ClinVar Miner

Variants in gene FANCM 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
150 24 0 23 11 1 1 32

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 risk factor
pathogenic 0 2 1 0 0 1
likely pathogenic 2 0 0 0 0 1
uncertain significance 1 0 0 8 6 0
likely benign 0 0 8 0 21 0
benign 0 0 6 21 0 0
risk factor 1 1 0 0 0 0

All variants with conflicting interpretations #

Total variants: 32
Download table as spreadsheet
HGVS dbSNP
NM_020937.3(FANCM):c.1040C>T (p.Pro347Leu) rs151071546
NM_020937.3(FANCM):c.1041G>A (p.Pro347=) rs140998495
NM_020937.3(FANCM):c.1397-3_1397-2delTA rs112326758
NM_020937.3(FANCM):c.1491dupA (p.Gln498Thrfs) rs797045116
NM_020937.3(FANCM):c.171G>C (p.Leu57Phe) rs142007602
NM_020937.3(FANCM):c.1964A>G (p.Asn655Ser) rs61753893
NM_020937.3(FANCM):c.2190A>G (p.Gln730=) rs117392855
NM_020937.3(FANCM):c.229A>G (p.Thr77Ala) rs61746895
NM_020937.3(FANCM):c.2445G>A (p.Ser815=) rs61745871
NM_020937.3(FANCM):c.2670T>C (p.Phe890=) rs8017226
NM_020937.3(FANCM):c.2749A>G (p.Ile917Val) rs148871932
NM_020937.3(FANCM):c.3040G>T (p.Gly1014Cys) rs77532752
NM_020937.3(FANCM):c.3758A>G (p.Asn1253Ser) rs45604036
NM_020937.3(FANCM):c.3863A>G (p.Asn1288Ser) rs116519044
NM_020937.3(FANCM):c.4222+7T>G rs148675704
NM_020937.3(FANCM):c.4378A>G (p.Ile1460Val) rs78211950
NM_020937.3(FANCM):c.4563A>C (p.Glu1521Asp) rs113986680
NM_020937.3(FANCM):c.4709G>A (p.Arg1570His) rs201803784
NM_020937.3(FANCM):c.4799C>T (p.Thr1600Ile) rs61746943
NM_020937.3(FANCM):c.4878T>C (p.Asp1626=) rs150389713
NM_020937.3(FANCM):c.4931G>A (p.Arg1644Gln) rs138151018
NM_020937.3(FANCM):c.5101C>T (p.Gln1701Ter) rs147021911
NM_020937.3(FANCM):c.5142G>A (p.Ala1714=) rs111894696
NM_020937.3(FANCM):c.5190G>A (p.Gln1730=) rs7142192
NM_020937.3(FANCM):c.5224A>G (p.Ile1742Val) rs143662421
NM_020937.3(FANCM):c.527C>T (p.Thr176Ile) rs77374493
NM_020937.3(FANCM):c.5434C>G (p.Pro1812Ala) rs3736772
NM_020937.3(FANCM):c.5627A>G (p.Asn1876Ser) rs45557033
NM_020937.3(FANCM):c.5656C>T (p.His1886Tyr) rs79343837
NM_020937.3(FANCM):c.5791C>T (p.Arg1931Ter) rs144567652
NM_020937.3(FANCM):c.6141T>C (p.Asp2047=) rs8018014
NM_020937.3(FANCM):c.926A>C (p.Glu309Ala) rs143006771

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