"FNDC3B-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060403	NM_022763.4(FNDC3B):c.536C>G (p.Thr179Ser)	FNDC3B (T179S)	Single nucleotide variant (missense variant)	FNDC3B-related condition	GBenign
Select item 3056937	NM_022763.4(FNDC3B):c.687T>C (p.His229=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition	GBenign
Select item 3044133	NM_022763.4(FNDC3B):c.771G>C (p.Ser257=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition	GBenign
Select item 773705	NM_022763.4(FNDC3B):c.1137C>T (p.Pro379=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition +1 more	GBenign
Select item 3039307	NM_022763.4(FNDC3B):c.1354G>T (p.Ala452Ser)	FNDC3B (A452S)	Single nucleotide variant (missense variant)	FNDC3B-related condition	GBenign
Select item 3059521	NM_022763.4(FNDC3B):c.1374T>C (p.Gly458=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition	GBenign
Select item 2654279	NM_022763.4(FNDC3B):c.1698G>A (p.Thr566=)	FNDC3B	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 782437	NM_022763.4(FNDC3B):c.1971+10G>A	FNDC3B	Single nucleotide variant (intron variant)	FNDC3B-related condition +1 more	GBenign
Select item 3038802	NM_022763.4(FNDC3B):c.2511A>G (p.Leu837=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition	GLikely benign
Select item 3045374	NM_022763.4(FNDC3B):c.2568G>T (p.Thr856=)	FNDC3B	Single nucleotide variant (synonymous variant)	FNDC3B-related condition	GLikely benign
Select item 3042904	NM_022763.4(FNDC3B):c.2590G>A (p.Val864Ile)	FNDC3B (V864I)	Single nucleotide variant (missense variant)	FNDC3B-related condition	GBenign
Select item 718734	NM_022763.4(FNDC3B):c.2967G>C (p.Glu989Asp)	FNDC3B (E989D)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign