Variant #0000524460 (NC_000005.9:g.140062794dup, NM_012208.3:c.-8440dup (HARS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.140062794dup
DNA change (hg38) g.140683209dup
Published as HARS(NM_002109.6):c.191dupA (p.D64Efs*3)
ISCN -
DB-ID HARS2_000010
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.191dup r.(?) p.(Asp64GlufsTer3)
HARS2 NM_012208.3 +?/. - c.-8440dup r.(?) p.(=)


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