REV3L[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656850	NM_001372078.1(REV3L):c.9342T>C (p.Asn3114=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2346445	NM_001372078.1(REV3L):c.9342T>G (p.Asn3114Lys)	REV3L (N3114K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469691	NM_001372078.1(REV3L):c.9278T>C (p.Phe3093Ser)	REV3L (F3015S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1243274	NM_001372078.1(REV3L):c.9219G>C (p.Arg3073=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3153258	NM_001372078.1(REV3L):c.9217C>T (p.Arg3073Trp)	REV3L (R2995W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3313787	NM_001372078.1(REV3L):c.9205A>C (p.Asn3069His)	REV3L (N2991H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1267973	NM_001372078.1(REV3L):c.9190G>A (p.Val3064Ile)	REV3L (V2986I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2286344	NM_001372078.1(REV3L):c.9122A>G (p.His3041Arg)	REV3L (H2963R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 707970	NM_001372078.1(REV3L):c.9108T>C (p.Tyr3036=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2535755	NM_001372078.1(REV3L):c.9106T>C (p.Tyr3036His)	REV3L (Y3036H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 724586	NM_001372078.1(REV3L):c.9100T>G (p.Ser3034Ala)	REV3L (S2956A +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 720269	NM_001372078.1(REV3L):c.9086G>A (p.Arg3029Gln)	REV3L (R2951Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3153257	NM_001372078.1(REV3L):c.9070A>T (p.Ser3024Cys)	REV3L (S2946C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3042556	NM_001372078.1(REV3L):c.9066G>A (p.Ser3022=)	REV3L	Single nucleotide variant (synonymous variant)	REV3L-related disorder	GLikely benign
Select item 729153	NM_001372078.1(REV3L):c.9045C>A (p.Ile3015=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3057510	NM_001372078.1(REV3L):c.8938C>T (p.Leu2980=)	REV3L	Single nucleotide variant (synonymous variant)	REV3L-related disorder	GLikely benign
Select item 3313789	NM_001372078.1(REV3L):c.8902C>T (p.Arg2968Cys)	REV3L (R2968C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153256	NM_001372078.1(REV3L):c.8857A>G (p.Ile2953Val)	REV3L (I2875V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 761777	NM_001372078.1(REV3L):c.8844A>G (p.Arg2948=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3313796	NM_001372078.1(REV3L):c.8816G>A (p.Arg2939Gln)	REV3L (R2939Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3052680	NM_001372078.1(REV3L):c.8805G>A (p.Leu2935=)	REV3L	Single nucleotide variant (synonymous variant)	REV3L-related disorder	GLikely benign
Select item 788998	NM_001372078.1(REV3L):c.8796-6G>A	REV3L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 737438	NM_001372078.1(REV3L):c.8796-7C>T	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3313797	NM_001372078.1(REV3L):c.8606T>C (p.Ile2869Thr)	REV3L (I2869T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 780992	NM_001372078.1(REV3L):c.8604+10A>C	REV3L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2291905	NM_001372078.1(REV3L):c.8576G>C (p.Arg2859Thr)	REV3L (R2859T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153255	NM_001372078.1(REV3L):c.8541C>G (p.Asp2847Glu)	REV3L (D2847E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3257885	NM_001372078.1(REV3L):c.8492C>G (p.Thr2831Arg)	REV3L (T2753R +1 more)	Single nucleotide variant (missense variant)	Neoplasm	OUncertain significance
