"Ambry Genetics"[submitter] AND "LOC126863184"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2592509	NM_012401.4(PLXNB2):c.3116C>T (p.Thr1039Met)	LOC126863184, PLXNB2 (T1008M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221092	NM_012401.4(PLXNB2):c.3059C>T (p.Ala1020Val)	LOC126863184, PLXNB2 (A989V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215649	NM_012401.4(PLXNB2):c.3011C>T (p.Thr1004Met)	LOC126863184, PLXNB2 (T1004M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215648	NM_012401.4(PLXNB2):c.2965G>A (p.Glu989Lys)	LOC126863184, PLXNB2 (E1012K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215647	NM_012401.4(PLXNB2):c.2960C>T (p.Ala987Val)	LOC126863184, PLXNB2 (A1010V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215646	NM_012401.4(PLXNB2):c.2957G>A (p.Arg986Gln)	LOC126863184, PLXNB2 (R986Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215645	NM_012401.4(PLXNB2):c.2950G>A (p.Val984Ile)	LOC126863184, PLXNB2 (V953I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379731	NM_012401.4(PLXNB2):c.2920G>A (p.Gly974Ser)	LOC126863184, PLXNB2 (G997S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2350992	NM_012401.4(PLXNB2):c.2877G>A (p.Met959Ile)	LOC126863184, PLXNB2 (M959I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251144	NM_012401.4(PLXNB2):c.2875A>T (p.Met959Leu)	LOC126863184, PLXNB2 (M928L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2546507	NM_012401.4(PLXNB2):c.2840A>G (p.Gln947Arg)	LOC126863184, PLXNB2 (Q970R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215644	NM_012401.4(PLXNB2):c.2807C>T (p.Pro936Leu)	LOC126863184, PLXNB2 (P905L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215643	NM_012401.4(PLXNB2):c.2791A>G (p.Thr931Ala)	LOC126863184, PLXNB2 (T900A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306921	NM_012401.4(PLXNB2):c.2728G>A (p.Gly910Ser)	LOC126863184, PLXNB2 (G879S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215642	NM_012401.4(PLXNB2):c.2723C>T (p.Ala908Val)	LOC126863184, PLXNB2 (A877V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215641	NM_012401.4(PLXNB2):c.2717C>T (p.Pro906Leu)	LOC126863184, PLXNB2 (P906L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance