ClinVar Miner

Variants in gene LTBP4 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
148 17 0 14 8 0 0 21

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 8 1
likely benign 8 0 14
benign 1 14 0

All variants with conflicting interpretations #

Total variants: 21
Download table as spreadsheet
HGVS dbSNP
NM_001042545.2(LTBP4):c.135C>T (p.Cys45=) rs185400394
NM_003573.2(LTBP4):c.1328G>A (p.Gly443Asp) rs114749335
NM_003573.2(LTBP4):c.1390T>A (p.Ser464Thr) rs34545902
NM_003573.2(LTBP4):c.1531A>G (p.Met511Val) rs116005784
NM_003573.2(LTBP4):c.1581G>T (p.Arg527=) rs117273116
NM_003573.2(LTBP4):c.1792C>G (p.Arg598Gly) rs33937741
NM_003573.2(LTBP4):c.1924C>G (p.Pro642Ala) rs34299942
NM_003573.2(LTBP4):c.2143G>A (p.Asp715Asn) rs34093919
NM_003573.2(LTBP4):c.2144-11C>A rs41470347
NM_003573.2(LTBP4):c.2265C>T (p.Cys755=) rs141810975
NM_003573.2(LTBP4):c.2328C>T (p.Pro776=) rs201588216
NM_003573.2(LTBP4):c.2389+9A>G rs73544980
NM_003573.2(LTBP4):c.2526G>A (p.Val842=) rs371083223
NM_003573.2(LTBP4):c.2655C>T (p.Asp885=) rs2077407
NM_003573.2(LTBP4):c.2771-10C>G rs200914063
NM_003573.2(LTBP4):c.2999C>G (p.Pro1000Arg) rs200667255
NM_003573.2(LTBP4):c.3219C>T (p.Val1073=) rs78745792
NM_003573.2(LTBP4):c.4388A>T (p.Tyr1463Phe) rs35809725
NM_003573.2(LTBP4):c.79C>T (p.Leu27=) rs370696272
NM_003573.2(LTBP4):c.948G>A (p.Gly316=) rs146234365
NM_003573.2(LTBP4):c.981C>T (p.Gly327=) rs374427407

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