Related gene-specific medical variations for Gene (Select 8897) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3216308	NM_021090.4(MTMR3):c.3331A>G (p.Thr1111Ala)	HORMAD2-AS1, MTMR3 (T1111A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216306	NM_021090.4(MTMR3):c.3089G>A (p.Arg1030His)	HORMAD2-AS1, MTMR3 (R1030H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216288	NM_021090.4(MTMR3):c.2864A>G (p.Asn955Ser)	HORMAD2-AS1, MTMR3 (N955S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216286	NM_021090.4(MTMR3):c.2863A>C (p.Asn955His)	HORMAD2-AS1, MTMR3 (N955H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216284	NM_021090.4(MTMR3):c.2794C>T (p.Pro932Ser)	HORMAD2-AS1, MTMR3 (P932S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216282	NM_021090.4(MTMR3):c.2786A>G (p.Asn929Ser)	HORMAD2-AS1, MTMR3 (N929S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216277	NM_021090.4(MTMR3):c.2591A>T (p.His864Leu)	HORMAD2-AS1, MTMR3 (H864L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216237	NM_021090.4(MTMR3):c.2311G>A (p.Gly771Arg)	HORMAD2-AS1, MTMR3 (G771R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216225	NM_021090.4(MTMR3):c.2240A>G (p.Asp747Gly)	HORMAD2-AS1, MTMR3 (D747G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216222	NM_021090.4(MTMR3):c.2164C>G (p.Leu722Val)	HORMAD2-AS1, MTMR3 (L722V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216202	NM_021090.4(MTMR3):c.1747A>G (p.Thr583Ala)	HORMAD2-AS1, MTMR3 (T583A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216193	NM_021090.4(MTMR3):c.1622G>A (p.Arg541Gln)	MTMR3, HORMAD2-AS1 (R541Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216188	NM_021090.4(MTMR3):c.1490A>G (p.Asn497Ser)	HORMAD2-AS1, MTMR3 (N497S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2653055	NM_021090.4(MTMR3):c.1510C>T (p.Leu504=)	HORMAD2-AS1, MTMR3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2612049	NM_021090.4(MTMR3):c.3322A>G (p.Lys1108Glu)	HORMAD2-AS1, MTMR3 (K1108E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601693	NM_021090.4(MTMR3):c.3125T>C (p.Val1042Ala)	HORMAD2-AS1, MTMR3 (V1042A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594415	NM_021090.4(MTMR3):c.2556T>G (p.Asp852Glu)	HORMAD2-AS1, MTMR3 (D852E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545216	NM_021090.4(MTMR3):c.1923G>T (p.Trp641Cys)	HORMAD2-AS1, MTMR3 (W641C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535560	NM_021090.4(MTMR3):c.1936C>T (p.Arg646Cys)	HORMAD2-AS1, MTMR3 (R646C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529976	NM_021090.4(MTMR3):c.2605G>T (p.Val869Leu)	HORMAD2-AS1, MTMR3 (V869L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522343	NM_021090.4(MTMR3):c.2281T>C (p.Phe761Leu)	HORMAD2-AS1, MTMR3 (F761L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490582	NM_021090.4(MTMR3):c.1883C>T (p.Ala628Val)	HORMAD2-AS1, MTMR3 (A628V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487656	NM_021090.4(MTMR3):c.2914C>T (p.Arg972Cys)	HORMAD2-AS1, MTMR3 (R972C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483136	NM_021090.4(MTMR3):c.2089A>G (p.Thr697Ala)	HORMAD2-AS1, MTMR3 (T697A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469648	NM_021090.4(MTMR3):c.2446G>A (p.Ala816Thr)	HORMAD2-AS1, MTMR3 (A816T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461692	NM_021090.4(MTMR3):c.2939G>C (p.Ser980Thr)	HORMAD2-AS1, MTMR3 (S980T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392061	NM_021090.4(MTMR3):c.2985T>G (p.His995Gln)	HORMAD2-AS1, MTMR3 (H995Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371728	NM_021090.4(MTMR3):c.2047G>A (p.Gly683Arg)	HORMAD2-AS1, MTMR3 (G683R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367093	NM_021090.4(MTMR3):c.3077C>T (p.Thr1026Met)	HORMAD2-AS1, MTMR3 (T1026M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342321	NM_021090.4(MTMR3):c.1933C>T (p.Arg645Trp)	HORMAD2-AS1, MTMR3 (R645W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337613	NM_021090.4(MTMR3):c.3539C>G (p.Pro1180Arg)	HORMAD2-AS1, MTMR3 (P1143R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331726	NM_021090.4(MTMR3):c.2559G>C (p.Lys853Asn)	HORMAD2-AS1, MTMR3 (K853N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326101	NM_021090.4(MTMR3):c.2968C>G (p.His990Asp)	HORMAD2-AS1, MTMR3 (H990D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322055	NM_021090.4(MTMR3):c.2224G>T (p.Asp742Tyr)	HORMAD2-AS1, MTMR3 (D742Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317907	NM_021090.4(MTMR3):c.3515A>C (p.Lys1172Thr)	HORMAD2-AS1, MTMR3 (K1135T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285884	NM_021090.4(MTMR3):c.2134A>G (p.Ile712Val)	HORMAD2-AS1, MTMR3 (I712V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285312	NM_021090.4(MTMR3):c.2663G>A (p.Ser888Asn)	HORMAD2-AS1, MTMR3 (S888N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265806	NM_021090.4(MTMR3):c.3196C>A (p.His1066Asn)	HORMAD2-AS1, MTMR3 (H1066N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251276	NM_021090.4(MTMR3):c.2945C>T (p.Ala982Val)	HORMAD2-AS1, MTMR3 (A982V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235393	NM_021090.4(MTMR3):c.2508G>C (p.Glu836Asp)	HORMAD2-AS1, MTMR3 (E836D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221341	NM_021090.4(MTMR3):c.3385G>A (p.Asp1129Asn)	HORMAD2-AS1, MTMR3 (D1092N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218050	NM_021090.4(MTMR3):c.2390G>A (p.Arg797Gln)	HORMAD2-AS1, MTMR3 (R797Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2204221	NM_021090.4(MTMR3):c.3034C>T (p.Arg1012Cys)	HORMAD2-AS1, MTMR3 (R1012C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1225402	NM_021090.4(MTMR3):c.*1670C>T	HORMAD2-AS1, MTMR3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 44