ATG16L2[gene] and "single gene"[properties] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3130894	NM_033388.2(ATG16L2):c.125A>G (p.His42Arg)	ATG16L2 (H42R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3130895	NM_033388.2(ATG16L2):c.127C>G (p.Leu43Val)	ATG16L2 (L43V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3130898	NM_033388.2(ATG16L2):c.176C>T (p.Pro59Leu)	ATG16L2 (P59L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2455541	NM_033388.2(ATG16L2):c.206A>G (p.His69Arg)	ATG16L2 (H69R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2309590	NM_033388.2(ATG16L2):c.262G>A (p.Ala88Thr)	ATG16L2 (A88T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2219139	NM_033388.2(ATG16L2):c.368C>T (p.Ser123Leu)	ATG16L2 (S123L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320838	NM_033388.2(ATG16L2):c.415G>C (p.Val139Leu)	ATG16L2 (V33L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320883	NM_033388.2(ATG16L2):c.448G>T (p.Ala150Ser)	ATG16L2 (A150S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130901	NM_033388.2(ATG16L2):c.494C>A (p.Ala165Glu)	ATG16L2 (A59E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384157	NM_033388.2(ATG16L2):c.563C>G (p.Ala188Gly)	ATG16L2 (A188G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381875	NM_033388.2(ATG16L2):c.586G>C (p.Val196Leu)	ATG16L2 (V196L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304851	NM_033388.2(ATG16L2):c.656C>T (p.Ala219Val)	ATG16L2 (A113V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253231	NM_033388.2(ATG16L2):c.829G>C (p.Ala277Pro)	ATG16L2 (A277P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320847	NM_033388.2(ATG16L2):c.845T>G (p.Leu282Arg)	ATG16L2 (L176R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206597	NM_033388.2(ATG16L2):c.848C>T (p.Thr283Met)	ATG16L2 (T177M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320830	NM_033388.2(ATG16L2):c.851T>C (p.Leu284Pro)	ATG16L2 (L178P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130903	NM_033388.2(ATG16L2):c.914T>C (p.Ile305Thr)	ATG16L2 (I305T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615832	NM_033388.2(ATG16L2):c.950C>G (p.Pro317Arg)	ATG16L2 (P211R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781025	NM_033388.2(ATG16L2):c.956G>C (p.Cys319Ser)	ATG16L2 (C213S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3320844	NM_033388.2(ATG16L2):c.968G>A (p.Arg323Gln)	ATG16L2 (R217Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456337	NM_033388.2(ATG16L2):c.979C>T (p.Arg327Trp)	ATG16L2 (R221W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515368	NM_033388.2(ATG16L2):c.1027C>G (p.Arg343Gly)	ATG16L2 (R237G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339298	NM_033388.2(ATG16L2):c.1073G>A (p.Arg358His)	ATG16L2 (R252H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130892	NM_033388.2(ATG16L2):c.1124C>T (p.Thr375Ile)	ATG16L2 (T375I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130893	NM_033388.2(ATG16L2):c.1229G>A (p.Gly410Glu)	ATG16L2 (G410E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494923	NM_033388.2(ATG16L2):c.1253T>C (p.Leu418Pro)	ATG16L2 (L418P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268401	NM_033388.2(ATG16L2):c.1298C>T (p.Thr433Met)	ATG16L2 (T327M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590557	NM_033388.2(ATG16L2):c.1324C>T (p.Arg442Cys)	ATG16L2 (R442C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320862	NM_033388.2(ATG16L2):c.1325G>A (p.Arg442His)	ATG16L2 (R336H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381650	NM_033388.2(ATG16L2):c.1331G>A (p.Arg444Gln)	ATG16L2 (R444Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642131	NM_033388.2(ATG16L2):c.1344G>A (p.Glu448=)	ATG16L2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3130897	NM_033388.2(ATG16L2):c.1426A>T (p.Ile476Phe)	ATG16L2 (I476F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223762	NM_033388.2(ATG16L2):c.1455C>G (p.Ile485Met)	ATG16L2 (I379M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612444	NM_033388.2(ATG16L2):c.1482C>A (p.His494Gln)	ATG16L2 (H388Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618167	NM_033388.2(ATG16L2):c.1514T>C (p.Val505Ala)	ATG16L2 (V505A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483523	NM_033388.2(ATG16L2):c.1565G>A (p.Arg522Gln)	ATG16L2 (R416Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320872	NM_033388.2(ATG16L2):c.1703G>A (p.Cys568Tyr)	ATG16L2 (C568Y +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2240801	NM_033388.2(ATG16L2):c.1736C>T (p.Thr579Ile)	ATG16L2 (T579I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403013	NM_033388.2(ATG16L2):c.1738G>A (p.Gly580Arg)	ATG16L2 (G474R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130899	NM_033388.2(ATG16L2):c.1773C>T (p.Cys591=)	ATG16L2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2355270	NM_033388.2(ATG16L2):c.1807G>A (p.Gly603Arg)	ATG16L2 (G603R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308823	NM_033388.2(ATG16L2):c.1816A>G (p.Met606Val)	ATG16L2 (M500V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3130900	NM_033388.2(ATG16L2):c.1838G>C (p.Arg613Thr)	ATG16L2 (R507T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 43