Variant #0000802758 (NC_000006.11:g.88226558del, NM_020320.3:c.1554del (RARS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88226558del
DNA change (hg38) -
Published as RARS2(NM_001350508.1):c.1029delC (p.R344Gfs*8)
ISCN -
DB-ID RARS2_000053
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 2021-09-17 14:40:49 +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     
SLC35A1 NM_001168398.1 +/. - c.*5314del r.(?) p.(=)
RARS2 NM_020320.3 +/. - c.1554del r.(?) p.(Arg519Glyfs*8)


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