Variant #0000306766 (NC_000006.11:g.88224671G>A, NC_000006.11(NM_020320.3):c.1650+4C>T (RARS2))

Chromosome 6
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.88224671G>A
DNA change (hg38) g.87514953G>A
Published as RARS2(NM_020320.4):c.1650+4C>T
ISCN -
DB-ID RARS2_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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 15:19:44 +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.*3427G>A r.(=) p.(=)
RARS2 NM_020320.3 -?/. - c.1650+4C>T r.spl? p.?


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