Variant #0000802763 (NC_000006.11:g.88299669A>G, NM_020320.3:c.7T>C (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.88299669A>G
DNA change (hg38) -
Published as RARS2(NM_020320.4):c.7T>C (p.C3R), RARS2(NM_020320.5):c.7T>C (p.C3R)
ISCN -
DB-ID ORC3_000010 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ORC3 NM_001197259.1 ?/. - c.-549A>G r.(?) p.(=)
RARS2 NM_020320.3 ?/. - c.7T>C r.(?) p.(Cys3Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.