Variant #0000331110 (NC_000006.11:g.88221114_88221124del, NM_020320.3:c.*3007_*3017del (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.88221114_88221124del
DNA change (hg38) g.87511396_87511406del
Published as SLC35A1(NM_001168398.1):c.710-3_717del (p.?)
ISCN -
DB-ID SLC35A1_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.710-3_717del r.spl? p.?
RARS2 NM_020320.3 ?/. - c.*3007_*3017del r.(=) p.(=)


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