Variant #0000520158 (NC_000003.11:g.49136126C>T, NM_017730.2:c.-4863G>A (QRICH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49136126C>T
DNA change (hg38) g.49098693C>T
Published as QARS1(NM_005051.3):c.1864-1G>A
ISCN -
DB-ID QRICH1_000003
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QARS NM_005051.1 +?/. - c.1864-1G>A r.spl? p.?
QRICH1 NM_017730.2 +?/. - c.-4863G>A r.(?) p.(=)


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