ClinVar Miner

List of variants in gene TERT reported as likely benign for Idiopathic fibrosing alveolitis, chronic form; Dyskeratosis congenita, autosomal dominant, 2

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Total variants: 38
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HGVS dbSNP
NM_198253.2(TERT):c.1119A>C (p.Pro373=) rs747342234
NM_198253.2(TERT):c.1389C>T (p.Gly463=) rs1554042821
NM_198253.2(TERT):c.1458C>T (p.Arg486=) rs1554042806
NM_198253.2(TERT):c.1476G>A (p.Lys492=) rs1060504789
NM_198253.2(TERT):c.1560G>A (p.Leu520=) rs753991999
NM_198253.2(TERT):c.1728C>T (p.Tyr576=) rs1554041291
NM_198253.2(TERT):c.1914C>T (p.Tyr638=) rs541931572
NM_198253.2(TERT):c.1917C>A (p.Val639=) rs142989562
NM_198253.2(TERT):c.2010G>A (p.Ala670=) rs759843505
NM_198253.2(TERT):c.2013G>A (p.Arg671=) rs34625402
NM_198253.2(TERT):c.2131-4A>C rs1030149805
NM_198253.2(TERT):c.2145C>A (p.Gly715=) rs769467251
NM_198253.2(TERT):c.2262C>T (p.His754=) rs778622091
NM_198253.2(TERT):c.2287-6C>T rs758808508
NM_198253.2(TERT):c.2307C>G (p.Leu769=) rs117662357
NM_198253.2(TERT):c.2538C>T (p.Tyr846=) rs778309923
NM_198253.2(TERT):c.2577G>C (p.Arg859=) rs1554039723
NM_198253.2(TERT):c.2701C>A (p.Arg901=) rs199422304
NM_198253.2(TERT):c.2736G>A (p.Glu912=) rs775289969
NM_198253.2(TERT):c.2740C>T (p.Leu914=) rs1554039274
NM_198253.2(TERT):c.2772C>T (p.Ala924=) rs367672336
NM_198253.2(TERT):c.2823G>A (p.Glu941=) rs1554039257
NM_198253.2(TERT):c.2938C>T (p.Leu980=) rs1554038808
NM_198253.2(TERT):c.3006C>T (p.Tyr1002=) rs760659103
NM_198253.2(TERT):c.3063T>C (p.Phe1021=) rs1554038261
NM_198253.2(TERT):c.3255C>T (p.His1085=) rs953571477
NM_198253.2(TERT):c.3296-4G>A rs780229179
NM_198253.2(TERT):c.3336G>C (p.Leu1112=) rs1554038061
NM_198253.2(TERT):c.3369G>A (p.Leu1123=) rs529179931
NM_198253.2(TERT):c.339G>A (p.Glu113=) rs757141480
NM_198253.2(TERT):c.391C>T (p.Leu131=) rs1018793583
NM_198253.2(TERT):c.444G>C (p.Val148=) rs1314321999
NM_198253.2(TERT):c.519G>A (p.Pro173=) rs763396974
NM_198253.2(TERT):c.522G>T (p.Pro174=) rs773784305
NM_198253.2(TERT):c.663G>T (p.Ala221=) rs35837567
NM_198253.2(TERT):c.897G>T (p.Val299=) rs1554042926
NM_198253.2(TERT):c.936G>A (p.Arg312=) rs1207164857
NM_198253.2(TERT):c.939A>G (p.Pro313=) rs1554042914

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