ClinVar Miner

Variants in gene ALDH7A1 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
449 27 0 16 16 0 5 35

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 2 2 0 0
likely pathogenic 2 0 3 0 0
uncertain significance 2 3 0 16 1
likely benign 0 0 16 0 14
benign 0 0 1 14 0

All variants with conflicting interpretations #

Total variants: 35
Download table as spreadsheet
NM_001182.4(ALDH7A1):c.-34G>C rs140627539
NM_001182.4(ALDH7A1):c.-80T>G rs563928852
NM_001182.5(ALDH7A1):c.-13T>G rs774190967
NM_001182.5(ALDH7A1):c.1009-6G>A rs138056453
NM_001182.5(ALDH7A1):c.1016A>G (p.His339Arg) rs199767457
NM_001182.5(ALDH7A1):c.1017T>C (p.His339=) rs200394848
NM_001182.5(ALDH7A1):c.1176T>C (p.Gly392=) rs935431600
NM_001182.5(ALDH7A1):c.1232C>T (p.Pro411Leu) rs780233639
NM_001182.5(ALDH7A1):c.1234A>G (p.Thr412Ala) rs2306618
NM_001182.5(ALDH7A1):c.1263G>A (p.Ala421=) rs587780850
NM_001182.5(ALDH7A1):c.1276A>G (p.Thr426Ala) rs150305320
NM_001182.5(ALDH7A1):c.1279G>C (p.Glu427Gln) rs121912707
NM_001182.5(ALDH7A1):c.1301_1302del (p.Tyr434fs)
NM_001182.5(ALDH7A1):c.1305C>G (p.Val435=) rs142975776
NM_001182.5(ALDH7A1):c.1315A>C (p.Lys439Gln) rs12514417
NM_001182.5(ALDH7A1):c.1406G>A (p.Arg469His) rs147940248
NM_001182.5(ALDH7A1):c.141_142insA (p.Arg48fs) rs1296037862
NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala) rs61757684
NM_001182.5(ALDH7A1):c.200C>T (p.Thr67Met) rs543181020
NM_001182.5(ALDH7A1):c.201G>T (p.Thr67=) rs747643987
NM_001182.5(ALDH7A1):c.243A>G (p.Arg81=) rs146438406
NM_001182.5(ALDH7A1):c.273T>C (p.Thr91=) rs60720055
NM_001182.5(ALDH7A1):c.34del (p.Ala12fs) rs750693623
NM_001182.5(ALDH7A1):c.39A>G (p.Ala13=) rs201566142
NM_001182.5(ALDH7A1):c.423G>C (p.Val141=) rs199653162
NM_001182.5(ALDH7A1):c.528T>C (p.His176=) rs757135576
NM_001182.5(ALDH7A1):c.552C>T (p.Pro184=) rs369859575
NM_001182.5(ALDH7A1):c.575C>T (p.Thr192Met) rs376917645
NM_001182.5(ALDH7A1):c.615C>T (p.Asn205=) rs369380330
NM_001182.5(ALDH7A1):c.63T>C (p.Pro21=) rs368427726
NM_001182.5(ALDH7A1):c.664A>G (p.Thr222Ala) rs777829351
NM_001182.5(ALDH7A1):c.675C>T (p.Leu225=) rs57902950
NM_001182.5(ALDH7A1):c.774-18G>A rs185333013
NM_001182.5(ALDH7A1):c.858G>A (p.Val286=) rs150623275
NM_001182.5(ALDH7A1):c.913+8T>C rs766528289

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