List of variants in gene TRDN reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1367A>G (p.Gln456Arg)	rs200243235	0.00128
NM_006073.4(TRDN):c.277C>T (p.Arg93Cys)	rs370788759	0.00060
NM_006073.4(TRDN):c.1895G>A (p.Arg632Lys)	rs181571822	0.00044
NM_006073.4(TRDN):c.1193A>T (p.Glu398Val)	rs374355537	0.00041
NM_006073.4(TRDN):c.71T>A (p.Val24Glu)	rs201097255	0.00034
NM_006073.4(TRDN):c.1811C>T (p.Thr604Ile)	rs763939252	0.00028
NM_006073.4(TRDN):c.2187G>T (p.Gln729His)	rs373439044	0.00026
NM_006073.4(TRDN):c.1537+1G>A	rs189125299	0.00019
NM_006073.4(TRDN):c.1282C>T (p.Arg428Ter)	rs202219343	0.00016
NM_006073.4(TRDN):c.85G>A (p.Gly29Arg)	rs763469367	0.00016
NM_006073.4(TRDN):c.239C>T (p.Ser80Phe)	rs181287533	0.00015
NM_006073.4(TRDN):c.1627C>A (p.Gln543Lys)	rs9398723	0.00013
NM_006073.4(TRDN):c.591A>C (p.Glu197Asp)	rs751143632	0.00013
NM_006073.4(TRDN):c.2093A>G (p.Asn698Ser)	rs377368177	0.00010
NM_006073.4(TRDN):c.1808G>C (p.Gly603Ala)	rs766406818	0.00009
NM_006073.4(TRDN):c.727A>G (p.Thr243Ala)	rs376208769	0.00009
NM_006073.4(TRDN):c.884C>T (p.Pro295Leu)	rs201899630	0.00009
NM_006073.4(TRDN):c.1137T>G (p.Asp379Glu)	rs200706450	0.00008
NM_006073.4(TRDN):c.1801C>G (p.Pro601Ala)	rs376214235	0.00007
NM_006073.4(TRDN):c.2084A>T (p.Asp695Val)	rs202040879	0.00006
NM_006073.4(TRDN):c.550G>T (p.Ala184Ser)	rs576028226	0.00006
NM_006073.4(TRDN):c.1276A>C (p.Thr426Pro)	rs1040336692	0.00005
NM_006073.4(TRDN):c.1136-1G>A	rs769776218	0.00004
NM_006073.4(TRDN):c.1589C>G (p.Ala530Gly)	rs367716594	0.00004
NM_006073.4(TRDN):c.2131C>T (p.Arg711Cys)	rs373408498	0.00004
NM_006073.4(TRDN):c.1420+1G>T	rs1375657667	0.00003
NM_006073.4(TRDN):c.1708A>G (p.Ile570Val)	rs915231524	0.00003
NM_006073.4(TRDN):c.1754G>A (p.Arg585Gln)	rs199986608	0.00003
NM_006073.4(TRDN):c.592A>G (p.Thr198Ala)	rs952211002	0.00003
NM_006073.4(TRDN):c.1975+5G>T	rs899940538	0.00002
NM_006073.4(TRDN):c.2164C>G (p.Pro722Ala)	rs774449661	0.00002
NM_006073.4(TRDN):c.1115A>G (p.Lys372Arg)	rs1259355217	0.00001
NM_006073.4(TRDN):c.1206A>T (p.Lys402Asn)	rs745563456	0.00001
NM_006073.4(TRDN):c.1475C>T (p.Pro492Leu)	rs1431462819	0.00001
NM_006073.4(TRDN):c.1682T>A (p.Val561Asp)	rs947096255	0.00001
NM_006073.4(TRDN):c.2122C>T (p.Pro708Ser)	rs751278695	0.00001
NM_006073.4(TRDN):c.335A>T (p.Asp112Val)	rs772376488	0.00001
NM_006073.4(TRDN):c.437A>G (p.Asp146Gly)	rs1449421617	0.00001
NM_006073.4(TRDN):c.853+3A>G	rs372783263	0.00001
NM_006073.4(TRDN):c.990A>G (p.Lys330=)	rs941068115	0.00001
NM_006073.4(TRDN):c.1055C>A (p.Pro352Gln)	rs754708708
NM_006073.4(TRDN):c.1233_1234dup (p.Lys412fs)	rs778198100
NM_006073.4(TRDN):c.1273+1G>A	rs2114394892
NM_006073.4(TRDN):c.1365G>A (p.Glu455=)	rs1452206168
NM_006073.4(TRDN):c.143C>A (p.Ala48Glu)
NM_006073.4(TRDN):c.1700C>A (p.Ala567Asp)	rs545470302
NM_006073.4(TRDN):c.1729A>G (p.Lys577Glu)	rs1554219149
NM_006073.4(TRDN):c.1922A>G (p.Glu641Gly)	rs1554217845
NM_006073.4(TRDN):c.545A>G (p.Lys182Arg)
NM_006073.4(TRDN):c.553A>G (p.Thr185Ala)	rs1064796444

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