Variant #0000721137 (NC_000006.11:g.88299673C>T, NM_020320.3:c.3G>A (RARS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88299673C>T
DNA change (hg38) -
Published as RARS2(NM_020320.4):c.3G>A (p.M1?)
ISCN -
DB-ID ORC3_000013 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ORC3 NM_001197259.1 +?/. - c.-545C>T r.(?) p.(=)
RARS2 NM_020320.3 +?/. - c.3G>A r.(?) p.(Met1?)


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