ClinVar Miner

List of variants in gene STK11 reported as likely benign by Counsyl

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_000455.4(STK11):c.1035C>T (p.His345=) rs751619208
NM_000455.4(STK11):c.1038C>T (p.Gly346=) rs767565606
NM_000455.4(STK11):c.1041G>A (p.Ala347=) rs537906142
NM_000455.4(STK11):c.1062C>T (p.Phe354=) rs59912467
NM_000455.4(STK11):c.1109-13G>A rs568152768
NM_000455.4(STK11):c.1109-14C>T rs780434041
NM_000455.4(STK11):c.1109-21C>T rs371145906
NM_000455.4(STK11):c.1137C>T (p.His379=) rs786201505
NM_000455.4(STK11):c.1185A>G (p.Thr395=) rs370207155
NM_000455.4(STK11):c.120C>T (p.Arg40=) rs878853984
NM_000455.4(STK11):c.1284G>A (p.Ser428=) rs369097329
NM_000455.4(STK11):c.237C>T (p.Ile79=) rs751859508
NM_000455.4(STK11):c.290+21_290+26dup6 rs1555735086
NM_000455.4(STK11):c.290+22C>T rs371255627
NM_000455.4(STK11):c.318G>A (p.Arg106=) rs777784520
NM_000455.4(STK11):c.357C>T (p.Asn119=) rs372511774
NM_000455.4(STK11):c.366G>A (p.Lys122=) rs376969448
NM_000455.4(STK11):c.375-5C>T rs1057517626
NM_000455.4(STK11):c.375-7G>A rs587781176
NM_000455.4(STK11):c.432G>A (p.Pro144=) rs376788924
NM_000455.4(STK11):c.464+10C>T rs587782445
NM_000455.4(STK11):c.464+20delG rs730881960
NM_000455.4(STK11):c.464+8C>T rs863224669
NM_000455.4(STK11):c.465-12_465-11delTG rs749644491
NM_000455.4(STK11):c.465-18G>T rs587781177
NM_000455.4(STK11):c.465-5C>T rs567202367
NM_000455.4(STK11):c.465-7C>T rs864622317
NM_000455.4(STK11):c.537G>A (p.Pro179=) rs528535500
NM_000455.4(STK11):c.594C>T (p.Ala198=) rs772940660
NM_000455.4(STK11):c.597+14del rs536282050
NM_000455.4(STK11):c.597+15G>T rs774187994
NM_000455.4(STK11):c.597+21dupG rs534445875
NM_000455.4(STK11):c.598-7G>A rs377502057
NM_000455.4(STK11):c.615G>A (p.Ala205=) rs532889728
NM_000455.4(STK11):c.618G>A (p.Ala206=) rs370976710
NM_000455.4(STK11):c.621C>T (p.Asp207=) rs569380138
NM_000455.4(STK11):c.666C>T (p.Pro222=) rs542189325
NM_000455.4(STK11):c.678C>T (p.Asn226=) rs748832988
NM_000455.4(STK11):c.723T>C (p.Ala241=) rs533550278
NM_000455.4(STK11):c.734+11C>T rs773604294
NM_000455.4(STK11):c.734+17C>A rs751929304
NM_000455.4(STK11):c.734+20G>A rs375315233
NM_000455.4(STK11):c.735-19C>T rs1057517576
NM_000455.4(STK11):c.787T>C (p.Leu263=) rs372378119
NM_000455.4(STK11):c.795G>A (p.Glu265=) rs730881963
NM_000455.4(STK11):c.828C>T (p.Gly276=) rs200824447
NM_000455.4(STK11):c.862+23C>T rs200302435
NM_000455.4(STK11):c.863-6C>T rs757276643
NM_000455.4(STK11):c.876C>T (p.Tyr292=) rs148928808
NM_000455.4(STK11):c.920+28C>T rs371039379
NM_000455.4(STK11):c.920+29G>A rs191273506
NM_000455.4(STK11):c.920+32G>A rs374147918
NM_000455.4(STK11):c.920+7G>A rs2075607
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.957A>G (p.Pro319=) rs755126393
NM_000455.4(STK11):c.96C>G (p.Thr32=) rs79175212

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