List of variants in gene GATA2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_032638.5(GATA2):c.1143+11C>T	rs367569053	0.00013
NM_032638.5(GATA2):c.30G>T (p.Trp10Cys)	rs367785289	0.00011
NM_032638.5(GATA2):c.445G>A (p.Gly149Arg)	rs753645971	0.00009
NM_032638.5(GATA2):c.829A>G (p.Ser277Gly)	rs141800945	0.00009
NM_032638.5(GATA2):c.1367C>T (p.Pro456Leu)	rs372912472	0.00007
NM_032638.5(GATA2):c.888C>T (p.Val296=)	rs574218913	0.00007
NM_032638.5(GATA2):c.1274C>T (p.Ser425Leu)	rs146554939	0.00006
NM_032638.5(GATA2):c.49C>T (p.Leu17=)	rs752025757	0.00005
NM_032638.5(GATA2):c.1017+485A>T	rs745812924	0.00004
NM_032638.5(GATA2):c.1391G>T (p.Ser464Ile)	rs770949428	0.00004
NM_032638.5(GATA2):c.358C>T (p.Pro120Ser)	rs144794596	0.00004
NM_032638.5(GATA2):c.-314G>A	rs1321601729	0.00003
NM_032638.5(GATA2):c.1286G>C (p.Ser429Thr)	rs201155045	0.00003
NM_032638.5(GATA2):c.-328del	rs1220195779	0.00002
NM_032638.5(GATA2):c.-179G>C	rs890513278	0.00001
NM_032638.5(GATA2):c.1017+512C>T	rs890419135	0.00001
NM_032638.5(GATA2):c.1179C>G (p.Ile393Met)	rs1553770437	0.00001
NM_032638.5(GATA2):c.1230G>T (p.Gly410=)	rs1461907039	0.00001
NM_032638.5(GATA2):c.371C>A (p.Thr124Lys)	rs569301892	0.00001
NM_032638.5(GATA2):c.409C>T (p.Pro137Ser)	rs113166293	0.00001
NM_032638.5(GATA2):c.1017+525C>T	rs916833024
NM_032638.5(GATA2):c.1017+530C>T	rs2107669883
NM_032638.5(GATA2):c.1018-5C>G	rs769196688
NM_032638.5(GATA2):c.1035C>T (p.Ala345=)	rs371599112
NM_032638.5(GATA2):c.1036G>A (p.Gly346Ser)	rs1559985135
NM_032638.5(GATA2):c.1407C>A (p.His469Gln)	rs772050518
NM_032638.5(GATA2):c.230-12_230-9del	rs760230147
NM_032638.5(GATA2):c.299_300delinsTT (p.Gly100Val)	rs1060500084
NM_032638.5(GATA2):c.331CAC[2] (p.His113del)	rs777017660
NM_032638.5(GATA2):c.346_351del (p.Trp116_Thr117del)	rs2107672791
NM_032638.5(GATA2):c.706A>G (p.Met236Val)	rs746737860
NM_032638.5(GATA2):c.774C>G (p.His258Gln)	rs1353328065
NM_032638.5(GATA2):c.802G>A (p.Gly268Arg)
NM_032638.5(GATA2):c.872-5T>G	rs886038417
NM_032638.5(GATA2):c.942C>T (p.Tyr314=)	rs2107670420

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