List of variants in gene combination LOC126806429, TTN reported as uncertain significance by Revvity Omics, Revvity

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19881G>A (p.Ser6627=)	rs371495674	0.00012
NM_001267550.2(TTN):c.19996C>T (p.Pro6666Ser)	rs571231816	0.00010
NM_001267550.2(TTN):c.20170G>A (p.Val6724Ile)	rs140143513	0.00004
NM_001267550.2(TTN):c.19786A>G (p.Ile6596Val)	rs369108292	0.00003
NM_001267550.2(TTN):c.19963G>A (p.Asp6655Asn)	rs397517493	0.00003
NM_001267550.2(TTN):c.19995A>T (p.Glu6665Asp)	rs146828735	0.00002
NM_001267550.2(TTN):c.19970G>T (p.Cys6657Phe)	rs776748717	0.00001
NM_001267550.2(TTN):c.20169C>T (p.Ala6723=)	rs727504776	0.00001
NM_001267550.2(TTN):c.19798A>G (p.Thr6600Ala)
NM_001267550.2(TTN):c.19799C>T (p.Thr6600Ile)
NM_001267550.2(TTN):c.19850G>A (p.Gly6617Asp)
NM_001267550.2(TTN):c.19856A>C (p.Lys6619Thr)
NM_001267550.2(TTN):c.19910A>G (p.Asp6637Gly)
NM_001267550.2(TTN):c.19996C>G (p.Pro6666Ala)
NM_001267550.2(TTN):c.20083C>T (p.Pro6695Ser)
NM_001267550.2(TTN):c.20099T>C (p.Val6700Ala)

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