"PreventionGenetics, part of Exact Sciences"[submitter] AND "RPS24"[ge - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1337223	NM_033022.4(RPS24):c.-4C>T	LOC130004144, RPS24	Single nucleotide variant (5 prime UTR variant)	RPS24-related condition +1 more	GConflicting classifications of pathogenicity
Select item 301093	NM_033022.4(RPS24):c.177A>G (p.Gly59=)	RPS24	Single nucleotide variant (synonymous variant)	RPS24-related condition +3 more	GBenign/Likely benign
Select item 436555	NM_033022.4(RPS24):c.189T>C (p.His63=)	RPS24	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 301094	NM_033022.4(RPS24):c.235C>T (p.Leu79=)	RPS24	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 416128	NM_033022.4(RPS24):c.363A>G (p.Ala121=)	RPS24	Single nucleotide variant (synonymous variant)	RPS24-related condition +2 more	GBenign
Select item 241728	NM_033022.4(RPS24):c.371A>G (p.Asn124Ser)	RPS24 (N124S)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 301097	NM_033022.4(RPS24):c.391-3C>A	RPS24	Single nucleotide variant (intron variant)	RPS24-related condition +3 more	GBenign
Select item 301098	NM_033022.4(RPS24):c.*21C>T	RPS24 (P131L)	Single nucleotide variant (missense variant +2 more)	RPS24-related condition +2 more	GBenign/Likely benign
Select item 2629329	NM_001142285.2(RPS24):c.428G>A (p.Arg143Lys)	RPS24 (R143K)	Single nucleotide variant (missense variant)	RPS24-related condition	GUncertain significance
Select item 3031763	NM_001142285.2(RPS24):c.468G>A (p.Ser156=)	RPS24	Single nucleotide variant (synonymous variant)	RPS24-related condition	GLikely benign
Select item 3049301	NM_001142285.2(RPS24):c.624G>A (p.Ala208=)	RPS24	Single nucleotide variant (synonymous variant)	RPS24-related condition	GLikely benign
Select item 2631423	NM_001142285.2(RPS24):c.629T>C (p.Leu210Pro)	RPS24 (L210P)	Single nucleotide variant (missense variant)	RPS24-related condition	GUncertain significance
Select item 3025335	NM_001142285.2(RPS24):c.668C>T (p.Ser223Leu)	RPS24 (S223L)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2635748	NM_001142285.2(RPS24):c.734C>T (p.Pro245Leu)	RPS24 (P245L)	Single nucleotide variant (missense variant)	RPS24-related condition	GUncertain significance
Select item 2636008	NM_001142285.2(RPS24):c.814C>T (p.His272Tyr)	RPS24 (H272Y)	Single nucleotide variant (missense variant)	RPS24-related condition	GUncertain significance
Select item 2634017	NM_001142285.2(RPS24):c.835T>G (p.Ser279Ala)	RPS24 (S279A)	Single nucleotide variant (missense variant)	RPS24-related condition	GUncertain significance