Variant #0000288934 (NC_000005.9:g.140070876G>T, NM_012208.3:c.-358G>T (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.140070876G>T
DNA change (hg38) g.140691291G>T
Published as HARS(NM_001258040.1):c.14C>A (p.(Ala5Glu)), HARS(NM_002109.6):c.14C>A (p.A5E), HARS1(NM_002109.6):c.14C>A (p.A5E)
ISCN -
DB-ID HARS_000006 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) 0.0054 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.14C>A r.(?) p.(Ala5Glu)
HARS2 NM_012208.3 -/. - c.-358G>T r.(?) p.(=)


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