FGFRL1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1509889	NM_001004356.3(FGFRL1):c.13C>T (p.Pro5Ser)	FGFRL1 (P5S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 721292	NM_001004356.3(FGFRL1):c.22C>T (p.Leu8=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3278684	NM_001004356.3(FGFRL1):c.29T>C (p.Leu10Pro)	FGFRL1 (L10P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548856	NM_001004356.3(FGFRL1):c.34C>T (p.Pro12Ser)	FGFRL1 (P12S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1924604	NM_001004356.3(FGFRL1):c.40C>T (p.Leu14=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2016950	NM_001004356.3(FGFRL1):c.45G>C (p.Leu15=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1169548	NM_001004356.3(FGFRL1):c.60G>A (p.Pro20=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2170296	NM_001004356.3(FGFRL1):c.64GCC[3] (p.Ala25del)	FGFRL1 (A25del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2890685	NM_001004356.3(FGFRL1):c.66C>T (p.Ala22=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1409881	NM_001004356.3(FGFRL1):c.74C>T (p.Ala25Val)	FGFRL1 (A25V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2087639	NM_001004356.3(FGFRL1):c.75C>T (p.Ala25=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1485221	NM_001004356.3(FGFRL1):c.76C>G (p.Arg26Gly)	FGFRL1 (R26G)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1658544	NM_001004356.3(FGFRL1):c.79+13G>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2044241	NM_001004356.3(FGFRL1):c.79+20C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 731918	NM_001004356.3(FGFRL1):c.80-9C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 748507	NM_001004356.3(FGFRL1):c.80-7C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3001338	NM_001004356.3(FGFRL1):c.80G>T (p.Gly27Val)	FGFRL1 (G27V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1504246	NM_001004356.3(FGFRL1):c.88A>G (p.Lys30Glu)	FGFRL1 (K30E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 710923	NM_001004356.3(FGFRL1):c.95C>T (p.Ala32Val)	FGFRL1 (A32V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2874940	NM_001004356.3(FGFRL1):c.96G>A (p.Ala32=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2421658	NM_001004356.3(FGFRL1):c.113G>A (p.Arg38Gln)	FGFRL1 (R38Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1927992	NM_001004356.3(FGFRL1):c.114G>A (p.Arg38=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1393767	NM_001004356.3(FGFRL1):c.117G>C (p.Gln39His)	FGFRL1 (Q39H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 816793	NM_001004356.3(FGFRL1):c.124C>T (p.Arg42Trp)	FGFRL1 (R42W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1408020	NM_001004356.3(FGFRL1):c.142C>T (p.Arg48Trp)	FGFRL1 (R48W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1987364	NM_001004356.3(FGFRL1):c.160G>A (p.Glu54Lys)	FGFRL1 (E54K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2184496	NM_001004356.3(FGFRL1):c.171G>A (p.Pro57=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2173733	NM_001004356.3(FGFRL1):c.173C>T (p.Pro58Leu)	FGFRL1 (P58L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 792854	NM_001004356.3(FGFRL1):c.178C>T (p.Leu60=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 711938	NM_001004356.3(FGFRL1):c.192C>T (p.Thr64=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1414799	NM_001004356.3(FGFRL1):c.202C>T (p.Arg68Cys)	FGFRL1 (R68C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 740418	NM_001004356.3(FGFRL1):c.216C>T (p.Ser72=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2818784	NM_001004356.3(FGFRL1):c.227G>C (p.Arg76Pro)	FGFRL1 (R76P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1920102	NM_001004356.3(FGFRL1):c.233G>A (p.Arg78His)	FGFRL1 (R78H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 719667	NM_001004356.3(FGFRL1):c.234C>A (p.Arg78=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2596453	NM_001004356.3(FGFRL1):c.238C>A (p.Leu80Met)	FGFRL1 (L80M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511439	NM_001004356.3(FGFRL1):c.242C>T (p.Pro81Leu)	FGFRL1 (P81L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1443528	NM_001004356.3(FGFRL1):c.261G>T (p.Lys87Asn)	FGFRL1 (K87N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1394468	NM_001004356.3(FGFRL1):c.283G>A (p.Gly95Ser)	FGFRL1 (G95S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2053091	NM_001004356.3(FGFRL1):c.285C>T (p.Gly95=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1958070	NM_001004356.3(FGFRL1):c.285C>A (p.Gly95=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2059216	NM_001004356.3(FGFRL1):c.286G>A (p.Val96Met)	FGFRL1 (V96M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 739396	NM_001004356.3(FGFRL1):c.291C>T (p.Tyr97=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1525546	NM_001004356.3(FGFRL1):c.292G>A (p.Val98Met)	FGFRL1 (V98M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1445081	NM_001004356.3(FGFRL1):c.292G>C (p.Val98Leu)	FGFRL1 (V98L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3023909	NM_001004356.3(FGFRL1):c.300G>A (p.Lys100=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2043815	NM_001004356.3(FGFRL1):c.304A>G (p.Thr102Ala)	FGFRL1 (T102A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 739216	NM_001004356.3(FGFRL1):c.309C>T (p.Asn103=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1541313	NM_001004356.3(FGFRL1):c.315C>T (p.Phe105=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1514869	NM_001004356.3(FGFRL1):c.323T>G (p.Leu108Arg)	FGFRL1 (L108R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3094820	NM_001004356.3(FGFRL1):c.326G>A (p.Ser109Asn)	FGFRL1 (S109N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2067392	NM_001004356.3(FGFRL1):c.327C>T (p.Ser109=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 813633	NM_001004356.3(FGFRL1):c.335A>G (p.Tyr112Cys)	FGFRL1 (Y112C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 736979	NM_001004356.3(FGFRL1):c.336C>T (p.Tyr112=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2056132	NM_001004356.3(FGFRL1):c.343G>A (p.Val115Ile)	FGFRL1 (V115I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2555670	NM_001004356.3(FGFRL1):c.344T>C (p.Val115Ala)	FGFRL1 (V115A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2080347	NM_001004356.3(FGFRL1):c.346G>A (p.Val116Met)	FGFRL1 (V116M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1940449	NM_001004356.3(FGFRL1):c.352+15C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2115928	NM_001004356.3(FGFRL1):c.352+16G>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1648410	NM_001004356.3(FGFRL1):c.352+16G>C	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1166954	NM_001004356.3(FGFRL1):c.352+16G>A	FGFRL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1903382	NM_001004356.3(FGFRL1):c.353-19C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1931825	NM_001004356.3(FGFRL1):c.353-17C>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1655120	NM_001004356.3(FGFRL1):c.353-12G>A	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2192424	NM_001004356.3(FGFRL1):c.353-8C>G	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3094821	NM_001004356.3(FGFRL1):c.365C>G (p.Pro122Arg)	FGFRL1 (P122R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1446360	NM_001004356.3(FGFRL1):c.368G>A (p.Gly123Glu)	FGFRL1 (G123E)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2082918	NM_001004356.3(FGFRL1):c.379C>T (p.Leu127=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1412693	NM_001004356.3(FGFRL1):c.388G>A (p.Asp130Asn)	FGFRL1 (D130N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2092151	NM_001004356.3(FGFRL1):c.399T>C (p.Ser133=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1981357	NM_001004356.3(FGFRL1):c.412G>A (p.Asp138Asn)	FGFRL1 (D138N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2723441	NM_001004356.3(FGFRL1):c.415C>A (p.Pro139Thr)	FGFRL1 (P139T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2097917	NM_001004356.3(FGFRL1):c.415C>T (p.Pro139Ser)	FGFRL1 (P139S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1589581	NM_001004356.3(FGFRL1):c.417C>T (p.Pro139=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1371212	NM_001004356.3(FGFRL1):c.418G>A (p.Ala140Thr)	FGFRL1 (A140T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 746827	NM_001004356.3(FGFRL1):c.433+7A>T	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1170809	NM_001004356.3(FGFRL1):c.433+10G>C	FGFRL1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1651257	NM_001004356.3(FGFRL1):c.433+17G>A	FGFRL1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3094822	NM_001004356.3(FGFRL1):c.437G>A (p.Arg146Gln)	FGFRL1 (R146Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1014653	NM_001004356.3(FGFRL1):c.442C>T (p.Arg148Cys)	FGFRL1 (R148C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2244965	NM_001004356.3(FGFRL1):c.469C>T (p.Arg157Cys)	FGFRL1 (R157C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384904	NM_001004356.3(FGFRL1):c.470G>A (p.Arg157His)	FGFRL1 (R157H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2147799	NM_001004356.3(FGFRL1):c.473G>A (p.Arg158Gln)	FGFRL1 (R158Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 764407	NM_001004356.3(FGFRL1):c.480C>T (p.Ile160=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1349107	NM_001004356.3(FGFRL1):c.485G>C (p.Arg162Pro)	FGFRL1 (R162P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1504066	NM_001004356.3(FGFRL1):c.489C>A (p.Pro163=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 792989	NM_001004356.3(FGFRL1):c.489C>T (p.Pro163=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045807	NM_001004356.3(FGFRL1):c.490G>A (p.Val164Met)	FGFRL1 (V164M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 775937	NM_001004356.3(FGFRL1):c.501C>T (p.Ser167=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2170491	NM_001004356.3(FGFRL1):c.502G>A (p.Val168Met)	FGFRL1 (V168M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006111	NM_001004356.3(FGFRL1):c.504G>A (p.Val168=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2054502	NM_001004356.3(FGFRL1):c.505C>T (p.Arg169Trp)	FGFRL1 (R169W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2063667	NM_001004356.3(FGFRL1):c.506G>A (p.Arg169Gln)	FGFRL1 (R169Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3234751	NM_001004356.3(FGFRL1):c.510C>T (p.Leu170=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2875029	NM_001004356.3(FGFRL1):c.512A>G (p.Lys171Arg)	FGFRL1 (K171R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 741108	NM_001004356.3(FGFRL1):c.516C>T (p.Cys172=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2593329	NM_001004356.3(FGFRL1):c.517G>A (p.Val173Met)	FGFRL1 (V173M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2325021	NM_001004356.3(FGFRL1):c.521C>T (p.Ala174Val)	FGFRL1 (A174V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1920284	NM_001004356.3(FGFRL1):c.522C>G (p.Ala174=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2111925	NM_001004356.3(FGFRL1):c.524G>A (p.Ser175Asn)	FGFRL1 (S175N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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