Related gene-specific medical variations for Gene (Select 167410) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290844	NM_153234.5(LIX1):c.88G>A (p.Val30Ile)	LIX1, LOC126807459 (V30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119126	NM_153234.5(LIX1):c.425T>A (p.Val142Asp)	LIX1, LIX1-AS1 (V142D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119125	NM_153234.5(LIX1):c.383C>T (p.Thr128Ile)	LIX1, LIX1-AS1 (T128I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119124	NM_153234.5(LIX1):c.274C>T (p.Arg92Trp)	LIX1, LIX1-AS1 (R92W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119123	NM_153234.5(LIX1):c.205T>G (p.Tyr69Asp)	LIX1, LOC126807459 (Y69D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599660	NM_153234.5(LIX1):c.275G>A (p.Arg92Gln)	LIX1, LIX1-AS1 (R92Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456043	NM_153234.5(LIX1):c.521G>A (p.Gly174Glu)	LIX1, LIX1-AS1 (G174E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287927	NM_153234.5(LIX1):c.352A>G (p.Met118Val)	LIX1, LIX1-AS1 (M118V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252913	NM_153234.5(LIX1):c.807T>A (p.Ser269Arg)	LIX1, LIX1-AS1 (S269R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233540	NM_153234.5(LIX1):c.608G>A (p.Arg203His)	LIX1, LIX1-AS1 (R203H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance