Variant #0000677414 (NC_000005.9:g.140056992T>A, NM_012208.3:c.-14242T>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.140056992T>A
DNA change (hg38) -
Published as HARS(NM_001258041.2):c.683A>T (p.E228V)
ISCN -
DB-ID DND1_000015
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 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.743A>T r.(?) p.(Glu248Val)
HARS2 NM_012208.3 ?/. - c.-14242T>A r.(?) p.(=)
WDR55 NM_017706.4 ?/. - c.*7753T>A r.(=) p.(=)
DND1 NM_194249.2 ?/. - c.-3865A>T r.(?) p.(=)


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