List of variants in gene TCIRG1 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.479G>A (p.Gly160Glu)	rs186758849	0.00601
NM_006019.4(TCIRG1):c.1515C>T (p.Thr505=)	rs34211419	0.00473
NM_006019.4(TCIRG1):c.1249G>A (p.Ala417Thr)	rs140963213	0.00275
NM_006019.4(TCIRG1):c.1800C>T (p.Ala600=)	rs145144233	0.00182
NM_006019.4(TCIRG1):c.90C>T (p.Gly30=)	rs141859450	0.00162
NM_006019.4(TCIRG1):c.1536C>T (p.Tyr512=)	rs138049763	0.00093
NM_006019.4(TCIRG1):c.1096C>T (p.Arg366Cys)	rs148619884	0.00035
NM_006019.4(TCIRG1):c.2193C>T (p.Thr731=)	rs141601593	0.00025
NM_006019.4(TCIRG1):c.1306-8C>T	rs188598855	0.00024
NM_006019.4(TCIRG1):c.1709C>T (p.Thr570Met)	rs61730880	0.00022
NM_006019.4(TCIRG1):c.2445C>T (p.Gly815=)	rs150788130	0.00022
NM_006019.4(TCIRG1):c.1674-1G>A	rs139617644	0.00019
NM_006019.4(TCIRG1):c.2008C>T (p.Arg670Ter)	rs371263807	0.00010
NM_006019.4(TCIRG1):c.2028C>T (p.Ala676=)	rs370181947	0.00006
NM_006019.4(TCIRG1):c.1972C>T (p.Arg658Cys)	rs769231419	0.00002
NM_006019.4(TCIRG1):c.2049C>T (p.Asp683=)	rs780969471	0.00001
NM_006019.4(TCIRG1):c.303G>C (p.Thr101=)	rs536494151	0.00001
NM_006019.4(TCIRG1):c.571C>T (p.Arg191Cys)	rs867224433	0.00001
NM_006019.4(TCIRG1):c.1162C>T (p.Pro388Ser)
NM_006019.4(TCIRG1):c.1463+5G>A
NM_006019.4(TCIRG1):c.2405G>A (p.Arg802Gln)
NM_006019.4(TCIRG1):c.630+7A>G
NM_006019.4(TCIRG1):c.806_807+1del	rs1554995891

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