ClinVar Miner

List of variants reported as uncertain significance for Maturity-onset diabetes of the young type 6; Type 2 diabetes mellitus by Fulgent Genetics, Fulgent Genetics

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_002500.5(NEUROD1):c.917C>T (p.Ala306Val) rs115159138 0.00022
NM_002500.5(NEUROD1):c.1031G>A (p.Arg344Gln) rs146389992 0.00018
NM_002500.5(NEUROD1):c.758T>C (p.Leu253Pro) rs147634094 0.00009
NM_002500.5(NEUROD1):c.646G>A (p.Val216Ile) rs755299574 0.00008
NM_002500.5(NEUROD1):c.1013G>C (p.Ser338Thr) rs767837260 0.00007
NM_002500.5(NEUROD1):c.741C>A (p.His247Gln) rs201542440 0.00004
NM_002500.5(NEUROD1):c.746A>G (p.Tyr249Cys) rs780520468 0.00004
NM_002500.5(NEUROD1):c.86C>G (p.Ser29Cys) rs138850469 0.00004
NM_002500.5(NEUROD1):c.973C>A (p.Arg325Ser) rs368727469 0.00004
NM_002500.5(NEUROD1):c.34G>C (p.Gly12Arg) rs556400603 0.00002
NM_002500.5(NEUROD1):c.357G>A (p.Ala119=) rs375774931 0.00002
NM_002500.5(NEUROD1):c.1043C>T (p.Ala348Val) rs771797718 0.00001
NM_002500.5(NEUROD1):c.1055C>A (p.Ala352Asp) rs774325551 0.00001
NM_002500.5(NEUROD1):c.37G>A (p.Glu13Lys) rs763871039 0.00001
NM_002500.5(NEUROD1):c.418A>G (p.Ile140Val) rs369575066 0.00001
NM_002500.5(NEUROD1):c.761A>C (p.Glu254Ala) rs767219230 0.00001
NM_002500.5(NEUROD1):c.766T>C (p.Phe256Leu) rs556602572 0.00001
NM_002500.5(NEUROD1):c.79C>T (p.Leu27Phe) rs766645933 0.00001
NM_002500.5(NEUROD1):c.814C>A (p.Pro272Thr) rs1365446719 0.00001
NM_002500.5(NEUROD1):c.931G>A (p.Ala311Thr) rs1475260624 0.00001
NM_002500.5(NEUROD1):c.1019C>T (p.Ser340Leu)
NM_002500.5(NEUROD1):c.1055C>T (p.Ala352Val) rs774325551
NM_002500.5(NEUROD1):c.112A>G (p.Lys38Glu) rs1013787986
NM_002500.5(NEUROD1):c.113A>G (p.Lys38Arg)
NM_002500.5(NEUROD1):c.136A>G (p.Met46Val)
NM_002500.5(NEUROD1):c.175G>C (p.Glu59Gln) rs553756272
NM_002500.5(NEUROD1):c.19G>A (p.Glu7Lys)
NM_002500.5(NEUROD1):c.205G>A (p.Glu69Lys)
NM_002500.5(NEUROD1):c.222GGA[1] (p.Glu75del) rs1190828671
NM_002500.5(NEUROD1):c.254G>A (p.Gly85Asp)
NM_002500.5(NEUROD1):c.260A>G (p.Lys87Arg) rs758515206
NM_002500.5(NEUROD1):c.278A>C (p.Lys93Thr)
NM_002500.5(NEUROD1):c.284G>A (p.Arg95His) rs1559135426
NM_002500.5(NEUROD1):c.29T>C (p.Leu10Pro)
NM_002500.5(NEUROD1):c.301T>A (p.Leu101Met)
NM_002500.5(NEUROD1):c.310A>C (p.Met104Leu)
NM_002500.5(NEUROD1):c.36C>T (p.Gly12=)
NM_002500.5(NEUROD1):c.425C>G (p.Thr142Ser)
NM_002500.5(NEUROD1):c.451T>C (p.Trp151Arg)
NM_002500.5(NEUROD1):c.487C>T (p.Pro163Ser) rs1225264254
NM_002500.5(NEUROD1):c.542C>T (p.Thr181Ile)
NM_002500.5(NEUROD1):c.554C>T (p.Ala185Val)
NM_002500.5(NEUROD1):c.603G>C (p.Gln201His)
NM_002500.5(NEUROD1):c.614C>A (p.Pro205His)
NM_002500.5(NEUROD1):c.616C>A (p.His206Asn) rs201174472
NM_002500.5(NEUROD1):c.616C>G (p.His206Asp) rs201174472
NM_002500.5(NEUROD1):c.61A>G (p.Ser21Gly)
NM_002500.5(NEUROD1):c.620T>C (p.Leu207Pro)
NM_002500.5(NEUROD1):c.631A>G (p.Ser211Gly)
NM_002500.5(NEUROD1):c.714T>G (p.His238Gln)
NM_002500.5(NEUROD1):c.715G>A (p.Val239Ile)
NM_002500.5(NEUROD1):c.722A>C (p.His241Pro)
NM_002500.5(NEUROD1):c.733C>A (p.Pro245Thr)
NM_002500.5(NEUROD1):c.790T>C (p.Cys264Arg)
NM_002500.5(NEUROD1):c.794C>G (p.Thr265Ser) rs1029071008
NM_002500.5(NEUROD1):c.827C>T (p.Pro276Leu)
NM_002500.5(NEUROD1):c.93C>A (p.Asp31Glu)
NM_002500.5(NEUROD1):c.94G>A (p.Glu32Lys) rs773755753
NM_002500.5(NEUROD1):c.950T>C (p.Ile317Thr)

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