Variant #0000923170 (NC_000001.10:g.33245085C>T, NM_003680.3:c.1374G>A (YARS))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33245085C>T
DNA change (hg38) -
Published as YARS1(NM_003680.3):c.1374G>A (p.P458=)
ISCN -
DB-ID KIAA1522_000016
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) 0.00095 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YARS NM_003680.3 -?/. - c.1374G>A r.(?) p.(Pro458=)
KIAA1522 NM_020888.2 -?/. - c.*6597C>T r.(=) p.(=)
S100PBP NM_022753.3 -?/. - c.-38325C>T r.(?) p.(=)


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