ClinVar Miner

Variants in gene NEXMIF 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 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
372 22 0 11 10 0 0 21

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 1 0 0 0
likely pathogenic 1 0 0 0 0
uncertain significance 0 0 0 6 4
likely benign 0 0 6 0 10
benign 0 0 4 10 0

All variants with conflicting interpretations #

Total variants: 21
Download table as spreadsheet
NM_001008537.3(NEXMIF):c.133G>A (p.Ala45Thr) rs199960807
NM_001008537.3(NEXMIF):c.1415C>G (p.Ser472Cys) rs770738202
NM_001008537.3(NEXMIF):c.151C>A (p.Pro51Thr) rs145018752
NM_001008537.3(NEXMIF):c.1882C>T (p.Arg628Ter) rs786205208
NM_001008537.3(NEXMIF):c.206C>T (p.Ser69Phe) rs201351157
NM_001008537.3(NEXMIF):c.2098G>C (p.Val700Leu) rs141776597
NM_001008537.3(NEXMIF):c.2130G>A (p.Lys710=) rs749479992
NM_001008537.3(NEXMIF):c.2373A>C (p.Thr791=) rs61742545
NM_001008537.3(NEXMIF):c.2598C>A (p.Ser866=) rs41298498
NM_001008537.3(NEXMIF):c.2669C>T (p.Pro890Leu) rs377201508
NM_001008537.3(NEXMIF):c.2672A>G (p.Asn891Ser) rs186535459
NM_001008537.3(NEXMIF):c.2895A>G (p.Gln965=) rs1556016407
NM_001008537.3(NEXMIF):c.2951A>G (p.Asn984Ser) rs375623451
NM_001008537.3(NEXMIF):c.3402C>A (p.His1134Gln) rs138632224
NM_001008537.3(NEXMIF):c.3555G>T (p.Gly1185=) rs142714242
NM_001008537.3(NEXMIF):c.3709A>T (p.Met1237Leu) rs61731613
NM_001008537.3(NEXMIF):c.381G>A (p.Glu127=) rs148717498
NM_001008537.3(NEXMIF):c.3823A>G (p.Ser1275Gly) rs201434271
NM_001008537.3(NEXMIF):c.4205A>G (p.Asn1402Ser) rs140532942
NM_001008537.3(NEXMIF):c.4406G>A (p.Arg1469Gln) rs151004644
NM_001008537.3(NEXMIF):c.4509T>C (p.Pro1503=) rs41303725

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