List of variants in gene TRPV3 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_145068.3(TRPV3):c.-279T>C	rs552876200	0.00042
NM_145068.3(TRPV3):c.-311A>T	rs538543296	0.00039
NM_145068.4(TRPV3):c.615C>T (p.Asn205=)	rs372599650	0.00015
NM_145068.4(TRPV3):c.*32C>T	rs368105861	0.00013
NM_145068.3(TRPV3):c.-220G>A	rs773689429	0.00012
NM_145068.3(TRPV3):c.-245G>A	rs886052859	0.00010
NM_145068.3(TRPV3):c.-313C>T	rs540741805	0.00005
NM_145068.3(TRPV3):c.-318A>G	rs112731342	0.00004
NM_145068.4(TRPV3):c.1401+9G>T	rs550564945	0.00003
NM_145068.3(TRPV3):c.-327T>G	rs1039178847	0.00002
NM_145068.4(TRPV3):c.1659G>A (p.Leu553=)	rs746336365	0.00002
NM_145068.4(TRPV3):c.1066-5C>G	rs778105648	0.00001
NM_145068.4(TRPV3):c.1487G>A (p.Cys496Tyr)	rs377485480	0.00001
NM_145068.4(TRPV3):c.1810+1G>A	rs773523427	0.00001
NM_145068.4(TRPV3):c.1971G>A (p.Leu657=)	rs749226142	0.00001
NM_145068.4(TRPV3):c.2050G>A (p.Val684Ile)	rs762399867	0.00001
NM_145068.4(TRPV3):c.20A>G (p.Glu7Gly)	rs779977306	0.00001
NM_145068.4(TRPV3):c.501G>A (p.Thr167=)	rs780723914	0.00001
NM_145068.4(TRPV3):c.619G>A (p.Glu207Lys)	rs770182855	0.00001
NM_145068.3(TRPV3):c.-177C>T	rs886052858
NM_145068.4(TRPV3):c.*49C>T	rs751585500
NM_145068.4(TRPV3):c.1243-4C>T	rs886052856
NM_145068.4(TRPV3):c.1700G>A (p.Arg567Gln)	rs199905369
NM_145068.4(TRPV3):c.2011A>G (p.Asn671Asp)	rs886052855
NM_145068.4(TRPV3):c.2197C>T (p.Arg733Trp)	rs776459642
NM_145068.4(TRPV3):c.2245C>G (p.Leu749Val)	rs1351736897
NM_145068.4(TRPV3):c.2278+3A>C	rs2074157253
NM_145068.4(TRPV3):c.276T>C (p.Asp92=)	rs2074504808
NM_145068.4(TRPV3):c.442C>G (p.Arg148Gly)	rs760726969
NM_145068.4(TRPV3):c.671A>G (p.Glu224Gly)	rs2074402995
NM_145068.4(TRPV3):c.682G>C (p.Gly228Arg)	rs1319398633
NM_145068.4(TRPV3):c.6A>C (p.Lys2Asn)	rs886052857

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