ClinVar Miner

Variants in gene ZFYVE26 with conflicting interpretations

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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
734 76 0 28 20 0 1 44

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 5 0 0 0
likely pathogenic 5 0 1 0 0
uncertain significance 0 1 0 16 8
likely benign 0 0 16 0 23
benign 0 0 8 23 0

All variants with conflicting interpretations #

Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_015346.4(ZFYVE26):c.1170G>A (p.Leu390=) rs532292359
NM_015346.4(ZFYVE26):c.1184G>T (p.Gly395Val) rs35512910
NM_015346.4(ZFYVE26):c.1224G>T (p.Gly408=) rs17104689
NM_015346.4(ZFYVE26):c.1819G>A (p.Gly607Arg) rs142015707
NM_015346.4(ZFYVE26):c.1945G>A (p.Val649Met) rs144790966
NM_015346.4(ZFYVE26):c.2067C>T (p.Leu689=) rs141880939
NM_015346.4(ZFYVE26):c.2254C>T (p.Gln752Ter) rs1057518016
NM_015346.4(ZFYVE26):c.2332+7del rs145183291
NM_015346.4(ZFYVE26):c.2396C>T (p.Thr799Met) rs200179480
NM_015346.4(ZFYVE26):c.2427C>T (p.Gly809=) rs144063215
NM_015346.4(ZFYVE26):c.2559G>A (p.Leu853=) rs7143196
NM_015346.4(ZFYVE26):c.2742C>T (p.Ser914=) rs140577908
NM_015346.4(ZFYVE26):c.2799C>T (p.Leu933=) rs146793500
NM_015346.4(ZFYVE26):c.2887G>C (p.Val963Leu) rs116890187
NM_015346.4(ZFYVE26):c.3118T>A (p.Ser1040Thr) rs112787369
NM_015346.4(ZFYVE26):c.3139+1G>A rs137907310
NM_015346.4(ZFYVE26):c.3139+2T>G rs767164213
NM_015346.4(ZFYVE26):c.3210C>G (p.Pro1070=) rs7156492
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.3308C>T (p.Pro1103Leu) rs3742885
NM_015346.4(ZFYVE26):c.3365C>T (p.Ala1122Val) rs3742884
NM_015346.4(ZFYVE26):c.3722G>A (p.Arg1241Gln) rs140756827
NM_015346.4(ZFYVE26):c.403G>A (p.Val135Met) rs771937001
NM_015346.4(ZFYVE26):c.4197C>T (p.Thr1399=) rs35018134
NM_015346.4(ZFYVE26):c.4293G>C (p.Gln1431His) rs373740172
NM_015346.4(ZFYVE26):c.4312C>T (p.Arg1438Ter) rs118204049
NM_015346.4(ZFYVE26):c.4370G>A (p.Cys1457Tyr) rs2235967
NM_015346.4(ZFYVE26):c.4401C>T (p.Pro1467=) rs138543433
NM_015346.4(ZFYVE26):c.443G>C (p.Arg148Pro) rs144919978
NM_015346.4(ZFYVE26):c.4502C>T (p.Thr1501Met) rs201034965
NM_015346.4(ZFYVE26):c.4734C>T (p.Ile1578=) rs200243306
NM_015346.4(ZFYVE26):c.4854C>T (p.Leu1618=) rs151287975
NM_015346.4(ZFYVE26):c.5485-1del rs878855013
NM_015346.4(ZFYVE26):c.5672A>G (p.Asn1891Ser) rs3742883
NM_015346.4(ZFYVE26):c.6405G>A (p.Leu2135=) rs76327447
NM_015346.4(ZFYVE26):c.677G>A (p.Arg226His) rs147919567
NM_015346.4(ZFYVE26):c.6849A>G (p.Thr2283=) rs74935043
NM_015346.4(ZFYVE26):c.7041C>A (p.Cys2347Ter) rs370837940
NM_015346.4(ZFYVE26):c.7055C>T (p.Thr2352Ile) rs151166497
NM_015346.4(ZFYVE26):c.7317C>T (p.Asp2439=) rs147321202
NM_015346.4(ZFYVE26):c.7417-5G>C rs201771769
NM_015346.4(ZFYVE26):c.7533C>T (p.Ser2511=) rs147494935
NM_015346.4(ZFYVE26):c.773G>A (p.Arg258Gln) rs150230201
NM_015346.4(ZFYVE26):c.879G>A (p.Ser293=) rs199794711

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