ClinVar Miner

List of variants reported as benign by King Laboratory, University of Washington

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.2440-6C>G rs139757930 0.00145
NM_004360.5(CDH1):c.2296-670T>A rs540884383 0.00078
NM_000249.4(MLH1):c.678-481C>T rs751119714 0.00051
NM_000051.4(ATM):c.5821G>C (p.Val1941Leu) rs147187700 0.00019
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
NM_000051.4(ATM):c.1009C>T (p.Arg337Cys) rs138398778 0.00017
NM_001130009.3(GEN1):c.1072-185G>A rs1305390435 0.00006
NM_000059.4(BRCA2):c.750G>A (p.Val250=) rs143214959 0.00005
NM_007294.4(BRCA1):c.199G>T (p.Asp67Tyr) rs80357102 0.00005
NM_007294.4(BRCA1):c.301+55G>A rs868735744 0.00005
NM_000546.6(TP53):c.783-60G>A rs898427453 0.00004
NM_007294.4(BRCA1):c.75C>T (p.Pro25=) rs80356839 0.00004
NM_024675.4(PALB2):c.1699C>T (p.His567Tyr) rs370422990 0.00004
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe) rs373478248 0.00004
NM_032043.3(BRIP1):c.297C>T (p.Asp99=) rs201617644 0.00004
NM_000059.4(BRCA2):c.9648+127G>A rs182622896 0.00003
NM_000314.8(PTEN):c.79+4229A>T rs973032283 0.00003
NM_007194.4(CHEK2):c.1130A>G (p.Glu377Gly) rs560973106 0.00003
NM_007294.4(BRCA1):c.81-6T>C rs80358179 0.00003
NM_000051.4(ATM):c.3963G>A (p.Met1321Ile) rs35184530 0.00002
NM_000051.4(ATM):c.5009C>T (p.Ala1670Val) rs375131360 0.00002
NM_000059.4(BRCA2):c.426-252A>G rs948639481 0.00002
NM_000314.8(PTEN):c.492+7414A>G rs1370122389 0.00002
NM_000059.4(BRCA2):c.7466A>G (p.Asp2489Gly) rs80358970 0.00001
NM_000059.4(BRCA2):c.8359C>T (p.Arg2787Cys) rs41293517 0.00001
NM_000059.4(BRCA2):c.9076C>G (p.Gln3026Glu) rs80359159 0.00001
NM_024675.4(PALB2):c.1551A>G (p.Lys517=) rs755845383 0.00001
NM_024675.4(PALB2):c.2204C>T (p.Pro735Leu) rs199743500 0.00001
NM_024675.4(PALB2):c.2587-703G>A rs371016034 0.00001
NM_032043.3(BRIP1):c.2390A>G (p.Lys797Arg) rs730881622 0.00001
NM_000051.4(ATM):c.7181C>T (p.Ser2394Leu) rs587779861
NM_000051.4(ATM):c.8011-6T>G rs762092284
NM_000059.4(BRCA2):c.128A>G (p.Asn43Ser) rs2072285447
NM_000059.4(BRCA2):c.28A>G (p.Thr10Ala) rs786203080
NM_000059.4(BRCA2):c.7559G>C (p.Arg2520Pro) rs80358982
NM_000059.4(BRCA2):c.7820C>T (p.Thr2607Ile) rs1555286821
NM_000059.4(BRCA2):c.7879A>T (p.Ile2627Phe) rs80359014
NM_000059.4(BRCA2):c.7902G>A (p.Met2634Ile) rs1483170360
NM_000059.4(BRCA2):c.8206C>T (p.Leu2736Phe) rs1555287042
NM_000059.4(BRCA2):c.8285C>G (p.Pro2762Arg) rs398122600
NM_000059.4(BRCA2):c.8510G>T (p.Gly2837Val) rs587780663
NM_000059.4(BRCA2):c.9344A>G (p.Lys3115Arg) rs276174923
NM_007194.4(CHEK2):c.231CCAAGAACCTGAGGA[1] (p.77DQEPE[1]) rs587780181
NM_007294.4(BRCA1):c.135-20T>G rs80358025
NM_007294.4(BRCA1):c.4185+31TG[3] rs760098710
NM_007294.4(BRCA1):c.4357+518_4357+521del rs558135126
NM_007294.4(BRCA1):c.5097G>A (p.Arg1699=) rs2051927969
NM_007294.4(BRCA1):c.5207T>G (p.Val1736Gly) rs45553935
NM_007294.4(BRCA1):c.5454C>T (p.Asp1818=) rs1555574705
NM_007294.4(BRCA1):c.81T>C (p.Cys27=) rs587780805
NM_024675.4(PALB2):c.2752C>T (p.Pro918Ser) rs515726094
NM_024675.4(PALB2):c.46A>G (p.Lys16Glu) rs1967230769
NM_032043.3(BRIP1):c.2372A>T (p.Asp791Val) rs876658934
NM_032043.3(BRIP1):c.2765T>C (p.Leu922Ser) rs587782410

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