Variant #0000524457 (NC_000005.9:g.140059387G>A, NM_012208.3:c.-11847G>A (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140059387G>A
DNA change (hg38) g.140679802G>A
Published as HARS(NM_002109.6):c.382C>T (p.R128C), HARS1(NM_002109.6):c.382C>T (p.R128C)
ISCN -
DB-ID HARS_000013 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) 0.00025 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 ?/. - c.382C>T r.(?) p.(Arg128Cys)
HARS2 NM_012208.3 ?/. - c.-11847G>A r.(?) p.(=)


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