ClinVar Miner

Variants in gene ATL1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP
NM_001127713.1(ATL1):c.1152A>G (p.Pro384=) rs377127492
NM_001127713.1(ATL1):c.1173C>T (p.His391=) rs149340140
NM_001127713.1(ATL1):c.1200G>A (p.Lys400=) rs144792471
NM_001127713.1(ATL1):c.1608T>G (p.Ala536=) rs777479928
NM_001127713.1(ATL1):c.322A>G (p.Thr108Ala) rs112496709
NM_001127713.1(ATL1):c.631-7T>A rs186528086
NM_001127713.1(ATL1):c.756C>T (p.Asn252=) rs771031586
NM_001127713.1(ATL1):c.969G>C (p.Arg323=) rs753145983

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