Variant #0000288933 (NC_000005.9:g.140054277G>A, NM_012208.3:c.-16957G>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.140054277G>A
DNA change (hg38) g.140674692G>A
Published as HARS(NM_002109.6):c.1445C>T (p.T482M)
ISCN -
DB-ID HARS_000008 See all 3 reported entries
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) 0.00063 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 ?/. - c.1445C>T r.(?) p.(Thr482Met)
HARS2 NM_012208.3 ?/. - c.-16957G>A r.(?) p.(=)
WDR55 NM_017706.4 ?/. - c.*5038G>A r.(=) p.(=)
DND1 NM_194249.2 ?/. - c.-1150C>T r.(?) p.(=)


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