ClinVar Miner

List of variants in gene STK11 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.-127T>C rs532196225 0.00374
NM_000455.5(STK11):c.597+14del rs536282050 0.00067
NM_000455.5(STK11):c.945G>A (p.Pro315=) rs376329042 0.00060
NM_000455.5(STK11):c.1211C>T (p.Ser404Phe) rs200078204 0.00051
NM_000455.5(STK11):c.1185A>G (p.Thr395=) rs370207155 0.00047
NM_000455.5(STK11):c.1108+531G>C rs925652247 0.00029
NM_000455.5(STK11):c.825G>A (p.Pro275=) rs202011521 0.00011
NM_000455.5(STK11):c.787T>C (p.Leu263=) rs372378119 0.00010
NM_000455.5(STK11):c.357C>T (p.Asn119=) rs372511774 0.00007
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.666C>T (p.Pro222=) rs542189325 0.00005
NM_000455.5(STK11):c.920+6C>T rs730881964 0.00005
NM_000455.5(STK11):c.723T>C (p.Ala241=) rs533550278 0.00004
NM_000455.5(STK11):c.795G>A (p.Glu265=) rs730881963 0.00004
NM_000455.5(STK11):c.876C>T (p.Tyr292=) rs148928808 0.00003
NM_000455.5(STK11):c.828C>T (p.Gly276=) rs200824447 0.00002
NM_000455.5(STK11):c.1108+521C>T rs572562074 0.00001
NM_000455.5(STK11):c.1128G>A (p.Glu376=) rs747018506 0.00001
NM_000455.5(STK11):c.147C>T (p.Tyr49=) rs751949296 0.00001
NM_000455.5(STK11):c.321C>T (p.His107=) rs878853987 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NC_000019.10:g.1201926G>A rs185744805
NM_000455.5(STK11):c.*475C>T rs2080840327
NM_000455.5(STK11):c.1108+460C>T
NM_000455.5(STK11):c.1108+527C>T
NM_000455.5(STK11):c.597+21dup rs534445875
NM_000455.5(STK11):c.96C>G (p.Thr32=) rs79175212

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