Variant #0000609529 (NC_000005.9:g.140075410T>C, NM_012208.3:c.613T>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.140075410T>C
DNA change (hg38) g.140695825T>C
Published as HARS2(NM_012208.3):c.613T>C (p.L205=)
ISCN -
DB-ID ZMAT2_000008
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 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 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.-4521A>G r.(?) p.(=)
HARS2 NM_012208.3 -?/. - c.613T>C r.(?) p.(Leu205=)
ZMAT2 NM_144723.1 -?/. - c.-4636T>C r.(?) p.(=)


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