Variant #0000610548 (NC_000006.11:g.88224146A>G, NM_020320.3:c.1722T>C (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.88224146A>G
DNA change (hg38) g.87514428A>G
Published as RARS2(NM_001350508.2):c.1197T>C (p.P399=)
ISCN -
DB-ID RARS2_000044
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*2902A>G r.(=) p.(=)
RARS2 NM_020320.3 -?/. - c.1722T>C r.(?) p.(Pro574=)


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