ClinVar for Gene (Select 4174) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3293684	NM_006739.4(MCM5):c.1880A>G (p.Lys627Arg)	MCM5 (K627R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3248114	NC_000022.10:g.(?_35776672)_(35799555_?)dup	HMOX1, MCM5	Duplication	not provided	GUncertain significance
Select item 3124366	NM_006739.4(MCM5):c.845G>A (p.Arg282His)	MCM5 (R282H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124365	NM_006739.4(MCM5):c.767A>G (p.Lys256Arg)	MCM5 (K256R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124364	NM_006739.4(MCM5):c.412C>T (p.Arg138Cys)	MCM5 (R138C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124363	NM_006739.4(MCM5):c.305C>T (p.Ala102Val)	MCM5 (A102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124362	NM_006739.4(MCM5):c.2053A>G (p.Ile685Val)	MCM5 (I685V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124361	NM_006739.4(MCM5):c.2041C>T (p.Arg681Cys)	MCM5 (R681C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124360	NM_006739.4(MCM5):c.1943C>T (p.Thr648Met)	MCM5 (T648M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124359	NM_006739.4(MCM5):c.1780C>G (p.Arg594Gly)	MCM5 (R594G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124358	NM_006739.4(MCM5):c.1364G>T (p.Arg455Leu)	MCM5 (R455L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124357	NM_006739.4(MCM5):c.1352G>A (p.Arg451Gln)	MCM5 (R451Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124356	NM_006739.4(MCM5):c.1060G>A (p.Ala354Thr)	MCM5 (A354T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3035691	NM_006739.4(MCM5):c.*8C>T	MCM5	Single nucleotide variant (3 prime UTR variant)	MCM5-related disorder	GLikely benign
Select item 3023205	NM_006739.4(MCM5):c.1027A>C (p.Ile343Leu)	MCM5 (I343L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3021944	NM_006739.4(MCM5):c.752+11C>G	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3017821	NM_006739.4(MCM5):c.1621G>A (p.Val541Met)	MCM5 (V541M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3009239	NM_006739.4(MCM5):c.712C>T (p.His238Tyr)	MCM5 (H238Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006096	NM_006739.4(MCM5):c.597-18_597-17del	MCM5	Deletion (intron variant)	not provided	GLikely benign
Select item 3004494	NM_006739.4(MCM5):c.632C>T (p.Pro211Leu)	MCM5 (P211L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2999389	NM_006739.4(MCM5):c.198G>T (p.Gly66=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2998001	NM_006739.4(MCM5):c.255C>T (p.Ala85=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996750	NM_006739.4(MCM5):c.1758C>T (p.Tyr586=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996446	NM_006739.4(MCM5):c.1091+2T>C	MCM5	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2993714	NM_006739.4(MCM5):c.1920C>A (p.Ala640=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2990944	NM_006739.4(MCM5):c.1472T>C (p.Val491Ala)	MCM5 (V491A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990853	NM_006739.4(MCM5):c.1723T>C (p.Ser575Pro)	MCM5 (S575P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990801	NM_006739.4(MCM5):c.1274G>A (p.Arg425Gln)	MCM5 (R425Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990518	NM_006739.4(MCM5):c.532A>T (p.Thr178Ser)	MCM5 (T178S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990107	NM_006739.4(MCM5):c.1414-4T>C	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986530	NM_006739.4(MCM5):c.1832+15A>G	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2985086	NM_006739.4(MCM5):c.79C>G (p.Arg27Gly)	MCM5 (R27G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2985005	NM_006739.4(MCM5):c.973C>T (p.Leu325=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984066	NM_006739.4(MCM5):c.841G>A (p.Gly281Ser)	MCM5 (G281S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2981481	NM_006739.4(MCM5):c.1323C>T (p.Val441=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2980462	NM_006739.4(MCM5):c.853G>A (p.Val285Met)	MCM5 (V285M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2979866	NM_006739.4(MCM5):c.1590+12G>T	MCM5	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2977609	NM_006739.4(MCM5):c.1894G>A (p.Ala632Thr)	MCM5 (A632T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976121	NM_006739.4(MCM5):c.237C>G (p.Ser79Arg)	MCM5 (S79R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2974723	NM_006739.4(MCM5):c.1975+13A>C	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974028	NM_006739.4(MCM5):c.2103+10C>T	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969583	NM_006739.4(MCM5):c.968G>A (p.Arg323His)	MCM5 (R323H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2969443	NM_006739.4(MCM5):c.920-11del	MCM5	Deletion (intron variant)	not provided	GLikely benign
