C0917713[trait identifier] AND "Myriad Genetics, Inc."[submitter] - ClinVar

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Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 984094	NM_004006.3(DMD):c.10807G>T (p.Glu3603Ter)	DMD (E1033* +11 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984095	NM_004006.3(DMD):c.10699C>T (p.Gln3567Ter)	DMD (Q1094* +11 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1726630	NM_004006.3(DMD):c.9957T>A (p.Cys3319Ter)	DMD (C1975* +8 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1725520	NM_004006.3(DMD):c.9856A>T (p.Arg3286Ter)	DMD (R1942* +8 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 984096	NM_004006.3(DMD):c.9743T>A (p.Leu3248Ter)	DMD (L180* +8 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1724995	NM_004006.3(DMD):c.9534T>A (p.Cys3178Ter)	DMD (C110* +8 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 984097	NM_004006.3(DMD):c.9362T>A (p.Leu3121Ter)	DMD (L1777* +8 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1424825	NM_004006.3(DMD):c.9311C>A (p.Ser3104Ter)	DMD (S1763* +8 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1725526	NM_004006.3(DMD):c.9284T>A (p.Leu3095Ter)	DMD (L1751* +8 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1726854	NM_004006.3(DMD):c.9219T>A (p.Tyr3073Ter)	DMD (Y1729* +7 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 650214	NM_004006.3(DMD):c.9094G>T (p.Glu3032Ter)	DMD (E3024* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984098	NM_004006.3(DMD):c.9014T>A (p.Leu3005Ter)	DMD (L1661* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +2 more	GPathogenic/Likely pathogenic
Select item 1448296	NM_004006.3(DMD):c.8965A>T (p.Lys2989Ter)	DMD (K1645* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984213	NM_004006.3(DMD):c.8659G>T (p.Glu2887Ter)	DMD (E1543* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984214	NM_004006.3(DMD):c.8483T>A (p.Leu2828Ter)	DMD (L1484* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984215	NM_004006.3(DMD):c.8329A>T (p.Arg2777Ter)	DMD (R1433* +7 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1685717	NM_004006.3(DMD):c.8206A>T (p.Lys2736Ter)	DMD (K1392* +6 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984216	NM_004006.3(DMD):c.8023A>T (p.Lys2675Ter)	DMD (K1331* +6 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984217	NM_004006.3(DMD):c.7833T>A (p.Tyr2611Ter)	DMD (Y1267* +6 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984218	NM_004006.3(DMD):c.6428G>A (p.Trp2143Ter)	DMD (W2020* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984219	NM_004006.3(DMD):c.6217A>T (p.Lys2073Ter)	DMD (K1950* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984220	NM_004006.3(DMD):c.6175A>T (p.Lys2059Ter)	DMD (K1936* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983654	NM_004006.3(DMD):c.6124A>T (p.Lys2042Ter)	DMD (K1919* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983655	NM_004006.3(DMD):c.5860A>T (p.Lys1954Ter)	DMD (K1831* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983656	NM_004006.3(DMD):c.5794C>T (p.Gln1932Ter)	DMD (Q591* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1724713	NM_004006.3(DMD):c.5767A>T (p.Lys1923Ter)	DMD (K1800* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 803859	NM_004006.3(DMD):c.5636G>A (p.Trp1879Ter)	DMD (W1879* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1724183	NM_004006.3(DMD):c.5584A>T (p.Lys1862Ter)	DMD (K1739* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1724896	NM_004006.3(DMD):c.5548A>T (p.Lys1850Ter)	DMD (K1727* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 983657	NM_004006.3(DMD):c.5383G>T (p.Glu1795Ter)	DMD (E1672* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1725030	NM_004006.3(DMD):c.5251A>T (p.Lys1751Ter)	DMD (K1628* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 983658	NM_004006.3(DMD):c.5114C>G (p.Ser1705Ter)	DMD (S1582* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983659	NM_004006.3(DMD):c.5026G>T (p.Glu1676Ter)	DMD (E1553* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983660	NM_004006.3(DMD):c.5012T>A (p.Leu1671Ter)	DMD (L1548* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 803866	NM_004006.3(DMD):c.4980G>A (p.Trp1660Ter)	DMD (W1537* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 983942	NM_004006.3(DMD):c.4979G>A (p.Trp1660Ter)	DMD (W1537* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1726596	NM_004006.3(DMD):c.4943T>A (p.Leu1648Ter)	DMD (L1525* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1724304	NM_004006.3(DMD):c.4715T>A (p.Leu1572Ter)	DMD (L1449* +5 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 983943	NM_004006.3(DMD):c.4656T>A (p.Tyr1552Ter)	DMD (Y1429* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983944	NM_004006.3(DMD):c.4649T>A (p.Leu1550Ter)	DMD (L1427* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983945	NM_004006.3(DMD):c.4454T>A (p.Leu1485Ter)	DMD (L1362* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1432376	NM_004006.3(DMD):c.4345A>T (p.Lys1449Ter)	DMD (K108* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 983946	NM_004006.3(DMD):c.4342C>T (p.Gln1448Ter)	DMD (Q104* +5 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1725516	NM_004006.3(DMD):c.3928G>T (p.Glu1310Ter)	DMD (E1187* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 983947	NM_004006.3(DMD):c.3898G>T (p.Glu1300Ter)	DMD (E1177* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 983948	NM_004006.3(DMD):c.3892G>T (p.Gly1298Ter)	DMD (G1175* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984107	NM_004006.3(DMD):c.3824T>A (p.Leu1275Ter)	DMD (L1152* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984108	NM_004006.3(DMD):c.3457A>T (p.Lys1153Ter)	DMD (K1030* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1724259	NM_004006.3(DMD):c.3184A>T (p.Lys1062Ter)	DMD (K1054* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 1725855	NM_004006.3(DMD):c.3160C>T (p.Gln1054Ter)	DMD (Q1046* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984109	NM_004006.3(DMD):c.3059C>A (p.Ser1020Ter)	DMD (S1012* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1724180	NM_004006.3(DMD):c.2873C>A (p.Ser958Ter)	DMD (S835* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1725491	NM_004006.3(DMD):c.2692A>T (p.Lys898Ter)	DMD (K775* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 984110	NM_004006.3(DMD):c.2626G>T (p.Glu876Ter)	DMD (E753* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1725239	NM_004006.3(DMD):c.1840A>T (p.Lys614Ter)	DMD (K491* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 933803	NM_004006.3(DMD):c.1837A>T (p.Lys613Ter)	DMD (K613* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984111	NM_004006.3(DMD):c.1819A>T (p.Lys607Ter)	DMD (K484* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 984112	NM_004006.3(DMD):c.1501G>T (p.Glu501Ter)	DMD (E378* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GPathogenic/Likely pathogenic
Select item 984113	NM_004006.3(DMD):c.1405G>T (p.Glu469Ter)	DMD (E346* +3 more)	Single nucleotide variant (nonsense)	Becker muscular dystrophy +1 more	GLikely pathogenic
Select item 1724244	NM_004006.3(DMD):c.1346T>A (p.Leu449Ter)	DMD (L326* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic
Select item 1725751	NM_004006.3(DMD):c.986C>A (p.Ser329Ter)	DMD (S206* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy +1 more	GLikely pathogenic

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Items: 61