Variant #0000605687 (NC_000001.10:g.33252687T>C, NC_000001.10(NM_003680.3):c.685-11A>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.33252687T>C
DNA change (hg38) g.32787086T>C
Published as YARS1(NM_003680.3):c.685-11A>G
ISCN -
DB-ID S100PBP_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) 2.0E-5 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 2019-12-04 14:54:23 +01:00 (CET)
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     
YARS NM_003680.3 -?/. - c.685-11A>G r.(=) p.(=)
S100PBP NM_022753.3 -?/. - c.-30723T>C r.(?) p.(=)


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