Related gene-specific medical variations for Gene (Select 100506083) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271262	NM_007242.7(DDX19B):c.1420A>G (p.Ile474Val)	DDX19A-DT, DDX19B +1 more (I448V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271261	NM_007242.7(DDX19B):c.610G>A (p.Glu204Lys)	DDX19A-DT, DDX19B (E173K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271260	NM_007242.7(DDX19B):c.899A>T (p.Glu300Val)	DDX19A-DT, DDX19B (E300V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080916	NM_007242.7(DDX19B):c.557G>A (p.Gly186Asp)	DDX19A-DT, DDX19B (G191D +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080915	NM_007242.7(DDX19B):c.464A>G (p.Gln155Arg)	DDX19A-DT, DDX19B (Q124R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080914	NM_007242.7(DDX19B):c.1416C>A (p.Asp472Glu)	DDX19A-DT, DDX19B +1 more (D363E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080913	NM_007242.7(DDX19B):c.1250A>G (p.Asn417Ser)	DDX19A-DT, DDX19B +1 more (N266S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557476	NM_007242.7(DDX19B):c.985G>A (p.Gly329Arg)	DDX19A-DT, DDX19B (G178R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550440	NM_007242.7(DDX19B):c.390C>G (p.Pro130=)	DDX19A-DT, DDX19B	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2527021	NM_007242.7(DDX19B):c.1091G>A (p.Ser364Asn)	DDX19A-DT, DDX19B (S333N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514314	NM_007242.7(DDX19B):c.1151A>G (p.Glu384Gly)	DDX19A-DT, DDX19B (E233G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488348	NM_007242.7(DDX19B):c.1148A>G (p.Lys383Arg)	DDX19A-DT, DDX19B (K274R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482167	NM_007242.7(DDX19B):c.340C>T (p.Arg114Cys)	DDX19A-DT, DDX19B (R5C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481979	NM_007242.7(DDX19B):c.580C>G (p.Leu194Val)	DDX19A-DT, DDX19B (L163V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396759	NM_007242.7(DDX19B):c.950G>A (p.Arg317Lys)	DDX19A-DT, DDX19B (R166K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378869	NM_007242.7(DDX19B):c.1198G>A (p.Glu400Lys)	DDX19A-DT, DDX19B +1 more (E291K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325436	NM_007242.7(DDX19B):c.697C>A (p.Pro233Thr)	DDX19A-DT, DDX19B (P207T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305435	NM_007242.7(DDX19B):c.1139G>A (p.Arg380Gln)	DDX19A-DT, DDX19B (R229Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance