ClinVar Miner

Variants in gene FOXP1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 19
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554 0.00016
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00015
NM_001349338.3(FOXP1):c.13T>C (p.Ser5Pro) rs762898505 0.00012
NM_001349338.3(FOXP1):c.1135G>A (p.Ala379Thr) rs149759021 0.00008
NM_001349338.3(FOXP1):c.107G>A (p.Arg36Gln) rs200643313 0.00005
NM_001349338.3(FOXP1):c.1359G>A (p.Ala453=) rs766683691 0.00004
NM_001349338.3(FOXP1):c.1383C>T (p.Asn461=) rs372403441 0.00004
NM_001349338.3(FOXP1):c.1344G>A (p.Ser448=) rs143503790 0.00003
NM_001349338.3(FOXP1):c.1902C>T (p.His634=) rs749771909 0.00003
NM_001349338.3(FOXP1):c.316G>A (p.Val106Ile) rs755709669 0.00002
NM_001349338.3(FOXP1):c.1964C>T (p.Ala655Val) rs762475508 0.00001
NM_001349338.3(FOXP1):c.321C>T (p.Ile107=) rs747108471 0.00001
NM_001349338.3(FOXP1):c.*1669dup rs886058842
NM_001349338.3(FOXP1):c.*3192del rs535202716
NM_001349338.3(FOXP1):c.*3391TG[10] rs143202281
NM_001349338.3(FOXP1):c.1162A>T (p.Ser388Cys)
NM_001349338.3(FOXP1):c.184C>T (p.Leu62Phe) rs538443416
NM_001349338.3(FOXP1):c.665-7_665-4del rs1453915867
NM_001349338.3(FOXP1):c.728A>G (p.Glu243Gly)

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