Variant #0000529977 (NC_000006.11:g.88221114C>T, NM_020320.3:c.*3017G>A (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.88221114C>T
DNA change (hg38) g.87511396C>T
Published as SLC35A1(NM_001168398.1):c.710-3C>T (p.?)
ISCN -
DB-ID RARS2_000031
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 15:18:47 +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.710-3C>T r.spl? p.?
RARS2 NM_020320.3 -?/. - c.*3017G>A r.(=) p.(=)


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