List of variants in gene TCIRG1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.528C>A (p.Pro176=)	rs538805960	0.00135
NM_006019.4(TCIRG1):c.412C>T (p.Pro138Ser)	rs35354504	0.00118
NM_006019.4(TCIRG1):c.813C>T (p.Leu271=)	rs377108710	0.00099
NM_006019.4(TCIRG1):c.1715C>T (p.Pro572Leu)	rs115854062	0.00098
NM_006019.4(TCIRG1):c.1209G>A (p.Met403Ile)	rs140191063	0.00095
NM_006019.4(TCIRG1):c.197-5C>T	rs183885218	0.00088
NM_006019.4(TCIRG1):c.611C>T (p.Pro204Leu)	rs373711940	0.00071
NM_006019.4(TCIRG1):c.1887+131G>A	rs78820476	0.00069
NM_006019.4(TCIRG1):c.274C>T (p.Arg92Trp)	rs371907380	0.00052
NM_006019.4(TCIRG1):c.2163C>T (p.Ile721=)	rs145718040	0.00029
NM_006019.4(TCIRG1):c.1227C>T (p.His409=)	rs145080707	0.00017
NM_006019.4(TCIRG1):c.118-6C>T	rs375317575	0.00014
NM_006019.4(TCIRG1):c.21C>T (p.Ser7=)	rs373244328	0.00011
NM_006019.4(TCIRG1):c.2333C>T (p.Ala778Val)	rs144775787	0.00010
NM_006019.4(TCIRG1):c.2119-10C>T	rs377606178	0.00009
NM_006019.4(TCIRG1):c.1195C>T (p.Leu399=)	rs151180675	0.00007
NM_006019.4(TCIRG1):c.1278A>G (p.Arg426=)	rs138527421	0.00007
NM_006019.4(TCIRG1):c.2028C>T (p.Ala676=)	rs370181947	0.00006
NM_006019.4(TCIRG1):c.307C>T (p.Arg103Cys)	rs771198568	0.00006
NM_006019.4(TCIRG1):c.1371C>T (p.Thr457=)	rs376526455	0.00004
NM_006019.4(TCIRG1):c.1904C>T (p.Thr635Met)	rs763119311	0.00004
NM_006019.4(TCIRG1):c.870G>A (p.Pro290=)	rs775370689	0.00004
NM_006019.4(TCIRG1):c.2118+10G>A	rs775491643	0.00003
NM_006019.4(TCIRG1):c.1548C>T (p.Ile516=)	rs759410959	0.00002
NM_006019.4(TCIRG1):c.2049C>T (p.Asp683=)	rs780969471	0.00001
NM_006019.4(TCIRG1):c.2475C>T (p.Phe825=)	rs886048602	0.00001
NM_006019.4(TCIRG1):c.1293C>T (p.Ala431=)	rs372063415
NM_006019.4(TCIRG1):c.1758C>T (p.Phe586=)
NM_006019.4(TCIRG1):c.1857C>T (p.Ser619=)
NM_006019.4(TCIRG1):c.1887+130C>T	rs928213157
NM_006019.4(TCIRG1):c.2448G>C (p.Thr816=)	rs139049989

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