"Ambry Genetics"[submitter] AND "MLST8"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2548990	NM_022372.6(MLST8):c.13C>T (p.Pro5Ser)	MLST8 (P5S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2223123	NM_022372.6(MLST8):c.155C>T (p.Pro52Leu)	MLST8 (P51L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3210415	NM_022372.6(MLST8):c.191A>G (p.His64Arg)	MLST8 (H63R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2517243	NM_022372.6(MLST8):c.396C>A (p.Asn132Lys)	MLST8 (N138K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261382	NM_022372.6(MLST8):c.509A>C (p.Glu170Ala)	MLST8 (E169A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210503	NM_022372.6(MLST8):c.510G>C (p.Glu170Asp)	MLST8 (E104D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3295213	NM_022372.6(MLST8):c.524C>T (p.Ser175Phe)	MLST8 (S181F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333513	NM_022372.6(MLST8):c.553A>G (p.Met185Val)	MLST8 (M184V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210558	NM_022372.6(MLST8):c.575G>A (p.Gly192Glu)	MLST8 (G191E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399427	NM_022372.6(MLST8):c.599C>T (p.Thr200Met)	MLST8 (T200M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210613	NM_022372.6(MLST8):c.661C>T (p.Arg221Cys)	MLST8 (R155C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210650	NM_022372.6(MLST8):c.679C>T (p.Arg227Cys)	MLST8 (R161C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524973	NM_022372.6(MLST8):c.690C>G (p.Pro230=)	MLST8	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3295212	NM_022372.6(MLST8):c.856G>A (p.Val286Ile)	MLST8 (V286I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3261763	NM_182563.4(BRICD5):c.682G>T (p.Asp228Tyr)	BRICD5, MLST8 (D228Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2323709	NM_182563.4(BRICD5):c.644G>A (p.Ser215Asn)	BRICD5, MLST8 (S215N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3261762	NM_182563.4(BRICD5):c.641C>T (p.Pro214Leu)	BRICD5, MLST8 (P214L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2394719	NM_182563.4(BRICD5):c.625A>G (p.Ile209Val)	BRICD5, MLST8 (I209V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3135058	NM_182563.4(BRICD5):c.617A>C (p.Tyr206Ser)	BRICD5, MLST8 (Y206S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2215915	NM_182563.4(BRICD5):c.607C>T (p.Arg203Trp)	BRICD5, MLST8 (R203W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3135057	NM_182563.4(BRICD5):c.598C>G (p.Arg200Gly)	BRICD5, MLST8 (R200G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 21