ClinVar Miner

List of variants in gene CHRNA4 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_000744.6(CHRNA4):c.105C>T (p.His35=) rs199541666
NM_000744.6(CHRNA4):c.1083G>A (p.Pro361=) rs202140852
NM_000744.6(CHRNA4):c.1104C>T (p.Cys368=) rs202166947
NM_000744.6(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652
NM_000744.6(CHRNA4):c.1160A>G (p.Glu387Gly) rs45604738
NM_000744.6(CHRNA4):c.132C>T (p.Leu44=) rs1555840462
NM_000744.6(CHRNA4):c.1359C>T (p.His453=) rs121912276
NM_000744.6(CHRNA4):c.1376G>A (p.Gly459Glu) rs753201154
NM_000744.6(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225
NM_000744.6(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498
NM_000744.6(CHRNA4):c.1527C>T (p.Ala509=) rs758693290
NM_000744.6(CHRNA4):c.1584G>A (p.Pro528=) rs199783192
NM_000744.6(CHRNA4):c.1635G>A (p.Thr545=) rs121912283
NM_000744.6(CHRNA4):c.1658C>T (p.Ala553Val) rs762808071
NM_000744.6(CHRNA4):c.1661C>T (p.Pro554Leu) rs56000199
NM_000744.6(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.6(CHRNA4):c.177G>A (p.Ser59=) rs138295365
NM_000744.6(CHRNA4):c.1860G>A (p.Pro620=) rs202203317
NM_000744.6(CHRNA4):c.1867C>T (p.Leu623=) rs878854142
NM_000744.6(CHRNA4):c.225C>T (p.Asp75=) rs113080067
NM_000744.6(CHRNA4):c.345C>T (p.Ser115=) rs201033859
NM_000744.6(CHRNA4):c.372C>T (p.Val124=) rs201386851
NM_000744.6(CHRNA4):c.384-9C>T rs199992800
NM_000744.6(CHRNA4):c.537C>T (p.Phe179=) rs747499031
NM_000744.6(CHRNA4):c.729G>A (p.Pro243=) rs121912253
NM_000744.6(CHRNA4):c.77-10C>T rs200490160
NM_000744.6(CHRNA4):c.777C>T (p.Cys259=) rs1555837947
NM_000744.6(CHRNA4):c.879C>T (p.Thr293=) rs371527699
NM_000744.6(CHRNA4):c.900A>G (p.Ser300=) rs878854143
NM_000744.6(CHRNA4):c.912A>G (p.Pro304=) rs1041716120

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