Related gene-specific medical variations for Gene (Select 83642) - ClinVar

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Links from Gene

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3159600	NM_031454.2(SELENOO):c.935G>A (p.Arg312Gln)	SELENOO, SELENOO-AS1 (R312Q)	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 3159598	NM_031454.2(SELENOO):c.806G>A (p.Arg269His)	SELENOO, SELENOO-AS1 (R269H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159597	NM_031454.2(SELENOO):c.799A>G (p.Thr267Ala)	SELENOO, SELENOO-AS1 (T267A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159596	NM_031454.2(SELENOO):c.719A>C (p.Gln240Pro)	SELENOO, SELENOO-AS1 (Q240P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159595	NM_031454.2(SELENOO):c.688G>A (p.Val230Met)	SELENOO, SELENOO-AS1 (V230M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159594	NM_031454.2(SELENOO):c.685G>A (p.Asp229Asn)	SELENOO, SELENOO-AS1 (D229N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159592	NM_031454.2(SELENOO):c.670T>G (p.Ser224Ala)	SELENOO, SELENOO-AS1 (S224A)	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 3159590	NM_031454.2(SELENOO):c.592C>T (p.Arg198Trp)	SELENOO, SELENOO-AS1 (R198W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159589	NM_031454.2(SELENOO):c.581G>A (p.Arg194Gln)	SELENOO, SELENOO-AS1 (R194Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159587	NM_031454.2(SELENOO):c.410C>T (p.Ala137Val)	LOC130067823, SELENOO (A137V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159585	NM_031454.2(SELENOO):c.380A>G (p.Asn127Ser)	LOC130067823, SELENOO (N127S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159584	NM_031454.2(SELENOO):c.376G>A (p.Gly126Ser)	LOC130067823, SELENOO (G126S)	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 2653368	NM_031454.2(SELENOO):c.880G>A (p.Glu294Lys)	SELENOO, SELENOO-AS1 (E294K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
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
Select item 2611243	NM_031454.2(SELENOO):c.671C>T (p.Ser224Phe)	SELENOO, SELENOO-AS1 (S224F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534536	NM_031454.2(SELENOO):c.397G>T (p.Ala133Ser)	LOC130067823, SELENOO (A133S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532074	NM_031454.2(SELENOO):c.730G>C (p.Val244Leu)	SELENOO, SELENOO-AS1 (V244L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514830	NM_031454.2(SELENOO):c.910G>A (p.Val304Met)	SELENOO, SELENOO-AS1 (V304M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2429004	NM_031454.2(SELENOO):c.441G>C (p.Gln147His)	LOC130067823, SELENOO (Q147H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Links from Gene

Items: 28