List of variants in gene BRIP1 reported as uncertain significance for Breast and/or ovarian cancer

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.3559G>A (p.Ala1187Thr)	rs367610893	0.00027
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.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.2087C>T (p.Pro696Leu)	rs147755155	0.00006
NM_032043.3(BRIP1):c.413T>C (p.Leu138Ser)	rs587780251	0.00006
NM_032043.3(BRIP1):c.590C>T (p.Ser197Phe)	rs533184563	0.00004
NM_032043.3(BRIP1):c.2285G>A (p.Arg762His)	rs200960251	0.00003
NM_032043.3(BRIP1):c.2324A>G (p.Asn775Ser)	rs571108955	0.00003
NM_032043.3(BRIP1):c.3571A>G (p.Ile1191Val)	rs761405340	0.00003
NM_032043.3(BRIP1):c.1377A>C (p.Arg459Ser)	rs780310294	0.00002
NM_032043.3(BRIP1):c.518G>A (p.Arg173His)	rs761432927	0.00002
NM_032043.3(BRIP1):c.778A>G (p.Thr260Ala)	rs138743097	0.00002
NM_032043.3(BRIP1):c.797C>T (p.Thr266Met)	rs550031006	0.00002
NM_032043.3(BRIP1):c.1742G>A (p.Arg581Gln)	rs587778133	0.00001
NM_032043.3(BRIP1):c.2056A>G (p.Thr686Ala)	rs769820537	0.00001
NM_032043.3(BRIP1):c.254C>T (p.Ser85Leu)	rs587781830	0.00001
NM_032043.3(BRIP1):c.2686A>G (p.Ile896Val)	rs764406913	0.00001
NM_032043.3(BRIP1):c.3199T>A (p.Cys1067Ser)	rs878855153	0.00001
NM_032043.3(BRIP1):c.655T>C (p.Cys219Arg)	rs730881630	0.00001
NM_032043.3(BRIP1):c.823A>G (p.Ile275Val)	rs587781425	0.00001
NM_032043.3(BRIP1):c.1040T>C (p.Leu347Pro)	rs786201819
NM_032043.3(BRIP1):c.1045G>A (p.Ala349Thr)	rs149364097
NM_032043.3(BRIP1):c.1141-7_1141-3del	rs1060501744
NM_032043.3(BRIP1):c.1430T>C (p.Leu477Ser)
NM_032043.3(BRIP1):c.1626C>G (p.Ser542Arg)
NM_032043.3(BRIP1):c.1629-4C>A
NM_032043.3(BRIP1):c.1795-12_1795-10del	rs1475317357
NM_032043.3(BRIP1):c.1972C>G (p.Arg658Gly)	rs786203170
NM_032043.3(BRIP1):c.2542C>G (p.Arg848Gly)	rs45572934
NM_032043.3(BRIP1):c.258_269del (p.Cys87_Cys90del)	rs730881648
NM_032043.3(BRIP1):c.2710G>A (p.Asp904Asn)	rs1555573413
NM_032043.3(BRIP1):c.2906-7T>C	rs1237575383
NM_032043.3(BRIP1):c.3374_3376del (p.Ala1125del)	rs745344948
NM_032043.3(BRIP1):c.3411_3412delinsCT (p.Asp1138Tyr)	rs1555572620
NM_032043.3(BRIP1):c.397A>G (p.Thr133Ala)	rs764256720
NM_032043.3(BRIP1):c.856C>T (p.Pro286Ser)	rs770289817

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