ClinVar Miner

Variants in gene MAGEL2 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:

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
1023 242 0 52 58 0 2 101

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 6 1 0 0
likely pathogenic 6 0 1 0 0
uncertain significance 1 1 0 57 12
likely benign 0 0 57 0 46
benign 0 0 12 46 0

All variants with conflicting interpretations #

Total variants: 101
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019066.5(MAGEL2):c.3151C>A (p.Leu1051Ile) rs2233070 0.03565
NM_019066.5(MAGEL2):c.901C>T (p.Pro301Ser) rs138154793 0.01279
NM_019066.5(MAGEL2):c.2611G>T (p.Ala871Ser) rs2233066 0.00969
NM_019066.5(MAGEL2):c.2612C>T (p.Ala871Val) rs74004212 0.00969
NM_019066.5(MAGEL2):c.3229T>C (p.Leu1077=) rs2233071 0.00936
NM_019066.5(MAGEL2):c.1446T>C (p.Ala482=) rs2233065 0.00866
NM_019066.5(MAGEL2):c.383T>C (p.Leu128Pro) rs191559595 0.00772
NM_019066.5(MAGEL2):c.1079C>T (p.Ala360Val) rs111759069 0.00733
NM_019066.5(MAGEL2):c.1038G>C (p.Arg346Ser) rs115892604 0.00564
NM_019066.5(MAGEL2):c.678T>G (p.Gly226=) rs367737053 0.00558
NM_019066.5(MAGEL2):c.2633C>T (p.Pro878Leu) rs2233067 0.00519
NM_019066.5(MAGEL2):c.3017C>G (p.Thr1006Ser) rs138628273 0.00437
NM_019066.5(MAGEL2):c.225G>A (p.Pro75=) rs564216035 0.00309
NM_019066.5(MAGEL2):c.1286C>T (p.Pro429Leu) rs2233061 0.00306
NM_019066.5(MAGEL2):c.539T>C (p.Val180Ala) rs58729661 0.00283
NM_019066.5(MAGEL2):c.2784C>T (p.Ile928=) rs189752384 0.00273
NM_019066.5(MAGEL2):c.2886C>T (p.Ser962=) rs2233068 0.00262
NM_019066.5(MAGEL2):c.853G>A (p.Gly285Arg) rs143908070 0.00185
NM_019066.5(MAGEL2):c.1470G>A (p.Pro490=) rs771501846 0.00154
NM_019066.5(MAGEL2):c.2074G>A (p.Val692Ile) rs200926181 0.00142
NM_019066.5(MAGEL2):c.3657G>A (p.Ala1219=) rs140288382 0.00133
NM_019066.5(MAGEL2):c.1304C>T (p.Pro435Leu) rs2233062 0.00132
NM_019066.5(MAGEL2):c.406G>A (p.Gly136Arg) rs570335069 0.00118
NM_019066.5(MAGEL2):c.385A>G (p.Met129Val) rs188762916 0.00109
NM_019066.5(MAGEL2):c.639A>C (p.Pro213=) rs886042708 0.00091
NM_019066.5(MAGEL2):c.2281G>C (p.Ala761Pro) rs146970674 0.00083
NM_019066.5(MAGEL2):c.2362A>T (p.Ser788Cys) rs113329438 0.00083
NM_019066.5(MAGEL2):c.3690G>C (p.Glu1230Asp) rs34875116 0.00083
NM_019066.5(MAGEL2):c.2290G>A (p.Ala764Thr) rs201984254 0.00072
NM_019066.5(MAGEL2):c.687G>A (p.Met229Ile) rs574367928 0.00070
NM_019066.5(MAGEL2):c.959C>A (p.Ala320Asp) rs541606785 0.00070
NM_019066.5(MAGEL2):c.919C>T (p.Pro307Ser) rs555920534 0.00062
NM_019066.5(MAGEL2):c.1524C>T (p.Ala508=) rs778438849 0.00059
NM_019066.5(MAGEL2):c.579C>T (p.Pro193=) rs113984257 0.00059
NM_019066.5(MAGEL2):c.1404C>A (p.Ala468=) rs2233064 0.00049
NM_019066.5(MAGEL2):c.1175C>T (p.Thr392Met) rs781777662 0.00040
NM_019066.5(MAGEL2):c.1423G>T (p.Ala475Ser) rs760039339 0.00040
NM_019066.5(MAGEL2):c.41C>A (p.Pro14Gln) rs769643348 0.00038
NM_019066.5(MAGEL2):c.3012T>C (p.Ser1004=) rs371333192 0.00036
NM_019066.5(MAGEL2):c.3046C>T (p.Pro1016Ser) rs2233069 0.00026
NM_019066.5(MAGEL2):c.135T>A (p.Asp45Glu) rs1273933786 0.00024
NM_019066.5(MAGEL2):c.434C>T (p.Pro145Leu) rs372352945 0.00019
NM_019066.5(MAGEL2):c.3140T>C (p.Val1047Ala) rs576711188 0.00017
NM_019066.5(MAGEL2):c.1305G>A (p.Pro435=) rs755945170 0.00015
NM_019066.5(MAGEL2):c.2660G>A (p.Arg887Gln) rs199772480 0.00014
NM_019066.5(MAGEL2):c.3721G>A (p.Gly1241Ser) rs555657199 0.00014
NM_019066.5(MAGEL2):c.680C>T (p.Thr227Ile) rs761097102 0.00014
