List of variants in gene TRDN reported as likely benign for not specified

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.383C>G (p.Thr128Ser)	rs9490809	0.50546
NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu)	rs17737379	0.17356
NM_006073.4(TRDN):c.1211T>G (p.Val404Gly)	rs28494009	0.16504
NM_006073.4(TRDN):c.1408C>A (p.Leu470Met)	rs6569336	0.09024
NM_006073.4(TRDN):c.1016G>A (p.Ser339Asn)	rs35766971	0.01214
NM_006073.4(TRDN):c.403G>A (p.Glu135Lys)	rs192289289	0.00900
NM_006073.4(TRDN):c.1567+19T>C	rs182813107	0.00459
NM_006073.4(TRDN):c.1510G>A (p.Gly504Ser)	rs150531306	0.00305
NM_006073.4(TRDN):c.430C>T (p.His144Tyr)	rs79182520	0.00232
NM_006073.4(TRDN):c.793+61T>C	rs572614305	0.00177
NM_006073.4(TRDN):c.84C>T (p.Pro28=)	rs145992727	0.00070
NM_006073.4(TRDN):c.1895G>A (p.Arg632Lys)	rs181571822	0.00044
NM_006073.4(TRDN):c.611-19A>T	rs142018848	0.00044
NM_006073.4(TRDN):c.546G>A (p.Lys182=)	rs377594350	0.00042
NM_006073.4(TRDN):c.1538-19T>A	rs142237914	0.00038
NM_006073.4(TRDN):c.1472-13C>T	rs367962513	0.00033
NM_006073.4(TRDN):c.129G>A (p.Thr43=)	rs373840513	0.00011
NM_006073.4(TRDN):c.793+27G>A	rs189106156	0.00011
NM_006073.4(TRDN):c.932-11G>T	rs954424960	0.00009
NM_006073.4(TRDN):c.1831+12C>A	rs368167703	0.00007
NM_006073.4(TRDN):c.1537+17C>T	rs369584691	0.00005
NM_006073.4(TRDN):c.1186+13A>T	rs374832854	0.00003
NM_006073.4(TRDN):c.2073T>C (p.Cys691=)	rs776628762	0.00003
NM_006073.4(TRDN):c.592A>G (p.Thr198Ala)	rs952211002	0.00003
NM_006073.4(TRDN):c.1220-3C>T	rs773907258	0.00002
NM_006073.4(TRDN):c.1951+16G>A	rs377046739	0.00002
NM_006073.4(TRDN):c.484+7del	rs764922806	0.00002
NM_006073.4(TRDN):c.551-4T>C	rs1413167708	0.00002
NM_006073.4(TRDN):c.1135+10A>T	rs765785141	0.00001
NM_006073.4(TRDN):c.1524G>A (p.Lys508=)	rs373408793	0.00001
NM_006073.4(TRDN):c.232+15A>T	rs769101414	0.00001
NM_006073.4(TRDN):c.991+11T>G	rs1245038855	0.00001
NM_006073.4(TRDN):c.1106-19G>T	rs754623877
NM_006073.4(TRDN):c.1313T>A (p.Ile438Asn)	rs2873479
NM_006073.4(TRDN):c.147C>A (p.Ala49=)	rs1554258804
NM_006073.4(TRDN):c.1511-14T>C	rs1252673540
NM_006073.4(TRDN):c.1597+10G>A	rs150165710
NM_006073.4(TRDN):c.1739-6C>T	rs1057524282
NM_006073.4(TRDN):c.1975+9G>A	rs111276785
NM_006073.4(TRDN):c.424+13_424+14delinsTC	rs1554256111
NM_006073.4(TRDN):c.551-20T>C	rs1554251627

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