Variant #0000994697 (NC_000005.9:g.140056997C>G, NM_012208.3:c.-14237C>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.140056997C>G
DNA change (hg38) -
Published as HARS(NM_002109.4):c.738G>C (p.(Trp246Cys))
ISCN -
DB-ID DND1_000023
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS2 NM_012208.3 ?/. - c.-14237C>G r.(?) p.(=)
WDR55 NM_017706.4 ?/. - c.*7758C>G r.(=) p.(=)
DND1 NM_194249.2 ?/. - c.-3870G>C r.(?) p.(=)


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