Variant #0000609527 (NC_000005.9:g.140062688T>C, NM_012208.3:c.-8546T>C (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.140062688T>C
DNA change (hg38) g.140683103T>C
Published as HARS(NM_001258041.2):c.297A>G (p.L99=)
ISCN -
DB-ID HARS2_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 -?/. - c.297A>G r.(?) p.(Leu99=)
HARS2 NM_012208.3 -?/. - c.-8546T>C r.(?) p.(=)


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