Variant #0000655305 (NC_000005.9:g.140073883G>A, NC_000005.9(NM_012208.3):c.399+18G>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.140073883G>A
DNA change (hg38) g.140694298G>A
Published as HARS2(NM_012208.4):c.399+18G>A
ISCN -
DB-ID HARS2_000002 See all 2 reported entries
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) 0.23767 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.-2994C>T r.(?) p.(=)
HARS2 NM_012208.3 -/. - c.399+18G>A r.(=) p.(=)
ZMAT2 NM_144723.1 -/. - c.-6163G>A r.(?) p.(=)


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