"Ambry Genetics"[submitter] AND "IFI16"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2474317	NM_001376587.1(IFI16):c.163A>G (p.Lys55Glu)	IFI16 (K55E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108116	NM_001376587.1(IFI16):c.212A>G (p.Asp71Gly)	IFI16 (D71G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285289	NM_001376587.1(IFI16):c.232C>G (p.Leu78Val)	IFI16 (L78V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483567	NM_001376587.1(IFI16):c.322G>T (p.Ala108Ser)	IFI16, LOC126805886 (A108S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494210	NM_001376587.1(IFI16):c.325C>G (p.Pro109Ala)	IFI16, LOC126805886 (P109A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218982	NM_001376587.1(IFI16):c.329C>T (p.Ser110Phe)	IFI16, LOC126805886 (S110F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309315	NM_001376587.1(IFI16):c.341C>T (p.Thr114Ile)	IFI16, LOC126805886 (T114I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285291	NM_001376587.1(IFI16):c.409G>T (p.Ala137Ser)	IFI16 (A137S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108118	NM_001376587.1(IFI16):c.409G>C (p.Ala137Pro)	IFI16 (A137P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276430	NM_001376587.1(IFI16):c.457T>G (p.Ser153Ala)	IFI16 (S153A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455030	NM_001376587.1(IFI16):c.472G>A (p.Gly158Ser)	IFI16 (G158S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2604913	NM_001376587.1(IFI16):c.489G>A (p.Met163Ile)	IFI16 (M163I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457845	NM_001376587.1(IFI16):c.554C>T (p.Pro185Leu)	IFI16 (P129L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589439	NM_001376587.1(IFI16):c.607C>T (p.Arg203Cys)	IFI16 (R147C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325165	NM_001376587.1(IFI16):c.805A>G (p.Ser269Gly)	IFI16 (S269G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2393641	NM_001376587.1(IFI16):c.825A>T (p.Glu275Asp)	IFI16 (E219D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292503	NM_001376587.1(IFI16):c.835G>A (p.Val279Ile)	IFI16 (V279I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108119	NM_001376587.1(IFI16):c.850C>A (p.Pro284Thr)	IFI16 (P284T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108120	NM_001376587.1(IFI16):c.868G>A (p.Val290Ile)	IFI16 (V234I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607615	NM_001376587.1(IFI16):c.876T>G (p.Asn292Lys)	IFI16 (N236K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108121	NM_001376587.1(IFI16):c.922C>T (p.His308Tyr)	IFI16 (H252Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212297	NM_001376587.1(IFI16):c.944T>C (p.Ile315Thr)	IFI16 (I259T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108122	NM_001376587.1(IFI16):c.990G>T (p.Lys330Asn)	IFI16 (K274N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285290	NM_001376587.1(IFI16):c.1003G>A (p.Glu335Lys)	IFI16 (E279K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325164	NM_001376587.1(IFI16):c.1051T>C (p.Cys351Arg)	IFI16 (C295R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226218	NM_001376587.1(IFI16):c.1112A>T (p.Lys371Ile)	IFI16 (K371I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285297	NM_001376587.1(IFI16):c.1136T>C (p.Ile379Thr)	IFI16 (I323T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285292	NM_001376587.1(IFI16):c.1181C>T (p.Pro394Leu)	IFI16 (P394L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232235	NM_001376587.1(IFI16):c.1226G>A (p.Arg409His)	IFI16 (R353H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108111	NM_001376587.1(IFI16):c.1280G>A (p.Arg427Gln)	IFI16 (R371Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404310	NM_001376587.1(IFI16):c.1325C>T (p.Thr442Ile)	IFI16 (T386I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2517481	NM_001376587.1(IFI16):c.1345A>G (p.Ile449Val)	IFI16 (I449V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3285296	NM_001376587.1(IFI16):c.1397A>G (p.His466Arg)	IFI16 (H410R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312464	NM_001376587.1(IFI16):c.1400T>C (p.Phe467Ser)	IFI16 (F467S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108112	NM_001376587.1(IFI16):c.1439G>A (p.Ser480Asn)	IFI16 (S424N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458211	NM_001376587.1(IFI16):c.1481G>A (p.Ser494Asn)	IFI16 (S438N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249917	NM_001376587.1(IFI16):c.1705A>G (p.Ile569Val)	IFI16 (I569V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263993	NM_001376587.1(IFI16):c.1784A>G (p.Glu595Gly)	IFI16 (E539G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285295	NM_001376587.1(IFI16):c.1786C>G (p.Gln596Glu)	IFI16 (Q596E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262064	NM_001376587.1(IFI16):c.1796T>G (p.Met599Arg)	IFI16 (M543R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412434	NM_001376587.1(IFI16):c.1814C>T (p.Ala605Val)	IFI16 (A493V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334715	NM_001376587.1(IFI16):c.1831T>C (p.Phe611Leu)	IFI16 (F499L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266140	NM_001376587.1(IFI16):c.1835G>A (p.Arg612Gln)	IFI16 (R500Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285294	NM_001376587.1(IFI16):c.1841A>T (p.Lys614Met)	IFI16 (K558M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108113	NM_001376587.1(IFI16):c.1888A>T (p.Ile630Phe)	IFI16 (I630F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108114	NM_001376587.1(IFI16):c.1894A>G (p.Ile632Val)	IFI16 (I520V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352885	NM_001376587.1(IFI16):c.1896A>G (p.Ile632Met)	IFI16 (I520M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465318	NM_001376587.1(IFI16):c.1951G>A (p.Ala651Thr)	IFI16 (A651T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285288	NM_001376587.1(IFI16):c.1976T>C (p.Met659Thr)	IFI16 (M547T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330285	NM_001376587.1(IFI16):c.2068G>A (p.Val690Met)	IFI16 (V578M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535496	NM_001376587.1(IFI16):c.2152G>C (p.Val718Leu)	IFI16 (V606L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561818	NM_001376587.1(IFI16):c.2162G>A (p.Arg721Gln)	IFI16 (R609Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275420	NM_001376587.1(IFI16):c.2182G>A (p.Glu728Lys)	IFI16 (E616K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270524	NM_001376587.1(IFI16):c.2184G>T (p.Glu728Asp)	IFI16 (E616D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108115	NM_001376587.1(IFI16):c.2185G>A (p.Glu729Lys)	IFI16 (E617K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285293	NM_001376587.1(IFI16):c.2264A>G (p.His755Arg)	IFI16 (H643R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108117	NM_001376587.1(IFI16):c.2321A>G (p.Asp774Gly)	IFI16 (D662G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455366	NM_001376587.1(IFI16):c.2346C>G (p.Asp782Glu)	IFI16 (D670E +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 58