All variants in the AARS gene

Information The variants shown are described using the NM_001605.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. - c.2900A>T r.(?) p.(Lys967Met) - benign g.70286631T>A g.70252728T>A AARS(NM_001605.2):c.2900A>T (p.K967M) - AARS_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
-?/. - c.2900A>T r.(?) p.(Lys967Met) - likely benign g.70286631T>A g.70252728T>A AARS(NM_001605.2):c.2900A>T (p.K967M) - AARS_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
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