MOSPD2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2365713	NM_152581.4(MOSPD2):c.242A>G (p.Asn81Ser)	MOSPD2 (N81S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330447	NM_152581.4(MOSPD2):c.364A>T (p.Ile122Leu)	MOSPD2 (I122L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295619	NM_152581.4(MOSPD2):c.460A>T (p.Thr154Ser)	MOSPD2 (T154S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487095	NM_152581.4(MOSPD2):c.733G>A (p.Val245Ile)	MOSPD2 (V182I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275431	NM_152581.4(MOSPD2):c.733G>T (p.Val245Leu)	MOSPD2 (V182L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712019	NM_152581.4(MOSPD2):c.891C>T (p.Thr297=)	MOSPD2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3200587	NM_152581.4(MOSPD2):c.956C>T (p.Pro319Leu)	MOSPD2 (P256L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515633	NM_152581.4(MOSPD2):c.956C>G (p.Pro319Arg)	MOSPD2 (P319R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712020	NM_152581.4(MOSPD2):c.993-5C>A	MOSPD2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2342428	NM_152581.4(MOSPD2):c.1211G>A (p.Arg404His)	MOSPD2 (R404H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200565	NM_152581.4(MOSPD2):c.1317G>A (p.Arg439=)	MOSPD2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3200567	NM_152581.4(MOSPD2):c.1373A>G (p.Asn458Ser)	MOSPD2 (N458S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295618	NM_152581.4(MOSPD2):c.1442A>G (p.Asn481Ser)	MOSPD2 (N481S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200571	NM_152581.4(MOSPD2):c.1469G>A (p.Arg490His)	MOSPD2 (R427H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3295617	NM_152581.4(MOSPD2):c.1477T>A (p.Trp493Arg)	MOSPD2 (W430R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance