MON1B[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295549	NM_014940.4(MON1B):c.35C>G (p.Pro12Arg)	MON1B (P12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596904	NM_014940.4(MON1B):c.52T>A (p.Leu18Met)	MON1B (L18M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241636	NM_014940.4(MON1B):c.67T>G (p.Phe23Val)	MON1B (F23V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511930	NM_014940.4(MON1B):c.116C>G (p.Pro39Arg)	MON1B (P39R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3295547	NM_014940.4(MON1B):c.130G>A (p.Glu44Lys)	MON1B (E44K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212584	NM_014940.4(MON1B):c.178C>G (p.Pro60Ala)	MON1B (P60A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616375	NM_014940.4(MON1B):c.242C>T (p.Pro81Leu)	MON1B (P81L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197879	NM_014940.4(MON1B):c.265C>T (p.Pro89Ser)	MON1B (P89S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246076	NM_014940.4(MON1B):c.275G>C (p.Ser92Thr)	MON1B (S92T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197937	NM_014940.4(MON1B):c.316C>T (p.Arg106Cys)	MON1B (R106C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621228	NM_014940.4(MON1B):c.326G>A (p.Arg109Gln)	MON1B (R109Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198011	NM_014940.4(MON1B):c.397T>A (p.Ser133Thr)	MON1B (S133T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231922	NM_014940.4(MON1B):c.472G>A (p.Ala158Thr)	MON1B (A158T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458400	NM_014940.4(MON1B):c.533G>A (p.Arg178Gln)	MON1B (R32Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198135	NM_014940.4(MON1B):c.535A>G (p.Thr179Ala)	MON1B (T179A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338830	NM_014940.4(MON1B):c.592G>T (p.Val198Leu)	MON1B (V198L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198203	NM_014940.4(MON1B):c.619G>A (p.Ala207Thr)	MON1B (A98T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325505	NM_014940.4(MON1B):c.620C>T (p.Ala207Val)	MON1B (A98V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288321	NM_014940.4(MON1B):c.755C>G (p.Pro252Arg)	MON1B (P106R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295550	NM_014940.4(MON1B):c.773G>A (p.Arg258Gln)	MON1B (R112Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480874	NM_014940.4(MON1B):c.1012G>A (p.Ala338Thr)	MON1B (A192T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197431	NM_014940.4(MON1B):c.1031A>G (p.Asp344Gly)	MON1B (D198G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235389	NM_014940.4(MON1B):c.1034C>T (p.Ala345Val)	MON1B (A199V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334647	NM_014940.4(MON1B):c.1142G>A (p.Arg381His)	MON1B (R381H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239467	NM_014940.4(MON1B):c.1208A>G (p.Gln403Arg)	MON1B (Q403R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296450	NM_014940.4(MON1B):c.1223C>T (p.Pro408Leu)	MON1B (P299L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479980	NM_014940.4(MON1B):c.1234C>T (p.His412Tyr)	MON1B (H266Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364268	NM_014940.4(MON1B):c.1360C>T (p.Arg454Cys)	MON1B (R308C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395534	NM_014940.4(MON1B):c.1397T>C (p.Leu466Pro)	MON1B (L357P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197715	NM_014940.4(MON1B):c.1423A>C (p.Lys475Gln)	MON1B (K366Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615690	NM_014940.4(MON1B):c.1459G>A (p.Glu487Lys)	MON1B (E341K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537323	NM_014940.4(MON1B):c.1551C>G (p.Asp517Glu)	MON1B (D408E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255086	NM_014940.4(MON1B):c.1588C>T (p.Pro530Ser)	MON1B (P384S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33