RSPO3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2569510	NM_032784.5(RSPO3):c.25C>T (p.Leu9Phe)	RSPO3 (L9F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3156758	NM_032784.5(RSPO3):c.46A>G (p.Met16Val)	RSPO3 (M16V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156757	NM_032784.5(RSPO3):c.103C>A (p.Pro35Thr)	RSPO3 (P35T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315586	NM_032784.5(RSPO3):c.229C>G (p.Leu77Val)	RSPO3 (L77V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610105	NM_032784.5(RSPO3):c.245G>A (p.Ser82Asn)	RSPO3 (S82N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513552	NM_032784.5(RSPO3):c.547C>T (p.Pro183Ser)	RSPO3 (P183S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339064	NM_032784.5(RSPO3):c.635G>C (p.Gly212Ala)	RSPO3 (G212A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487373	NM_032784.5(RSPO3):c.689A>C (p.Glu230Ala)	RSPO3 (E230A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156759	NM_032784.5(RSPO3):c.754C>G (p.Gln252Glu)	RSPO3 (Q252E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232144	NM_032784.5(RSPO3):c.770G>A (p.Arg257Gln)	RSPO3 (R257Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156760	NM_032784.5(RSPO3):c.794C>T (p.Ser265Leu)	RSPO3 (S265L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 980786	GRCh37/hg19 6q22.33(chr6:127289665-127570560)x1	RSPO3	Copy number loss	not provided	GUncertain significance