ClinVar Miner

List of variants in gene ALMS1 reported as benign for not provided

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Gene type:
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Total variants: 41
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HGVS dbSNP
NM_001378454.1(ALMS1):c.10209T>A (p.Thr3403=) rs34617744
NM_001378454.1(ALMS1):c.10272G>C (p.Lys3424Asn) rs34398445
NM_001378454.1(ALMS1):c.10628C>G (p.Thr3543Ser) rs45501594
NM_001378454.1(ALMS1):c.11054G>A (p.Ser3685Asn) rs11896293
NM_001378454.1(ALMS1):c.11266G>A (p.Gly3756Ser) rs34927702
NM_001378454.1(ALMS1):c.1871A>G (p.His624Arg) rs41291187
NM_001378454.1(ALMS1):c.1899A>G (p.Gln633=) rs116033693
NM_001378454.1(ALMS1):c.2535C>T (p.Asp845=) rs77517267
NM_001378454.1(ALMS1):c.36_38GGA[11] (p.Glu27_Glu28del) rs55889738
NM_001378454.1(ALMS1):c.36_38GGA[12] (p.Glu28del) rs55889738
NM_001378454.1(ALMS1):c.4962G>T (p.Lys1654Asn) rs28730853
NM_001378454.1(ALMS1):c.5786G>A (p.Arg1929Gln) rs17009061
NM_001378454.1(ALMS1):c.6302C>T (p.Ser2101Leu) rs28730854
NM_001378454.1(ALMS1):c.8835C>G (p.Asn2945Lys) rs35062203
NM_001378454.1(ALMS1):c.9782-9C>T rs10199680
NM_015120.4(ALMS1):c.10306A>G (p.Lys3436Glu) rs34071195
NM_015120.4(ALMS1):c.10338C>T (p.Pro3446=) rs78108069
NM_015120.4(ALMS1):c.10388-239C>A rs6725385
NM_015120.4(ALMS1):c.1147A>G (p.Thr383Ala) rs28730849
NM_015120.4(ALMS1):c.11671+119A>G rs11901974
NM_015120.4(ALMS1):c.12301+183C>T rs7576245
NM_015120.4(ALMS1):c.12365+23A>T rs116733486
NM_015120.4(ALMS1):c.12365+24C>T rs114375547
NM_015120.4(ALMS1):c.12365+27A>G rs17848872
NM_015120.4(ALMS1):c.12365+57C>T rs116327057
NM_015120.4(ALMS1):c.1270G>A (p.Val424Ile) rs45630557
NM_015120.4(ALMS1):c.2664A>G (p.Val888=) rs76266696
NM_015120.4(ALMS1):c.3196T>C (p.Ser1066Pro) rs28730852
NM_015120.4(ALMS1):c.4157C>G (p.Thr1386Arg) rs115517108
NM_015120.4(ALMS1):c.5172A>G (p.Gln1724=) rs75434052
NM_015120.4(ALMS1):c.5466G>A (p.Pro1822=) rs62151609
NM_015120.4(ALMS1):c.64del (p.Glu22fs) rs753006733
NM_015120.4(ALMS1):c.674C>A (p.Pro225His) rs11889925
NM_015120.4(ALMS1):c.7544-163A>G rs76317790
NM_015120.4(ALMS1):c.7678-144C>G rs2056750
NM_015120.4(ALMS1):c.8448A>G (p.Ser2816=) rs137932254
NM_015120.4(ALMS1):c.8549G>A (p.Arg2850Lys) rs200009686
NM_015120.4(ALMS1):c.9543-259T>C rs6711033
NM_015120.4(ALMS1):c.9785-70G>A rs3738848
NM_015120.4(ALMS1):c.9910+160A>G rs10178678
NM_015120.4(ALMS1):c.9910+309G>A rs34032338

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