ClinVar Miner

List of variants in gene PLXNA1 reported as benign for not provided

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_032242.4(PLXNA1):c.5595+10G>A rs6439031 0.99022
NM_032242.4(PLXNA1):c.3792C>A (p.Leu1264=) rs4679323 0.60169
NM_032242.4(PLXNA1):c.2061A>G (p.Thr687=) rs9876615 0.10984
NM_032242.4(PLXNA1):c.1614C>T (p.His538=) rs28710010 0.10077
NM_032242.4(PLXNA1):c.3108C>T (p.Thr1036=) rs9858521 0.10042
NM_032242.4(PLXNA1):c.1509C>T (p.Thr503=) rs41266467 0.10019
NM_032242.4(PLXNA1):c.4362+13G>A rs60819734 0.07847
NM_032242.4(PLXNA1):c.1023C>T (p.Phe341=) rs61746811 0.05924
NM_032242.4(PLXNA1):c.4122G>A (p.Thr1374=) rs9289290 0.05336
NM_032242.4(PLXNA1):c.2613C>T (p.Pro871=) rs80308004 0.03995
NM_032242.4(PLXNA1):c.5062-7C>T rs7625998 0.03982
NM_032242.4(PLXNA1):c.1194+17C>T rs57299665 0.03970
NM_032242.4(PLXNA1):c.3015-13C>T rs73861744 0.03957
NM_032242.4(PLXNA1):c.4782C>T (p.Asp1594=) rs6776842 0.03850
NM_032242.4(PLXNA1):c.4510-9C>T rs114317796 0.02820
NM_032242.4(PLXNA1):c.939G>A (p.Gln313=) rs6809502 0.02508
NM_032242.4(PLXNA1):c.1305C>T (p.Thr435=) rs116342901 0.00962
NM_032242.4(PLXNA1):c.4152C>T (p.Arg1384=) rs150052583 0.00818
NM_032242.4(PLXNA1):c.2562G>A (p.Ala854=) rs182679484 0.00777
NM_032242.4(PLXNA1):c.3786T>C (p.Ala1262=) rs112490369 0.00741
NM_032242.4(PLXNA1):c.4669+7G>A rs73196573 0.00728
NM_032242.4(PLXNA1):c.3896-15C>T rs149529631 0.00465
NM_032242.4(PLXNA1):c.1989C>T (p.Val663=) rs61744428 0.00403
NM_032242.4(PLXNA1):c.5583G>A (p.Lys1861=) rs149838873 0.00391
NM_032242.4(PLXNA1):c.3606G>A (p.Ser1202=) rs76967585 0.00358
NM_032242.4(PLXNA1):c.4510-4G>A rs75945701 0.00342
NM_032242.4(PLXNA1):c.369C>T (p.Ala123=) rs141064930 0.00314
NM_032242.4(PLXNA1):c.2410+15C>T rs112410743 0.00250
NM_032242.4(PLXNA1):c.4239C>T (p.Ser1413=) rs147741166 0.00238
NM_032242.4(PLXNA1):c.4887G>A (p.Thr1629=) rs143448130 0.00187
NM_032242.4(PLXNA1):c.2802C>T (p.Asp934=) rs141302156 0.00152
NM_032242.4(PLXNA1):c.3293A>G (p.Asn1098Ser) rs200818881 0.00129
NM_032242.4(PLXNA1):c.5232-9C>T rs370468399 0.00120
NM_032242.4(PLXNA1):c.1653C>T (p.Asp551=) rs147582354 0.00107
NM_032242.4(PLXNA1):c.3759G>A (p.Gly1253=) rs138074920 0.00096
NM_032242.4(PLXNA1):c.4670-10C>A rs141727345 0.00068
NM_032242.4(PLXNA1):c.3666G>A (p.Arg1222=) rs148887289 0.00059
NM_032242.4(PLXNA1):c.3924C>T (p.His1308=) rs532069081 0.00010
NM_032242.4(PLXNA1):c.1734C>T (p.Ser578=) rs368596147 0.00007
NM_032242.4(PLXNA1):c.4669+19G>A rs573158849 0.00007
NM_032242.4(PLXNA1):c.2646C>T (p.Leu882=) rs774535244 0.00006
NM_032242.4(PLXNA1):c.1625C>T (p.Ser542Leu) rs559370201 0.00001
NM_032242.4(PLXNA1):c.1017T>C (p.Thr339=) rs6773789
NM_032242.4(PLXNA1):c.118C>G (p.Pro40Ala)
NM_032242.4(PLXNA1):c.14C>T (p.Pro5Leu)
NM_032242.4(PLXNA1):c.1518+20_1518+21del rs749482082
NM_032242.4(PLXNA1):c.2439C>T (p.Arg813=) rs11719489
NM_032242.4(PLXNA1):c.2640G>A (p.Thr880=)
NM_032242.4(PLXNA1):c.4039-19G>A
NM_032242.4(PLXNA1):c.4295+10G>C
NM_032242.4(PLXNA1):c.4410G>A (p.Gln1470=)
NM_032242.4(PLXNA1):c.4509+7G>A
NM_032242.4(PLXNA1):c.4510-5C>T
NM_032242.4(PLXNA1):c.5049A>T (p.Leu1683=)
NM_032242.4(PLXNA1):c.5061+24dup
NM_032242.4(PLXNA1):c.5415C>T (p.Asp1805=)
NM_032242.4(PLXNA1):c.5499G>A (p.Ala1833=)
NM_032242.4(PLXNA1):c.906C>T (p.Cys302=)

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