Variant #0000331111 (NC_000006.11:g.88226602A>G, NC_000006.11(NM_020320.3):c.1512-4T>C (RARS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.88226602A>G
DNA change (hg38) g.87516884A>G
Published as RARS2(NM_020320.3):c.1512-4T>C (p.?)
ISCN -
DB-ID RARS2_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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 15:20:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35A1 NM_001168398.1 ?/. - c.*5358A>G r.(=) p.(=)
RARS2 NM_020320.3 ?/. - c.1512-4T>C r.spl? p.?


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