ClinVar Miner

Variants in gene FAT4 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:
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
270 44 0 26 14 0 0 37

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 0 13 4
likely benign 13 0 26
benign 4 26 0

All variants with conflicting interpretations #

Total variants: 37
Download table as spreadsheet
HGVS dbSNP
NM_024582.4(FAT4):c.10101A>G (p.Glu3367=) rs147646369
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.10804A>C (p.Ile3602Leu) rs76491994
NM_024582.4(FAT4):c.10847C>T (p.Thr3616Met) rs111423173
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
NM_024582.4(FAT4):c.11664C>T (p.Cys3888=) rs150894545
NM_024582.4(FAT4):c.12060C>T (p.Gly4020=) rs144476127
NM_024582.4(FAT4):c.12064C>T (p.Arg4022Trp) rs138019311
NM_024582.4(FAT4):c.12641G>A (p.Arg4214His) rs148170326
NM_024582.4(FAT4):c.12849T>C (p.Asp4283=) rs78040862
NM_024582.4(FAT4):c.12980A>G (p.Asp4327Gly) rs114234553
NM_024582.4(FAT4):c.13398G>A (p.Val4466=) rs149993049
NM_024582.4(FAT4):c.13548G>A (p.Leu4516=) rs78235204
NM_024582.4(FAT4):c.14657C>G (p.Ala4886Gly) rs35340865
NM_024582.4(FAT4):c.14660G>A (p.Arg4887Lys) rs35845544
NM_024582.4(FAT4):c.14682C>T (p.His4894=) rs35862879
NM_024582.4(FAT4):c.2316A>G (p.Gln772=) rs187427286
NM_024582.4(FAT4):c.2322C>T (p.Pro774=) rs200593370
NM_024582.4(FAT4):c.2811G>T (p.Lys937Asn) rs112454576
NM_024582.4(FAT4):c.2896A>G (p.Ile966Val) rs778631726
NM_024582.4(FAT4):c.3402A>T (p.Glu1134Asp) rs144768563
NM_024582.4(FAT4):c.3424G>A (p.Val1142Met) rs202188213
NM_024582.4(FAT4):c.4154T>C (p.Leu1385Ser) rs139883132
NM_024582.4(FAT4):c.4219G>A (p.Val1407Ile) rs114227532
NM_024582.4(FAT4):c.4303A>G (p.Ile1435Val) rs142747281
NM_024582.4(FAT4):c.524G>T (p.Arg175Leu) rs143534324
NM_024582.4(FAT4):c.5275A>G (p.Ile1759Val) rs145639192
NM_024582.4(FAT4):c.5367C>T (p.Ile1789=) rs144922340
NM_024582.4(FAT4):c.5987A>G (p.Lys1996Arg) rs140055438
NM_024582.4(FAT4):c.6478A>G (p.Lys2160Glu) rs75942329
NM_024582.4(FAT4):c.6733G>A (p.Val2245Ile) rs112971995
NM_024582.4(FAT4):c.7225A>T (p.Thr2409Ser) rs147297895
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.7781T>C (p.Leu2594Ser) rs111501860
NM_024582.4(FAT4):c.7929C>T (p.Asp2643=) rs146157250
NM_024582.4(FAT4):c.9822C>T (p.Pro3274=) rs73849226
NM_024582.4(FAT4):c.9885G>A (p.Val3295=) rs139704889

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