Related gene-specific medical variations for Gene (Select 128077) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290845	NM_153713.3(LIX1L):c.115C>G (p.Pro39Ala)	LIX1L, LOC129931340 (P39A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119130	NM_153713.3(LIX1L):c.856A>C (p.Ser286Arg)	LIX1L, LIX1L-AS1 (S286R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119129	NM_153713.3(LIX1L):c.670G>A (p.Gly224Ser)	LIX1L, LIX1L-AS1 (G224S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477240	NM_153713.3(LIX1L):c.98C>T (p.Ala33Val)	LIX1L, LOC129931340 (A33V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477239	NM_153713.3(LIX1L):c.103A>G (p.Thr35Ala)	LIX1L, LOC129931340 (T35A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2339631	NM_153713.3(LIX1L):c.233G>C (p.Arg78Pro)	LIX1L, LOC129931340 (R78P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322096	NM_153713.3(LIX1L):c.128C>A (p.Pro43Gln)	LIX1L, LOC129931340 (P43Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313303	NM_153713.3(LIX1L):c.920T>G (p.Leu307Arg)	LIX1L, LIX1L-AS1 (L307R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297528	NM_153713.3(LIX1L):c.50G>A (p.Gly17Glu)	LIX1L, LOC129931340 (G17E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296395	NM_153713.3(LIX1L):c.863C>T (p.Pro288Leu)	LIX1L, LIX1L-AS1 (P288L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279988	NM_153713.3(LIX1L):c.205G>A (p.Gly69Ser)	LIX1L, LOC129931340 (G69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271356	NM_153713.3(LIX1L):c.154C>A (p.Pro52Thr)	LIX1L, LOC129931340 (P52T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261613	NM_153713.3(LIX1L):c.612A>T (p.Glu204Asp)	LIX1L, LIX1L-AS1 (E204D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217566	NM_153713.3(LIX1L):c.901G>C (p.Glu301Gln)	LIX1L, LIX1L-AS1 (E301Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance