"PreventionGenetics, part of Exact Sciences"[submitter] AND "FGFRL1"[g - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1169548	NM_001004356.3(FGFRL1):c.60G>A (p.Pro20=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign
Select item 710923	NM_001004356.3(FGFRL1):c.95C>T (p.Ala32Val)	FGFRL1 (A32V)	Single nucleotide variant (missense variant)	FGFRL1-related condition +1 more	GBenign
Select item 739396	NM_001004356.3(FGFRL1):c.291C>T (p.Tyr97=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 746827	NM_001004356.3(FGFRL1):c.433+7A>T	FGFRL1	Single nucleotide variant (intron variant)	FGFRL1-related condition +1 more	GLikely benign
Select item 1170809	NM_001004356.3(FGFRL1):c.433+10G>C	FGFRL1	Single nucleotide variant (intron variant)	FGFRL1-related condition +1 more	GBenign
Select item 728655	NM_001004356.3(FGFRL1):c.541G>A (p.Asp181Asn)	FGFRL1 (D181N)	Single nucleotide variant (missense variant)	4p partial monosomy syndrome +2 more	GBenign/Likely benign
Select item 746636	NM_001004356.3(FGFRL1):c.576G>A (p.Thr192=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign
Select item 780905	NM_001004356.3(FGFRL1):c.588C>T (p.Ala196=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign/Likely benign
Select item 790551	NM_001004356.3(FGFRL1):c.723G>A (p.Arg241=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign
Select item 713302	NM_001004356.3(FGFRL1):c.738C>T (p.Pro246=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 787268	NM_001004356.3(FGFRL1):c.828G>A (p.Pro276=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign
Select item 2056225	NM_001004356.3(FGFRL1):c.865G>A (p.Glu289Lys)	FGFRL1 (E289K)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1170810	NM_001004356.3(FGFRL1):c.891T>C (p.Asp297=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition +1 more	GBenign
Select item 736534	NM_001004356.3(FGFRL1):c.948C>T (p.Asp316=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3040612	NM_001004356.3(FGFRL1):c.1072+7G>C	FGFRL1	Single nucleotide variant (intron variant)	FGFRL1-related condition	GLikely benign
Select item 3058404	NM_001004356.3(FGFRL1):c.1224C>T (p.Pro408=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition	GLikely benign
Select item 736361	NM_001004356.3(FGFRL1):c.1227G>A (p.Ala409=)	FGFRL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1170311	NM_001004356.3(FGFRL1):c.1271G>T (p.Arg424Leu)	FGFRL1 (R424L)	Single nucleotide variant (missense variant)	FGFRL1-related condition +1 more	GBenign
Select item 3046075	NM_001004356.3(FGFRL1):c.1359G>A (p.Pro453=)	FGFRL1	Single nucleotide variant (synonymous variant)	FGFRL1-related condition	GLikely benign
Select item 2416515	NM_001004356.3(FGFRL1):c.1366C>T (p.Pro456Ser)	FGFRL1 (P456S)	Single nucleotide variant (missense variant)	FGFRL1-related condition +1 more	GLikely benign
Select item 3056461	NM_001004356.3(FGFRL1):c.1454_1455dup (p.Ser486fs)	FGFRL1 (S486fs)	Microsatellite (frameshift variant)	FGFRL1-related condition	GLikely benign
Select item 725937	NM_001004356.3(FGFRL1):c.1452_1455dup (p.Ser486fs)	FGFRL1 (S486fs)	Microsatellite (frameshift variant)	FGFRL1-related condition +1 more	GLikely benign
Select item 1618744	NM_001004356.3(FGFRL1):c.1474G>A (p.Val492Met)	FGFRL1 (V492M)	Single nucleotide variant (missense variant)	FGFRL1-related condition +1 more	GBenign

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Items: 23