ClinVar Miner

List of variants in gene BRIP1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_032043.3(BRIP1):c.1735C>T (p.Arg579Cys) rs28997571 0.00034
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala) rs28903098 0.00024
NM_032043.3(BRIP1):c.1899C>G (p.Ile633Met) rs28997572 0.00002
NM_032043.3(BRIP1):c.2648A>C (p.Glu883Ala) rs1453990721 0.00001
NM_032043.3(BRIP1):c.1432C>T (p.His478Tyr) rs761452695
NM_032043.3(BRIP1):c.2365G>T (p.Val789Leu) rs876661097
NM_032043.3(BRIP1):c.2498T>C (p.Ile833Thr) rs876660936
NM_032043.3(BRIP1):c.2519G>A (p.Gly840Glu)
NM_032043.3(BRIP1):c.3284C>G (p.Ser1095Cys) rs1479296707

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