Select item 2969303	NM_006739.4(MCM5):c.1092-3C>T	MCM5	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2967923	NM_006739.4(MCM5):c.1535C>T (p.Ser512Leu)	MCM5 (S512L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2966835	NM_006739.4(MCM5):c.447G>A (p.Val149=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965345	NM_006739.4(MCM5):c.970C>T (p.Arg324Cys)	MCM5 (R324C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2965166	NM_006739.4(MCM5):c.752+3G>A	MCM5	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2964547	NM_006739.4(MCM5):c.982C>T (p.Leu328Phe)	MCM5 (L328F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964505	NM_006739.4(MCM5):c.919+11T>C	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963641	NM_006739.4(MCM5):c.167+19C>T	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963159	NM_006739.4(MCM5):c.1833-16G>A	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961561	NM_006739.4(MCM5):c.1199T>C (p.Ile400Thr)	MCM5 (I400T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2958580	NM_006739.4(MCM5):c.1092-10C>T	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2958355	NM_006739.4(MCM5):c.1954G>A (p.Ala652Thr)	MCM5 (A652T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2915898	NM_006739.4(MCM5):c.483C>G (p.Val161=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902244	NM_006739.4(MCM5):c.389C>T (p.Ser130Leu)	MCM5 (S130L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901734	NM_006739.4(MCM5):c.1272C>T (p.Ser424=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900722	NM_006739.4(MCM5):c.1542C>T (p.Phe514=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896854	NM_006739.4(MCM5):c.1002C>T (p.Val334=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2893138	NM_006739.4(MCM5):c.1944G>A (p.Thr648=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2890816	NM_006739.4(MCM5):c.1449C>T (p.Ser483=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889407	NM_006739.4(MCM5):c.1753C>T (p.Arg585Cys)	MCM5 (R585C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2889088	NM_006739.4(MCM5):c.675G>T (p.Gln225His)	MCM5 (Q225H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888612	NM_006739.4(MCM5):c.1092-9G>A	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2885208	NM_006739.4(MCM5):c.1557C>T (p.Ile519=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2883279	NM_006739.4(MCM5):c.2136G>T (p.Leu712=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2882986	NM_006739.4(MCM5):c.2109C>T (p.Tyr703=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880237	NM_006739.4(MCM5):c.1109C>A (p.Thr370Asn)	MCM5 (T370N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2875033	NM_006739.4(MCM5):c.869G>A (p.Arg290Gln)	MCM5 (R290Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2874818	NM_006739.4(MCM5):c.141C>T (p.Asp47=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873680	NM_006739.4(MCM5):c.1975+8G>A	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873142	NM_006739.4(MCM5):c.1477G>A (p.Gly493Ser)	MCM5 (G493S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2871795	NM_006739.4(MCM5):c.1224C>T (p.Gly408=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868774	NM_006739.4(MCM5):c.1061C>T (p.Ala354Val)	MCM5 (A354V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2867663	NM_006739.4(MCM5):c.753-15C>G	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2852836	NM_006739.4(MCM5):c.1715C>T (p.Pro572Leu)	MCM5 (P572L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2845198	NM_006739.4(MCM5):c.2140C>T (p.Leu714Phe)	MCM5 (L714F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2844753	NM_006739.4(MCM5):c.1204-11C>T	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2821004	NM_006739.4(MCM5):c.529A>C (p.Asn177His)	MCM5 (N177H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2816902	NM_006739.4(MCM5):c.1729G>A (p.Glu577Lys)	MCM5 (E577K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2809634	NM_006739.4(MCM5):c.2160G>C (p.Glu720Asp)	MCM5 (E720D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802995	NM_006739.4(MCM5):c.425C>A (p.Ser142Ter)	MCM5 (S142*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2801857	NM_006739.4(MCM5):c.1609A>G (p.Ile537Val)	MCM5 (I537V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2795485	NM_006739.4(MCM5):c.167+16G>T	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2794982	NM_006739.4(MCM5):c.502A>G (p.Ile168Val)	MCM5 (I168V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2788882	NM_006739.4(MCM5):c.874T>G (p.Ser292Ala)	MCM5 (S292A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2786107	NM_006739.4(MCM5):c.347C>T (p.Ser116Phe)	MCM5 (S116F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2783616	NM_006739.4(MCM5):c.2157C>T (p.Gly719=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780618	NM_006739.4(MCM5):c.597-8T>C	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2780354	NM_006739.4(MCM5):c.1064G>C (p.Cys355Ser)	MCM5 (C355S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2766922	NM_006739.4(MCM5):c.975G>C (p.Leu325=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2764924	NM_006739.4(MCM5):c.87G>T (p.Ser29=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2754184	NM_006739.4(MCM5):c.1572C>T (p.His524=)	MCM5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2747598	NM_006739.4(MCM5):c.437C>T (p.Ser146Leu)	MCM5 (S146L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2742690	NM_006739.4(MCM5):c.62C>T (p.Ala21Val)	MCM5 (A21V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2742656	NM_006739.4(MCM5):c.423+9G>A	MCM5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2739292	NM_006739.4(MCM5):c.500G>A (p.Arg167His)	MCM5 (R167H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2733034	NM_006739.4(MCM5):c.1198A>G (p.Ile400Val)	MCM5 (I400V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2729495	NM_006739.4(MCM5):c.710C>T (p.Pro237Leu)	MCM5 (P237L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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