STK19[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3171293	NM_032454.1(STK19):c.166T>G (p.Trp56Gly)	STK19 (W56G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323285	NM_032454.1(STK19):c.200G>C (p.Arg67Pro)	STK19 (R67P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323286	NM_032454.1(STK19):c.236A>G (p.Glu79Gly)	STK19 (E79G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263166	NM_032454.1(STK19):c.238A>T (p.Thr80Ser)	STK19 (T80S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 76320	NM_004197.1(STK19):c.265G>A (p.Asp89Asn)	STK19 (D89N)	Single nucleotide variant (missense variant +1 more)	Malignant melanoma of skin +1 more	GLikely pathogenic
Select item 3171294	NM_004197.2(STK19):c.-30C>G	STK19 (P58A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2283808	NM_004197.2(STK19):c.-5G>T	STK19 (R109L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2462463	NM_004197.2(STK19):c.-3G>A	STK19 (D67N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3171295	NM_004197.2(STK19):c.4A>G (p.Ser2Gly)	STK19 (S112G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214408	NM_004197.2(STK19):c.38T>C (p.Phe13Ser)	STK19 (F80S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171296	NM_004197.2(STK19):c.81T>G (p.Asp27Glu)	STK19 (D137E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171298	NM_004197.2(STK19):c.83C>T (p.Pro28Leu)	STK19 (P138L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490314	NM_004197.2(STK19):c.104C>G (p.Ser35Trp)	STK19 (S35W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171299	NM_004197.2(STK19):c.106G>T (p.Ala36Ser)	STK19 (A103S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171300	NM_004197.2(STK19):c.107C>T (p.Ala36Val)	STK19 (A103V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171301	NM_004197.2(STK19):c.271G>A (p.Val91Ile)	STK19 (V158I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3171302	NM_004197.2(STK19):c.286G>A (p.Asp96Asn)	STK19 (D96N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233321	NM_004197.2(STK19):c.317A>G (p.Glu106Gly)	STK19 (E106G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615402	NM_004197.2(STK19):c.323A>G (p.Tyr108Cys)	STK19 (Y218C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347892	NM_004197.2(STK19):c.343G>T (p.Ala115Ser)	STK19 (A229S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590748	NM_004197.2(STK19):c.356G>A (p.Arg119Gln)	STK19 (R186Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553553	NM_004197.2(STK19):c.397C>T (p.Leu133Phe)	STK19 (L133F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379122	NM_004197.2(STK19):c.438G>A (p.Met146Ile)	STK19 (M213I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404144	NM_004197.2(STK19):c.614G>A (p.Arg205Gln)	STK19 (R272Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466032	NM_004197.2(STK19):c.646C>T (p.Arg216Trp)	STK19 (R216W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227053	NM_004197.2(STK19):c.665G>A (p.Arg222Gln)	STK19 (R222Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344536	NM_004197.2(STK19):c.698T>C (p.Ile233Thr)	STK19 (I300T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 27