ClinVar Miner

List of variants in gene STK11 reported as benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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NM_000455.4(STK11):c.-2G>T rs774072752
NM_000455.4(STK11):c.1041G>A (p.Ala347=) rs537906142
NM_000455.4(STK11):c.1109-5C>T rs587782020
NM_000455.4(STK11):c.1185A>G (p.Thr395=) rs370207155
NM_000455.4(STK11):c.1194G>A (p.Ala398=) rs184271025
NM_000455.4(STK11):c.1211C>T (p.Ser404Phe) rs200078204
NM_000455.4(STK11):c.1257C>T (p.Ser419=) rs375328708
NM_000455.4(STK11):c.1284G>A (p.Ser428=) rs369097329
NM_000455.4(STK11):c.1296G>A (p.Gln432=) rs587781179
NM_000455.4(STK11):c.357C>T (p.Asn119=) rs372511774
NM_000455.4(STK11):c.464+10C>T rs587782445
NM_000455.4(STK11):c.464+9G>A rs376313955
NM_000455.4(STK11):c.552C>T (p.Leu184=) rs587780719
NM_000455.4(STK11):c.598-8C>T rs373610101
NM_000455.4(STK11):c.651G>A (p.Pro217=) rs368348370
NM_000455.4(STK11):c.666C>T (p.Pro222=) rs542189325
NM_000455.4(STK11):c.723T>C (p.Ala241=) rs533550278
NM_000455.4(STK11):c.920+6C>T rs730881964
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.96C>G (p.Thr32=) rs79175212
NM_000455.4(STK11):c.972G>A (p.Pro324=) rs553474397

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