List of variants reported as uncertain significance for Familial cancer of breast; Fanconi anemia complementation group J by Fulgent Genetics, Fulgent Genetics

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1255C>T (p.Arg419Trp)	rs150624408	0.00026
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	rs28903098	0.00024
NM_032043.3(BRIP1):c.380-5A>G	rs587782131	0.00019
NM_032043.3(BRIP1):c.550G>T (p.Asp184Tyr)	rs201047375	0.00006
NM_032043.3(BRIP1):c.1619A>T (p.Gln540Leu)	rs4988349	0.00003
NM_032043.3(BRIP1):c.2285G>A (p.Arg762His)	rs200960251	0.00003
NM_032043.3(BRIP1):c.2469G>T (p.Arg823Ser)	rs587780239	0.00003
NM_032043.3(BRIP1):c.2543G>A (p.Arg848His)	rs374334794	0.00003
NM_032043.3(BRIP1):c.3730_3731del (p.Met1244fs)	rs730881646	0.00003
NM_032043.3(BRIP1):c.797C>T (p.Thr266Met)	rs550031006	0.00002
NM_032043.3(BRIP1):c.1105T>C (p.Tyr369His)	rs587781325	0.00001
NM_032043.3(BRIP1):c.1A>G (p.Met1Val)	rs764585550	0.00001
NM_032043.3(BRIP1):c.2867C>T (p.Ser956Leu)	rs761639530	0.00001
NM_032043.3(BRIP1):c.3149C>A (p.Thr1050Asn)	rs373040333	0.00001
NM_032043.3(BRIP1):c.3178G>A (p.Val1060Ile)	rs149016505	0.00001
NM_032043.3(BRIP1):c.3238G>A (p.Asp1080Asn)	rs786204230	0.00001
NM_032043.3(BRIP1):c.3274C>T (p.Pro1092Ser)	rs768065626	0.00001
NM_032043.3(BRIP1):c.3464G>A (p.Gly1155Glu)	rs45603843	0.00001
NM_032043.3(BRIP1):c.752G>A (p.Arg251His)	rs780834054	0.00001
NM_032043.3(BRIP1):c.823A>G (p.Ile275Val)	rs587781425	0.00001
NM_032043.3(BRIP1):c.110A>G (p.Asn37Ser)	rs876659105
NM_032043.3(BRIP1):c.1219A>G (p.Ser407Gly)	rs1555607156
NM_032043.3(BRIP1):c.1941G>T (p.Trp647Cys)	rs786202760
NM_032043.3(BRIP1):c.2216T>C (p.Leu739Pro)	rs587780234
NM_032043.3(BRIP1):c.2380G>T (p.Val794Phe)	rs1261005517
NM_032043.3(BRIP1):c.2990C>T (p.Thr997Ile)	rs749978235
NM_032043.3(BRIP1):c.340C>T (p.Pro114Ser)	rs2145827137
NM_032043.3(BRIP1):c.3439A>G (p.Asn1147Asp)	rs1258403817
NM_032043.3(BRIP1):c.3622G>C (p.Asp1208His)	rs760589795
NM_032043.3(BRIP1):c.3651G>T (p.Trp1217Cys)	rs542698396
NM_032043.3(BRIP1):c.485G>A (p.Arg162Gln)	rs61757643
NM_032043.3(BRIP1):c.93+8T>G	rs1567878012

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