ClinVar Miner

List of variants in gene ALMS1 reported as likely benign by Personalized Diabetes Medicine Program,University of Maryland School of Medicine

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Total variants: 38
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HGVS dbSNP
NM_001378454.1(ALMS1):c.11323C>G (p.Leu3775Val)
NM_001378454.1(ALMS1):c.12103G>A (p.Ala4035Thr)
NM_001378454.1(ALMS1):c.2973G>T (p.Lys991Asn)
NM_001378454.1(ALMS1):c.4988C>T (p.Thr1663Ile) rs188807564
NM_001378454.1(ALMS1):c.8117A>G (p.Glu2706Gly)
NM_001378454.1(ALMS1):c.9779A>C (p.Asp3260Ala)
NM_001378454.1(ALMS1):c.9976G>C (p.Ala3326Pro)
NM_015120.4(ALMS1):c.10754A>T (p.Gln3585Leu) rs144486524
NM_015120.4(ALMS1):c.11410C>T (p.Pro3804Ser) rs189032342
NM_015120.4(ALMS1):c.11644C>T (p.His3882Tyr) rs142278066
NM_015120.4(ALMS1):c.11768A>G (p.Asn3923Ser) rs199874928
NM_015120.4(ALMS1):c.12079A>G (p.Arg4027Gly) rs754439156
NM_015120.4(ALMS1):c.12298A>G (p.Arg4100Gly) rs1057524885
NM_015120.4(ALMS1):c.1270G>A (p.Val424Ile) rs45630557
NM_015120.4(ALMS1):c.1612C>G (p.Leu538Val) rs202111717
NM_015120.4(ALMS1):c.1841G>A (p.Gly614Asp) rs148040591
NM_015120.4(ALMS1):c.2039A>G (p.Tyr680Cys) rs199573929
NM_015120.4(ALMS1):c.2041C>G (p.Arg681Gly) rs115444326
NM_015120.4(ALMS1):c.2215G>A (p.Glu739Lys) rs1057524883
NM_015120.4(ALMS1):c.3005G>T (p.Gly1002Val) rs773630367
NM_015120.4(ALMS1):c.3467A>C (p.His1156Pro) rs553406974
NM_015120.4(ALMS1):c.3815C>A (p.Pro1272Gln) rs372563916
NM_015120.4(ALMS1):c.4166C>T (p.Pro1389Leu) rs377354387
NM_015120.4(ALMS1):c.4225G>A (p.Val1409Ile) rs200529564
NM_015120.4(ALMS1):c.4253G>A (p.Arg1418Gln) rs771362238
NM_015120.4(ALMS1):c.4319A>C (p.Tyr1440Ser) rs201971114
NM_015120.4(ALMS1):c.4403G>T (p.Gly1468Val) rs78102263
NM_015120.4(ALMS1):c.5465C>T (p.Pro1822Leu) rs200266868
NM_015120.4(ALMS1):c.5921C>A (p.Pro1974Gln) rs199615641
NM_015120.4(ALMS1):c.6010A>G (p.Ile2004Val) rs7587103
NM_015120.4(ALMS1):c.6040G>T (p.Ala2014Ser) rs1057524884
NM_015120.4(ALMS1):c.604C>G (p.Gln202Glu) rs376989302
NM_015120.4(ALMS1):c.6085T>C (p.Ser2029Pro) rs149096794
NM_015120.4(ALMS1):c.614A>C (p.Glu205Ala) rs200054604
NM_015120.4(ALMS1):c.6364G>C (p.Val2122Leu) rs200368564
NM_015120.4(ALMS1):c.8260C>A (p.His2754Asn) rs200718841
NM_015120.4(ALMS1):c.9115C>G (p.Pro3039Ala) rs370622410
NM_015120.4(ALMS1):c.9392C>G (p.Pro3131Arg) rs200586877

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