"Laboratory for Molecular Medicine, Mass General Brigham Personalized - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 402611	NM_001372106.1(DNAH10):c.682T>C (p.Ser228Pro)	DNAH10 (S167P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 402612	NM_001372106.1(DNAH10):c.842-16A>G	DNAH10	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 402613	NM_001372106.1(DNAH10):c.891T>C (p.Ser297=)	DNAH10	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 402628	NM_001372106.1(DNAH10):c.901G>A (p.Ala301Thr)	DNAH10 (A240T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 402614	NM_001372106.1(DNAH10):c.1621A>G (p.Ile541Val)	DNAH10 (I480V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 402615	NM_001372106.1(DNAH10):c.5245T>G (p.Leu1749Val)	DNAH10 (L1631V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 402616	NM_001372106.1(DNAH10):c.5525C>T (p.Thr1842Met)	DNAH10 (T1724M +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 402617	NM_001372106.1(DNAH10):c.6311C>T (p.Thr2104Met)	DNAH10 (T1986M +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 402618	NM_001372106.1(DNAH10):c.9030A>G (p.Lys3010=)	DNAH10	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 402619	NM_001372106.1(DNAH10):c.9199+9G>A	DNAH10	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 402620	NM_001372106.1(DNAH10):c.9540C>T (p.Asp3180=)	DNAH10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 402621	NM_001372106.1(DNAH10):c.9729G>A (p.Glu3243=)	DNAH10	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 402622	NM_001372106.1(DNAH10):c.9741A>G (p.Ala3247=)	DNAH10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 402623	NM_001372106.1(DNAH10):c.9815+9C>T	DNAH10	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 402627	NM_001372106.1(DNAH10):c.9848C>T (p.Thr3283Met)	DNAH10 (T3165M +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 402624	NM_001372106.1(DNAH10):c.10722+4T>C	DNAH10	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 402625	NM_001372106.1(DNAH10):c.13308C>T (p.Ser4436=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 402626	NM_001372106.1(DNAH10):c.13392C>T (p.Asn4464=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign