Related gene-specific medical variations for Gene (Select 100291105) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3152343	NM_017495.6(RBM38):c.320A>G (p.Asn107Ser)	RBM38, RBM38-AS1 (N107S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3152342	NM_017495.6(RBM38):c.158A>G (p.Tyr53Cys)	RBM38, RBM38-AS1 (Y53C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541061	NM_017495.6(RBM38):c.49C>T (p.Pro17Ser)	RBM38, RBM38-AS1 (P17S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466095	NM_017495.6(RBM38):c.53T>C (p.Leu18Pro)	RBM38, RBM38-AS1 (L18P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2219158	NM_017495.6(RBM38):c.23G>A (p.Cys8Tyr)	RBM38, RBM38-AS1 (C8Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789858	NM_017495.6(RBM38):c.62C>T (p.Pro21Leu)	RBM38, RBM38-AS1 (P21L)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar