SIDT2[gene] and "single gene"[properties] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603934	NM_001040455.2(SIDT2):c.138G>C (p.Glu46Asp)	SIDT2 (E46D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401991	NM_001040455.2(SIDT2):c.189G>C (p.Glu63Asp)	SIDT2 (E63D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295015	NM_001040455.2(SIDT2):c.233C>T (p.Ala78Val)	SIDT2 (A78V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457708	NM_001040455.2(SIDT2):c.256C>A (p.Gln86Lys)	SIDT2 (Q86K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487423	NM_001040455.2(SIDT2):c.306G>A (p.Met102Ile)	SIDT2 (M102I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368899	NM_001040455.2(SIDT2):c.358C>T (p.Pro120Ser)	SIDT2 (P120S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162082	NM_001040455.2(SIDT2):c.392A>C (p.Tyr131Ser)	SIDT2 (Y131S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162083	NM_001040455.2(SIDT2):c.394G>A (p.Val132Met)	SIDT2 (V132M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509127	NM_001040455.2(SIDT2):c.451A>G (p.Met151Val)	SIDT2 (M151V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162084	NM_001040455.2(SIDT2):c.457G>A (p.Asp153Asn)	SIDT2 (D153N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282092	NM_001040455.2(SIDT2):c.524A>C (p.Lys175Thr)	SIDT2 (K175T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318449	NM_001040455.2(SIDT2):c.544G>A (p.Val182Met)	SIDT2 (V182M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319987	NM_001040455.2(SIDT2):c.565G>A (p.Val189Met)	SIDT2 (V189M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591969	NM_001040455.2(SIDT2):c.622C>G (p.Pro208Ala)	SIDT2 (P208A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475802	NM_001040455.2(SIDT2):c.638A>G (p.Asp213Gly)	SIDT2 (D213G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545643	NM_001040455.2(SIDT2):c.646G>A (p.Val216Ile)	SIDT2 (V216I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333970	NM_001040455.2(SIDT2):c.703C>T (p.Arg235Cys)	SIDT2 (R235C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162085	NM_001040455.2(SIDT2):c.784T>G (p.Phe262Val)	SIDT2 (F262V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789211	NM_001040455.2(SIDT2):c.963-6A>G	SIDT2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3162086	NM_001040455.2(SIDT2):c.992T>C (p.Ile331Thr)	SIDT2 (I331T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228027	NM_001040455.2(SIDT2):c.1020C>A (p.His340Gln)	SIDT2 (H340Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318452	NM_001040455.2(SIDT2):c.1057C>T (p.Pro353Ser)	SIDT2 (P353S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522087	NM_001040455.2(SIDT2):c.1108G>A (p.Asp370Asn)	SIDT2 (D370N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642404	NM_001040455.2(SIDT2):c.1149C>T (p.Tyr383=)	SIDT2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2514434	NM_001040455.2(SIDT2):c.1162C>T (p.Arg388Cys)	SIDT2 (R388C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162080	NM_001040455.2(SIDT2):c.1163G>A (p.Arg388His)	SIDT2 (R388H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389297	NM_001040455.2(SIDT2):c.1183A>G (p.Thr395Ala)	SIDT2 (T395A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318450	NM_001040455.2(SIDT2):c.1187G>A (p.Arg396Gln)	SIDT2 (R396Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318453	NM_001040455.2(SIDT2):c.1418C>T (p.Thr473Met)	SIDT2 (T473M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162081	NM_001040455.2(SIDT2):c.1423G>C (p.Val475Leu)	SIDT2 (V475L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510748	NM_001040455.2(SIDT2):c.1494C>T (p.Ser498=)	SIDT2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496479	NM_001040455.2(SIDT2):c.1620A>T (p.Glu540Asp)	SIDT2 (E540D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318451	NM_001040455.2(SIDT2):c.1762G>A (p.Gly588Arg)	SIDT2 (G588R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620392	NM_001040455.2(SIDT2):c.1815C>T (p.Ser605=)	SIDT2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2373667	NM_001040455.2(SIDT2):c.1882A>C (p.Lys628Gln)	SIDT2 (K628Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 779316	NM_001040455.2(SIDT2):c.1892C>T (p.Thr631Met)	SIDT2 (T631M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 779317	NM_001040455.2(SIDT2):c.1923C>T (p.His641=)	SIDT2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2222792	NM_001040455.2(SIDT2):c.1949C>T (p.Thr650Met)	SIDT2 (T650M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616082	NM_001040455.2(SIDT2):c.1985C>T (p.Ser662Leu)	SIDT2 (S662L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404174	NM_001040455.2(SIDT2):c.1996C>T (p.Arg666Cys)	SIDT2 (R666C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379488	NM_001040455.2(SIDT2):c.2011G>A (p.Val671Met)	SIDT2 (V671M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642405	NM_001040455.2(SIDT2):c.2128C>T (p.Arg710Cys)	SIDT2 (R710C)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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Items: 42