Variant #0000655304 (NC_000005.9:g.140057509C>T, NM_012208.3:c.-13725C>T (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.140057509C>T
DNA change (hg38) g.140677924C>T
Published as HARS(NM_001258041.2):c.554G>A (p.G185D), HARS1(NM_002109.6):c.614G>A (p.G205D)
ISCN -
DB-ID DND1_000012 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) 0.00289 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 2020-03-23 16:13:27 +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.614G>A r.(?) p.(Gly205Asp)
HARS2 NM_012208.3 -?/. - c.-13725C>T r.(?) p.(=)
WDR55 NM_017706.4 -?/. - c.*8270C>T r.(=) p.(=)
DND1 NM_194249.2 -?/. - c.-4382G>A r.(?) p.(=)


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