"Ambry Genetics"[submitter] AND "RPL10"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2609304	NM_006013.5(RPL10):c.42C>A (p.Asn14Lys)	RPL10 (N14K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2234615	NM_006013.5(RPL10):c.224A>T (p.Tyr75Phe)	RPL10 (Y39F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1792661	NM_006013.5(RPL10):c.252C>T (p.Gly84=)	RPL10	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 588816	NM_006013.5(RPL10):c.264G>A (p.Arg88=)	RPL10	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 167612	NM_006013.5(RPL10):c.291C>T (p.Ile97=)	RPL10	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 985712	NM_006013.5(RPL10):c.479C>G (p.Pro160Arg)	RPL10 (P124R +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2291356	NM_006013.5(RPL10):c.561A>C (p.Glu187Asp)	RPL10 (E151D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 95327	NM_006013.5(RPL10):c.605= (p.Ser202=)	RPL10	Single nucleotide variant (no sequence alteration)	not specified +1 more	GBenign
Select item 1752694	NM_006013.5(RPL10):c.629G>A (p.Arg210Gln)	RPL10 (R174Q +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GBenign
Select item 589527	NM_006013.5(RPL10):c.633C>T (p.Ala211=)	RPL10 (P157L)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases +1 more	GBenign