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 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
234 35 0 33 23 0 1 52

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 12
likely benign 0 0 16 0 28
benign 0 0 12 28 0

All variants with conflicting interpretations #

Total variants: 52
Download table as spreadsheet
HGVS dbSNP
NM_015346.3(ZFYVE26):c.-70A>T rs17192296
NM_015346.3(ZFYVE26):c.1184G>T (p.Gly395Val) rs35512910
NM_015346.3(ZFYVE26):c.1224G>T (p.Gly408=) rs17104689
NM_015346.3(ZFYVE26):c.1844C>T (p.Ser615Phe) rs117228915
NM_015346.3(ZFYVE26):c.2067C>T (p.Leu689=) rs141880939
NM_015346.3(ZFYVE26):c.2254C>T (p.Gln752Ter) rs1057518016
NM_015346.3(ZFYVE26):c.2332+7delT rs145183291
NM_015346.3(ZFYVE26):c.2401+11T>A rs191741115
NM_015346.3(ZFYVE26):c.2427C>T (p.Gly809=) rs144063215
NM_015346.3(ZFYVE26):c.2450delT (p.Leu817Cysfs) rs768176054
NM_015346.3(ZFYVE26):c.2559G>A (p.Leu853=) rs7143196
NM_015346.3(ZFYVE26):c.2692A>T (p.Thr898Ser) rs17192170
NM_015346.3(ZFYVE26):c.2852C>T (p.Thr951Met) rs35471427
NM_015346.3(ZFYVE26):c.2887G>C (p.Val963Leu) rs116890187
NM_015346.3(ZFYVE26):c.30T>G (p.Ala10=) rs141905183
NM_015346.3(ZFYVE26):c.3118T>A (p.Ser1040Thr) rs112787369
NM_015346.3(ZFYVE26):c.3139+1G>A rs137907310
NM_015346.3(ZFYVE26):c.3139+2T>G rs767164213
NM_015346.3(ZFYVE26):c.3210C>G (p.Pro1070=) rs7156492
NM_015346.3(ZFYVE26):c.3308C>T (p.Pro1103Leu) rs3742885
NM_015346.3(ZFYVE26):c.3365C>T (p.Ala1122Val) rs3742884
NM_015346.3(ZFYVE26):c.3722G>A (p.Arg1241Gln) rs140756827
NM_015346.3(ZFYVE26):c.3757C>T (p.Leu1253=) rs34296097
NM_015346.3(ZFYVE26):c.4035G>T (p.Val1345=) rs374530573
NM_015346.3(ZFYVE26):c.4066T>G (p.Cys1356Gly) rs149276487
NM_015346.3(ZFYVE26):c.4197C>T (p.Thr1399=) rs35018134
NM_015346.3(ZFYVE26):c.4293G>C (p.Gln1431His) rs373740172
NM_015346.3(ZFYVE26):c.4312C>T (p.Arg1438Ter) rs118204049
NM_015346.3(ZFYVE26):c.4324G>A (p.Asp1442Asn) rs534497092
NM_015346.3(ZFYVE26):c.4370G>A (p.Cys1457Tyr) rs2235967
NM_015346.3(ZFYVE26):c.4502C>T (p.Thr1501Met) rs201034965
NM_015346.3(ZFYVE26):c.453C>T (p.Ser151=) rs75391113
NM_015346.3(ZFYVE26):c.4734C>T (p.Ile1578=) rs200243306
NM_015346.3(ZFYVE26):c.4854C>T (p.Leu1618=) rs151287975
NM_015346.3(ZFYVE26):c.5121A>C (p.Gly1707=) rs143981992
NM_015346.3(ZFYVE26):c.5484+13G>A rs140117984
NM_015346.3(ZFYVE26):c.5485-1delG rs878855013
NM_015346.3(ZFYVE26):c.5672A>G (p.Asn1891Ser) rs3742883
NM_015346.3(ZFYVE26):c.5784T>C (p.Tyr1928=) rs34852231
NM_015346.3(ZFYVE26):c.6135C>T (p.Ala2045=) rs146209388
NM_015346.3(ZFYVE26):c.6405G>A (p.Leu2135=) rs76327447
NM_015346.3(ZFYVE26):c.677G>A (p.Arg226His) rs147919567
NM_015346.3(ZFYVE26):c.6819G>A (p.Arg2273=) rs144007962
NM_015346.3(ZFYVE26):c.6849A>G (p.Thr2283=) rs74935043
NM_015346.3(ZFYVE26):c.6921C>T (p.Ser2307=) rs35917338
NM_015346.3(ZFYVE26):c.6987-3C>T rs76728509
NM_015346.3(ZFYVE26):c.7055C>T (p.Thr2352Ile) rs151166497
NM_015346.3(ZFYVE26):c.7232G>A (p.Arg2411His) rs34373049
NM_015346.3(ZFYVE26):c.7407T>C (p.Asp2469=) rs35106153
NM_015346.3(ZFYVE26):c.7417-5G>C rs201771769
NM_015346.3(ZFYVE26):c.7533C>T (p.Ser2511=) rs147494935
NM_015346.3(ZFYVE26):c.7586C>G (p.Pro2529Arg) rs143198225

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