NM_019066.5(MAGEL2):c.263C>T (p.Pro88Leu) rs780815292 0.00013
NM_019066.5(MAGEL2):c.2884A>G (p.Ser962Gly) rs368008966 0.00013
NM_019066.5(MAGEL2):c.807C>A (p.Thr269=) rs377155487 0.00011
NM_019066.5(MAGEL2):c.137C>T (p.Pro46Leu) rs1433820460 0.00010
NM_019066.5(MAGEL2):c.2426C>A (p.Ala809Asp) rs201811165 0.00009
NM_019066.5(MAGEL2):c.474A>G (p.Pro158=) rs750481560 0.00009
NM_019066.5(MAGEL2):c.2870G>T (p.Gly957Val) rs560259716 0.00007
NM_019066.5(MAGEL2):c.2641C>T (p.Arg881Cys) rs372275206 0.00006
NM_019066.5(MAGEL2):c.3483T>C (p.Phe1161=) rs185139848 0.00006
NM_019066.5(MAGEL2):c.3746G>A (p.Arg1249His) rs745776063 0.00006
NM_019066.5(MAGEL2):c.979G>A (p.Ala327Thr) rs1185550236 0.00005
NM_019066.5(MAGEL2):c.1054C>G (p.Pro352Ala) rs1045111596 0.00004
NM_019066.5(MAGEL2):c.273G>A (p.Pro91=) rs374554976 0.00004
NM_019066.5(MAGEL2):c.3256G>A (p.Ala1086Thr) rs753866114 0.00004
NM_019066.5(MAGEL2):c.1894G>A (p.Ala632Thr) rs777626175 0.00003
NM_019066.5(MAGEL2):c.3228A>G (p.Gln1076=) rs780869732 0.00003
NM_019066.5(MAGEL2):c.3257C>A (p.Ala1086Asp) rs373819727 0.00003
NM_019066.5(MAGEL2):c.765G>A (p.Pro255=) rs760536434 0.00003
NM_019066.5(MAGEL2):c.3406C>A (p.Leu1136Met) rs778703892 0.00002
NM_019066.5(MAGEL2):c.504G>A (p.Pro168=) rs757734525 0.00002
NM_019066.5(MAGEL2):c.1942C>T (p.Pro648Ser) rs866333931 0.00001
NM_019066.5(MAGEL2):c.2092G>A (p.Gly698Arg) rs752045093 0.00001
NM_019066.5(MAGEL2):c.2296C>T (p.Arg766Ter) rs1249139977 0.00001
NM_019066.5(MAGEL2):c.2919G>A (p.Pro973=) rs544938560 0.00001
NM_019066.5(MAGEL2):c.3706G>A (p.Gly1236Ser) rs753063313 0.00001
NM_019066.5(MAGEL2):c.42G>A (p.Pro14=) rs794726942 0.00001
NM_019066.5(MAGEL2):c.789T>C (p.Pro263=) rs993057859 0.00001
NM_019066.5(MAGEL2):c.1021C>T (p.Gln341Ter) rs2140717169
NM_019066.5(MAGEL2):c.1344ACCCGTGATCCGCCAGGCCCC[1] (p.442PVIRQAP[2]) rs794726941
NM_019066.5(MAGEL2):c.1344_1385del (p.442PVIRQAP[1]) rs794726941
NM_019066.5(MAGEL2):c.1386_1406del (p.Ala463_Pro469del) rs1273738588
NM_019066.5(MAGEL2):c.1404CCCACCTGTGATCCGCCAGGC[1] (p.464VIRQAPP[3]) rs1386125417
NM_019066.5(MAGEL2):c.1407A>C (p.Pro469=) rs1227406471
NM_019066.5(MAGEL2):c.1446_1466del (p.464VIRQAPP[3])
NM_019066.5(MAGEL2):c.1601C>G (p.Pro534Arg) rs976206096
NM_019066.5(MAGEL2):c.1621C>T (p.Gln541Ter) rs1555374290
NM_019066.5(MAGEL2):c.1808C>G (p.Ser603Ter) rs1595332731
NM_019066.5(MAGEL2):c.1912C>T (p.Gln638Ter) rs797044883
NM_019066.5(MAGEL2):c.1922C>G (p.Pro641Arg) rs556296973
NM_019066.5(MAGEL2):c.1923dup (p.Val643fs) rs2503979002
NM_019066.5(MAGEL2):c.1991C>T (p.Pro664Leu) rs201935129
NM_019066.5(MAGEL2):c.1996C>T (p.Gln666Ter) rs752097874
NM_019066.5(MAGEL2):c.2057G>A (p.Trp686Ter) rs768844200
NM_019066.5(MAGEL2):c.2408C>A (p.Ala803Asp) rs371119917
NM_019066.5(MAGEL2):c.2543C>G (p.Ser848Trp) rs777433159
NM_019066.5(MAGEL2):c.2642G>A (p.Arg881His) rs368034669
NM_019066.5(MAGEL2):c.2727G>C (p.Gln909His) rs2503976271
NM_019066.5(MAGEL2):c.290G>A (p.Gly97Asp) rs771078069
NM_019066.5(MAGEL2):c.2989G>A (p.Ala997Thr) rs558186319
NM_019066.5(MAGEL2):c.44C>T (p.Ala15Val) rs758805784
NM_019066.5(MAGEL2):c.479CCCATCCTCCTCCTCCGGGGACCCCGATGG[1] (p.160AHPPPPGTPM[1]) rs751352401
NM_019066.5(MAGEL2):c.579CCCTCCGGGGACACCGATGGCTCATCCTCC[1] (p.181HPPPPGTPMA[4]) rs758291032
NM_019066.5(MAGEL2):c.6G>A (p.Ser2=) rs1222522082
NM_019066.5(MAGEL2):c.939CCCACCTGCACAGCCGATGGC[1] (p.314PPAQPMA[1]) rs528108868

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