Variant #0000689441 (NC_000005.9:g.140056935A>G, NM_012208.3:c.-14299A>G (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.140056935A>G
DNA change (hg38) -
Published as HARS1(NM_001258041.3):c.740T>C (p.I247T)
ISCN -
DB-ID DND1_000016
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 ?/. - c.800T>C r.(?) p.(Ile267Thr)
HARS2 NM_012208.3 ?/. - c.-14299A>G r.(?) p.(=)
WDR55 NM_017706.4 ?/. - c.*7696A>G r.(=) p.(=)
DND1 NM_194249.2 ?/. - c.-3808T>C r.(?) p.(=)


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