List of variants in gene combination LOC101927055, TTN reported by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 98

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.4209-223A>G	rs7570526	0.99883
NM_001267550.2(TTN):c.3730-115C>T	rs2035496	0.95067
NM_001267550.2(TTN):c.3884C>T (p.Ser1295Leu)	rs1552280	0.94810
NM_001267550.2(TTN):c.3964-41T>C	rs2291302	0.94808
NM_001267550.2(TTN):c.3963+22T>C	rs2291301	0.94740
NM_001267550.2(TTN):c.4480+6C>T	rs719201	0.94321
NM_001267550.2(TTN):c.3759A>G (p.Arg1253=)	rs2291308	0.04988
NM_001267550.2(TTN):c.4715G>A (p.Arg1572Gln)	rs12476289	0.04792
NM_001267550.2(TTN):c.4208+56A>G	rs56180285	0.03905
NM_001267550.2(TTN):c.4209-180A>G	rs140462764	0.03773
NM_001267550.2(TTN):c.4177A>G (p.Ile1393Val)	rs16866531	0.03468
NM_001267550.2(TTN):c.3730-238G>A	rs6709235	0.02269
NM_001267550.2(TTN):c.4246C>T (p.Arg1416Cys)	rs72647875	0.01559
NM_001267550.2(TTN):c.3993C>T (p.Ile1331=)	rs55757622	0.01419
NM_001267550.2(TTN):c.4630A>G (p.Ile1544Val)	rs72647877	0.01178
NM_001267550.2(TTN):c.4034G>A (p.Gly1345Asp)	rs36021856	0.01079
NM_001267550.2(TTN):c.4347A>G (p.Ser1449=)	rs719202	0.01042
NM_001267550.2(TTN):c.4739C>T (p.Thr1580Met)	rs73973147	0.00558
NM_001267550.2(TTN):c.3730-266T>G	rs75885953	0.00443
NM_001267550.2(TTN):c.4328T>C (p.Leu1443Pro)	rs142317580	0.00198
NM_001267550.2(TTN):c.4199G>C (p.Ser1400Thr)	rs138506461	0.00197
NM_001267550.2(TTN):c.4815-26T>C	rs149453892	0.00110
NM_001267550.2(TTN):c.4671G>A (p.Met1557Ile)	rs139192633	0.00091
NM_001267550.2(TTN):c.4396T>C (p.Phe1466Leu)	rs151310601	0.00089
NM_001267550.2(TTN):c.4208G>C (p.Arg1403Thr)	rs531590921	0.00029
NM_001267550.2(TTN):c.4645+8G>T	rs144456585	0.00029
NM_001267550.2(TTN):c.4359A>T (p.Arg1453Ser)	rs376857956	0.00028
NM_001267550.2(TTN):c.4262G>A (p.Arg1421Gln)	rs147254212	0.00027
NM_001267550.2(TTN):c.4291C>T (p.Arg1431Trp)	rs139636676	0.00015
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.4261C>T (p.Arg1421Trp)	rs144672482	0.00011
NM_001267550.2(TTN):c.4668G>A (p.Pro1556=)	rs145709534	0.00011
NM_001267550.2(TTN):c.3864T>G (p.Ala1288=)	rs368702156	0.00010
NM_001267550.2(TTN):c.4150G>T (p.Ala1384Ser)	rs144609506	0.00010
NM_001267550.2(TTN):c.4049G>A (p.Arg1350His)	rs539470256	0.00008
NM_001267550.2(TTN):c.4081A>C (p.Ile1361Leu)	rs145308734	0.00006
NM_001267550.2(TTN):c.4247G>A (p.Arg1416His)	rs750278602	0.00006
NM_001267550.2(TTN):c.4462A>G (p.Thr1488Ala)	rs146732280	0.00006
NM_001267550.2(TTN):c.4709G>C (p.Gly1570Ala)	rs199910114	0.00006
NM_001267550.2(TTN):c.4153G>A (p.Ala1385Thr)	rs140760859	0.00005
NM_001267550.2(TTN):c.4087A>G (p.Thr1363Ala)	rs768249663	0.00004
NM_001267550.2(TTN):c.4646-7C>A	rs758516007	0.00004
NM_001267550.2(TTN):c.3798A>C (p.Thr1266=)	rs527497634	0.00003
NM_001267550.2(TTN):c.3899A>G (p.Tyr1300Cys)	rs188090472	0.00003
NM_001267550.2(TTN):c.3913G>T (p.Gly1305Trp)	rs199889888	0.00003
NM_001267550.2(TTN):c.4274C>T (p.Ala1425Val)	rs746063269	0.00003
NM_001267550.2(TTN):c.4463C>T (p.Thr1488Met)	rs111282958	0.00003
NM_001267550.2(TTN):c.4532G>A (p.Gly1511Asp)	rs751606948	0.00003
NM_001267550.2(TTN):c.4650G>A (p.Val1550=)	rs915170239	0.00003
NM_001267550.2(TTN):c.4764A>G (p.Val1588=)	rs1410819176	0.00003
NM_001267550.2(TTN):c.3989G>A (p.Arg1330His)	rs761402128	0.00002
NM_001267550.2(TTN):c.4602C>T (p.Asn1534=)	rs546385657	0.00002
NM_001267550.2(TTN):c.4889C>T (p.Ala1630Val)	rs371601918	0.00002
NM_001267550.2(TTN):c.3737A>T (p.His1246Leu)	rs201988645	0.00001
NM_001267550.2(TTN):c.4076A>G (p.Glu1359Gly)	rs370978752	0.00001
NM_001267550.2(TTN):c.4110A>G (p.Lys1370=)	rs1554011877	0.00001
NM_001267550.2(TTN):c.4142T>C (p.Val1381Ala)	rs794729252	0.00001
NM_001267550.2(TTN):c.4209-17G>A	rs373298221	0.00001
NM_001267550.2(TTN):c.4292G>A (p.Arg1431Gln)	rs373690688	0.00001
NM_001267550.2(TTN):c.4429G>C (p.Asp1477His)	rs532313981	0.00001
NM_001267550.2(TTN):c.4547T>C (p.Ile1516Thr)	rs1464496143	0.00001
NM_001267550.2(TTN):c.4612A>G (p.Arg1538Gly)	rs766463184	0.00001
NM_001267550.2(TTN):c.4639G>A (p.Val1547Met)	rs750678272	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.4843C>T (p.Leu1615Phe)	rs777977684	0.00001
NM_001267550.2(TTN):c.4851C>T (p.Ile1617=)	rs756286153	0.00001
NM_001267550.2(TTN):c.3913G>C (p.Gly1305Arg)	rs199889888
NM_001267550.2(TTN):c.3963+4A>G	rs2154347664
NM_001267550.2(TTN):c.3963+9T>C	rs1554012412
NM_001267550.2(TTN):c.3968C>T (p.Ala1323Val)	rs774954394
NM_001267550.2(TTN):c.3972G>C (p.Trp1324Cys)	rs1561323791
NM_001267550.2(TTN):c.3976A>T (p.Lys1326Ter)
NM_001267550.2(TTN):c.4032T>A (p.Asp1344Glu)
NM_001267550.2(TTN):c.4081A>G (p.Ile1361Val)	rs145308734
NM_001267550.2(TTN):c.4100G>A (p.Ser1367Asn)	rs1015028448
NM_001267550.2(TTN):c.4130G>A (p.Gly1377Glu)	rs794729573
NM_001267550.2(TTN):c.4208+18T>C	rs1057523992
NM_001267550.2(TTN):c.4227A>G (p.Ser1409=)	rs2154346890
NM_001267550.2(TTN):c.4247G>C (p.Arg1416Pro)	rs750278602
NM_001267550.2(TTN):c.4270C>T (p.Pro1424Ser)	rs772479207
NM_001267550.2(TTN):c.4289C>A (p.Ala1430Glu)	rs577298130
NM_001267550.2(TTN):c.4322G>C (p.Arg1441Pro)	rs72647876
NM_001267550.2(TTN):c.4330del (p.Glu1444fs)	rs2532971415
NM_001267550.2(TTN):c.4412G>A (p.Gly1471Glu)
NM_001267550.2(TTN):c.4414C>A (p.Gln1472Lys)
NM_001267550.2(TTN):c.4441G>A (p.Val1481Ile)	rs794729574
NM_001267550.2(TTN):c.4451C>G (p.Pro1484Arg)
NM_001267550.2(TTN):c.4476T>C (p.His1492=)	rs759703630
NM_001267550.2(TTN):c.4526A>C (p.Glu1509Ala)	rs794729575
NM_001267550.2(TTN):c.4529A>G (p.Asp1510Gly)
NM_001267550.2(TTN):c.4560C>A (p.Ala1520=)	rs1554009279
NM_001267550.2(TTN):c.4561A>C (p.Thr1521Pro)	rs1574674545
NM_001267550.2(TTN):c.4592_4596del (p.Val1531fs)	rs1131691910
NM_001267550.2(TTN):c.4624T>G (p.Ser1542Ala)
NM_001267550.2(TTN):c.4714C>T (p.Arg1572Ter)	rs1554008881
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs)	rs756433029

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