Variant #0000277542 (NC_000005.9:g.140056377C>T, NM_012208.3:c.-14857C>T (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.140056377C>T
DNA change (hg38) g.140676792C>T
Published as HARS1(NM_002109.6):c.1056G>A (p.L352=)
ISCN -
DB-ID HARS_000011
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 ?/. - c.1056G>A r.(?) p.(Leu352=)
HARS2 NM_012208.3 ?/. - c.-14857C>T r.(?) p.(=)
WDR55 NM_017706.4 ?/. - c.*7138C>T r.(=) p.(=)
DND1 NM_194249.2 ?/. - c.-3250G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.