ClinVar Miner

Variants in gene TRDN 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 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
191 37 0 18 11 0 0 28

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 3 0 0 0
likely pathogenic 3 0 0 0 0
uncertain significance 0 0 0 11 1
likely benign 0 0 11 0 15
benign 0 0 1 15 0

All variants with conflicting interpretations #

Total variants: 28
Download table as spreadsheet
HGVS dbSNP
NM_001251987.1(TRDN):c.568dupA (p.Ile190Asnfs) rs1085307100
NM_006073.3(TRDN):c.-26A>G rs372934247
NM_006073.3(TRDN):c.1105+5G>A rs41284430
NM_006073.3(TRDN):c.1188A>G (p.Lys396=) rs6901953
NM_006073.3(TRDN):c.1211T>G (p.Val404Gly) rs28494009
NM_006073.3(TRDN):c.1219+4A>G rs189551080
NM_006073.3(TRDN):c.1257C>A (p.Asp419Glu) rs17737379
NM_006073.3(TRDN):c.1282C>T (p.Arg428Ter) rs202219343
NM_006073.3(TRDN):c.1313T>A (p.Ile438Asn) rs2873479
NM_006073.3(TRDN):c.1408C>A (p.Leu470Met) rs6569336
NM_006073.3(TRDN):c.1472-12G>A rs375364108
NM_006073.3(TRDN):c.1510G>A (p.Gly504Ser) rs150531306
NM_006073.3(TRDN):c.1538-13T>G rs55704802
NM_006073.3(TRDN):c.1568-4T>A rs764779610
NM_006073.3(TRDN):c.1598-3dupT rs147062785
NM_006073.3(TRDN):c.1620A>G (p.Ile540Met) rs7771303
NM_006073.3(TRDN):c.1713A>C (p.Glu571Asp) rs201115952
NM_006073.3(TRDN):c.1871-15G>A rs59935057
NM_006073.3(TRDN):c.1895G>A (p.Arg632Lys) rs181571822
NM_006073.3(TRDN):c.1900_1903delGAAA (p.Glu634Lysfs) rs750469686
NM_006073.3(TRDN):c.1975+9G>A rs111276785
NM_006073.3(TRDN):c.277C>T (p.Arg93Cys) rs370788759
NM_006073.3(TRDN):c.367G>A (p.Asp123Asn) rs201021891
NM_006073.3(TRDN):c.375C>T (p.Asp125=) rs377440434
NM_006073.3(TRDN):c.430C>T (p.His144Tyr) rs79182520
NM_006073.3(TRDN):c.503_508delAAAAAG (p.Glu168_Lys169del) rs148596612
NM_006073.3(TRDN):c.510A>G (p.Gly170=) rs773658957
NM_006073.3(TRDN):c.932-4C>G rs77768246

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