GREM2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282669	NM_022469.4(GREM2):c.489C>A (p.Ser163Arg)	GREM2 (S163R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351554	NM_022469.4(GREM2):c.413C>G (p.Pro138Arg)	GREM2 (P138R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 374885	NM_022469.4(GREM2):c.408G>T (p.Glu136Asp)	GREM2 (E136D)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 9	GPathogenic
Select item 2318886	NM_022469.4(GREM2):c.263G>A (p.Arg88Gln)	GREM2 (R88Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102279	NM_022469.4(GREM2):c.250G>A (p.Glu84Lys)	GREM2 (E84K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1098865	NM_022469.4(GREM2):c.238C>G (p.Gln80Glu)	GREM2 (Q80E)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 9	GUncertain significance
Select item 2920777	NM_022469.4(GREM2):c.226C>G (p.Gln76Glu)	GREM2 (Q76E)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 9	GUncertain significance
Select item 3048496	NM_022469.4(GREM2):c.225G>A (p.Thr75=)	GREM2	Single nucleotide variant (synonymous variant)	GREM2-related disorder	GLikely benign
Select item 2375958	NM_022469.4(GREM2):c.178C>G (p.Leu60Val)	GREM2 (L60V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289063	NM_022469.4(GREM2):c.154G>T (p.Val52Leu)	GREM2 (V52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461718	NM_022469.4(GREM2):c.109G>A (p.Gly37Ser)	GREM2 (G37S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 374884	NM_022469.4(GREM2):c.38C>T (p.Ala13Val)	GREM2 (A13V)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 9	GPathogenic
Select item 2324465	NM_022469.4(GREM2):c.30C>A (p.Phe10Leu)	GREM2 (F10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102278	NM_022469.4(GREM2):c.17C>G (p.Ser6Cys)	GREM2 (S6C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406236	NM_022469.4(GREM2):c.7T>G (p.Trp3Gly)	GREM2 (W3G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 873242	NM_022469.4(GREM2):c.-1-16027A>C	GREM2	Single nucleotide variant (intron variant)	not specified	GBenign