ClinVar Miner

Variants in gene MET with conflicting interpretations

See also:
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
1415 28 7 16 16 0 0 27

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 4 11 10
likely benign 11 0 16
benign 10 16 3

All variants with conflicting interpretations #

Total variants: 27
Download table as spreadsheet
HGVS dbSNP
NM_000245.4(MET):c.-14-4G>A rs144126521
NM_000245.4(MET):c.1019A>G (p.Asp340Gly) rs200690492
NM_000245.4(MET):c.1039G>A (p.Ala347Thr) rs200074800
NM_000245.4(MET):c.1076G>A (p.Arg359Gln) rs201274041
NM_000245.4(MET):c.110T>C (p.Val37Ala) rs201315884
NM_000245.4(MET):c.1124A>G (p.Asn375Ser) rs33917957
NM_000245.4(MET):c.1306G>C (p.Glu436Gln) rs200740468
NM_000245.4(MET):c.1715G>A (p.Ser572Asn) rs199771406
NM_000245.4(MET):c.1932C>T (p.His644=) rs45520237
NM_000245.4(MET):c.2584-7del rs587780736
NM_000245.4(MET):c.2715C>T (p.Ser905=) rs45572835
NM_000245.4(MET):c.2908C>T (p.Arg970Cys) rs34589476
NM_000245.4(MET):c.2975C>T (p.Thr992Ile) rs56391007
NM_000245.4(MET):c.36C>T (p.Leu12=) rs188625702
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987
NM_000245.4(MET):c.4087G>A (p.Ala1363Thr) rs45578433
NM_000245.4(MET):c.4105T>C (p.Leu1369=) rs45575438
NM_000245.4(MET):c.467C>T (p.Ser156Leu) rs56311081
NM_000245.4(MET):c.504G>T (p.Glu168Asp) rs55985569
NM_000245.4(MET):c.607T>A (p.Ser203Thr) rs200861145
NM_000245.4(MET):c.654G>A (p.Arg218=) rs35284565
NM_000245.4(MET):c.689C>T (p.Thr230Met) rs587780740
NM_000245.4(MET):c.71G>A (p.Gly24Glu) rs180985111
NM_000245.4(MET):c.789G>A (p.Thr263=) rs554190225
NM_000245.4(MET):c.948A>G (p.Ile316Met) rs35225896
NM_000245.4(MET):c.959C>T (p.Ala320Val) rs35776110
NM_000245.4(MET):c.967A>G (p.Ser323Gly) rs201467281

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