MORN1[gene] and "single gene"[properties] - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2599417	NM_024848.3(MORN1):c.1490G>A (p.Arg497Gln)	MORN1 (R497Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607174	NM_024848.3(MORN1):c.1483G>C (p.Ala495Pro)	MORN1 (A495P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200327	NM_024848.3(MORN1):c.1469C>A (p.Thr490Asn)	MORN1 (T490N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200324	NM_024848.3(MORN1):c.1400G>C (p.Gly467Ala)	MORN1 (G467A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371634	NM_024848.3(MORN1):c.1400G>A (p.Gly467Asp)	MORN1 (G467D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3295597	NM_024848.3(MORN1):c.1384G>A (p.Val462Ile)	MORN1 (V462I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342952	NM_024848.3(MORN1):c.1379G>A (p.Arg460Gln)	MORN1 (R460Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487471	NM_024848.3(MORN1):c.1364C>A (p.Ala455Asp)	MORN1 (A455D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200308	NM_024848.3(MORN1):c.1348C>T (p.Arg450Cys)	MORN1 (R450C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295596	NM_024848.3(MORN1):c.1334C>T (p.Pro445Leu)	MORN1 (P445L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366198	NM_024848.3(MORN1):c.1319G>A (p.Arg440His)	MORN1 (R440H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3200304	NM_024848.3(MORN1):c.1306G>C (p.Val436Leu)	MORN1 (V436L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266335	NM_024848.3(MORN1):c.1214C>A (p.Thr405Lys)	MORN1 (T405K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233921	NM_024848.3(MORN1):c.1195G>A (p.Gly399Ser)	MORN1 (G399S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200295	NM_024848.3(MORN1):c.1180G>A (p.Gly394Ser)	MORN1 (G394S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2481884	NM_024848.3(MORN1):c.1127C>T (p.Pro376Leu)	MORN1 (P376L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225237	NM_024848.3(MORN1):c.1123C>T (p.Pro375Ser)	MORN1 (P375S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200284	NM_024848.3(MORN1):c.1084C>A (p.Gln362Lys)	MORN1 (Q362K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556921	NM_024848.3(MORN1):c.1069T>C (p.Cys357Arg)	MORN1 (C357R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371661	NM_024848.3(MORN1):c.1049C>T (p.Ala350Val)	MORN1 (A350V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336784	NM_024848.3(MORN1):c.1000C>T (p.Leu334Phe)	MORN1 (L334F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378883	NM_024848.3(MORN1):c.955G>A (p.Asp319Asn)	MORN1 (D319N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295595	NM_024848.3(MORN1):c.926C>T (p.Pro309Leu)	MORN1 (P309L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215517	NM_024848.3(MORN1):c.907G>A (p.Ala303Thr)	MORN1 (A303T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295598	NM_024848.3(MORN1):c.866C>T (p.Pro289Leu)	MORN1 (P289L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398161	NM_024848.3(MORN1):c.803C>T (p.Ala268Val)	MORN1 (A268V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274889	NM_024848.3(MORN1):c.730G>A (p.Gly244Arg)	MORN1 (G244R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489590	NM_024848.3(MORN1):c.653T>A (p.Val218Glu)	MORN1 (V218E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592360	NM_024848.3(MORN1):c.652G>A (p.Val218Met)	MORN1 (V218M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343594	NM_024848.3(MORN1):c.620A>G (p.Asn207Ser)	MORN1 (N207S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331725	NM_024848.3(MORN1):c.553G>A (p.Asp185Asn)	MORN1 (D185N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389305	NM_024848.3(MORN1):c.520G>A (p.Asp174Asn)	MORN1 (D174N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459497	NM_024848.3(MORN1):c.491G>A (p.Arg164His)	MORN1 (R164H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200370	NM_024848.3(MORN1):c.490C>T (p.Arg164Cys)	MORN1 (R164C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 782837	NM_024848.3(MORN1):c.465C>T (p.Tyr155=)	MORN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2396944	NM_024848.3(MORN1):c.454G>A (p.Gly152Ser)	MORN1 (G152S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200362	NM_024848.3(MORN1):c.439A>G (p.Met147Val)	MORN1 (M147V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326465	NM_024848.3(MORN1):c.430C>G (p.Pro144Ala)	MORN1 (P144A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200356	NM_024848.3(MORN1):c.415A>G (p.Asn139Asp)	MORN1 (N139D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597852	NM_024848.3(MORN1):c.379C>T (p.Arg127Trp)	MORN1 (R127W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200348	NM_024848.3(MORN1):c.364G>A (p.Gly122Arg)	MORN1 (G122R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 782838	NM_024848.3(MORN1):c.345C>T (p.His115=)	MORN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2389012	NM_024848.3(MORN1):c.298G>A (p.Val100Ile)	MORN1 (V100I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2620787	NM_024848.3(MORN1):c.265C>A (p.Gln89Lys)	MORN1 (Q89K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200342	NM_024848.3(MORN1):c.251A>G (p.Asp84Gly)	MORN1 (D84G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200291	NM_024848.3(MORN1):c.115T>C (p.Tyr39His)	MORN1 (Y39H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304214	NM_024848.3(MORN1):c.44G>A (p.Arg15His)	MORN1 (R15H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350510	NM_024848.3(MORN1):c.16G>C (p.Glu6Gln)	MORN1 (E6Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314268	NM_024848.3(MORN1):c.8C>G (p.Ala3Gly)	MORN1 (A3G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 49