STK32C[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 716418	NM_173575.4(STK32C):c.1455C>T (p.Ser485=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2520458	NM_173575.4(STK32C):c.1430G>T (p.Gly477Val)	STK32C (G490V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171366	NM_173575.4(STK32C):c.1421C>T (p.Pro474Leu)	STK32C (P474L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323315	NM_173575.4(STK32C):c.1411T>C (p.Ser471Pro)	STK32C (S354P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2366721	NM_173575.4(STK32C):c.1409G>A (p.Arg470His)	STK32C (R353H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3323312	NM_173575.4(STK32C):c.1408C>T (p.Arg470Cys)	STK32C (R353C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 783587	NM_173575.4(STK32C):c.1400A>G (p.Glu467Gly)	STK32C (E350G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3171365	NM_173575.4(STK32C):c.1388C>A (p.Pro463His)	STK32C (P476H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171364	NM_173575.4(STK32C):c.1385A>G (p.Glu462Gly)	STK32C (E462G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171363	NM_173575.4(STK32C):c.1346G>A (p.Arg449Lys)	STK32C (R332K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 708796	NM_173575.4(STK32C):c.1341C>G (p.Leu447=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2459655	NM_173575.4(STK32C):c.1339C>T (p.Leu447Phe)	STK32C (L460F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295529	NM_173575.4(STK32C):c.1126C>G (p.Arg376Gly)	STK32C (R376G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491160	NM_173575.4(STK32C):c.1105G>A (p.Gly369Ser)	STK32C (G382S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291151	NM_173575.4(STK32C):c.1094G>T (p.Arg365Met)	STK32C (R248M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225179	NM_173575.4(STK32C):c.1085G>C (p.Ser362Thr)	STK32C (S245T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171362	NM_173575.4(STK32C):c.1070T>C (p.Leu357Pro)	STK32C (L240P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546069	NM_173575.4(STK32C):c.943G>A (p.Val315Ile)	STK32C (V328I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323313	NM_173575.4(STK32C):c.937G>A (p.Val313Met)	STK32C (V196M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553191	NM_173575.4(STK32C):c.637A>C (p.Ile213Leu)	STK32C (I226L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 768402	NM_173575.4(STK32C):c.624C>T (p.Arg208=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3171367	NM_173575.4(STK32C):c.574A>T (p.Thr192Ser)	STK32C (T205S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790633	NM_173575.4(STK32C):c.519A>C (p.Leu173=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2257229	NM_173575.4(STK32C):c.452T>A (p.Val151Asp)	STK32C (V34D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3064185	NM_173575.4(STK32C):c.451G>C (p.Val151Leu)	STK32C (V151L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2460708	NM_173575.4(STK32C):c.400G>A (p.Glu134Lys)	STK32C (E147K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484505	NM_173575.4(STK32C):c.388A>G (p.Ile130Val)	STK32C (I13V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493046	NM_173575.4(STK32C):c.338G>A (p.Arg113Gln)	STK32C (R113Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3323316	NM_173575.4(STK32C):c.280C>G (p.Gln94Glu)	STK32C (Q94E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2256192	NM_173575.4(STK32C):c.128C>T (p.Pro43Leu)	STK32C (P43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609124	NM_173575.4(STK32C):c.112C>G (p.Pro38Ala)	STK32C (P38A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313131	NM_173575.4(STK32C):c.80C>G (p.Ala27Gly)	STK32C (A27G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323314	NM_173575.4(STK32C):c.70G>A (p.Ala24Thr)	STK32C (A24T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 33