Genomic variant #0000558916

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70285776C>A
DNA change (hg38) -
Published as EXOSC6(NM_058219.2):c.28G>T (p.(Gly10Cys))
ISCN -
DB-ID AARS_000029
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
AARS NM_001605.2 -?/. - c.*848G>T likely benign r.(=) p.(=)
EXOSC6 NM_058219.2 -?/. - c.28G>T likely benign r.(?) p.(Gly10Cys)