Variant #0000288939 (NC_000005.9:g.140070850G>T, NM_012208.3:c.-384G>T (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140070850G>T
DNA change (hg38) g.140691265G>T
Published as HARS(NM_002109.6):c.40C>A (p.Q14K), HARS1(NM_002109.6):c.40C>A (p.Q14K)
ISCN -
DB-ID HARS_000020 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) 0.00098 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +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.40C>A r.(?) p.(Gln14Lys)
HARS2 NM_012208.3 ?/. - c.-384G>T r.(?) p.(=)


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