MRPL50[gene] - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 147624	GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3	ABCA1, ABHD17B +1072 more	Copy number gain	See cases	GPathogenic
Select item 151006	GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3	ABCA1, ABHD17B +1188 more	Copy number gain	See cases	GPathogenic
Select item 59881	GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3	LOC130002218, LOC130002219 +994 more	Copy number gain	See cases	GPathogenic
Select item 144971	GRCh38/hg38 9q22.32-31.3(chr9:95061030-108695569)x1	LOC130002205, LOC130002206 +417 more	Copy number loss	See cases	GPathogenic
Select item 149230	GRCh38/hg38 9q22.33-31.3(chr9:99024205-109947890)x1	ABCA1, ABITRAM +253 more	Copy number loss	See cases	GPathogenic
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
Select item 32222	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	ABCA1, ABITRAM +514 more	Copy number loss	See cases	GPathogenic
Select item 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 2268074	NM_019051.3(MRPL50):c.458A>C (p.Lys153Thr)	MRPL50 (K153T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294788	NM_019051.3(MRPL50):c.443T>C (p.Leu148Pro)	MRPL50 (L148P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623926	NM_019051.3(MRPL50):c.410G>A (p.Arg137Lys)	MRPL50 (R137K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608351	NM_019051.3(MRPL50):c.362G>A (p.Cys121Tyr)	MRPL50 (C121Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809800	NM_019051.3(MRPL50):c.335T>A (p.Val112Asp)	MRPL50 (V112D)	Single nucleotide variant (missense variant)	See cases	GLikely pathogenic
Select item 3296046	NM_019051.3(MRPL50):c.307C>T (p.His103Tyr)	MRPL50 (H103Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296045	NM_019051.3(MRPL50):c.296A>G (p.Asn99Ser)	MRPL50 (N99S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3208297	NM_019051.3(MRPL50):c.284G>C (p.Arg95Pro)	MRPL50 (R95P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208290	NM_019051.3(MRPL50):c.284G>A (p.Arg95His)	MRPL50 (R95H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3296042	NM_019051.3(MRPL50):c.263A>T (p.Asp88Val)	MRPL50 (D88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208284	NM_019051.3(MRPL50):c.229G>A (p.Val77Ile)	MRPL50 (V77I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3296047	NM_019051.3(MRPL50):c.218A>C (p.Tyr73Ser)	MRPL50 (Y73S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472913	NM_019051.3(MRPL50):c.212A>T (p.Glu71Val)	MRPL50 (E71V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223461	NM_019051.3(MRPL50):c.208T>G (p.Leu70Val)	MRPL50 (L70V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473349	NM_019051.3(MRPL50):c.206G>A (p.Arg69His)	MRPL50 (R69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296044	NM_019051.3(MRPL50):c.49A>G (p.Thr17Ala)	MRPL50 (T17A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 3063058	GRCh37/hg19 9q31.1-31.2(chr9:102606857-109839724)x1	ABCA1, ALDOB +34 more	Copy number loss	not specified	GPathogenic
Select item 2671591	Single allele	CARD19, MIR24-1 +106 more	Deletion	not provided	GPathogenic
Select item 2422164	NC_000009.11:g.(?_104124710)_(104500261_?)del	ALDOB, BAAT +6 more	Deletion	Hereditary fructosuria	GPathogenic
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 1341973	GRCh37/hg19 9q22.2-31.1(chr9:93864974-106661581)x1	ALDOB, ALG2 +87 more	Copy number loss	Gorlin syndrome	GPathogenic
Select item 1341248	GRCh37/hg19 9q31.1-31.2(chr9:102858276-110624997)x3	ABCA1, ALDOB +34 more	Copy number gain	not provided	GUncertain significance
Select item 997816	Single allele	PRXL2C, TBC1D2 +55 more	Deletion	Intellectual disability	GPathogenic
Select item 979862	GRCh37/hg19 9q31.1(chr9:103872812-104974365)x3	GRIN3A, ALDOB +6 more	Copy number gain	not provided	GUncertain significance
Select item 929316	GRCh37/hg19 9q22.31-31.2(chr9:96126075-108535272)x1	TSTD2, XPA +84 more	Copy number loss	See cases	GPathogenic
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 394229	GRCh37/hg19 9q31.1-31.3(chr9:103271401-113948226)x1	ABCA1, ABITRAM +48 more	Copy number loss	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic

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Items: 53