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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1049767	NC_000016.10:g.31257008_31257021delinsC	ITGAM	Indel	not provided	GUncertain significance
Select item 1049353	NC_000016.10:g.31258314_31258316dup	ITGAM	Duplication	not provided	GUncertain significance
Select item 2707877	NM_000632.4(ITGAM):c.4G>T (p.Ala2Ser)	ITGAM (A2S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2168374	NM_000632.4(ITGAM):c.7C>T (p.Leu3Phe)	ITGAM (L3F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2052199	NM_000632.4(ITGAM):c.8T>G (p.Leu3Arg)	ITGAM (L3R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1490534	NM_000632.4(ITGAM):c.14T>C (p.Val5Ala)	ITGAM (V5A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2695140	NM_000632.4(ITGAM):c.15C>G (p.Val5=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1434930	NM_000632.4(ITGAM):c.28+5A>C	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1657194	NM_000632.4(ITGAM):c.28+7G>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1550918	NM_000632.4(ITGAM):c.28+13G>C	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1670129	NM_000632.4(ITGAM):c.28+14_28+15insCAC	ITGAM	Insertion (intron variant)	not provided	GLikely benign
Select item 2802165	NM_000632.4(ITGAM):c.28+17T>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1538088	NM_000632.4(ITGAM):c.29-13A>C	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2877900	NM_000632.4(ITGAM):c.29-6C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784047	NM_000632.4(ITGAM):c.55T>C (p.Leu19=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2006976	NM_000632.4(ITGAM):c.58G>A (p.Asp20Asn)	ITGAM (D20N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1378132	NM_000632.4(ITGAM):c.59A>G (p.Asp20Gly)	ITGAM (D20G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2192967	NM_000632.4(ITGAM):c.62C>T (p.Thr21Ile)	ITGAM (T21I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1898123	NM_000632.4(ITGAM):c.69C>T (p.Asn23=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1968348	NM_000632.4(ITGAM):c.90C>T (p.Asn30=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1655598	NM_000632.4(ITGAM):c.96G>A (p.Arg32=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1638909	NM_000632.4(ITGAM):c.102C>T (p.Phe34=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1524198	NM_000632.4(ITGAM):c.103G>A (p.Gly35Arg)	ITGAM (G35R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1652756	NM_000632.4(ITGAM):c.111C>T (p.Ser37=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1412109	NM_000632.4(ITGAM):c.112G>A (p.Val38Met)	ITGAM (V38M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1354817	NM_000632.4(ITGAM):c.122T>A (p.Leu41His)	ITGAM (L41H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2809948	NM_000632.4(ITGAM):c.132C>A (p.Ser44=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901249	NM_000632.4(ITGAM):c.134G>A (p.Arg45Lys)	ITGAM (R45K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1477971	NM_000632.4(ITGAM):c.134+4A>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1170102	NM_000632.4(ITGAM):c.134+11T>C	ITGAM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2114534	NM_000632.4(ITGAM):c.134+19G>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871766	NM_000632.4(ITGAM):c.428-13T>C	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2716281	NM_000632.4(ITGAM):c.428-9C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3017792	NM_000632.4(ITGAM):c.428-3C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2026243	NM_000632.4(ITGAM):c.428-2A>G	ITGAM	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 1938561	NM_000632.4(ITGAM):c.429G>T (p.Gly143=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2090324	NM_000632.4(ITGAM):c.432T>A (p.Cys144Ter)	ITGAM (C144*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1100963	NM_000632.4(ITGAM):c.444T>C (p.Asp148=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1423232	NM_000632.4(ITGAM):c.451A>T (p.Ile151Phe)	ITGAM (I151F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1346021	NM_000632.4(ITGAM):c.452T>C (p.Ile151Thr)	ITGAM (I151T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1541781	NM_000632.4(ITGAM):c.489A>C (p.Pro163=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1485227	NM_000632.4(ITGAM):c.491A>G (p.His164Arg)	ITGAM (H164R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1465772	NM_000632.4(ITGAM):c.499C>T (p.Arg167Trp)	ITGAM (R167W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2737676	NM_000632.4(ITGAM):c.500G>A (p.Arg167Gln)	ITGAM (R167Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1570551	NM_000632.4(ITGAM):c.501G>A (p.Arg167=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1389435	NM_000632.4(ITGAM):c.502C>T (p.Arg168Trp)	ITGAM (R168W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1494103	NM_000632.4(ITGAM):c.503G>A (p.Arg168Gln)	ITGAM (R168Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1672860	NM_000632.4(ITGAM):c.510G>A (p.Lys170=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2837228	NM_000632.4(ITGAM):c.513G>A (p.Glu171=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1553177	NM_000632.4(ITGAM):c.519C>G (p.Val173=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2557870	NM_000632.4(ITGAM):c.526G>A (p.Val176Met)	ITGAM (V176M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1422669	NM_000632.4(ITGAM):c.540A>T (p.Leu180Phe)	ITGAM (L180F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1380844	NM_000632.4(ITGAM):c.557del (p.Leu186fs)	ITGAM (L186fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2012770	NM_000632.4(ITGAM):c.558+7G>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2155971	NM_000632.4(ITGAM):c.558+10C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1096882	NM_000632.4(ITGAM):c.558+11del	ITGAM	Deletion (intron variant)	not provided	GLikely benign
