TFIP11[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605281	NM_012143.4(TFIP11):c.1970A>T (p.His657Leu)	TFIP11 (H657L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176546	NM_012143.4(TFIP11):c.1966A>G (p.Lys656Glu)	TFIP11 (K656E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320653	NM_012143.4(TFIP11):c.1933A>G (p.Ile645Val)	TFIP11 (I614V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325642	NM_012143.4(TFIP11):c.1916T>C (p.Ile639Thr)	TFIP11 (I608T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366032	NM_012143.4(TFIP11):c.1894A>G (p.Met632Val)	TFIP11 (M632V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472097	NM_012143.4(TFIP11):c.1850G>A (p.Gly617Glu)	TFIP11 (G617E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176545	NM_012143.4(TFIP11):c.1766A>G (p.Lys589Arg)	TFIP11 (K558R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553952	NM_012143.4(TFIP11):c.1711C>T (p.Arg571Cys)	TFIP11 (R571C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509880	NM_012143.4(TFIP11):c.1508C>T (p.Pro503Leu)	TFIP11 (P472L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250563	NM_012143.4(TFIP11):c.1469G>A (p.Arg490Gln)	TFIP11 (R459Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176543	NM_012143.4(TFIP11):c.1405G>C (p.Gly469Arg)	TFIP11 (G438R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2653009	NM_012143.4(TFIP11):c.1347C>T (p.Thr449=)	TFIP11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2559336	NM_012143.4(TFIP11):c.1346C>T (p.Thr449Ile)	TFIP11 (T449I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623501	NM_012143.4(TFIP11):c.1330G>A (p.Asp444Asn)	TFIP11 (D444N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306766	NM_012143.4(TFIP11):c.1312G>A (p.Glu438Lys)	TFIP11 (E438K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313571	NM_012143.4(TFIP11):c.1205G>A (p.Arg402His)	TFIP11 (R371H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373847	NM_012143.4(TFIP11):c.1204C>T (p.Arg402Cys)	TFIP11 (R402C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361963	NM_012143.4(TFIP11):c.1153C>T (p.Arg385Trp)	TFIP11 (R354W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537860	NM_012143.4(TFIP11):c.1142A>G (p.Glu381Gly)	TFIP11 (E350G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325640	NM_012143.4(TFIP11):c.1028A>G (p.Gln343Arg)	TFIP11 (Q343R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3325641	NM_012143.4(TFIP11):c.997C>G (p.Gln333Glu)	TFIP11 (Q333E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176553	NM_012143.4(TFIP11):c.955G>A (p.Glu319Lys)	TFIP11 (E319K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176552	NM_012143.4(TFIP11):c.639A>C (p.Glu213Asp)	TFIP11 (E213D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314996	NM_012143.4(TFIP11):c.615C>G (p.Phe205Leu)	TFIP11 (F174L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322194	NM_012143.4(TFIP11):c.584C>G (p.Ser195Cys)	TFIP11 (S164C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176544	NM_012143.4(TFIP11):c.149C>T (p.Thr50Ile)	TFIP11 (T50I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461385	NM_012143.4(TFIP11):c.83A>G (p.Asp28Gly)	TFIP11 (D28G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790472	NM_012143.4(TFIP11):c.23G>A (p.Arg8Gln)	TFIP11 (R8Q)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign

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Items: 28