Related gene-specific medical variations for Gene (Select 9645) - ClinVar

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Items: 55

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294746	NM_001393937.1(MICAL2):c.5669G>A (p.Arg1890Lys)	MICAL2, MICALCL (R1890K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294742	NM_001393937.1(MICAL2):c.3979T>C (p.Phe1327Leu)	MICAL2, MICALCL (F1327L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294740	NM_001393937.1(MICAL2):c.4061A>T (p.Glu1354Val)	MICAL2, MICALCL (E1354V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294739	NM_001393937.1(MICAL2):c.5779G>A (p.Asp1927Asn)	MICAL2, MICALCL (D1927N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3294737	NM_001393937.1(MICAL2):c.4091G>T (p.Gly1364Val)	MICAL2, MICALCL (G1364V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294730	NM_001393937.1(MICAL2):c.5455C>T (p.Arg1819Trp)	MICAL2, MICALCL (R1819W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126195	NM_001393937.1(MICAL2):c.4784C>A (p.Ser1595Tyr)	MICAL2, MICALCL (S1595Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126194	NM_001393937.1(MICAL2):c.4715G>C (p.Arg1572Pro)	MICAL2, MICALCL (R1572P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126193	NM_001393937.1(MICAL2):c.4700C>T (p.Ala1567Val)	MICAL2, MICALCL (A1567V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126192	NM_001393937.1(MICAL2):c.4666G>A (p.Ala1556Thr)	MICAL2, MICALCL (A1556T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126191	NM_001393937.1(MICAL2):c.4619G>C (p.Arg1540Pro)	MICAL2, MICALCL (R1540P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126190	NM_001393937.1(MICAL2):c.4577C>A (p.Pro1526His)	MICAL2, MICALCL (P1526H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126188	NM_001393937.1(MICAL2):c.4547C>A (p.Ala1516Glu)	MICAL2, MICALCL (A1516E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126186	NM_001393937.1(MICAL2):c.4474C>G (p.Leu1492Val)	MICAL2, MICALCL (L1492V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126182	NM_001393937.1(MICAL2):c.4247G>A (p.Arg1416Gln)	MICAL2, MICALCL (R1416Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3126181	NM_001393937.1(MICAL2):c.4225T>A (p.Ser1409Thr)	MICAL2, MICALCL (S1409T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126180	NM_001393937.1(MICAL2):c.4198G>A (p.Asp1400Asn)	MICAL2, MICALCL (D1400N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126179	NM_001393937.1(MICAL2):c.3824T>A (p.Leu1275His)	MICAL2, MICALCL (L1275H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126178	NM_001393937.1(MICAL2):c.4158C>G (p.Ile1386Met)	MICAL2, MICALCL (I1386M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126172	NM_001393937.1(MICAL2):c.4066T>A (p.Cys1356Ser)	MICAL2, MICALCL (C1356S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126166	NM_001393937.1(MICAL2):c.4042C>T (p.Pro1348Ser)	MICAL2, MICALCL (P1348S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126159	NM_001393937.1(MICAL2):c.5839G>A (p.Val1947Ile)	MICAL2, MICALCL (V1947I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3126158	NM_001393937.1(MICAL2):c.5837T>C (p.Phe1946Ser)	MICAL2, MICALCL (F1946S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126156	NM_001393937.1(MICAL2):c.5740G>A (p.Glu1914Lys)	MICAL2, MICALCL (E1914K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126154	NM_001393937.1(MICAL2):c.5731G>A (p.Val1911Ile)	MICAL2, MICALCL (V1911I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3126153	NM_001393937.1(MICAL2):c.5696A>G (p.Gln1899Arg)	MICAL2, MICALCL (Q1899R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126150	NM_001393937.1(MICAL2):c.5620C>G (p.Gln1874Glu)	MICAL2, MICALCL (Q1874E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126147	NM_001393937.1(MICAL2):c.5504G>C (p.Arg1835Pro)	MICAL2, MICALCL (R1835P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126146	NM_001393937.1(MICAL2):c.5498C>T (p.Ala1833Val)	MICAL2, MICALCL (A1833V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126145	NM_001393937.1(MICAL2):c.5480G>A (p.Gly1827Asp)	MICAL2, MICALCL (G1827D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126144	NM_001393937.1(MICAL2):c.5464G>A (p.Ala1822Thr)	MICAL2, MICALCL (A1822T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126143	NM_001393937.1(MICAL2):c.5344A>G (p.Arg1782Gly)	MICAL2, MICALCL (R1782G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126142	NM_001393937.1(MICAL2):c.5144G>A (p.Arg1715His)	MICAL2, MICALCL (R1715H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126141	NM_001393937.1(MICAL2):c.5101G>C (p.Ala1701Pro)	MICAL2, MICALCL (A1701P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3126139	NM_001393937.1(MICAL2):c.3910C>T (p.Pro1304Ser)	MICAL2, MICALCL (P1304S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126136	NM_001393937.1(MICAL2):c.4927G>A (p.Glu1643Lys)	MICAL2, MICALCL (E1643K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126134	NM_001393937.1(MICAL2):c.4817G>A (p.Arg1606His)	MICAL2, MICALCL (R1606H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641614	NM_001393937.1(MICAL2):c.5172T>C (p.Pro1724=)	MICAL2, MICALCL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2641613	NM_001393937.1(MICAL2):c.4838G>A (p.Arg1613Gln)	MICAL2, MICALCL (R1613Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2641612	NM_001393937.1(MICAL2):c.4450C>T (p.Arg1484Cys)	MICAL2, MICALCL (R1484C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2624345	NM_001393937.1(MICAL2):c.4326G>T (p.Lys1442Asn)	MICAL2, MICALCL (K1442N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597389	NM_001393937.1(MICAL2):c.4451G>A (p.Arg1484His)	MICAL2, MICALCL (R1484H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595340	NM_001393937.1(MICAL2):c.4264G>A (p.Gly1422Arg)	MICAL2, MICALCL (G1422R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2595146	NM_001393937.1(MICAL2):c.4511C>T (p.Thr1504Ile)	MICAL2, MICALCL (T1504I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593686	NM_001393937.1(MICAL2):c.4556C>T (p.Ala1519Val)	MICAL2, MICALCL (A1519V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593360	NM_001393937.1(MICAL2):c.4094T>G (p.Leu1365Arg)	MICAL2, MICALCL (L1365R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589207	NM_001393937.1(MICAL2):c.4597C>T (p.Arg1533Trp)	MICAL2, MICALCL (R1533W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557441	NM_001393937.1(MICAL2):c.4330G>A (p.Val1444Ile)	MICAL2, MICALCL (V1444I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540704	NM_001393937.1(MICAL2):c.4364A>T (p.Asp1455Val)	MICAL2, MICALCL (D1455V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531334	NM_001393937.1(MICAL2):c.4816C>T (p.Arg1606Cys)	MICAL2, MICALCL (R1606C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530070	NM_001393937.1(MICAL2):c.4246C>T (p.Arg1416Trp)	MICAL2, MICALCL (R1416W)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2528851	NM_001393937.1(MICAL2):c.5580T>A (p.Asn1860Lys)	MICAL2, MICALCL (N1860K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521339	NM_001393937.1(MICAL2):c.4730G>T (p.Arg1577Leu)	MICAL2, MICALCL (R1577L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511070	NM_001393937.1(MICAL2):c.5614A>T (p.Met1872Leu)	MICAL2, MICALCL (M1872L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484878	NM_001393937.1(MICAL2):c.4850T>C (p.Val1617Ala)	MICAL2, MICALCL (V1617A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 55