Variant #0000246659 (NC_000007.13:g.30655580A>G, NM_002047.2:c.1100A>G (GARS))

Chromosome 7
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.30655580A>G
DNA change (hg38) g.30615964A>G
Published as GARS1(NM_001316772.1):c.938A>G (p.N313S), GARS1(NM_002047.4):c.1100A>G (p.N367S)
ISCN -
DB-ID GARS_000035
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) 0.00025 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GARS NM_002047.2 ?/. - c.1100A>G r.(?) p.(Asn367Ser)


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