ClinVar Miner

List of variants in gene GRXCR1 reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001080476.3(GRXCR1):c.140C>T (p.Ala47Val) rs57655409 0.07551
NM_001080476.3(GRXCR1):c.777C>T (p.Ser259=) rs61733348 0.01525
NM_001080476.3(GRXCR1):c.272G>T (p.Gly91Val) rs113203706 0.00339
NM_001080476.3(GRXCR1):c.785G>A (p.Arg262Gln) rs146696590 0.00067
NM_001080476.3(GRXCR1):c.774G>A (p.Met258Ile) rs200029324 0.00021
NM_001080476.3(GRXCR1):c.331T>C (p.Tyr111His) rs201002003 0.00016
NM_001080476.3(GRXCR1):c.753C>T (p.Ser251=) rs374667597 0.00012
NM_001080476.3(GRXCR1):c.825G>A (p.Thr275=) rs370629848 0.00012
NM_001080476.3(GRXCR1):c.*13C>G rs368464416 0.00006
NM_001080476.3(GRXCR1):c.231G>T (p.Gln77His) rs368876169 0.00005
NM_001080476.3(GRXCR1):c.747A>G (p.Pro249=) rs369500517 0.00005
NM_001080476.3(GRXCR1):c.152G>A (p.Gly51Glu) rs727505186 0.00001
NM_001080476.3(GRXCR1):c.296T>C (p.Ile99Thr) rs727503088 0.00001
NM_001080476.3(GRXCR1):c.358T>C (p.Phe120Leu) rs529420082 0.00001
NM_001080476.3(GRXCR1):c.75T>C (p.Ser25=) rs876657475 0.00001
NM_001080476.3(GRXCR1):c.784C>T (p.Arg262Ter) rs761349153 0.00001
NM_001080476.3(GRXCR1):c.813C>A (p.Ala271=) rs727503090 0.00001
NM_001080476.2(GRXCR1):c.(?_-62)_*(153_?)dup
NM_001080476.3(GRXCR1):c.234T>C (p.Asp78=) rs376086928
NM_001080476.3(GRXCR1):c.25G>A (p.Glu9Lys) rs78136490
NM_001080476.3(GRXCR1):c.58A>G (p.Ile20Val) rs1746274698
NM_001080476.3(GRXCR1):c.594_597dup (p.Val200fs) rs1553941938
NM_001080476.3(GRXCR1):c.597T>A (p.Pro199=) rs1553941946
NM_001080476.3(GRXCR1):c.627+8A>C rs10213360
NM_001080476.3(GRXCR1):c.627+8A>T rs10213360
NM_001080476.3(GRXCR1):c.628-11C>T rs727503089
NM_001080476.3(GRXCR1):c.785G>T (p.Arg262Leu) rs146696590
NM_001080476.3(GRXCR1):c.822T>C (p.Cys274=) rs1441618706

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