Variant #0000850364 (NC_000003.11:g.49136630C>A, NM_017730.2:c.-5367G>T (QRICH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49136630C>A
DNA change (hg38) -
Published as QARS1(NM_005051.3):c.1671G>T (p.V557=)
ISCN -
DB-ID QARS_000037
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) 0.00058 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QARS NM_005051.1 -/. - c.1671G>T r.(?) p.(Val557=)
QRICH1 NM_017730.2 -/. - c.-5367G>T r.(?) p.(=)


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