ClinVar Miner

List of variants reported as likely benign for Familial cancer of breast by MGZ Medical Genetics Center

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.5414A>G (p.Asn1805Ser) rs80358765 0.00010
NM_007294.4(BRCA1):c.3649T>C (p.Ser1217Pro) rs273900712 0.00008
NM_000059.4(BRCA2):c.8092G>A (p.Ala2698Thr) rs80359052 0.00005
NM_000059.4(BRCA2):c.6739A>G (p.Ser2247Gly) rs80358896 0.00004
NM_000059.4(BRCA2):c.3910A>G (p.Thr1304Ala) rs28897723 0.00003
NM_000059.4(BRCA2):c.6847C>G (p.Pro2283Ala) rs80358909 0.00003
NM_000059.4(BRCA2):c.179A>G (p.Asn60Ser) rs80358463 0.00002
NM_000059.4(BRCA2):c.353G>A (p.Arg118His) rs80358603 0.00002
NM_000059.4(BRCA2):c.6550C>G (p.Gln2184Glu) rs80358887 0.00002
NM_007294.4(BRCA1):c.2808T>G (p.Asp936Glu) rs730881485 0.00002
NM_007294.4(BRCA1):c.994C>T (p.Arg332Trp) rs80357176 0.00002
NM_000059.4(BRCA2):c.10054C>G (p.Leu3352Val) rs1475702169 0.00001
NM_000059.4(BRCA2):c.1124C>T (p.Pro375Leu) rs80358409 0.00001
NM_000059.4(BRCA2):c.1159G>T (p.Val387Phe) rs869320791 0.00001
NM_000059.4(BRCA2):c.2599A>G (p.Thr867Ala) rs80358522 0.00001
NM_000059.4(BRCA2):c.3085A>G (p.Met1029Val) rs80358553 0.00001
NM_000059.4(BRCA2):c.4685A>C (p.Gln1562Pro) rs544688816 0.00001
NM_000059.4(BRCA2):c.5225A>T (p.Asn1742Ile) rs756463217 0.00001
NM_000059.4(BRCA2):c.5487G>T (p.Leu1829Phe) rs779967765 0.00001
NM_000059.4(BRCA2):c.5683G>A (p.Glu1895Lys) rs146351301 0.00001
NM_000059.4(BRCA2):c.6458C>T (p.Pro2153Leu) rs276174873 0.00001
NM_000059.4(BRCA2):c.6467C>T (p.Ser2156Phe) rs765575482 0.00001
NM_000059.4(BRCA2):c.6772G>A (p.Glu2258Lys) rs730881549 0.00001
NM_000059.4(BRCA2):c.7222C>T (p.Pro2408Ser) rs398122577 0.00001
NM_000059.4(BRCA2):c.7633G>A (p.Val2545Ile) rs80358990 0.00001
NM_000059.4(BRCA2):c.8798G>C (p.Arg2933Thr) rs553440338 0.00001
NM_000059.4(BRCA2):c.959T>C (p.Leu320Pro) rs1334767632 0.00001
NM_000059.4(BRCA2):c.9983T>G (p.Phe3328Cys) rs770826575 0.00001
NM_007294.4(BRCA1):c.2362G>A (p.Val788Ile) rs80357060 0.00001
NM_007294.4(BRCA1):c.2765C>G (p.Thr922Arg) rs80357460 0.00001
NM_007294.4(BRCA1):c.4417T>C (p.Ser1473Pro) rs398122686 0.00001
NM_000059.4(BRCA2):c.10072G>A (p.Gly3358Arg) rs1593202253
NM_000059.4(BRCA2):c.1117C>A (p.Gln373Lys)
NM_000059.4(BRCA2):c.1942T>A (p.Ser648Thr) rs1593895835
NM_000059.4(BRCA2):c.2024C>G (p.Thr675Arg) rs80358484
NM_000059.4(BRCA2):c.2091A>C (p.Lys697Asn) rs876659230
NM_000059.4(BRCA2):c.2515T>C (p.Tyr839His) rs587778125
NM_000059.4(BRCA2):c.2743A>T (p.Thr915Ser)
NM_000059.4(BRCA2):c.2779A>G (p.Met927Val) rs786201837
NM_000059.4(BRCA2):c.305A>G (p.Lys102Arg) rs80358549
NM_000059.4(BRCA2):c.3503T>C (p.Met1168Thr) rs80358598
