AKR1B15[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3107640	NM_001080538.3(AKR1B15):c.155T>G (p.Leu52Arg)	AKR1B15 (L24R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224959	NM_001080538.3(AKR1B15):c.163A>G (p.Lys55Glu)	AKR1B15 (K55E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508334	NM_001080538.3(AKR1B15):c.167T>C (p.Val56Ala)	AKR1B15 (V28A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408085	NM_001080538.3(AKR1B15):c.176C>T (p.Ala59Val)	AKR1B15 (A31V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282619	NM_001080538.3(AKR1B15):c.206G>A (p.Arg69His)	AKR1B15 (R69H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784119	NM_001080538.3(AKR1B15):c.255A>G (p.Glu85=)	AKR1B15	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3282649	NM_001080538.3(AKR1B15):c.295G>A (p.Glu99Lys)	AKR1B15 (E71K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 717221	NM_001080538.3(AKR1B15):c.307A>G (p.Ile103Val)	AKR1B15 (I103V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2264602	NM_001080538.3(AKR1B15):c.310G>A (p.Val104Ile)	AKR1B15 (V104I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536044	NM_001080538.3(AKR1B15):c.338A>C (p.Glu113Ala)	AKR1B15 (E113A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615587	NM_001080538.3(AKR1B15):c.407A>G (p.Tyr136Cys)	AKR1B15 (Y108C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282647	NM_001080538.3(AKR1B15):c.425A>G (p.Gln142Arg)	AKR1B15 (Q142R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773498	NM_001080538.3(AKR1B15):c.495G>A (p.Thr165=)	AKR1B15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3107652	NM_001080538.3(AKR1B15):c.517A>G (p.Met173Val)	AKR1B15 (M145V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405637	NM_001080538.3(AKR1B15):c.535G>A (p.Glu179Lys)	AKR1B15 (E151K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368655	NM_001080538.3(AKR1B15):c.586G>A (p.Glu196Lys)	AKR1B15 (E196K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543252	NM_001080538.3(AKR1B15):c.604C>G (p.Pro202Ala)	AKR1B15 (P174A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107659	NM_001080538.3(AKR1B15):c.692A>C (p.Lys231Thr)	AKR1B15 (K203T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282630	NM_001080538.3(AKR1B15):c.731C>T (p.Pro244Leu)	AKR1B15 (P244L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364916	NM_001080538.3(AKR1B15):c.815C>A (p.Thr272Asn)	AKR1B15 (T244N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282641	NM_001080538.3(AKR1B15):c.821C>G (p.Ala274Gly)	AKR1B15 (A274G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206174	NM_001080538.3(AKR1B15):c.836G>A (p.Arg279His)	AKR1B15 (R251H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545734	NM_001080538.3(AKR1B15):c.862G>T (p.Val288Leu)	AKR1B15 (V260L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107674	NM_001080538.3(AKR1B15):c.881C>T (p.Thr294Ile)	AKR1B15 (T266I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241676	NM_001080538.3(AKR1B15):c.892A>C (p.Ile298Leu)	AKR1B15 (I298L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331775	NM_001080538.3(AKR1B15):c.902A>G (p.Asn301Ser)	AKR1B15 (N273S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 712007	NM_001080538.3(AKR1B15):c.909+10C>T	AKR1B15	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 27