Select item 1924242	NM_000632.4(ITGAM):c.558+16T>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2042257	NM_000632.4(ITGAM):c.558+19G>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1649689	NM_000632.4(ITGAM):c.559-14C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974021	NM_000632.4(ITGAM):c.559-13G>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2732038	NM_000632.4(ITGAM):c.559-11C>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1947429	NM_000632.4(ITGAM):c.559-11C>G	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2994377	NM_000632.4(ITGAM):c.559-10C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1395508	NM_000632.4(ITGAM):c.559-10C>G	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1577533	NM_000632.4(ITGAM):c.559-9C>G	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1557754	NM_000632.4(ITGAM):c.559-5C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1164966	NM_000632.4(ITGAM):c.559-4G>A	ITGAM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2893192	NM_000632.4(ITGAM):c.561del (p.Ser188fs)	ITGAM (S188fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1560446	NM_000632.4(ITGAM):c.579T>C (p.Ser193=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1934193	NM_000632.4(ITGAM):c.588C>T (p.Phe196=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1647366	NM_000632.4(ITGAM):c.589C>T (p.Arg197Trp)	ITGAM (R197W)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2891738	NM_000632.4(ITGAM):c.590G>A (p.Arg197Gln)	ITGAM (R197Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2416165	NM_000632.4(ITGAM):c.595C>T (p.His199Tyr)	ITGAM (H199Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1381480	NM_000632.4(ITGAM):c.596A>C (p.His199Pro)	ITGAM (H199P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1375816	NM_000632.4(ITGAM):c.599T>G (p.Phe200Cys)	ITGAM (F200C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1348720	NM_000632.4(ITGAM):c.607A>G (p.Lys203Glu)	ITGAM (K203E)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1969251	NM_000632.4(ITGAM):c.623A>G (p.Asn208Ser)	ITGAM (N208S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1502195	NM_000632.4(ITGAM):c.624C>A (p.Asn208Lys)	ITGAM (N208K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1412199	NM_000632.4(ITGAM):c.628A>G (p.Asn210Asp)	ITGAM (N210D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3111362	NM_000632.4(ITGAM):c.630C>A (p.Asn210Lys)	ITGAM (N210K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1721251	NM_000632.4(ITGAM):c.632C>A (p.Pro211Gln)	ITGAM (P211Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1923136	NM_000632.4(ITGAM):c.651A>G (p.Pro217=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1393285	NM_000632.4(ITGAM):c.656C>T (p.Thr219Met)	ITGAM (T219M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1387435	NM_000632.4(ITGAM):c.656C>A (p.Thr219Lys)	ITGAM (T219K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 741398	NM_000632.4(ITGAM):c.657G>A (p.Thr219=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2052559	NM_000632.4(ITGAM):c.670C>T (p.Arg224Trp)	ITGAM (R224W)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1428639	NM_000632.4(ITGAM):c.671G>A (p.Arg224Gln)	ITGAM (R224Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2483133	NM_000632.4(ITGAM):c.680C>T (p.Thr227Met)	ITGAM (T227M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1636827	NM_000632.4(ITGAM):c.681G>A (p.Thr227=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1462522	NM_000632.4(ITGAM):c.682G>A (p.Ala228Thr)	ITGAM (A228T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1407869	NM_000632.4(ITGAM):c.686C>T (p.Thr229Met)	ITGAM (T229M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1392871	NM_000632.4(ITGAM):c.694C>T (p.Arg232Cys)	ITGAM (R232C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1369544	NM_000632.4(ITGAM):c.695G>A (p.Arg232His)	ITGAM (R232H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2063772	NM_000632.4(ITGAM):c.700G>C (p.Val234Leu)	ITGAM (V234L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2984022	NM_000632.4(ITGAM):c.702G>A (p.Val234=)	ITGAM	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2630050	NM_000632.4(ITGAM):c.704+5G>A	ITGAM	Single nucleotide variant (intron variant)	ITGAM-related disorder	GUncertain significance
Select item 1514583	NM_000632.4(ITGAM):c.704+6C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1923435	NM_000632.4(ITGAM):c.704+9_704+10delinsTG	ITGAM	Indel (intron variant)	not provided	GUncertain significance
Select item 1164967	NM_000632.4(ITGAM):c.704+10C>G	ITGAM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2838989	NM_000632.4(ITGAM):c.704+11C>T	ITGAM	Single nucleotide variant (intron variant)	not provided	GLikely benign

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