Select item 750781	NM_001372078.1(REV3L):c.8467G>C (p.Val2823Leu)	REV3L (V2745L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 748811	NM_001372078.1(REV3L):c.8466+9A>G	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 715342	NM_001372078.1(REV3L):c.8285G>A (p.Arg2762Gln)	REV3L (R2762Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2402461	NM_001372078.1(REV3L):c.8110A>G (p.Met2704Val)	REV3L (M2626V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2626871	NM_001372078.1(REV3L):c.8080_8081del (p.Leu2694fs)	REV3L (L2616fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 3153254	NM_001372078.1(REV3L):c.8080T>G (p.Leu2694Val)	REV3L (L2616V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153253	NM_001372078.1(REV3L):c.8001C>G (p.Ile2667Met)	REV3L (I2589M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224801	NM_001372078.1(REV3L):c.7999A>G (p.Ile2667Val)	REV3L (I2667V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 725199	NM_001372078.1(REV3L):c.7971A>C (p.Pro2657=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3313792	NM_001372078.1(REV3L):c.7906C>G (p.His2636Asp)	REV3L (H2558D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 755949	NM_001372078.1(REV3L):c.7538+4C>T	REV3L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2479332	NM_001372078.1(REV3L):c.7532T>A (p.Leu2511Gln)	REV3L (L2433Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 775240	NM_001372078.1(REV3L):c.7420-3dup	REV3L	Duplication (intron variant)	not provided	GBenign
Select item 3313804	NM_001372078.1(REV3L):c.7413A>C (p.Arg2471Ser)	REV3L (R2471S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2541802	NM_001372078.1(REV3L):c.7359G>C (p.Met2453Ile)	REV3L (M2375I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3313803	NM_001372078.1(REV3L):c.7357A>G (p.Met2453Val)	REV3L (M2375V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3313806	NM_001372078.1(REV3L):c.7285A>G (p.Ile2429Val)	REV3L (I2351V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2560175	NM_001372078.1(REV3L):c.7280G>A (p.Arg2427Gln)	REV3L (R2427Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 794140	NM_001372078.1(REV3L):c.7257C>A (p.Ala2419=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 732525	NM_001372078.1(REV3L):c.7257C>T (p.Ala2419=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2718008	NM_001372078.1(REV3L):c.7185-5T>A	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 723094	NM_001372078.1(REV3L):c.7185-6T>C	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 713968	NM_001372078.1(REV3L):c.7122C>T (p.Leu2374=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2253131	NM_001372078.1(REV3L):c.7113T>G (p.Ile2371Met)	REV3L (I2293M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 710732	NM_001372078.1(REV3L):c.6954T>C (p.Phe2318=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2321013	NM_001372078.1(REV3L):c.6893C>G (p.Thr2298Ser)	REV3L (T2298S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 714091	NM_001372078.1(REV3L):c.6880-9C>T	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 753658	NM_001372078.1(REV3L):c.6879+9G>A	REV3L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2541920	NM_001372078.1(REV3L):c.6856C>G (p.Gln2286Glu)	REV3L (Q2286E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488161	NM_001372078.1(REV3L):c.6803A>T (p.Asp2268Val)	REV3L (D2190V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2353864	NM_001372078.1(REV3L):c.6755A>G (p.Asn2252Ser)	REV3L (N2252S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 775241	NM_001372078.1(REV3L):c.6754-5dup	REV3L	Duplication (intron variant)	not provided	GBenign
Select item 718999	NM_001372078.1(REV3L):c.6723T>C (p.Thr2241=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 772883	NM_001372078.1(REV3L):c.6639T>C (p.Leu2213=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 752004	NM_001372078.1(REV3L):c.6628C>T (p.Leu2210=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 760813	NM_001372078.1(REV3L):c.6627T>C (p.Leu2209=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 725495	NM_001372078.1(REV3L):c.6601A>G (p.Ser2201Gly)	REV3L (S2123G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2509121	NM_001372078.1(REV3L):c.6553A>G (p.Ile2185Val)	REV3L (I2107V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 709413	NM_001372078.1(REV3L):c.6516C>G (p.Pro2172=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3153251	NM_001372078.1(REV3L):c.6453G>T (p.Glu2151Asp)	REV3L (E2073D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 737581	