ClinVar Miner

Variants in gene FOXP1 with conflicting interpretations

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Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
213 10 0 11 4 0 3 16

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 4 2 0 0
likely pathogenic 4 0 0 1 0
uncertain significance 2 0 0 3 2
likely benign 0 1 3 0 7
benign 0 0 2 7 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
NM_001349338.3(FOXP1):c.1321_1324del (p.Asp441fs)
NM_032682.5(FOXP1):c.1652+5G>A rs794727216
NM_032682.5(FOXP1):c.1890-5T>C rs187666567
NM_032682.6(FOXP1):c.1217C>G (p.Thr406Ser) rs200355554
NM_032682.6(FOXP1):c.123G>A (p.Thr41=) rs201155996
NM_032682.6(FOXP1):c.1240_1241del (p.Leu414fs) rs1064793130
NM_032682.6(FOXP1):c.13T>C (p.Ser5Pro) rs762898505
NM_032682.6(FOXP1):c.1541G>A (p.Arg514His) rs797045586
NM_032682.6(FOXP1):c.1574G>A (p.Arg525Gln) rs1553663084
NM_032682.6(FOXP1):c.1630C>T (p.Arg544Ter) rs1559602356
NM_032682.6(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680
NM_032682.6(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845
NM_032682.6(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892
NM_032682.6(FOXP1):c.1825G>A (p.Ala609Thr) rs147537388
NM_032682.6(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.6(FOXP1):c.643C>G (p.Pro215Ala) rs146606219

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