Variant #0000982084 (NC_000016.9:g.75669880G>A, NM_005548.2:c.599C>T (KARS))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75669880G>A
DNA change (hg38) -
Published as KARS(NM_005548.3):c.599C>T (p.(Pro200Leu)), KARS1(NM_001130089.2):c.683C>T (p.P228L)
ISCN -
DB-ID KARS_000041 See all 9 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) 0.00014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KARS NM_005548.2 +/. - c.599C>T r.(?) p.(Pro200Leu)


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