NM_000059.4(BRCA2):c.3521G>A (p.Gly1174Asp) rs1555283272
NM_000059.4(BRCA2):c.3524A>G (p.Gln1175Arg)
NM_000059.4(BRCA2):c.362A>T (p.Lys121Ile)
NM_000059.4(BRCA2):c.3762G>T (p.Glu1254Asp) rs777028631
NM_000059.4(BRCA2):c.3767A>G (p.His1256Arg) rs80358618
NM_000059.4(BRCA2):c.3836A>G (p.Asn1279Ser) rs1060502384
NM_000059.4(BRCA2):c.397C>A (p.Pro133Thr) rs571823764
NM_000059.4(BRCA2):c.4028A>G (p.Lys1343Arg)
NM_000059.4(BRCA2):c.4059A>C (p.Glu1353Asp)
NM_000059.4(BRCA2):c.454A>G (p.Thr152Ala) rs886037806
NM_000059.4(BRCA2):c.4644A>C (p.Glu1548Asp)
NM_000059.4(BRCA2):c.464G>A (p.Arg155Lys) rs377639990
NM_000059.4(BRCA2):c.5081G>A (p.Arg1694Lys) rs753721331
NM_000059.4(BRCA2):c.5386G>T (p.Asp1796Tyr) rs1064793715
NM_000059.4(BRCA2):c.5860A>G (p.Thr1954Ala) rs1566233345
NM_000059.4(BRCA2):c.5987C>G (p.Ala1996Gly) rs80358834
NM_000059.4(BRCA2):c.6034T>C (p.Ser2012Pro)
NM_000059.4(BRCA2):c.6144T>G (p.Asn2048Lys) rs587782775
NM_000059.4(BRCA2):c.622G>C (p.Val208Leu) rs1593887544
NM_000059.4(BRCA2):c.631+7A>G rs431825339
NM_000059.4(BRCA2):c.6469C>G (p.Gln2157Glu) rs397507859
NM_000059.4(BRCA2):c.6742C>T (p.His2248Tyr)
NM_000059.4(BRCA2):c.6842G>T (p.Gly2281Val) rs80358908
NM_000059.4(BRCA2):c.6884G>C (p.Arg2295Thr) rs1555285151
NM_000059.4(BRCA2):c.6916G>C (p.Ala2306Pro) rs730881550
NM_000059.4(BRCA2):c.7033C>G (p.Gln2345Glu) rs886040685
NM_000059.4(BRCA2):c.7095T>A (p.His2365Gln) rs370708814
NM_000059.4(BRCA2):c.9613_9614delinsCT (p.Ala3205Leu) rs276174926
NM_000059.4(BRCA2):c.9749C>T (p.Ser3250Leu)
NM_000059.4(BRCA2):c.9998T>C (p.Leu3333Pro) rs1555290016
NM_007294.4(BRCA1):c.*39G>A
NM_007294.4(BRCA1):c.1099A>G (p.Thr367Ala) rs878854929
NM_007294.4(BRCA1):c.1119A>G (p.Ile373Met)
NM_007294.4(BRCA1):c.1232A>T (p.Asp411Val) rs730881469
NM_007294.4(BRCA1):c.1441C>G (p.Leu481Val) rs1397842308
NM_007294.4(BRCA1):c.2069A>G (p.Lys690Arg) rs2154401162
NM_007294.4(BRCA1):c.2079C>G (p.Asp693Glu)
NM_007294.4(BRCA1):c.2663A>T (p.His888Leu) rs876658843
NM_007294.4(BRCA1):c.3058C>T (p.Pro1020Ser)
NM_007294.4(BRCA1):c.3113A>C (p.Glu1038Ala) rs16941
NM_007294.4(BRCA1):c.3365C>T (p.Thr1122Ile) rs2053599251
NM_007294.4(BRCA1):c.3681A>T (p.Gln1227His) rs730881488
NM_007294.4(BRCA1):c.3728G>C (p.Arg1243Thr)
NM_007294.4(BRCA1):c.4273C>T (p.Pro1425Ser) rs768327850
NM_007294.4(BRCA1):c.4697C>A (p.Ser1566Tyr) rs1060502325
NM_007294.4(BRCA1):c.4921G>T (p.Ala1641Ser) rs1800726
NM_007294.4(BRCA1):c.523A>G (p.Lys175Glu) rs1567806027
NM_007294.4(BRCA1):c.556T>G (p.Ser186Ala) rs397509298
NM_007294.4(BRCA1):c.724A>G (p.Ser242Gly) rs1555593258
NM_007294.4(BRCA1):c.827C>T (p.Thr276Ile)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.