List of variants in gene BRIP1 reported as uncertain significance by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.587A>G (p.Asn196Ser)	rs550707862	0.00017
NM_032043.3(BRIP1):c.2440C>T (p.Arg814Cys)	rs201869624	0.00016
NM_032043.3(BRIP1):c.2324A>G (p.Asn775Ser)	rs571108955	0.00003
NM_032043.3(BRIP1):c.2830C>G (p.Gln944Glu)	rs140233356	0.00003
NM_032043.3(BRIP1):c.2854A>G (p.Ile952Val)	rs200239986	0.00003
NM_032043.3(BRIP1):c.1442G>A (p.Gly481Asp)	rs200062099	0.00001
NM_032043.3(BRIP1):c.2441G>A (p.Arg814His)	rs45468199	0.00001
NM_032043.3(BRIP1):c.2569A>G (p.Ile857Val)	rs28904918	0.00001
NM_032043.3(BRIP1):c.3505G>T (p.Asp1169Tyr)	rs587782029	0.00001
NM_032043.3(BRIP1):c.1114C>A (p.Leu372Ile)	rs786202637
NM_032043.3(BRIP1):c.1427C>G (p.Thr476Ser)	rs1567825164
NM_032043.3(BRIP1):c.2131A>G (p.Thr711Ala)	rs760515227
NM_032043.3(BRIP1):c.2266C>T (p.Leu756Phe)	rs2077009187
NM_032043.3(BRIP1):c.2301G>C (p.Glu767Asp)	rs369434185
NM_032043.3(BRIP1):c.2531T>C (p.Leu844Pro)	rs1555574776
NM_032043.3(BRIP1):c.3508C>G (p.Leu1170Val)	rs587782552
NM_032043.3(BRIP1):c.650G>C (p.Cys217Ser)	rs587782156
NM_032043.3(BRIP1):c.87G>T (p.Met29Ile)	rs769585673

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