Related gene-specific medical variations for Gene (Select 26281) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3514944	NM_019851.3(FGF20):c.123G>C (p.Arg41Ser)	FGF20, LOC129999926 (R41S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3514943	NM_019851.3(FGF20):c.155C>A (p.Pro52Gln)	FGF20, LOC129999926 (P52Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094713	NM_019851.3(FGF20):c.152G>T (p.Gly51Val)	FGF20, LOC129999926 (G51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094712	NM_019851.3(FGF20):c.140G>A (p.Ser47Asn)	FGF20, LOC129999926 (S47N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094711	NM_019851.3(FGF20):c.104C>A (p.Pro35Gln)	FGF20, LOC129999926 (P35Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2985501	NM_019851.3(FGF20):c.127_128delinsAA (p.Ala43Lys)	FGF20, LOC129999926 (A43K)	Indel (missense variant)	not provided	GUncertain significance
Select item 2958709	NM_019851.3(FGF20):c.151G>C (p.Gly51Arg)	FGF20, LOC129999926 (G51R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2887699	NM_019851.3(FGF20):c.163G>A (p.Ala55Thr)	FGF20, LOC129999926 (A55T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2815320	NM_019851.3(FGF20):c.154C>G (p.Pro52Ala)	FGF20, LOC129999926 (P52A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2557108	NM_019851.3(FGF20):c.161C>T (p.Ala54Val)	FGF20, LOC129999926 (A54V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2420456	NM_019851.3(FGF20):c.144_145delinsCA (p.Arg49Ser)	FGF20, LOC129999926 (R49S)	Indel (missense variant)	not provided	GUncertain significance
Select item 2394092	NM_019851.3(FGF20):c.152G>A (p.Gly51Glu)	FGF20, LOC129999926 (G51E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2290716	NM_019851.3(FGF20):c.137G>A (p.Arg46Gln)	FGF20, LOC129999926 (R46Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267057	NM_019851.3(FGF20):c.134A>G (p.Glu45Gly)	FGF20, LOC129999926 (E45G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2084376	NM_019851.3(FGF20):c.121A>G (p.Arg41Gly)	FGF20, LOC129999926 (R41G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1246783	NM_019851.3(FGF20):c.144G>C (p.Ala48=)	FGF20, LOC129999926	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1231868	NM_019851.3(FGF20):c.102G>A (p.Pro34=)	LOC129999926, FGF20	Single nucleotide variant (synonymous variant)	not provided	GBenign