ClinVar Miner

Variants in gene MYOM1 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
248 66 0 10 6 0 1 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.

likely pathogenic uncertain significance likely benign benign
likely pathogenic 0 0 0 1
uncertain significance 0 0 5 2
likely benign 0 5 0 10
benign 1 2 10 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_003803.3(MYOM1):c.117C>T (p.Tyr39=) rs375113650
NM_003803.3(MYOM1):c.1900+3A>C rs77613865
NM_003803.3(MYOM1):c.1978C>G (p.Pro660Ala) rs201104206
NM_003803.3(MYOM1):c.2062A>T (p.Thr688Ser) rs188677538
NM_003803.3(MYOM1):c.2384+4A>T rs73373171
NM_003803.3(MYOM1):c.2727G>A (p.Pro909=) rs72860212
NM_003803.3(MYOM1):c.3038C>T (p.Ala1013Val) rs557671408
NM_003803.3(MYOM1):c.3190C>T (p.His1064Tyr) rs755409090
NM_003803.3(MYOM1):c.3308G>A (p.Arg1103Gln) rs186972208
NM_003803.3(MYOM1):c.3539A>G (p.Asp1180Gly) rs188319622
NM_003803.3(MYOM1):c.3548G>A (p.Arg1183Gln) rs147050513
NM_003803.3(MYOM1):c.3572A>G (p.Asn1191Ser) rs200480164
NM_003803.3(MYOM1):c.3639A>G (p.Thr1213=) rs558779097
NM_003803.3(MYOM1):c.4776C>G (p.Leu1592=) rs1143658
NM_003803.3(MYOM1):c.5019C>T (p.Ala1673=) rs199980922
NM_003803.3(MYOM1):c.739G>A (p.Glu247Lys) rs139422575

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