Variant #0000850802 (NC_000005.9:g.140058699C>T, NM_012208.3:c.-12535C>T (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.140058699C>T
DNA change (hg38) -
Published as HARS(NM_002109.4):c.410G>A (p.(Arg137Gln)), HARS(NM_002109.6):c.410G>A (p.R137Q), HARS1(NM_002109.6):c.410G>A (p.R137Q)
ISCN -
DB-ID HARS_000005 See all 8 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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 ?/. - c.410G>A r.(?) p.(Arg137Gln)
HARS2 NM_012208.3 ?/. - c.-12535C>T r.(?) p.(=)


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