ClinVar Miner

Variants in gene FYCO1 with conflicting interpretations

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 Variants with at least 2 submissions 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 kind of conflict
131 15 0 11 7 0 0 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.

uncertain significance likely benign benign
uncertain significance 0 5 4
likely benign 5 0 11
benign 4 11 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_024513.4(FYCO1):c.1439C>T (p.Thr480Met) rs146711260
NM_024513.4(FYCO1):c.1474C>T (p.Arg492Trp) rs143704916
NM_024513.4(FYCO1):c.1843C>T (p.Arg615Trp) rs149507450
NM_024513.4(FYCO1):c.2179C>A (p.His727Asn) rs36014492
NM_024513.4(FYCO1):c.2980G>A (p.Glu994Lys) rs34801630
NM_024513.4(FYCO1):c.3001_3003delinsGAA (p.Asn1001Glu) rs71622515
NM_024513.4(FYCO1):c.3419G>A (p.Arg1140Gln) rs41289620
NM_024513.4(FYCO1):c.3705C>A (p.Gly1235=) rs367690473
NM_024513.4(FYCO1):c.3779C>G (p.Pro1260Arg) rs144182297
NM_024513.4(FYCO1):c.3789A>G (p.Thr1263=) rs41289618
NM_024513.4(FYCO1):c.3825G>A (p.Pro1275=) rs748985200
NM_024513.4(FYCO1):c.4086G>A (p.Glu1362=) rs137986696
NM_024513.4(FYCO1):c.4319C>T (p.Thr1440Ile) rs41289612
NM_024513.4(FYCO1):c.713A>C (p.Glu238Ala) rs117543659
NM_024513.4(FYCO1):c.753G>T (p.Glu251Asp) rs3821885
NM_024513.4(FYCO1):c.845G>A (p.Arg282His) rs9875356

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