C1863659[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 899476	NM_002473.6(MYH9):c.*1330A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341458	NM_002473.6(MYH9):c.*1329C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign/Likely benign
Select item 341459	NM_002473.6(MYH9):c.*1314C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GBenign
Select item 341460	NM_002473.6(MYH9):c.*1204A>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341461	NM_002473.6(MYH9):c.*1193A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341463	NM_002473.6(MYH9):c.*1099A>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341464	NM_002473.6(MYH9):c.*1026C>G	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 341465	NM_002473.6(MYH9):c.*978A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 341466	NM_002473.6(MYH9):c.*975A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341467	NM_002473.6(MYH9):c.*906G>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GBenign
Select item 341468	NM_002473.6(MYH9):c.*802T>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341469	NM_002473.6(MYH9):c.*800T>C	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GBenign
Select item 341470	NM_002473.6(MYH9):c.*748A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341471	NM_002473.6(MYH9):c.*732C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 341472	NM_002473.6(MYH9):c.*686C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign/Likely benign
Select item 341473	NM_002473.6(MYH9):c.*656T>C	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 341474	NM_002473.6(MYH9):c.*645C>G	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 899543	NM_002473.6(MYH9):c.*639C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341475	NM_002473.6(MYH9):c.*596G>A	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 341476	NM_002473.6(MYH9):c.*539G>A	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 341477	NM_002473.6(MYH9):c.*474C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341478	NM_002473.6(MYH9):c.*329C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GBenign/Likely benign
Select item 900679	NM_002473.6(MYH9):c.*325C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GBenign/Likely benign
Select item 341479	NM_002473.6(MYH9):c.*312C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 902362	NM_002473.6(MYH9):c.*273C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341480	NM_002473.6(MYH9):c.*261G>C	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 902363	NM_002473.6(MYH9):c.*248C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341481	NM_002473.6(MYH9):c.*243C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 341482	NM_002473.6(MYH9):c.*238G>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 903228	NM_002473.6(MYH9):c.*195T>C	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GConflicting classifications of pathogenicity
Select item 341484	NM_002473.6(MYH9):c.*193C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 341485	NM_002473.6(MYH9):c.*137C>A	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 341486	NM_002473.6(MYH9):c.*136C>A	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign
Select item 341487	NM_002473.6(MYH9):c.*107A>G	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 341488	NM_002473.6(MYH9):c.*81C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +2 more	GBenign/Likely benign
Select item 341489	NM_002473.6(MYH9):c.*74G>A	MYH9	Single nucleotide variant (3 prime UTR variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 900751	NM_002473.6(MYH9):c.*73C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 900752	NM_002473.6(MYH9):c.*13G>A	MYH9	Single nucleotide variant (3 prime UTR variant)	MYH9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 228922	NM_002473.6(MYH9):c.*8C>T	MYH9	Single nucleotide variant (3 prime UTR variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 902430	NM_002473.6(MYH9):c.5878G>A (p.Glu1960Lys)	MYH9 (E1960K)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341490	NM_002473.6(MYH9):c.5877C>T (p.Ala1959=)	MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +4 more	GBenign/Likely benign
Select item 44573	NM_002473.6(MYH9):c.5818G>A (p.Gly1940Arg)	MYH9 (G1940R)	Single nucleotide variant (missense variant)	MYH9-related disorder +4 more	GBenign/Likely benign
Select item 178424	NM_002473.6(MYH9):c.5815G>A (p.Ala1939Thr)	MYH9 (A1939T)	Single nucleotide variant (missense variant)	MYH9-related condition +5 more	GBenign
Select item 903289	NM_002473.6(MYH9):c.5787C>T (p.Val1929=)	MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +4 more	GConflicting classifications of pathogenicity
Select item 44572	NM_002473.6(MYH9):c.5781G>T (p.Pro1927=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +4 more	GBenign
Select item 903290	NM_002473.6(MYH9):c.5769C>T (p.Arg1923=)	MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GConflicting classifications of pathogenicity
Select item 258760	NM_002473.6(MYH9):c.5766-5C>T	MYH9	Single nucleotide variant (intron variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 341491	NM_002473.6(MYH9):c.5765+9C>T	MYH9	Single nucleotide variant (intron variant)	MYH9-related disorder +3 more	GBenign/Likely benign
Select item 341492	NM_002473.6(MYH9):c.5717C>T (p.Thr1906Met)	MYH9 (T1906M)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 258758	NM_002473.6(MYH9):c.5709C>T (p.Ala1903=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 829957	NM_002473.6(MYH9):c.5671G>A (p.Ala1891Thr)	MYH9 (A1891T)	Single nucleotide variant (missense variant)	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss +3 more	GConflicting classifications of pathogenicity
Select item 341493	NM_002473.6(MYH9):c.5593-14G>A	MYH9	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 17 +2 more	GConflicting classifications of pathogenicity
Select item 900833	NM_002473.6(MYH9):c.5489G>A (p.Arg1830His)	MYH9 (R1830H)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 44570	NM_002473.6(MYH9):c.5483+4C>G	MYH9	Single nucleotide variant (intron variant)	MYH9-related disorder +4 more	GBenign
Select item 341494	NM_002473.6(MYH9):c.5456T>G (p.Leu1819Arg)	MYH9 (L1819R)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 902509	NM_002473.6(MYH9):c.5378A>G (p.Lys1793Arg)	MYH9 (K1793R)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 44569	NM_002473.6(MYH9):c.5323A>G (p.Lys1775Glu)	MYH9 (K1775E)	Single nucleotide variant (missense variant)	MYH9-related disorder +3 more	GLikely benign
Select item 341495	NM_002473.6(MYH9):c.5271G>T (p.Leu1757=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 902510	NM_002473.6(MYH9):c.5191A>G (p.Ile1731Val)	MYH9 (I1731V)	Single nucleotide variant (missense variant)	MYH9-related condition +2 more	GUncertain significance
Select item 178425	NM_002473.6(MYH9):c.5143G>A (p.Gly1715Ser)	MYH9 (G1715S)	Single nucleotide variant (missense variant)	MYH9-related condition +5 more	GBenign/Likely benign
Select item 903365	NM_002473.6(MYH9):c.5108G>A (p.Arg1703Gln)	MYH9 (R1703Q)	Single nucleotide variant (missense variant)	MYH9-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 627083	NM_002473.6(MYH9):c.5074G>A (p.Ala1692Thr)	MYH9 (A1692T)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 164421	NM_002473.6(MYH9):c.5026A>G (p.Lys1676Glu)	MYH9 (K1676E)	Single nucleotide variant (missense variant)	MYH9-related condition +5 more	GConflicting classifications of pathogenicity
Select item 178428	NM_002473.6(MYH9):c.5010G>A (p.Glu1670=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +4 more	GBenign/Likely benign
Select item 341496	NM_002473.6(MYH9):c.4972C>T (p.Arg1658Cys)	MYH9 (R1658C)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 899753	NM_002473.6(MYH9):c.4959G>C (p.Glu1653Asp)	MYH9 (E1653D)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 178429	NM_002473.6(MYH9):c.4956C>T (p.Arg1652=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +3 more	GBenign/Likely benign
Select item 341497	NM_002473.6(MYH9):c.4955G>A (p.Arg1652His)	MYH9 (R1652H)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 44567	NM_002473.6(MYH9):c.4952T>C (p.Met1651Thr)	MYH9 (M1651T)	Single nucleotide variant (missense variant)	MYH9-related disorder +5 more	GBenign/Likely benign
