Related gene-specific medical variations for Gene (Select 10009) - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333913	NM_001184742.2(ZBTB33):c.1189A>G (p.Arg397Gly)	TMEM255A, ZBTB33 (R397G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333912	NM_001184742.2(ZBTB33):c.836A>G (p.Asn279Ser)	TMEM255A, ZBTB33 (N279S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192007	NM_001184742.2(ZBTB33):c.787G>A (p.Gly263Arg)	TMEM255A, ZBTB33 (G263R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192006	NM_001184742.2(ZBTB33):c.458A>G (p.Lys153Arg)	TMEM255A, ZBTB33 (K153R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192005	NM_001184742.2(ZBTB33):c.389C>T (p.Ala130Val)	TMEM255A, ZBTB33 (A130V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192004	NM_001184742.2(ZBTB33):c.1979G>A (p.Gly660Asp)	TMEM255A, ZBTB33 (G660D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192003	NM_001184742.2(ZBTB33):c.1882G>A (p.Gly628Arg)	TMEM255A, ZBTB33 (G628R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192002	NM_001184742.2(ZBTB33):c.1843A>G (p.Ile615Val)	TMEM255A, ZBTB33 (I615V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192001	NM_001184742.2(ZBTB33):c.1707A>G (p.Ile569Met)	TMEM255A, ZBTB33 (I569M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192000	NM_001184742.2(ZBTB33):c.163A>G (p.Thr55Ala)	TMEM255A, ZBTB33 (T55A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191998	NM_001184742.2(ZBTB33):c.1229T>C (p.Met410Thr)	TMEM255A, ZBTB33 (M410T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191997	NM_001184742.2(ZBTB33):c.1200T>G (p.Asn400Lys)	TMEM255A, ZBTB33 (N400K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661321	NM_001184742.2(ZBTB33):c.*1127T>G	TMEM255A, ZBTB33	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 2661320	NM_001184742.2(ZBTB33):c.1326T>C (p.Tyr442=)	TMEM255A, ZBTB33	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661319	NM_001184742.2(ZBTB33):c.105C>T (p.Thr35=)	TMEM255A, ZBTB33	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661318	NM_001184742.2(ZBTB33):c.-105+814G>A	TMEM255A, ZBTB33	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2604129	NM_001184742.2(ZBTB33):c.592T>G (p.Cys198Gly)	TMEM255A, ZBTB33 (C198G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602779	NM_001184742.2(ZBTB33):c.623T>C (p.Leu208Ser)	TMEM255A, ZBTB33 (L208S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558412	NM_001184742.2(ZBTB33):c.1048G>A (p.Val350Ile)	TMEM255A, ZBTB33 (V350I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474427	NM_001184742.2(ZBTB33):c.856A>G (p.Thr286Ala)	TMEM255A, ZBTB33 (T286A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404204	NM_001184742.2(ZBTB33):c.1408G>A (p.Glu470Lys)	TMEM255A, ZBTB33 (E470K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375761	NM_001184742.2(ZBTB33):c.1912A>G (p.Met638Val)	TMEM255A, ZBTB33 (M638V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342083	NM_001184742.2(ZBTB33):c.1705A>G (p.Ile569Val)	TMEM255A, ZBTB33 (I569V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313070	NM_001184742.2(ZBTB33):c.1003A>C (p.Ile335Leu)	TMEM255A, ZBTB33 (I335L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297677	NM_001184742.2(ZBTB33):c.1397C>A (p.Thr466Lys)	TMEM255A, ZBTB33 (T466K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1279050	NM_001184742.2(ZBTB33):c.564_565insTGA (p.Asp189Ter)	TMEM255A, ZBTB33 (D189*)	Insertion (nonsense)	not provided	GBenign
Select item 783911	NM_001184742.2(ZBTB33):c.676A>G (p.Ile226Val)	TMEM255A, ZBTB33 (I226V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 781643	NM_001184742.2(ZBTB33):c.1873C>A (p.Pro625Thr)	TMEM255A, ZBTB33 (P625T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 493544	NM_001184742.2(ZBTB33):c.653A>T (p.Gln218Leu)	TMEM255A, ZBTB33 (Q218L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 373722	NM_001184742.2(ZBTB33):c.37C>G (p.Gln13Glu)	TMEM255A, ZBTB33 (Q13E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30