ClinVar Miner

List of variants in gene combination LOC101927055, TTN reported as likely benign for Cardiovascular phenotype

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.4199G>C (p.Ser1400Thr) rs138506461 0.00219
NM_001267550.2(TTN):c.4671G>A (p.Met1557Ile) rs139192633 0.00097
NM_001267550.2(TTN):c.4396T>C (p.Phe1466Leu) rs151310601 0.00089
NM_001267550.2(TTN):c.4359A>T (p.Arg1453Ser) rs376857956 0.00028
NM_001267550.2(TTN):c.3835A>T (p.Met1279Leu) rs374497665 0.00014
NM_001267550.2(TTN):c.4160T>C (p.Leu1387Pro) rs115303497 0.00012
NM_001267550.2(TTN):c.4668G>A (p.Pro1556=) rs145709534 0.00011
NM_001267550.2(TTN):c.4150G>T (p.Ala1384Ser) rs144609506 0.00010
NM_001267550.2(TTN):c.3813T>C (p.Leu1271=) rs773274762 0.00008
NM_001267550.2(TTN):c.4081A>C (p.Ile1361Leu) rs145308734 0.00007
NM_001267550.2(TTN):c.4709G>C (p.Gly1570Ala) rs199910114 0.00006
NM_001267550.2(TTN):c.4239T>G (p.Ser1413=) rs372187889 0.00004
NM_001267550.2(TTN):c.4284T>A (p.Ser1428=) rs771454835 0.00004
NM_001267550.2(TTN):c.4764A>G (p.Val1588=) rs1410819176 0.00004
NM_001267550.2(TTN):c.4650G>A (p.Val1550=) rs915170239 0.00003
NM_001267550.2(TTN):c.3777A>G (p.Glu1259=) rs755728462 0.00002
NM_001267550.2(TTN):c.3810T>C (p.Leu1270=) rs878883624 0.00001
NM_001267550.2(TTN):c.3876A>G (p.Gly1292=) rs755784209 0.00001
NM_001267550.2(TTN):c.4110A>G (p.Lys1370=) rs1554011877 0.00001
NM_001267550.2(TTN):c.4131G>A (p.Gly1377=) rs777874876 0.00001
NM_001267550.2(TTN):c.4170G>A (p.Pro1390=) rs369005241 0.00001
NM_001267550.2(TTN):c.4188A>G (p.Leu1396=) rs192329423 0.00001
NM_001267550.2(TTN):c.4197G>C (p.Val1399=) rs770601569 0.00001
NM_001267550.2(TTN):c.4452T>C (p.Pro1484=) rs727503695 0.00001
NM_001267550.2(TTN):c.4641G>T (p.Val1547=) rs1012929202 0.00001
NM_001267550.2(TTN):c.4740G>A (p.Thr1580=) rs765087240 0.00001
NM_001267550.2(TTN):c.3990C>T (p.Arg1330=)
NM_001267550.2(TTN):c.4002A>C (p.Gly1334=)
NM_001267550.2(TTN):c.4011C>T (p.Tyr1337=) rs1246677370
NM_001267550.2(TTN):c.4182C>G (p.Pro1394=) rs775070186
NM_001267550.2(TTN):c.4213C>G (p.Leu1405Val)
NM_001267550.2(TTN):c.4227A>G (p.Ser1409=) rs2154346890
NM_001267550.2(TTN):c.4401A>G (p.Lys1467=)
NM_001267550.2(TTN):c.4464G>A (p.Thr1488=) rs1287524221
NM_001267550.2(TTN):c.4575T>C (p.Ser1525=)
NM_001267550.2(TTN):c.4590G>C (p.Val1530=)
NM_001267550.2(TTN):c.4752C>A (p.Asn1584Lys)
NM_001267550.2(TTN):c.4752C>T (p.Asn1584=) rs879252955
NM_001267550.2(TTN):c.4929C>T (p.Cys1643=)

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