Variant #0000675817 (NC_000001.10:g.33236322G>A, NM_003680.3:c.*5260C>T (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.33236322G>A
DNA change (hg38) -
Published as KIAA1522(NM_020888.3):c.1542G>A (p.V514=)
ISCN -
DB-ID KIAA1522_000021
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +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.*5260C>T r.(=) p.(=)
KIAA1522 NM_020888.2 -?/. - c.1542G>A r.(?) p.(Val514=)
S100PBP NM_022753.3 -?/. - c.-47088G>A r.(?) p.(=)


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