Variant #0000246384 (NC_000005.9:g.140057256A>G, NM_012208.3:c.-13978A>G (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140057256A>G
DNA change (hg38) g.140677671A>G
Published as HARS1(NM_002109.6):c.713T>C (p.V238A)
ISCN -
DB-ID HARS_000003 See all 4 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) 1.0E-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 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.713T>C r.(?) p.(Val238Ala)
HARS2 NM_012208.3 -?/. - c.-13978A>G r.(?) p.(=)
WDR55 NM_017706.4 -?/. - c.*8017A>G r.(=) p.(=)
DND1 NM_194249.2 -?/. - c.-4129T>C r.(?) p.(=)


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