List of variants in gene combination LOC101927055, TTN reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
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	0.01259
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.4328T>C (p.Leu1443Pro)	rs142317580	0.00188
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.3963+8A>G	rs746377261	0.00001
NM_001267550.2(TTN):c.4322G>C (p.Arg1441Pro)	rs72647876
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs)	rs756433029

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