ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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NM_001127713.1(ATL1):c.1173C>T (p.His391=) rs149340140
NM_001127713.1(ATL1):c.351G>A (p.Glu117=) rs1060197
NM_001127713.1(ATL1):c.669C>T (p.Tyr223=) rs146975855
NM_001127713.1(ATL1):c.84A>G (p.Pro28=) rs35014209
NM_001127713.1(ATL1):c.991-6T>G rs192428744

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