ClinVar Miner

List of variants in gene TMPRSS6 reported as uncertain significance for Microcytic anemia

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Total variants: 58
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HGVS dbSNP
NM_001374504.1(TMPRSS6):c.*212T>A
NM_001374504.1(TMPRSS6):c.*24G>A
NM_001374504.1(TMPRSS6):c.*251T>A
NM_001374504.1(TMPRSS6):c.-1-218C>G
NM_001374504.1(TMPRSS6):c.1086G>A (p.Thr362=)
NM_001374504.1(TMPRSS6):c.124C>T (p.Leu42Phe)
NM_001374504.1(TMPRSS6):c.1309C>G (p.Arg437Gly)
NM_001374504.1(TMPRSS6):c.1355A>G (p.Glu452Gly)
NM_001374504.1(TMPRSS6):c.1440C>T (p.Cys480=)
NM_001374504.1(TMPRSS6):c.1633C>T (p.Arg545Trp)
NM_001374504.1(TMPRSS6):c.163G>T (p.Val55Leu)
NM_001374504.1(TMPRSS6):c.1651G>A (p.Gly551Ser)
NM_001374504.1(TMPRSS6):c.1687G>A (p.Gly563Ser)
NM_001374504.1(TMPRSS6):c.183G>A (p.Val61=)
NM_001374504.1(TMPRSS6):c.1851C>T (p.Ser617=)
NM_001374504.1(TMPRSS6):c.1999C>T (p.His667Tyr)
NM_001374504.1(TMPRSS6):c.2004G>A (p.Pro668=)
NM_001374504.1(TMPRSS6):c.2014T>C (p.Ser672Pro)
NM_001374504.1(TMPRSS6):c.2099C>T (p.Ala700Val)
NM_001374504.1(TMPRSS6):c.212C>T (p.Ala71Val)
NM_001374504.1(TMPRSS6):c.2204G>A (p.Arg735His)
NM_001374504.1(TMPRSS6):c.2250+15C>T
NM_001374504.1(TMPRSS6):c.2250+7C>A
NM_001374504.1(TMPRSS6):c.2374G>A (p.Gly792Ser)
NM_001374504.1(TMPRSS6):c.251G>C (p.Arg84Pro)
NM_001374504.1(TMPRSS6):c.287G>A (p.Arg96His)
NM_001374504.1(TMPRSS6):c.334A>G (p.Met112Val)
NM_001374504.1(TMPRSS6):c.530C>T (p.Ser177Leu)
NM_001374504.1(TMPRSS6):c.549G>A (p.Arg183=)
NM_001374504.1(TMPRSS6):c.648C>A (p.Ser216Arg)
NM_001374504.1(TMPRSS6):c.656G>A (p.Gly219Asp)
NM_001374504.1(TMPRSS6):c.752G>T (p.Arg251Leu)
NM_001374504.1(TMPRSS6):c.780G>A (p.Arg260=)
NM_001374504.1(TMPRSS6):c.865G>A (p.Val289Met)
NM_001374504.1(TMPRSS6):c.928T>C (p.Tyr310His)
NM_153609.3(TMPRSS6):c.*140C>T rs886057491
NM_153609.3(TMPRSS6):c.*303T>G rs886057490
NM_153609.3(TMPRSS6):c.*35T>C rs199957731
NM_153609.3(TMPRSS6):c.*499C>T rs560949530
NM_153609.3(TMPRSS6):c.1000+11del rs780218999
NM_153609.3(TMPRSS6):c.1096T>C (p.Cys366Arg) rs886057492
NM_153609.3(TMPRSS6):c.1224-4C>G rs529716198
NM_153609.3(TMPRSS6):c.1233C>T (p.Gly411=) rs146266448
NM_153609.3(TMPRSS6):c.1365G>A (p.Ser455=) rs776737568
NM_153609.3(TMPRSS6):c.1520C>T (p.Pro507Leu) rs138915369
NM_153609.3(TMPRSS6):c.154C>T (p.Arg52Cys) rs750274321
NM_153609.3(TMPRSS6):c.170T>A (p.Phe57Tyr) rs745388319
NM_153609.3(TMPRSS6):c.1789C>T (p.Arg597Trp) rs773272073
NM_153609.3(TMPRSS6):c.2085C>G (p.Phe695Leu) rs375189210
NM_153609.3(TMPRSS6):c.270C>A (p.Gly90=) rs147397866
NM_153609.3(TMPRSS6):c.438A>G (p.Gly146=) rs375681801
NM_153609.3(TMPRSS6):c.478G>A (p.Glu160Lys) rs752163489
NM_153609.3(TMPRSS6):c.616+9T>C rs377665035
NM_153609.3(TMPRSS6):c.659-8C>T rs375234781
NM_153609.3(TMPRSS6):c.720C>T (p.His240=) rs769301726
NM_153609.3(TMPRSS6):c.865G>T (p.Val289Leu) rs201148397
NM_153609.3(TMPRSS6):c.909G>A (p.Ala303=) rs370192027
NM_153609.3(TMPRSS6):c.984_985insGGAGACC (p.Pro329fs) rs1569012596

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