ClinVar Miner

List of variants in gene combination NKX2-1, SFTA3 reported as likely benign for not provided

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_001079668.3(NKX2-1):c.463+278G>A rs114814082 0.01086
NM_001079668.3(NKX2-1):c.464-306G>A rs186809227 0.00514
NM_001079668.3(NKX2-1):c.78-48C>T rs147791173 0.00503
NM_001079668.3(NKX2-1):c.1093G>T (p.Ala365Ser) rs147542347 0.00389
NM_001079668.3(NKX2-1):c.464-64C>T rs372806369 0.00354
NM_001079668.3(NKX2-1):c.190C>A (p.Leu64Ile) rs201631950 0.00103
NM_001079668.3(NKX2-1):c.1106C>T (p.Ala369Val) rs537209983 0.00009
NM_001079668.3(NKX2-1):c.463+15C>T rs765190713 0.00009
NM_001079668.3(NKX2-1):c.1054G>A (p.Gly352Ser) rs200560568 0.00006
NM_001079668.3(NKX2-1):c.867G>A (p.Ala289=) rs746780018 0.00004
NM_001079668.3(NKX2-1):c.1155G>C (p.Ser385=) rs371404638 0.00003
NM_001079668.3(NKX2-1):c.435C>G (p.Gly145=) rs886050484 0.00003
NM_001079668.3(NKX2-1):c.464-15G>A rs370921485 0.00003
NM_001079668.3(NKX2-1):c.1029T>C (p.Leu343=) rs1292638363 0.00002
NM_001079668.3(NKX2-1):c.1131G>A (p.Leu377=) rs756582124 0.00001
NM_001079668.3(NKX2-1):c.1152C>A (p.Gly384=) rs766670160 0.00001
NM_001079668.3(NKX2-1):c.1200C>T (p.Thr400=) rs886050481 0.00001
NM_001079668.3(NKX2-1):c.282C>A (p.Val94=) rs1306310829 0.00001
NM_001079668.3(NKX2-1):c.810G>C (p.Gly270=) rs1398331119 0.00001
NM_001079668.3(NKX2-1):c.996G>C (p.Ala332=) rs1170518090 0.00001
NM_001079668.3(NKX2-1):c.*143C>A rs564521320
NM_001079668.3(NKX2-1):c.*184_*186C[4]ACCC[1]
NM_001079668.3(NKX2-1):c.*184_*186C[6]ACCC[1]
NM_001079668.3(NKX2-1):c.*186_*187insCCACTC
NM_001079668.3(NKX2-1):c.1005C>T (p.Ser335=) rs1364390122
NM_001079668.3(NKX2-1):c.1041G>A (p.Pro347=)
NM_001079668.3(NKX2-1):c.1062A>C (p.Ala354=)
NM_001079668.3(NKX2-1):c.1074G>C (p.Pro358=)
NM_001079668.3(NKX2-1):c.1122A>G (p.Val374=)
NM_001079668.3(NKX2-1):c.1131G>C (p.Leu377=) rs756582124
NM_001079668.3(NKX2-1):c.1161C>T (p.Tyr387=) rs566854717
NM_001079668.3(NKX2-1):c.174C>T (p.Gly58=)
NM_001079668.3(NKX2-1):c.192C>T (p.Leu64=)
NM_001079668.3(NKX2-1):c.207G>A (p.Ala69=)
NM_001079668.3(NKX2-1):c.279C>A (p.Ala93=) rs1346114723
NM_001079668.3(NKX2-1):c.297C>T (p.His99=)
NM_001079668.3(NKX2-1):c.324C>T (p.Leu108=) rs779655723
NM_001079668.3(NKX2-1):c.336C>T (p.Ala112=)
NM_001079668.3(NKX2-1):c.339G>A (p.Val113=) rs779417680
NM_001079668.3(NKX2-1):c.339G>T (p.Val113=) rs779417680
NM_001079668.3(NKX2-1):c.399C>G (p.Thr133=)
NM_001079668.3(NKX2-1):c.420C>T (p.Gly140=)
NM_001079668.3(NKX2-1):c.464-4A>G rs780157161
NM_001079668.3(NKX2-1):c.528G>T (p.Leu176=)
NM_001079668.3(NKX2-1):c.555G>A (p.Pro185=)
NM_001079668.3(NKX2-1):c.567G>A (p.Ala189=)
NM_001079668.3(NKX2-1):c.567G>T (p.Ala189=) rs1594404310
NM_001079668.3(NKX2-1):c.574A>C (p.Arg192=)
NM_001079668.3(NKX2-1):c.615G>A (p.Glu205=)
NM_001079668.3(NKX2-1):c.621G>A (p.Glu207=) rs1438796223
NM_001079668.3(NKX2-1):c.651G>C (p.Ser217=)
NM_001079668.3(NKX2-1):c.651G>T (p.Ser217=)
NM_001079668.3(NKX2-1):c.759G>A (p.Lys253=)
NM_001079668.3(NKX2-1):c.776T>A (p.Leu259Gln)
NM_001079668.3(NKX2-1):c.796GGCGGGGGC[1] (p.Gly269_Gly271del) rs577015120
NM_001079668.3(NKX2-1):c.796GGCGGGGGC[3] (p.Gly269_Gly271dup) rs577015120
NM_001079668.3(NKX2-1):c.825G>T (p.Pro275=)
NM_001079668.3(NKX2-1):c.879G>A (p.Leu293=)
NM_001079668.3(NKX2-1):c.951G>A (p.Gln317=) rs1594403473
NM_001079668.3(NKX2-1):c.981G>T (p.Ala327=)

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