Related gene-specific medical variations for Gene (Select 130067822) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3317238	NM_031454.2(SELENOO):c.169G>C (p.Ala57Pro)	LOC130067822, SELENOO (A57P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159599	NM_031454.2(SELENOO):c.85C>T (p.Pro29Ser)	LOC130067822, SELENOO (P29S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159591	NM_031454.2(SELENOO):c.5C>T (p.Ala2Val)	LOC130067822, SELENOO (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159578	NM_031454.2(SELENOO):c.26G>A (p.Gly9Glu)	LOC130067822, SELENOO (G9E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159577	NM_031454.2(SELENOO):c.25G>C (p.Gly9Arg)	LOC130067822, SELENOO (G9R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159576	NM_031454.2(SELENOO):c.22C>G (p.Leu8Val)	LOC130067822, SELENOO (L8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159575	NM_031454.2(SELENOO):c.209C>T (p.Ala70Val)	LOC130067822, SELENOO (A70V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159550	NM_031454.2(SELENOO):c.128G>C (p.Arg43Pro)	LOC130067822, SELENOO (R43P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159544	NM_031454.2(SELENOO):c.112A>G (p.Met38Val)	LOC130067822, SELENOO (M38V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2653367	NM_031454.2(SELENOO):c.105C>G (p.Gly35=)	LOC130067822, SELENOO	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620873	NM_031454.2(SELENOO):c.160G>T (p.Ala54Ser)	LOC130067822, SELENOO (A54S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance