ClinVar Miner

List of variants in gene STK11 reported as likely pathogenic for not provided

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Total variants: 11
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HGVS dbSNP
NM_000455.4(STK11):c.199del (p.Leu67fs) rs1555735014
NM_000455.4(STK11):c.407T>C (p.Met136Thr) rs1060499958
NM_000455.4(STK11):c.481A>T (p.Ile161Phe) rs1131690938
NM_000455.4(STK11):c.527A>G (p.Asp176Gly) rs1064794805
NM_000455.4(STK11):c.580G>A (p.Asp194Asn) rs121913315
NM_000455.4(STK11):c.582C>A (p.Asp194Glu) rs786202134
NM_000455.4(STK11):c.630C>A (p.Cys210Ter) rs786201213
NM_000455.4(STK11):c.711C>G (p.Asp237Glu) rs1057520379
NM_000455.4(STK11):c.781_788dup (p.Leu263fs) rs1568709203
NM_000455.4(STK11):c.869T>C (p.Leu290Pro) rs1057524439
NM_000455.4(STK11):c.908T>G (p.Ile303Ser) rs727504171

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