Variant #0000655303 (NC_000005.9:g.140054652G>C, NM_012208.3:c.-16582G>C (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.140054652G>C
DNA change (hg38) g.140675067G>C
Published as HARS1(NM_001258041.3):c.1201C>G (p.L401V)
ISCN -
DB-ID DND1_000013
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) 0.00081 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 2020-03-23 16:13:27 +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.1261C>G r.(?) p.(Leu421Val)
HARS2 NM_012208.3 -/. - c.-16582G>C r.(?) p.(=)
WDR55 NM_017706.4 -/. - c.*5413G>C r.(=) p.(=)
DND1 NM_194249.2 -/. - c.-1525C>G r.(?) p.(=)


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