Select item 900909	NM_002473.6(MYH9):c.4902C>T (p.Asp1634=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related condition +3 more	GConflicting classifications of pathogenicity
Select item 44566	NM_002473.6(MYH9):c.4899G>A (p.Arg1633=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +3 more	GBenign
Select item 178431	NM_002473.6(MYH9):c.4878C>T (p.Ile1626=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 38967	NM_002473.6(MYH9):c.4876A>G (p.Ile1626Val)	MYH9 (I1626V)	Single nucleotide variant (missense variant)	MYH9-related disorder +4 more	GBenign
Select item 44565	NM_002473.6(MYH9):c.4872G>T (p.Ala1624=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +4 more	GBenign
Select item 902577	NM_002473.6(MYH9):c.4855C>T (p.Leu1619=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 341498	NM_002473.6(MYH9):c.4830C>T (p.Ala1610=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related condition +3 more	GConflicting classifications of pathogenicity
Select item 290063	NM_002473.6(MYH9):c.4818G>A (p.Ser1606=)	MYH9	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 903427	NM_002473.6(MYH9):c.4817C>T (p.Ser1606Leu)	MYH9 (S1606L)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 903428	NM_002473.6(MYH9):c.4728G>A (p.Arg1576=)	MYH9	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 164426	NM_002473.6(MYH9):c.4727G>A (p.Arg1576Gln)	MYH9 (R1576Q)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 341499	NM_002473.6(MYH9):c.4654G>A (p.Glu1552Lys)	MYH9 (E1552K)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 44563	NM_002473.6(MYH9):c.4563C>T (p.His1521=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +4 more	GBenign
Select item 341500	NM_002473.6(MYH9):c.4474A>G (p.Lys1492Glu)	MYH9 (K1492E)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 900977	NM_002473.6(MYH9):c.4466T>C (p.Met1489Thr)	MYH9 (M1489T)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 164435	NM_002473.6(MYH9):c.4396C>T (p.Arg1466Trp)	MYH9 (R1466W)	Single nucleotide variant (missense variant)	MYH9-related condition +4 more	GConflicting classifications of pathogenicity
Select item 341501	NM_002473.6(MYH9):c.4391G>A (p.Arg1464His)	MYH9 (R1464H)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341502	NM_002473.6(MYH9):c.4359G>A (p.Glu1453=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +2 more	GBenign/Likely benign
Select item 341503	NM_002473.6(MYH9):c.4348C>T (p.Leu1450=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341504	NM_002473.6(MYH9):c.4345-11C>G	MYH9	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 227612	NM_002473.6(MYH9):c.4344+10C>T	MYH9	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 341505	NM_002473.6(MYH9):c.4305C>T (p.Ser1435=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 164438	NM_002473.6(MYH9):c.4297C>T (p.Arg1433Cys)	MYH9 (R1433C)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 903480	NM_002473.6(MYH9):c.4283A>G (p.Asp1428Gly)	MYH9 (D1428G)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 17 +1 more	GUncertain significance
Select item 228928	NM_002473.6(MYH9):c.4247C>T (p.Thr1416Met)	MYH9 (T1416M)	Single nucleotide variant (missense variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 164439	NM_002473.6(MYH9):c.4225G>A (p.Asp1409Asn)	MYH9 (D1409N)	Single nucleotide variant (missense variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 44562	NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp)	MYH9 (R1400W)	Single nucleotide variant (missense variant)	MYH9-related disorder +5 more	GBenign/Likely benign
Select item 341506	NM_002473.6(MYH9):c.4126A>G (p.Ser1376Gly)	MYH9 (S1376G)	Single nucleotide variant (missense variant)	MYH9-related disorder +1 more	GUncertain significance
Select item 899867	NM_002473.6(MYH9):c.4077C>T (p.Ile1359=)	MYH9	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 341507	NM_002473.6(MYH9):c.4025G>A (p.Arg1342Gln)	MYH9 (R1342Q)	Single nucleotide variant (missense variant)	MYH9-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 341508	NM_002473.6(MYH9):c.3915G>A (p.Ala1305=)	MYH9	Single nucleotide variant (synonymous variant)	MYH9-related disorder +3 more	GConflicting classifications of pathogenicity

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