"DDX10-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 777859	NM_004398.4(DDX10):c.131C>G (p.Pro44Arg)	DDX10 (P44R)	Single nucleotide variant (missense variant)	DDX10-related disorder +1 more	GBenign/Likely benign
Select item 3049135	NM_004398.4(DDX10):c.240A>G (p.Thr80=)	DDX10, LOC106865368	Single nucleotide variant (synonymous variant)	DDX10-related disorder	GLikely benign
Select item 3041086	NM_004398.4(DDX10):c.378+7A>G	DDX10, LOC106865368	Single nucleotide variant (intron variant)	DDX10-related disorder	GBenign
Select item 3037106	NM_004398.4(DDX10):c.1139-4G>A	DDX10	Single nucleotide variant (intron variant)	DDX10-related disorder	GLikely benign
Select item 218632	NM_004398.4(DDX10):c.1334A>G (p.Glu445Gly)	DDX10 (E445G)	Single nucleotide variant (missense variant)	DDX10-related disorder +1 more	GBenign/Likely benign
Select item 790364	NM_004398.4(DDX10):c.1563C>T (p.Thr521=)	DDX10	Single nucleotide variant (synonymous variant)	DDX10-related disorder +1 more	GBenign/Likely benign
Select item 3037141	NM_004398.4(DDX10):c.1698C>T (p.Leu566=)	DDX10	Single nucleotide variant (synonymous variant)	DDX10-related disorder	GBenign
Select item 3040175	NM_004398.4(DDX10):c.1723A>G (p.Asn575Asp)	DDX10 (N575D)	Single nucleotide variant (missense variant)	DDX10-related disorder	GBenign
Select item 3040076	NM_004398.4(DDX10):c.1749AGA[3] (p.Glu586del)	DDX10 (E586del)	Microsatellite (inframe deletion)	DDX10-related disorder	GLikely benign
Select item 3057636	NM_004398.4(DDX10):c.1761C>T (p.Asp587=)	DDX10	Single nucleotide variant (synonymous variant)	DDX10-related disorder	GLikely benign
Select item 3043585	NM_004398.4(DDX10):c.1964A>G (p.Gln655Arg)	DDX10 (Q655R)	Single nucleotide variant (missense variant)	DDX10-related disorder	GLikely benign
Select item 3049863	NM_004398.4(DDX10):c.2505C>T (p.Asp835=)	DDX10	Single nucleotide variant (synonymous variant)	DDX10-related disorder	GLikely benign
Select item 3045017	NM_004398.4(DDX10):c.2514A>G (p.Pro838=)	DDX10	Single nucleotide variant (synonymous variant)	DDX10-related disorder	GBenign