Related gene-specific medical variations for Gene (Select 441381) - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3120470	NM_001024678.4(LRRC24):c.982G>T (p.Gly328Cys)	LOC130001413, LRRC14 +1 more (G328C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120469	NM_001024678.4(LRRC24):c.944T>A (p.Leu315Gln)	LRRC14, LRRC24 (L315Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120468	NM_001024678.4(LRRC24):c.908G>A (p.Arg303Gln)	LRRC14, LRRC24 (R303Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120467	NM_001024678.4(LRRC24):c.817C>A (p.Leu273Met)	LRRC14, LRRC24 (L273M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120466	NM_001024678.4(LRRC24):c.565G>A (p.Ala189Thr)	LRRC14, LRRC24 (A189T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120465	NM_001024678.4(LRRC24):c.428T>C (p.Leu143Ser)	LRRC14, LRRC24 (L143S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120464	NM_001024678.4(LRRC24):c.407G>A (p.Arg136Gln)	LRRC14, LRRC24 (R136Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3120463	NM_001024678.4(LRRC24):c.373C>A (p.Arg125Ser)	LRRC14, LRRC24 (R125S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120462	NM_001024678.4(LRRC24):c.350C>T (p.Ala117Val)	LRRC14, LRRC24 (A117V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120461	NM_001024678.4(LRRC24):c.29C>T (p.Pro10Leu)	LRRC14, LRRC24 (P10L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3120460	NM_001024678.4(LRRC24):c.1433C>T (p.Pro478Leu)	LRRC14, LRRC24 (P478L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120459	NM_001024678.4(LRRC24):c.1399G>A (p.Gly467Ser)	LRRC14, LRRC24 (G467S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120458	NM_001024678.4(LRRC24):c.1319G>A (p.Gly440Glu)	LRRC14, LRRC24 (G440E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120456	NM_001024678.4(LRRC24):c.1288C>G (p.Arg430Gly)	LRRC14, LRRC24 (R430G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2658998	NM_001024678.4(LRRC24):c.837T>A (p.Val279=)	LRRC14, LRRC24	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658997	NM_001024678.4(LRRC24):c.1113G>A (p.Gln371=)	LOC130001413, LRRC14 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2603397	NM_001024678.4(LRRC24):c.574C>A (p.Pro192Thr)	LRRC14, LRRC24 (P192T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591389	NM_001024678.4(LRRC24):c.1490C>G (p.Ala497Gly)	LRRC14, LRRC24 (A497G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588138	NM_001024678.4(LRRC24):c.1272G>C (p.Met424Ile)	LRRC14, LRRC24 (M424I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536753	NM_001024678.4(LRRC24):c.64G>C (p.Gly22Arg)	LRRC14, LRRC24 (G22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526234	NM_001024678.4(LRRC24):c.1378G>C (p.Glu460Gln)	LRRC14, LRRC24 (E460Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390344	NM_001024678.4(LRRC24):c.41T>C (p.Leu14Pro)	LRRC14, LRRC24 (L14P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381359	NM_001024678.4(LRRC24):c.340C>G (p.Arg114Gly)	LRRC14, LRRC24 (R114G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374193	NM_001024678.4(LRRC24):c.998G>A (p.Ser333Asn)	LOC130001413, LRRC14 +1 more (S333N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353498	NM_001024678.4(LRRC24):c.319A>C (p.Ser107Arg)	LRRC14, LRRC24 (S107R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329333	NM_001024678.4(LRRC24):c.646G>C (p.Gly216Arg)	LRRC14, LRRC24 (G216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329064	NM_001024678.4(LRRC24):c.1304C>T (p.Ala435Val)	LRRC14, LRRC24 (A435V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322557	NM_001024678.4(LRRC24):c.1486G>A (p.Gly496Arg)	LRRC14, LRRC24 (G496R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322231	NM_001024678.4(LRRC24):c.1165C>T (p.Pro389Ser)	LOC130001413, LRRC14 +1 more (P389S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320949	NM_001024678.4(LRRC24):c.1454C>A (p.Ala485Glu)	LRRC14, LRRC24 (A485E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301733	NM_001024678.4(LRRC24):c.562G>C (p.Glu188Gln)	LRRC14, LRRC24 (E188Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283850	NM_001024678.4(LRRC24):c.1304C>A (p.Ala435Glu)	LRRC14, LRRC24 (A435E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258489	NM_001024678.4(LRRC24):c.660G>C (p.Lys220Asn)	LRRC24, LRRC14 (K220N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230251	NM_001024678.4(LRRC24):c.1316C>T (p.Pro439Leu)	LRRC14, LRRC24 (P439L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216441	NM_001024678.4(LRRC24):c.1292G>A (p.Arg431Lys)	LRRC14, LRRC24 (R431K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 35