ClinVar Miner

Variants in gene combination LOC101927055, TTN with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 17
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HGVS dbSNP
NM_001267550.2(TTN):c.3835A>T (p.Met1279Leu) rs374497665
NM_001267550.2(TTN):c.3913G>T (p.Gly1305Trp) rs199889888
NM_001267550.2(TTN):c.3989G>A (p.Arg1330His) rs761402128
NM_001267550.2(TTN):c.4076A>G (p.Glu1359Gly) rs370978752
NM_001267550.2(TTN):c.4081A>C (p.Ile1361Leu) rs145308734
NM_001267550.2(TTN):c.4150G>T (p.Ala1384Ser) rs144609506
NM_001267550.2(TTN):c.4153G>A (p.Ala1385Thr) rs140760859
NM_001267550.2(TTN):c.4160T>C (p.Leu1387Pro) rs115303497
NM_001267550.2(TTN):c.4208G>C (p.Arg1403Thr) rs531590921
NM_001267550.2(TTN):c.4261C>T (p.Arg1421Trp) rs144672482
NM_001267550.2(TTN):c.4262G>A (p.Arg1421Gln) rs147254212
NM_001267550.2(TTN):c.4291C>T (p.Arg1431Trp) rs139636676
NM_001267550.2(TTN):c.4359A>T (p.Arg1453Ser) rs376857956
NM_001267550.2(TTN):c.4396T>C (p.Phe1466Leu) rs151310601
NM_001267550.2(TTN):c.4641G>T (p.Val1547=) rs1012929202
NM_001267550.2(TTN):c.4671G>A (p.Met1557Ile) rs139192633
NM_001267550.2(TTN):c.4709G>C (p.Gly1570Ala) rs199910114

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