ClinVar Miner

List of variants in gene TINF2 reported as uncertain significance for Dyskeratosis congenita

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Total variants: 58
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HGVS dbSNP
NM_001099274.3(TINF2):c.1010del (p.Gly337fs) rs756029660
NM_001099274.3(TINF2):c.1016C>T (p.Ala339Val) rs1566366492
NM_001099274.3(TINF2):c.1025A>C (p.Glu342Ala) rs1555303978
NM_001099274.3(TINF2):c.1030C>T (p.Pro344Ser) rs200454893
NM_001099274.3(TINF2):c.1073_1081dup (p.Met361_Asp362insAsnCysTyr) rs776727691
NM_001099274.3(TINF2):c.1081A>G (p.Met361Val)
NM_001099274.3(TINF2):c.1083G>A (p.Met361Ile)
NM_001099274.3(TINF2):c.1130-1G>T
NM_001099274.3(TINF2):c.1139C>T (p.Pro380Leu)
NM_001099274.3(TINF2):c.1156G>A (p.Val386Ile) rs749534744
NM_001099274.3(TINF2):c.115C>G (p.Arg39Gly) rs1367518236
NM_001099274.3(TINF2):c.1221+3G>C
NM_001099274.3(TINF2):c.1222G>C (p.Glu408Gln) rs1594548909
NM_001099274.3(TINF2):c.1253T>C (p.Phe418Ser) rs773286175
NM_001099274.3(TINF2):c.127G>A (p.Ala43Thr) rs35653076
NM_001099274.3(TINF2):c.1288C>A (p.Pro430Thr)
NM_001099274.3(TINF2):c.1288C>T (p.Pro430Ser) rs374776408
NM_001099274.3(TINF2):c.1292del (p.Pro431fs) rs770529422
NM_001099274.3(TINF2):c.1307C>T (p.Ala436Val) rs369249473
NM_001099274.3(TINF2):c.1312C>G (p.Pro438Ala)
NM_001099274.3(TINF2):c.1331G>A (p.Cys444Tyr)
NM_001099274.3(TINF2):c.1337A>T (p.Asp446Val) rs532096263
NM_001099274.3(TINF2):c.141C>T (p.Gly47=)
NM_001099274.3(TINF2):c.163G>A (p.Glu55Lys)
NM_001099274.3(TINF2):c.167G>A (p.Arg56His)
NM_001099274.3(TINF2):c.217G>C (p.Gly73Arg)
NM_001099274.3(TINF2):c.218G>A (p.Gly73Asp) rs1566369238
NM_001099274.3(TINF2):c.257_258del (p.His86fs)
NM_001099274.3(TINF2):c.28G>T (p.Ala10Ser) rs746625511
NM_001099274.3(TINF2):c.302A>G (p.Lys101Arg) rs1375036989
NM_001099274.3(TINF2):c.318G>C (p.Lys106Asn)
NM_001099274.3(TINF2):c.37C>T (p.Arg13Cys)
NM_001099274.3(TINF2):c.400-3T>C
NM_001099274.3(TINF2):c.403C>T (p.Leu135Phe) rs199740488
NM_001099274.3(TINF2):c.500C>T (p.Ala167Val)
NM_001099274.3(TINF2):c.507+6G>A
NM_001099274.3(TINF2):c.517G>A (p.Val173Met)
NM_001099274.3(TINF2):c.569G>A (p.Arg190Lys) rs1382407347
NM_001099274.3(TINF2):c.586A>G (p.Met196Val)
NM_001099274.3(TINF2):c.61C>G (p.Gln21Glu) rs767648367
NM_001099274.3(TINF2):c.62A>G (p.Gln21Arg) rs367835995
NM_001099274.3(TINF2):c.631C>G (p.Leu211Val) rs746287594
NM_001099274.3(TINF2):c.640C>T (p.Pro214Ser) rs372610524
NM_001099274.3(TINF2):c.659C>T (p.Pro220Leu)
NM_001099274.3(TINF2):c.684C>A (p.His228Gln) rs370555134
NM_001099274.3(TINF2):c.707C>T (p.Pro236Leu)
NM_001099274.3(TINF2):c.718C>T (p.Leu240Phe) rs1594551965
NM_001099274.3(TINF2):c.778C>G (p.Leu260Val) rs1594551733
NM_001099274.3(TINF2):c.793C>T (p.Arg265Ter)
NM_001099274.3(TINF2):c.910G>A (p.Glu304Lys) rs1566366788
NM_001099274.3(TINF2):c.914G>C (p.Ser305Thr)
NM_001099274.3(TINF2):c.917A>G (p.Lys306Arg) rs1555304016
NM_001099274.3(TINF2):c.922G>C (p.Glu308Gln) rs1232383398
NM_001099274.3(TINF2):c.922G>T (p.Glu308Ter)
NM_001099274.3(TINF2):c.929C>T (p.Ala310Val)
NM_001099274.3(TINF2):c.936C>A (p.Tyr312Ter) rs201677741
NM_001099274.3(TINF2):c.937A>T (p.Thr313Ser)
NM_001099274.3(TINF2):c.967G>C (p.Ala323Pro)

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