Variant #0000850804 (NC_000005.9:g.140073804G>T, NM_012208.3:c.338G>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.140073804G>T
DNA change (hg38) -
Published as HARS2(NM_001363535.1):c.356G>T (p.G119V)
ISCN -
DB-ID ZMAT2_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) 2.0E-5 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 2022-05-09 15:40:45 +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.338G>T r.(?) p.(Gly113Val)
ZMAT2 NM_144723.1 ?/. - c.-6242G>T r.(?) p.(=)


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