Variant #0000677413 (NC_000005.9:g.140054276C>T, NM_012208.3:c.-16958C>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.140054276C>T
DNA change (hg38) -
Published as HARS(NM_001258041.2):c.1386G>A (p.T462=)
ISCN -
DB-ID DND1_000014
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) 3.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.1446G>A r.(?) p.(Thr482=)
HARS2 NM_012208.3 -?/. - c.-16958C>T r.(?) p.(=)
WDR55 NM_017706.4 -?/. - c.*5037C>T r.(=) p.(=)
DND1 NM_194249.2 -?/. - c.-1149G>A r.(?) p.(=)


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