RPS15A[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2904148	NM_001019.5(RPS15A):c.240C>T (p.Asp80=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2414709	NM_001019.5(RPS15A):c.214-8T>C	RPS15A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1903144	NM_001019.5(RPS15A):c.214-21GTT[5]	RPS15A	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2867658	NM_001019.5(RPS15A):c.214-21GTT[2]	RPS15A	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2746992	NM_001019.5(RPS15A):c.214-21GTT[3]	RPS15A	Microsatellite (intron variant)	not provided	GLikely benign
Select item 617665	NM_001019.5(RPS15A):c.213G>A (p.Lys71=)	RPS15A	Single nucleotide variant (synonymous variant)	Diamond-Blackfan anemia 20	GPathogenic
Select item 2177617	NM_001019.5(RPS15A):c.183T>A (p.Ile61=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1977655	NM_001019.5(RPS15A):c.144C>T (p.Gly48=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1259635	NM_001019.5(RPS15A):c.134-151G>T	RPS15A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2975320	NM_001019.5(RPS15A):c.133+14C>T	RPS15A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963083	NM_001019.5(RPS15A):c.120G>C (p.Val40=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646266	NM_001019.5(RPS15A):c.114C>T (p.Leu38=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646267	NM_001019.5(RPS15A):c.108G>C (p.Arg36=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2784941	NM_001019.5(RPS15A):c.106C>A (p.Arg36=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2997133	NM_001019.5(RPS15A):c.105C>G (p.Val35=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2993763	NM_001019.5(RPS15A):c.61G>A (p.Gly21Ser)	RPS15A (G21S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1899577	NM_001019.5(RPS15A):c.51C>A (p.Ala17=)	RPS15A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2127841	NM_001019.5(RPS15A):c.14A>G (p.Asn5Ser)	RPS15A (N5S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1290255	NM_001019.5(RPS15A):c.-5-198C>G	RPS15A	Single nucleotide variant (intron variant)	not provided	GBenign