OLA1[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2218989	NM_013341.5(OLA1):c.1145T>C (p.Ile382Thr)	OLA1 (I361T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522709	NM_013341.5(OLA1):c.1072T>A (p.Ser358Thr)	OLA1 (S200T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351267	NM_013341.5(OLA1):c.950G>A (p.Arg317His)	OLA1 (R159H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302249	NM_013341.5(OLA1):c.899T>A (p.Phe300Tyr)	OLA1 (F279Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304634	NM_013341.5(OLA1):c.866A>G (p.Gln289Arg)	OLA1 (Q289R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302254	NM_013341.5(OLA1):c.854C>A (p.Ala285Glu)	OLA1 (A127E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526826	NM_013341.5(OLA1):c.852A>C (p.Glu284Asp)	OLA1 (E263D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302253	NM_013341.5(OLA1):c.836G>A (p.Arg279Lys)	OLA1 (R258K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302252	NM_013341.5(OLA1):c.820T>A (p.Leu274Met)	OLA1 (L274M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302251	NM_013341.5(OLA1):c.819A>T (p.Glu273Asp)	OLA1 (E115D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161492	NM_013341.5(OLA1):c.787T>G (p.Phe263Val)	OLA1 (F105V +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 3204181	NM_013341.5(OLA1):c.776T>C (p.Leu259Ser)	OLA1 (L259S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204180	NM_013341.5(OLA1):c.766C>T (p.Pro256Ser)	OLA1 (P98S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302250	NM_013341.5(OLA1):c.760T>C (p.Tyr254His)	OLA1 (Y254H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604593	NM_013341.5(OLA1):c.608A>G (p.Tyr203Cys)	OLA1 (Y203C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204179	NM_013341.5(OLA1):c.556A>C (p.Met186Leu)	OLA1 (M28L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217938	NM_013341.5(OLA1):c.482G>A (p.Gly161Glu)	OLA1 (G161E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223393	NM_013341.5(OLA1):c.434T>C (p.Ile145Thr)	OLA1 (I145T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3204178	NM_013341.5(OLA1):c.366T>A (p.His122Gln)	OLA1 (H122Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2304814	NM_013341.5(OLA1):c.301C>T (p.His101Tyr)	OLA1 (H101Y)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2557128	NM_013341.5(OLA1):c.299C>T (p.Ala100Val)	OLA1 (A100V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2239188	NM_013341.5(OLA1):c.199C>T (p.Pro67Ser)	OLA1 (P67S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3302248	NM_013341.5(OLA1):c.74T>C (p.Ile25Thr)	OLA1 (I25T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366071	NM_013341.5(OLA1):c.38C>T (p.Pro13Leu)	OLA1 (P13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24