List of variants in gene BRIP1 reported as likely benign by Counsyl

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.517C>T (p.Arg173Cys)	rs4988345	0.00363
NM_032043.3(BRIP1):c.2097+7G>A	rs4988352	0.00271
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=)	rs75091137	0.00194
NM_032043.3(BRIP1):c.2286T>C (p.Arg762=)	rs61754141	0.00173
NM_032043.3(BRIP1):c.2061G>C (p.Val687=)	rs112414873	0.00153
NM_032043.3(BRIP1):c.890A>G (p.Lys297Arg)	rs28997570	0.00113
NM_032043.3(BRIP1):c.790C>T (p.Arg264Trp)	rs28997569	0.00104
NM_032043.3(BRIP1):c.195A>G (p.Gln65=)	rs141436143	0.00076
NM_032043.3(BRIP1):c.3459T>C (p.Asp1153=)	rs4987050	0.00069
NM_032043.3(BRIP1):c.1935+11G>A	rs79121306	0.00051
NM_032043.3(BRIP1):c.852C>T (p.Val284=)	rs144940449	0.00021
NM_032043.3(BRIP1):c.36G>T (p.Gly12=)	rs45566938	0.00019
NM_032043.3(BRIP1):c.1890A>G (p.Thr630=)	rs145796331	0.00017
NM_032043.3(BRIP1):c.595C>T (p.Leu199=)	rs144969738	0.00014
NM_032043.3(BRIP1):c.3099T>C (p.Pro1033=)	rs202228407	0.00013
NM_032043.3(BRIP1):c.93+15G>A	rs113052745	0.00009
NM_032043.3(BRIP1):c.1629-11T>C	rs375710640	0.00007
NM_032043.3(BRIP1):c.3336T>C (p.Asp1112=)	rs369843642	0.00007
NM_032043.3(BRIP1):c.1140+11G>A	rs369153270	0.00006
NM_032043.3(BRIP1):c.2232C>T (p.Asp744=)	rs374362388	0.00006
NM_032043.3(BRIP1):c.297C>T (p.Asp99=)	rs201617644	0.00004
NM_032043.3(BRIP1):c.3051G>A (p.Pro1017=)	rs776990704	0.00004
NM_032043.3(BRIP1):c.312T>G (p.Thr104=)	rs769190318	0.00003
NM_032043.3(BRIP1):c.702G>A (p.Lys234=)	rs45512798	0.00003
NM_032043.2(BRIP1):c.2097+8A>C	rs730881642	0.00001
NM_032043.3(BRIP1):c.1455T>C (p.Ala485=)	rs773489367	0.00001
NM_032043.3(BRIP1):c.1795-9T>G	rs777006706	0.00001
NM_032043.3(BRIP1):c.612C>G (p.Ser204=)	rs587780832	0.00001
NM_032043.3(BRIP1):c.1629-500G>A	rs1057517645
NM_032043.3(BRIP1):c.1935+5GTT[2]	rs730881641
NM_032043.3(BRIP1):c.2576-17T>G	rs1057517647
NM_032043.3(BRIP1):c.2991A>G (p.Thr997=)	rs45466996
NM_032043.3(BRIP1):c.380-17dup	rs545021924

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