NM_001372078.1(REV3L):c.6438A>G (p.Ser2146=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2543351	NM_001372078.1(REV3L):c.6437C>T (p.Ser2146Leu)	REV3L (S2146L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2620082	NM_001372078.1(REV3L):c.6401C>T (p.Pro2134Leu)	REV3L (P2134L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517628	NM_001372078.1(REV3L):c.6370G>A (p.Val2124Ile)	REV3L (V2124I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298947	NM_001372078.1(REV3L):c.6344T>G (p.Ile2115Ser)	REV3L (I2037S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 724736	NM_001372078.1(REV3L):c.6338A>G (p.Tyr2113Cys)	REV3L (Y2035C +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3055335	NM_001372078.1(REV3L):c.6309C>T (p.Pro2103=)	REV3L	Single nucleotide variant (synonymous variant)	REV3L-related disorder	GBenign
Select item 3153250	NM_001372078.1(REV3L):c.6245C>T (p.Thr2082Met)	REV3L (T2082M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1072419	NM_001372078.1(REV3L):c.6220_6221del (p.Gln2074fs)	REV3L (Q1996fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2332828	NM_001372078.1(REV3L):c.6190G>A (p.Ala2064Thr)	REV3L (A1986T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 735135	NM_001372078.1(REV3L):c.6182C>A (p.Pro2061His)	REV3L (P2061H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3057225	NM_001372078.1(REV3L):c.6064C>T (p.Leu2022=)	REV3L	Single nucleotide variant (synonymous variant)	REV3L-related disorder	GBenign
Select item 709899	NM_001372078.1(REV3L):c.6044A>T (p.Glu2015Val)	REV3L (E1937V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 718912	NM_001372078.1(REV3L):c.5991C>T (p.Cys1997=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 713895	NM_001372078.1(REV3L):c.5984T>C (p.Met1995Thr)	REV3L (M1917T +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2621020	NM_001372078.1(REV3L):c.5972A>G (p.Lys1991Arg)	REV3L (K1913R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248064	NM_001372078.1(REV3L):c.5957T>C (p.Met1986Thr)	REV3L (M1986T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153249	NM_001372078.1(REV3L):c.5923G>A (p.Val1975Ile)	REV3L (V1897I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3041385	NM_001372078.1(REV3L):c.5909G>A (p.Arg1970His)	REV3L (R1892H +1 more)	Single nucleotide variant (missense variant)	REV3L-related disorder	GBenign
Select item 2656851	NM_001372078.1(REV3L):c.5908C>T (p.Arg1970Cys)	REV3L (R1892C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3153248	NM_001372078.1(REV3L):c.5863G>A (p.Ala1955Thr)	REV3L (A1877T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525922	NM_001372078.1(REV3L):c.5848C>T (p.Arg1950Cys)	REV3L (R1872C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 756225	NM_001372078.1(REV3L):c.5778C>T (p.Leu1926=)	REV3L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3153247	NM_001372078.1(REV3L):c.5699C>G (p.Ser1900Cys)	REV3L (S1822C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280543	NM_001372078.1(REV3L):c.5660G>A (p.Arg1887Lys)	REV3L (R1809K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338873	NM_001372078.1(REV3L):c.5606G>T (p.Ser1869Ile)	REV3L (S1869I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3313800	NM_001372078.1(REV3L):c.5591A>T (p.Gln1864Leu)	REV3L (Q1864L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2312633	NM_001372078.1(REV3L):c.5516T>C (p.Leu1839Pro)	REV3L (L1761P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3313807	NM_001372078.1(REV3L):c.5505A>T (p.Glu1835Asp)	REV3L (E1757D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492456	NM_001372078.1(REV3L):c.5474C>T (p.Pro1825Leu)	REV3L (P1825L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153245	NM_001372078.1(REV3L):c.5461A>G (p.Ile1821Val)	REV3L (I1743V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3153244	NM_001372078.1(REV3L):c.5459C>T (p.Ala1820Val)	REV3L (A1742V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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