000020
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +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     
HARS2 NM_012208.3 -?/. - c.-13733G>A r.(?) p.(=)
WDR55 NM_017706.4 -?/. - c.*8262G>A r.(=) p.(=)
DND1 NM_194249.2 -?/. - c.-4374C>T r.(?) p.(=)


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