List of variants in gene TACR3 reported as uncertain significance for Kallmann syndrome

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_001059.3(TACR3):c.-20G>A	rs201377092	0.00433
NM_001059.3(TACR3):c.579C>T (p.Pro193=)	rs62340657	0.00164
NM_001059.3(TACR3):c.1246A>T (p.Asn416Tyr)	rs143073792	0.00151
NM_001059.3(TACR3):c.*138G>A	rs200193311	0.00041
NM_001059.3(TACR3):c.1321C>T (p.Arg441Cys)	rs146482011	0.00024
NM_001059.3(TACR3):c.-10A>T	rs200498239	0.00017
NM_001059.3(TACR3):c.1290G>A (p.Thr430=)	rs138661164	0.00015
NM_001059.3(TACR3):c.918G>A (p.Met306Ile)	rs201088165	0.00006
NM_001059.3(TACR3):c.*87T>C	rs199959009	0.00004
NM_001059.3(TACR3):c.*143G>A	rs145839786	0.00003
NM_001059.3(TACR3):c.1206C>T (p.Thr402=)	rs201120800	0.00003
NM_001059.3(TACR3):c.737C>T (p.Thr246Ile)	rs200991185	0.00003
NM_001059.3(TACR3):c.*125A>G	rs201125726	0.00001
NM_001059.3(TACR3):c.-111C>A	rs371989130	0.00001
NM_001059.3(TACR3):c.114G>T (p.Glu38Asp)	rs886058977	0.00001
NM_001059.3(TACR3):c.1234G>A (p.Val412Met)	rs151158699	0.00001
NM_001059.3(TACR3):c.1289C>T (p.Thr430Met)	rs200736098	0.00001
NM_001059.3(TACR3):c.150C>T (p.Asn50=)	rs201531776	0.00001
NM_001059.3(TACR3):c.688C>T (p.Arg230Cys)	rs1195516345	0.00001
NM_001059.3(TACR3):c.*202G>C	rs886058970
NM_001059.3(TACR3):c.*94T>G	rs1723845345
NM_001059.3(TACR3):c.-20G>C	rs201377092
NM_001059.3(TACR3):c.-86C>A	rs886058978
NM_001059.3(TACR3):c.-93A>G	rs1723174170
NM_001059.3(TACR3):c.1188G>A (p.Arg396=)	rs886058974
NM_001059.3(TACR3):c.1225A>G (p.Met409Val)	rs201828791
NM_001059.3(TACR3):c.1230A>T (p.Thr410=)	rs886058973
NM_001059.3(TACR3):c.1311T>C (p.Asn437=)	rs886058972
NM_001059.3(TACR3):c.1345G>T (p.Ala449Ser)	rs17033889
NM_001059.3(TACR3):c.138C>T (p.Asp46=)	rs181951458
NM_001059.3(TACR3):c.548+2T>A	rs772508077
NM_001059.3(TACR3):c.703G>A (p.Val235Met)	rs886058976

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