ZNF138[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2390686	NM_001271639.2(ZNF138):c.8C>A (p.Pro3Gln)	ZNF138 (P3Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3194028	NM_001271639.2(ZNF138):c.20T>C (p.Met7Thr)	ZNF138 (M7T +1 more)	Single nucleotide variant (missense variant +4 more)	not specified	GUncertain significance
Select item 2411850	NM_001271639.2(ZNF138):c.76C>T (p.Arg26Trp)	ZNF138 (R26W +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2517144	NM_001271639.2(ZNF138):c.77G>A (p.Arg26Gln)	ZNF138 (R20Q +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 2556911	NM_001271639.2(ZNF138):c.105G>C (p.Glu35Asp)	ZNF138 (E29D +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2250902	NM_001271639.2(ZNF138):c.115A>G (p.Asn39Asp)	ZNF138 (N33D +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3334950	NM_001271639.2(ZNF138):c.121G>A (p.Val41Ile)	ZNF138 (V35I +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3194027	NM_001271639.2(ZNF138):c.125T>C (p.Phe42Ser)	ZNF138 (F42S +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2361708	NM_001271639.2(ZNF138):c.209C>T (p.Ala70Val)	ZNF138 (A38V +8 more)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 2590932	NM_001271639.2(ZNF138):c.234C>T (p.Asp78=)	ZNF138 (T118I +4 more)	Single nucleotide variant (missense variant +4 more)	not specified	GLikely benign
Select item 2348068	NM_001271639.2(ZNF138):c.274G>A (p.Val92Met)	ZNF138 (V60M +3 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2267090	NM_001271639.2(ZNF138):c.328G>A (p.Gly110Ser)	ZNF138 (G78S +3 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GLikely benign
Select item 2457135	NM_001271639.2(ZNF138):c.354G>C (p.Lys118Asn)	ZNF138 (K118N +3 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2205210	NM_001271639.2(ZNF138):c.529T>C (p.Cys177Arg)	ZNF138 (C177R +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194029	NM_001271639.2(ZNF138):c.541C>T (p.Arg181Cys)	ZNF138 (R181C +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2364640	NM_001271639.2(ZNF138):c.594A>T (p.Glu198Asp)	ZNF138 (E172D +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3334951	NM_001271639.2(ZNF138):c.674G>A (p.Cys225Tyr)	ZNF138 (C193Y +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2313867	NM_001271639.2(ZNF138):c.709A>G (p.Ile237Val)	ZNF138 (I205V +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2367108	NM_001271639.2(ZNF138):c.727A>G (p.Ile243Val)	ZNF138 (I217V +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2557693	NM_001271639.2(ZNF138):c.757T>G (p.Cys253Gly)	ZNF138 (C196G +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194030	NM_001271639.2(ZNF138):c.826G>A (p.Glu276Lys)	ZNF138 (E129K +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2335800	NM_001271639.2(ZNF138):c.832C>T (p.Pro278Ser)	ZNF138 (P246S +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3194031	NM_001271639.2(ZNF138):c.949A>G (p.Asn317Asp)	ZNF138 (N285D +4 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 23