Variant #0000247389 (NC_000016.9:g.70316567A>G, AARS(NM_001605.2):c.100T>C)

Chromosome 16
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.70316567A>G
DNA change (hg38) g.70282664A>G
Published as AARS(NM_001605.2):c.100T>C (p.L34=)
ISCN -
DB-ID AARS_000021
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AARS NM_001605.2 -?/. - c.100T>C r.(?) p.(Leu34=)