ClinVar Miner

List of variants in gene CHRNA4 reported as benign for not provided

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Total variants: 36
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1758+191C>T rs114426220
NM_000744.6(CHRNA4):c.1758+192G>C rs3899053
NM_000744.6(CHRNA4):c.1759-309A>G rs6090380
NM_000744.6(CHRNA4):c.228+26A>G rs6090384
NM_000744.6(CHRNA4):c.228+317C>G rs6011788
NM_000744.6(CHRNA4):c.229-163T>C rs45449494
NM_000744.6(CHRNA4):c.229-294C>T rs2273504
NM_000744.6(CHRNA4):c.384-117A>G rs13041103
NM_000744.6(CHRNA4):c.384-135_384-134insCGTGGGCATGGGTGTGGATGTGGGCGTGGGACGTGGG rs1568811491
NM_000744.6(CHRNA4):c.384-143dup rs11483691
NM_000744.6(CHRNA4):c.384-153A>C rs370897210
NM_000744.6(CHRNA4):c.384-157A>G rs8115452
NM_000744.6(CHRNA4):c.384-166G>A rs77645330
NM_000744.6(CHRNA4):c.384-171T>C rs55658831
NM_000744.6(CHRNA4):c.384-172_384-171insCGTGGGGCGTGGGCGTGGC rs1555838260
NM_000744.6(CHRNA4):c.384-177T>C rs77439870
NM_000744.6(CHRNA4):c.384-184A>G rs8115455
NM_000744.6(CHRNA4):c.384-189C>T rs78581196
NM_000744.6(CHRNA4):c.384-196G>A rs8124039
NM_000744.6(CHRNA4):c.384-201T>C rs59145036
NM_000744.6(CHRNA4):c.384-202A>C rs8115495
NM_000744.6(CHRNA4):c.384-211T>G rs866354873
NM_000744.6(CHRNA4):c.384-213C>T rs79124348
NM_000744.6(CHRNA4):c.384-232A>G rs55781913
NM_000744.6(CHRNA4):c.384-23C>T rs56151028
NM_000744.6(CHRNA4):c.384-313G>A rs6011772
NM_000744.6(CHRNA4):c.711C>T (p.Phe237=) rs144446511
NM_000744.6(CHRNA4):c.77-250T>G rs45457196
NM_000744.6(CHRNA4):c.77-90C>T rs3818204
NM_000744.7(CHRNA4):c.1629C>T (p.Ser543=) rs1044396
NM_000744.7(CHRNA4):c.1659G>A (p.Ala553=) rs1044397
NM_000744.7(CHRNA4):c.225C>T (p.Asp75=) rs113080067
NM_000744.7(CHRNA4):c.402G>A (p.Ala134=) rs201488442
NM_000744.7(CHRNA4):c.639T>C (p.Asp213=) rs1044393
NM_000744.7(CHRNA4):c.678T>C (p.Cys226=) rs1044394
NM_000744.7(CHRNA4):c.858C>T (p.Thr286=) rs121912257

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