Related gene-specific medical variations for Gene (Select 64951) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296098	NM_032014.3(MRPS24):c.280A>G (p.Lys94Glu)	MRPS24, URGCP-MRPS24 (K94E)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3296097	NM_032014.3(MRPS24):c.260T>A (p.Val87Glu)	MRPS24, URGCP-MRPS24 (V87E)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3296096	NM_032014.3(MRPS24):c.364G>A (p.Val122Met)	MRPS24, URGCP-MRPS24 (V122M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3209108	NM_032014.3(MRPS24):c.65C>T (p.Pro22Leu)	MRPS24, URGCP-MRPS24 (P22L)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3209094	NM_032014.3(MRPS24):c.445T>C (p.Cys149Arg)	MRPS24, URGCP-MRPS24 (C149R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3209091	NM_032014.3(MRPS24):c.437T>C (p.Phe146Ser)	MRPS24, URGCP-MRPS24 (F146S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3209086	NM_032014.3(MRPS24):c.286A>T (p.Met96Leu)	MRPS24, URGCP-MRPS24 (M96L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3186967	NM_001204871.2(URGCP-MRPS24):c.274G>A (p.Gly92Arg)	MRPS24, URGCP-MRPS24 (G92R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592808	NM_032014.3(MRPS24):c.277C>T (p.Arg93Cys)	MRPS24, URGCP-MRPS24 (R93C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2507537	NM_032014.3(MRPS24):c.238G>A (p.Asp80Asn)	MRPS24, URGCP-MRPS24 (D80N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2389246	NM_001204871.2(URGCP-MRPS24):c.181G>A (p.Val61Ile)	MRPS24, URGCP-MRPS24 (V61I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374327	NM_032014.3(MRPS24):c.455G>A (p.Arg152Gln)	MRPS24, URGCP-MRPS24 (R152Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2278174	NM_032014.3(MRPS24):c.481A>G (p.Lys161Glu)	MRPS24, URGCP-MRPS24 (K161E)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance