List of variants in gene TCIRG1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.1249G>A (p.Ala417Thr)	rs140963213	0.00275
NM_006019.4(TCIRG1):c.90C>T (p.Gly30=)	rs141859450	0.00162
NM_006019.4(TCIRG1):c.707C>T (p.Thr236Met)	rs116001129	0.00026
NM_006019.4(TCIRG1):c.1883G>A (p.Arg628Gln)	rs201661352	0.00020
NM_006019.4(TCIRG1):c.629C>T (p.Thr210Met)	rs372826788	0.00015
NM_006019.4(TCIRG1):c.1978C>T (p.Arg660Cys)	rs528045019	0.00009
NM_006019.4(TCIRG1):c.1382A>G (p.Tyr461Cys)	rs771395837	0.00007
NM_006019.4(TCIRG1):c.1020G>A (p.Ser340=)	rs144158792	0.00006
NM_006019.4(TCIRG1):c.1061G>C (p.Cys354Ser)	rs369222109	0.00006
NM_006019.4(TCIRG1):c.1981C>T (p.Arg661Cys)	rs770889100	0.00006
NM_006019.4(TCIRG1):c.851G>A (p.Arg284Gln)	rs146244480	0.00006
NM_006019.4(TCIRG1):c.2344G>A (p.Val782Met)	rs779910642	0.00005
NM_006019.4(TCIRG1):c.763G>A (p.Gly255Arg)	rs376201635	0.00005
NM_006019.4(TCIRG1):c.1627G>A (p.Val543Ile)	rs763319140	0.00004
NM_006019.4(TCIRG1):c.1438G>A (p.Ala480Thr)	rs537359796	0.00003
NM_006019.4(TCIRG1):c.1087C>T (p.Arg363Cys)	rs375809635	0.00002
NM_006019.4(TCIRG1):c.59C>T (p.Ala20Val)	rs377034463	0.00002
NM_006019.4(TCIRG1):c.1088G>A (p.Arg363His)	rs755474518	0.00001
NM_006019.4(TCIRG1):c.16C>T (p.Arg6Trp)	rs563996115	0.00001
NM_006019.4(TCIRG1):c.1985G>A (p.Arg662His)	rs763065648	0.00001
NM_006019.4(TCIRG1):c.260C>T (p.Pro87Leu)	rs982462013	0.00001
NM_006019.4(TCIRG1):c.911T>C (p.Leu304Pro)	rs1449131788	0.00001
NM_006019.4(TCIRG1):c.991G>A (p.Ala331Thr)	rs773402451	0.00001
NM_006019.4(TCIRG1):c.1630G>A (p.Val544Met)	rs371505143
NM_006019.4(TCIRG1):c.656T>C (p.Phe219Ser)	rs748465503

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