Related gene-specific medical variations for Gene (Select 55778) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198746	NM_018335.6(ZNF839):c.62C>G (p.Pro21Arg)	LOC130056512, ZNF839 (P21R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198741	NM_018335.6(ZNF839):c.284C>T (p.Pro95Leu)	LOC130056513, ZNF839 (P95L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198734	NM_018335.6(ZNF839):c.136G>C (p.Glu46Gln)	LOC130056512, ZNF839 (E46Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2491535	NM_018335.6(ZNF839):c.118C>A (p.Gln40Lys)	LOC130056512, ZNF839 (Q40K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2480321	NM_018335.6(ZNF839):c.44G>A (p.Gly15Asp)	LOC130056512, ZNF839 (G15D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2396564	NM_018335.6(ZNF839):c.206T>G (p.Leu69Arg)	LOC130056513, ZNF839 (L69R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2273793	NM_018335.6(ZNF839):c.87C>A (p.Ser29Arg)	LOC130056512, ZNF839 (S29R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2255003	NM_018335.6(ZNF839):c.221A>C (p.Gln74Pro)	LOC130056513, ZNF839 (Q74P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2232776	NM_018335.6(ZNF839):c.83G>T (p.Gly28Val)	LOC130056512, ZNF839 (G28V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2231097	NM_018335.6(ZNF839):c.55G>T (p.Gly19Cys)	LOC130056512, ZNF839 (G19C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2225047	NM_018335.6(ZNF839):c.212A>G (p.Asp71Gly)	LOC130056513, ZNF839 (D71G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance