ClinVar for Gene (Select 642475) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295931	NM_001100878.2(MROH6):c.306T>C (p.Ser102=)	MROH6	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3295930	NM_001100878.2(MROH6):c.333C>G (p.Asp111Glu)	MROH6 (D111E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295929	NM_001100878.2(MROH6):c.535G>A (p.Ala179Thr)	MROH6 (A179T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295928	NM_001100878.2(MROH6):c.2117G>T (p.Ser706Ile)	MROH6 (S706I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295927	NM_001100878.2(MROH6):c.1247C>T (p.Thr416Ile)	MROH6 (T416I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295926	NM_001100878.2(MROH6):c.2110C>T (p.Arg704Cys)	MROH6 (R704C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295925	NM_001100878.2(MROH6):c.621G>T (p.Trp207Cys)	MROH6 (W207C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295924	NM_001100878.2(MROH6):c.389C>G (p.Ala130Gly)	MROH6 (A130G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295923	NM_001100878.2(MROH6):c.622C>A (p.Arg208Ser)	MROH6 (R208S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295922	NM_001100878.2(MROH6):c.1348G>T (p.Gly450Cys)	MROH6 (G450C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295920	NM_001100878.2(MROH6):c.965C>T (p.Thr322Met)	MROH6 (T322M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295919	NM_001100878.2(MROH6):c.80G>C (p.Gly27Ala)	MROH6 (G27A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295918	NM_001100878.2(MROH6):c.191C>T (p.Pro64Leu)	MROH6 (P64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295917	NM_001100878.2(MROH6):c.46G>A (p.Val16Met)	MROH6 (V16M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295916	NM_001100878.2(MROH6):c.1759C>T (p.Arg587Cys)	MROH6 (R587C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206148	NM_001100878.2(MROH6):c.937A>T (p.Thr313Ser)	MROH6 (T313S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206145	NM_001100878.2(MROH6):c.902C>G (p.Ala301Gly)	MROH6 (A301G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206122	NM_001100878.2(MROH6):c.728G>A (p.Arg243His)	MROH6 (R243H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206116	NM_001100878.2(MROH6):c.727C>T (p.Arg243Cys)	MROH6 (R243C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206110	NM_001100878.2(MROH6):c.662T>C (p.Leu221Pro)	MROH6 (L221P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206103	NM_001100878.2(MROH6):c.643C>T (p.Arg215Cys)	MROH6 (R215C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206092	NM_001100878.2(MROH6):c.622C>T (p.Arg208Cys)	MROH6 (R208C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206086	NM_001100878.2(MROH6):c.616C>A (p.Leu206Ile)	MROH6 (L206I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206077	NM_001100878.2(MROH6):c.598G>A (p.Asp200Asn)	MROH6 (D200N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3206072	NM_001100878.2(MROH6):c.595G>T (p.Ala199Ser)	MROH6 (A199S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206068	NM_001100878.2(MROH6):c.595G>A (p.Ala199Thr)	MROH6 (A199T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206062	NM_001100878.2(MROH6):c.583C>T (p.Arg195Cys)	MROH6 (R195C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206057	NM_001100878.2(MROH6):c.562G>A (p.Val188Met)	MROH6 (V188M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206051	NM_001100878.2(MROH6):c.502A>T (p.Arg168Trp)	MROH6 (R168W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206038	NM_001100878.2(MROH6):c.371G>A (p.Gly124Asp)	MROH6 (G124D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206028	NM_001100878.2(MROH6):c.292C>G (p.Gln98Glu)	MROH6 (Q98E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206024	NM_001100878.2(MROH6):c.241G>A (p.Glu81Lys)	MROH6 (E81K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206006	NM_001100878.2(MROH6):c.2122G>A (p.Ala708Thr)	MROH6 (A708T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3206003	NM_001100878.2(MROH6):c.211C>T (p.Arg71Cys)	MROH6 (R71C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3205991	NM_001100878.2(MROH6):c.2075G>A (p.Arg692Gln)	MROH6 (R692Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205987	NM_001100878.2(MROH6):c.2059G>A (p.Ala687Thr)	MROH6 (A687T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205979	NM_001100878.2(MROH6):c.2018G>A (p.Arg673His)	MROH6 (R673H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205949	NM_001100878.2(MROH6):c.1786G>A (p.Val596Met)	MROH6 (V596M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205942	NM_001100878.2(MROH6):c.1744A>G (p.Ser582Gly)	MROH6 (S582G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205939	NM_001100878.2(MROH6):c.1699G>C (p.Glu567Gln)	MROH6 (E567Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205925	NM_001100878.2(MROH6):c.1568C>A (p.Pro523His)	MROH6 (P523H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205875	NM_001100878.2(MROH6):c.1049T>C (p.Met350Thr)	MROH6 (M350T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063034	GRCh37/hg19 8q24.3(chr8:144090414-145900544)x3	ADCK5, ARHGAP39 +63 more	Copy number gain	not specified	GUncertain significance
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	NRBP2, NSMCE2 +173 more	Copy number gain	not provided	GPathogenic
Select item 2684561	GRCh37/hg19 8q24.3(chr8:144282591-144740223)x3	EEF1D, GFUS +14 more	Copy number gain	not provided	GUncertain significance
Select item 2684556	GRCh37/hg19 8q24.3(chr8:141419599-146295771)x3	ADCK5, ADGRB1 +95 more	Copy number gain	not provided	GPathogenic
Select item 2620654	NM_001100878.2(MROH6):c.1624C>T (p.Pro542Ser)	MROH6 (P542S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594024	NM_001100878.2(MROH6):c.133C>G (p.Pro45Ala)	MROH6 (P45A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592565	NM_001100878.2(MROH6):c.1701G>C (p.Glu567Asp)	MROH6 (E567D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590522	NM_001100878.2(MROH6):c.425G>A (p.Arg142Gln)	MROH6 (R142Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590066	NM_001100878.2(MROH6):c.628C>G (p.Leu210Val)	MROH6 (L210V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560167	NM_001100878.2(MROH6):c.688G>A (p.Gly230Ser)	MROH6 (G230S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558287	NM_001100878.2(MROH6):c.2149C>T (p.Arg717Cys)	MROH6 (R717C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557030	NM_001100878.2(MROH6):c.1184G>A (p.Arg395Gln)	MROH6 (R395Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556959	NM_001100878.2(MROH6):c.1130G>A (p.Arg377His)	MROH6 (R377H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556875	NM_001100878.2(MROH6):c.427G>C (p.Gly143Arg)	MROH6 (G143R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555339	NM_001100878.2(MROH6):c.778G>A (p.Gly260Ser)	MROH6 (G260S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550951	NM_001100878.2(MROH6):c.2119G>A (p.Val707Ile)	MROH6 (V707I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550379	NM_001100878.2(MROH6):c.2065C>T (p.Arg689Cys)	MROH6 (R689C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549458	NM_001100878.2(MROH6):c.1898G>A (p.Cys633Tyr)	MROH6 (C633Y)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2531662	NM_001100878.2(MROH6):c.1114G>A (p.Ala372Thr)	MROH6 (A372T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530511	NM_001100878.2(MROH6):c.2063C>T (p.Pro688Leu)	MROH6 (P688L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522597	NM_001100878.2(MROH6):c.1040C>T (p.Ala347Val)	MROH6 (A347V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519605	NM_001100878.2(MROH6):c.1667G>A (p.Arg556His)	MROH6 (R556H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516895	NM_001100878.2(MROH6):c.773C>T (p.Thr258Met)	MROH6 (T258M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512432	NM_001100878.2(MROH6):c.80G>T (p.Gly27Val)	MROH6 (G27V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511506	NM_001100878.2(MROH6):c.634C>T (p.Arg212Cys)	MROH6 (R212C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510690	NM_001100878.2(MROH6):c.338C>A (p.Ala113Glu)	MROH6 (A113E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490581	NM_001100878.2(MROH6):c.548A>G (p.Glu183Gly)	MROH6 (E183G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490482	NM_001100878.2(MROH6):c.1513C>T (p.Leu505Phe)	MROH6 (L505F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488463	NM_001100878.2(MROH6):c.1987G>A (p.Val663Met)	MROH6 (V663M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482280	NM_001100878.2(MROH6):c.880C>G (p.Arg294Gly)	MROH6 (R294G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474728	NM_001100878.2(MROH6):c.803C>A (p.Ala268Glu)	MROH6 (A268E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464068	NM_001100878.2(MROH6):c.2038G>A (p.Gly680Arg)	MROH6 (G680R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460365	NM_001100878.2(MROH6):c.1975G>A (p.Ala659Thr)	MROH6 (A659T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403589	NM_001100878.2(MROH6):c.22C>T (p.Arg8Trp)	MROH6 (R8W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393649	NM_001100878.2(MROH6):c.1481G>A (p.Arg494Gln)	MROH6 (R494Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387934	NM_001100878.2(MROH6):c.1846C>T (p.Arg616Trp)	MROH6 (R616W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384043	NM_001100878.2(MROH6):c.1969G>A (p.Val657Met)	MROH6 (V657M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382746	NM_001100878.2(MROH6):c.1387G>T (p.Ala463Ser)	MROH6 (A463S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381474	NM_001100878.2(MROH6):c.29G>A (p.Arg10Gln)	MROH6 (R10Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371429	NM_001100878.2(MROH6):c.1976C>T (p.Ala659Val)	MROH6 (A659V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369709	NM_001100878.2(MROH6):c.848C>T (p.Pro283Leu)	MROH6 (P283L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369359	NM_001100878.2(MROH6):c.400A>G (p.Thr134Ala)	MROH6 (T134A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366379	NM_001100878.2(MROH6):c.1894G>A (p.Gly632Ser)	MROH6 (G632S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2359269	NM_001100878.2(MROH6):c.2006C>T (p.Ala669Val)	MROH6 (A669V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358471	NM_001100878.2(MROH6):c.2128C>T (p.Arg710Cys)	MROH6 (R710C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356856	NM_001100878.2(MROH6):c.1883A>C (p.His628Pro)	MROH6 (H628P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354746	NM_001100878.2(MROH6):c.803C>T (p.Ala268Val)	MROH6 (A268V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2351855	NM_001100878.2(MROH6):c.2129G>A (p.Arg710His)	MROH6 (R710H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351654	NM_001100878.2(MROH6):c.755C>T (p.Ser252Leu)	MROH6 (S252L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344603	NM_001100878.2(MROH6):c.416T>C (p.Leu139Pro)	MROH6 (L139P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344475	NM_001100878.2(MROH6):c.2077C>A (p.Pro693Thr)	MROH6 (P693T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337508	NM_001100878.2(MROH6):c.37G>A (p.Glu13Lys)	MROH6 (E13K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336049	NM_001100878.2(MROH6):c.2092G>A (p.Ala698Thr)	MROH6 (A698T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333919	NM_001100878.2(MROH6):c.1081C>G (p.Leu361Val)	MROH6 (L361V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289073	NM_001100878.2(MROH6):c.600T>G (p.Asp200Glu)	MROH6 (D200E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286492	NM_001100878.2(MROH6):c.584G>T (p.Arg195Leu)	MROH6 (R195L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284216	NM_001100878.2(MROH6):c.1499C>T (p.Ser500Leu)	MROH6 (S500L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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