Variant #0000507123 (NC_000001.10:g.33237892T>C, NM_003680.3:c.*3690A>G (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.33237892T>C
DNA change (hg38) g.32772291T>C
Published as KIAA1522(NM_001198972.1):c.2935T>C (p.(Ser979Pro))
ISCN -
DB-ID KIAA1522_000011
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +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.*3690A>G r.(=) p.(=)
KIAA1522 NM_020888.2 -?/. - c.3112T>C r.(?) p.(Ser1038Pro)
S100PBP NM_022753.3 -?/. - c.-45518T>C r.(?) p.(=)


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