Related gene-specific medical variations for Gene (Select 84624) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3096024	NM_032532.3(FNDC1):c.32C>G (p.Ala11Gly)	FNDC1, FNDC1-AS1 (A11G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390576	NM_032532.3(FNDC1):c.106T>A (p.Ser36Thr)	FNDC1, FNDC1-AS1 (S36T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390575	NM_032532.3(FNDC1):c.101C>A (p.Ala34Glu)	FNDC1, FNDC1-AS1 (A34E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363209	NM_032532.3(FNDC1):c.85G>T (p.Val29Phe)	FNDC1, FNDC1-AS1 (V29F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809131	GRCh37/hg19 6q25.3(chr6:159555545-159671284)x1	FNDC1	Copy number loss	not provided	GUncertain significance

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