ClinVar Miner

List of variants in gene GAD2 reported as uncertain significance for not specified

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001134366.2(GAD2):c.1580C>T (p.Ser527Leu) rs149742560 0.00060
NM_001134366.2(GAD2):c.372A>C (p.Lys124Asn) rs8190600 0.00037
NM_001134366.2(GAD2):c.1348G>A (p.Val450Ile) rs369617935 0.00018
NM_001134366.2(GAD2):c.121G>A (p.Gly41Arg) rs764530401 0.00011
NM_001134366.2(GAD2):c.814A>T (p.Arg272Trp) rs150392847 0.00011
NM_001134366.2(GAD2):c.1724T>C (p.Ile575Thr) rs145419731 0.00009
NM_001134366.2(GAD2):c.1237G>A (p.Gly413Arg) rs185111133 0.00007
NM_001134366.2(GAD2):c.173G>C (p.Ser58Thr) rs753506834 0.00003
NM_001134366.2(GAD2):c.304G>A (p.Asp102Asn) rs139888003 0.00003
NM_001134366.2(GAD2):c.1246C>G (p.Gln416Glu) rs1564671677 0.00001
NM_001134366.2(GAD2):c.1538T>G (p.Leu513Trp) rs1262383631 0.00001
NM_001134366.2(GAD2):c.1573C>T (p.Arg525Cys) rs762107590 0.00001
NM_001134366.2(GAD2):c.1738C>T (p.Arg580Cys) rs564481006 0.00001
NM_001134366.2(GAD2):c.178G>A (p.Gly60Arg) rs773194823 0.00001
NM_001134366.2(GAD2):c.264C>A (p.Asn88Lys) rs755051252 0.00001
NM_001134366.2(GAD2):c.566T>C (p.Val189Ala) rs375300049 0.00001
NM_001134366.2(GAD2):c.610A>G (p.Met204Val) rs553646520 0.00001
NM_001134366.2(GAD2):c.1036C>T (p.Pro346Ser)
NM_001134366.2(GAD2):c.1037C>G (p.Pro346Arg)
NM_001134366.2(GAD2):c.1088T>C (p.Val363Ala)
NM_001134366.2(GAD2):c.1113A>C (p.Leu371Phe) rs1045840765
NM_001134366.2(GAD2):c.1124G>T (p.Arg375Leu)
NM_001134366.2(GAD2):c.1172C>T (p.Thr391Met)
NM_001134366.2(GAD2):c.1432G>A (p.Ala478Thr) rs1050757379
NM_001134366.2(GAD2):c.1477A>G (p.Met493Val) rs1834228230
NM_001134366.2(GAD2):c.1541G>A (p.Arg514His)
NM_001134366.2(GAD2):c.1549G>A (p.Glu517Lys)
NM_001134366.2(GAD2):c.157G>A (p.Glu53Lys) rs1844397943
NM_001134366.2(GAD2):c.1655A>T (p.Asp552Val)
NM_001134366.2(GAD2):c.1681A>G (p.Ile561Val)
NM_001134366.2(GAD2):c.1694C>T (p.Ala565Val) rs1834322290
NM_001134366.2(GAD2):c.1747C>A (p.Gln583Lys)
NM_001134366.2(GAD2):c.188C>A (p.Pro63His) rs781515916
NM_001134366.2(GAD2):c.278A>C (p.His93Pro) rs1357321101
NM_001134366.2(GAD2):c.344T>G (p.Met115Arg)
NM_001134366.2(GAD2):c.379G>A (p.Asp127Asn) rs747528687
NM_001134366.2(GAD2):c.550A>G (p.Thr184Ala)
NM_001134366.2(GAD2):c.590C>A (p.Thr197Lys) rs2494342642
NM_001134366.2(GAD2):c.70G>C (p.Gly24Arg) rs766470128
NM_001134366.2(GAD2):c.751A>G (p.Met251Val)
NM_001134366.2(GAD2):c.83C>T (p.Ala28Val)
NM_001134366.2(GAD2):c.857A>G (p.Lys286Arg) rs8190671
NM_001134366.2(GAD2):c.881T>C (p.Ile294Thr)
NM_001134366.2(GAD2):c.953G>A (p.Arg318Lys)
NM_001134366.2(GAD2):c.983T>C (p.Val328Ala) rs766748892

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