Variant #0000277547 (NC_000005.9:g.140062751G>A, NM_012208.3:c.-8483G>A (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140062751G>A
DNA change (hg38) g.140683166G>A
Published as HARS1(NM_002109.6):c.234C>T (p.D78=)
ISCN -
DB-ID HARS_000016
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) 0.00146 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 -/. - c.234C>T r.(?) p.(Asp78=)
HARS2 NM_012208.3 -/. - c.-8483G>A r.(?) p.(=)


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