ClinVar Miner

List of variants in gene ALMS1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 147
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HGVS dbSNP
NC_000002.12:g.73424408_73424411del
NM_015120.4(ALMS1):c.-21C>T rs530120421
NM_015120.4(ALMS1):c.-27_-25dupCTC rs746980000
NM_015120.4(ALMS1):c.-45C>G rs539250179
NM_015120.4(ALMS1):c.10082-11C>T rs368250605
NM_015120.4(ALMS1):c.10216+12G>A rs527508238
NM_015120.4(ALMS1):c.10216+22C>T
NM_015120.4(ALMS1):c.10216+7A>G rs1553416882
NM_015120.4(ALMS1):c.10217-214G>A
NM_015120.4(ALMS1):c.10221C>T (p.Ser3407=)
NM_015120.4(ALMS1):c.1035A>G (p.Ser345=)
NM_015120.4(ALMS1):c.10467A>G (p.Val3489=) rs28730858
NM_015120.4(ALMS1):c.10631C>G (p.Thr3544Ser) rs45501594
NM_015120.4(ALMS1):c.10754A>T (p.Gln3585Leu) rs144486524
NM_015120.4(ALMS1):c.10791G>C (p.Val3597=) rs45445398
NM_015120.4(ALMS1):c.11076G>A (p.Glu3692=) rs1421582809
NM_015120.4(ALMS1):c.11226G>A (p.Glu3742=) rs28730859
NM_015120.4(ALMS1):c.11331C>T (p.His3777=) rs45596541
NM_015120.4(ALMS1):c.11382T>C (p.Ala3794=) rs377090880
NM_015120.4(ALMS1):c.11604C>T (p.Phe3868=) rs80009262
NM_015120.4(ALMS1):c.11613A>G (p.Ser3871=) rs188172095
NM_015120.4(ALMS1):c.1164T>C (p.His388=) rs191091347
NM_015120.4(ALMS1):c.11748C>T (p.Ser3916=) rs147831309
NM_015120.4(ALMS1):c.11751G>A (p.Glu3917=) rs373364340
NM_015120.4(ALMS1):c.11775T>C (p.Asp3925=)
NM_015120.4(ALMS1):c.11824G>A (p.Gly3942Ser) rs61741524
NM_015120.4(ALMS1):c.1185T>C (p.Tyr395=) rs139512700
NM_015120.4(ALMS1):c.11871T>C (p.His3957=) rs370489767
NM_015120.4(ALMS1):c.1200A>G (p.Thr400=) rs756136557
NM_015120.4(ALMS1):c.12117+14G>T rs1057524070
NM_015120.4(ALMS1):c.12117+33G>A
NM_015120.4(ALMS1):c.12118-100C>T
NM_015120.4(ALMS1):c.12129G>A (p.Gln4043=) rs763332177
NM_015120.4(ALMS1):c.12150C>T (p.Ile4050=) rs374328093
NM_015120.4(ALMS1):c.12225C>T (p.Thr4075=) rs199638718
NM_015120.4(ALMS1):c.12301+5G>A rs371853987
NM_015120.4(ALMS1):c.12302-19C>T rs1553422031
NM_015120.4(ALMS1):c.12324C>T (p.Asn4108=) rs767420244
NM_015120.4(ALMS1):c.12365+16_12365+27delCAAGAGTACGTAinsTGAGTTTGTG rs1064795877
NM_015120.4(ALMS1):c.12365+16_12365+29delCAAGAGTACGTATAinsTGAGTTTGTGTG rs1064795814
NM_015120.4(ALMS1):c.12365+17_12365+27delAAGAGTACGTAinsGAGTTTGTG rs1064796118
NM_015120.4(ALMS1):c.12365+181G>A
NM_015120.4(ALMS1):c.12366-294A>C
NM_015120.4(ALMS1):c.12441G>T (p.Arg4147=) rs35902379
NM_015120.4(ALMS1):c.12465+205G>C
NM_015120.4(ALMS1):c.1248G>T (p.Leu416=) rs1553400953
NM_015120.4(ALMS1):c.1270G>A (p.Val424Ile) rs45630557
NM_015120.4(ALMS1):c.1436-10_1436-9insCTT rs1064795386
NM_015120.4(ALMS1):c.1436-9_1436-8insCTT rs1064795791
NM_015120.4(ALMS1):c.1524A>C (p.Gly508=) rs760374410
NM_015120.4(ALMS1):c.1560G>A (p.Gln520=) rs764869245
NM_015120.4(ALMS1):c.1574_1576CTC[1] (p.Pro526del) rs34628045
NM_015120.4(ALMS1):c.1710A>G (p.Thr570=) rs752130351
NM_015120.4(ALMS1):c.1713A>C (p.Val571=) rs201095989
NM_015120.4(ALMS1):c.1734T>C (p.His578=) rs768761501
NM_015120.4(ALMS1):c.1776C>T (p.Asp592=)
NM_015120.4(ALMS1):c.1874A>G (p.His625Arg) rs41291187
NM_015120.4(ALMS1):c.1977G>A (p.Lys659=)
NM_015120.4(ALMS1):c.2041C>G (p.Arg681Gly) rs115444326
NM_015120.4(ALMS1):c.2097G>A (p.Val699=) rs200535382
NM_015120.4(ALMS1):c.2199C>T (p.Asp733=) rs754758293
NM_015120.4(ALMS1):c.2325C>T (p.Tyr775=) rs752503817
NM_015120.4(ALMS1):c.2419G>C (p.Val807Leu) rs138921247
NM_015120.4(ALMS1):c.2439A>G (p.Ser813=) rs925267503
NM_015120.4(ALMS1):c.2661A>G (p.Lys887=) rs80133984
NM_015120.4(ALMS1):c.2733C>T (p.His911=) rs189923349
NM_015120.4(ALMS1):c.2767C>T (p.Leu923=) rs143885319
NM_015120.4(ALMS1):c.2877C>T (p.Ser959=) rs541122374
NM_015120.4(ALMS1):c.3099C>A (p.Gly1033=) rs368659119
NM_015120.4(ALMS1):c.3196T>C (p.Ser1066Pro) rs28730852
NM_015120.4(ALMS1):c.3269C>G (p.Thr1090Arg) rs556855697
NM_015120.4(ALMS1):c.3270A>G (p.Thr1090=)
NM_015120.4(ALMS1):c.3314G>A (p.Gly1105Asp) rs201074268
NM_015120.4(ALMS1):c.3378A>G (p.Val1126=) rs189914793
NM_015120.4(ALMS1):c.3402G>A (p.Lys1134=) rs376683428
NM_015120.4(ALMS1):c.3423C>T (p.Thr1141=)
NM_015120.4(ALMS1):c.3594A>G (p.Lys1198=) rs773852068
NM_015120.4(ALMS1):c.3693G>A (p.Gly1231=) rs1057523614
NM_015120.4(ALMS1):c.36_38GGA[10] (p.Glu26_Glu29del) rs55889738
NM_015120.4(ALMS1):c.36_38GGA[9] (p.Glu25_Glu29del) rs55889738
NM_015120.4(ALMS1):c.3735G>A (p.Lys1245=) rs140670994
NM_015120.4(ALMS1):c.3870T>C (p.Tyr1290=) rs369314182
NM_015120.4(ALMS1):c.3945A>C (p.Ser1315=) rs186449817
NM_015120.4(ALMS1):c.39_77= (p.Glu13_Glu26=) rs55889738
NM_015120.4(ALMS1):c.4137T>C (p.Ser1379=) rs200491758
NM_015120.4(ALMS1):c.4152A>G (p.Gln1384=) rs370508895
NM_015120.4(ALMS1):c.4188G>A (p.Ser1396=)
NM_015120.4(ALMS1):c.41_42insAGA (p.Glu29dup) rs1553396124
NM_015120.4(ALMS1):c.4332G>T (p.Leu1444Phe) rs192499639
NM_015120.4(ALMS1):c.4347A>G (p.Leu1449=) rs200459890
NM_015120.4(ALMS1):c.4608A>G (p.Gln1536=) rs144720929
NM_015120.4(ALMS1):c.474T>C (p.Cys158=) rs367648094
NM_015120.4(ALMS1):c.4860A>G (p.Ala1620=) rs367772965
NM_015120.4(ALMS1):c.4991C>T (p.Thr1664Ile) rs188807564
NM_015120.4(ALMS1):c.4992T>C (p.Thr1664=) rs774538998
NM_015120.4(ALMS1):c.5637T>C (p.Val1879=) rs1057524275
NM_015120.4(ALMS1):c.6010A>G (p.Ile2004Val) rs7587103
NM_015120.4(ALMS1):c.6085T>C (p.Ser2029Pro) rs149096794
NM_015120.4(ALMS1):c.6444A>G (p.Lys2148=) rs776254949
NM_015120.4(ALMS1):c.6467A>G (p.Asp2156Gly) rs58093963
NM_015120.4(ALMS1):c.6540C>T (p.Thr2180=) rs371511963
NM_015120.4(ALMS1):c.66G>A (p.Glu22=) rs1004961829
NM_015120.4(ALMS1):c.6755A>G (p.Asp2252Gly) rs28730855
NM_015120.4(ALMS1):c.7271A>G (p.Asn2424Ser) rs75145370
NM_015120.4(ALMS1):c.7380C>T (p.Ser2460=) rs867561704
NM_015120.4(ALMS1):c.7467A>G (p.Gln2489=) rs765766155
NM_015120.4(ALMS1):c.7544-180G>C
NM_015120.4(ALMS1):c.7544-33T>C
NM_015120.4(ALMS1):c.767+17G>T rs1057524596
NM_015120.4(ALMS1):c.767+18C>T rs1553400459
NM_015120.4(ALMS1):c.7678-64A>T
NM_015120.4(ALMS1):c.7678-66A>T
NM_015120.4(ALMS1):c.7713A>C (p.Pro2571=) rs750225944
NM_015120.4(ALMS1):c.7746C>T (p.Ser2582=) rs370740871
NM_015120.4(ALMS1):c.7929T>C (p.Val2643=) rs749406009
NM_015120.4(ALMS1):c.8214T>C (p.Thr2738=) rs759935089
NM_015120.4(ALMS1):c.825T>C (p.Ser275=) rs145009331
NM_015120.4(ALMS1):c.8277A>G (p.Gln2759=) rs181226362
NM_015120.4(ALMS1):c.8448A>G (p.Ser2816=) rs137932254
NM_015120.4(ALMS1):c.8745A>G (p.Val2915=) rs142611294
NM_015120.4(ALMS1):c.8782C>A (p.Arg2928=) rs376244626
NM_015120.4(ALMS1):c.8838C>G (p.Asn2946Lys) rs35062203
NM_015120.4(ALMS1):c.8886G>A (p.Pro2962=) rs367862140
NM_015120.4(ALMS1):c.8922G>A (p.Ala2974=) rs116854981
NM_015120.4(ALMS1):c.8983G>A (p.Val2995Ile) rs45566838
NM_015120.4(ALMS1):c.9141T>C (p.Cys3047=) rs779818117
NM_015120.4(ALMS1):c.9307T>C (p.Leu3103=) rs537370242
NM_015120.4(ALMS1):c.9321T>G (p.Pro3107=) rs771679163
NM_015120.4(ALMS1):c.948T>C (p.Ser316=) rs183390773
NM_015120.4(ALMS1):c.94_96GCG[3] (p.Ala35_Ala36del)
NM_015120.4(ALMS1):c.94_96GCG[7] (p.Ala35_Ala36dup) rs746896173
NM_015120.4(ALMS1):c.9636G>A (p.Lys3212=) rs373013570
NM_015120.4(ALMS1):c.9642A>G (p.Leu3214=) rs566943393
NM_015120.4(ALMS1):c.9696G>A (p.Glu3232=) rs764518519
NM_015120.4(ALMS1):c.9770C>G (p.Ser3257Cys) rs200922218
NM_015120.4(ALMS1):c.9780A>C (p.Thr3260=) rs183325464
NM_015120.4(ALMS1):c.9784+19A>G rs895296631
NM_015120.4(ALMS1):c.9784+19delA rs751238172
NM_015120.4(ALMS1):c.9785-19C>A rs777706370
NM_015120.4(ALMS1):c.9825C>G (p.Thr3275=) rs201446579
NM_015120.4(ALMS1):c.9864A>G (p.Pro3288=) rs114687298
NM_015120.4(ALMS1):c.9870G>A (p.Pro3290=) rs773900415
NM_015120.4(ALMS1):c.9900C>T (p.Ser3300=) rs1217540541
NM_015120.4(ALMS1):c.9910+129T>G
NM_015120.4(ALMS1):c.9911-12G>A rs376627151
NM_015120.4:c.11551-3T>C
NM_015120.4:c.12365+18A>T

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