ClinVar Miner

List of variants in gene SLC17A8 reported as benign for not provided

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_139319.3(SLC17A8):c.474-300G>A rs1969927 0.56419
NM_139319.3(SLC17A8):c.677-244A>G rs7966317 0.55293
NM_139319.3(SLC17A8):c.1054-331A>G rs1887276 0.55272
NM_139319.3(SLC17A8):c.1426-106A>G rs7967828 0.50970
NM_139319.3(SLC17A8):c.*39A>C rs11568537 0.45975
NM_139319.3(SLC17A8):c.763+153A>G rs11110366 0.45784
NM_139319.3(SLC17A8):c.1187-45C>T rs11568536 0.42236
NM_139319.3(SLC17A8):c.1298-80C>T rs11110371 0.41016
NM_139319.3(SLC17A8):c.474-52T>C rs1998925 0.30498
NM_139319.3(SLC17A8):c.-218T>C rs10860582 0.18033
NM_139319.3(SLC17A8):c.474-197C>T rs10860588 0.10195
NM_139319.3(SLC17A8):c.1298-58A>C rs61941805 0.08416
NM_139319.3(SLC17A8):c.*71T>C rs75599713 0.05167
NM_139319.3(SLC17A8):c.677-281C>T rs76372830 0.04619
NM_139319.3(SLC17A8):c.1187-258G>A rs73376055 0.02328
NM_139319.3(SLC17A8):c.764-49C>T rs7970087 0.01833
NM_139319.3(SLC17A8):c.711G>A (p.Leu237=) rs11568542 0.01720
NM_139319.3(SLC17A8):c.1054-46C>G rs11568549 0.01715
NM_139319.3(SLC17A8):c.354+173C>G rs372598021 0.01206
NM_139319.3(SLC17A8):c.54G>A (p.Lys18=) rs11568528 0.00987
NM_139319.3(SLC17A8):c.355-4C>A rs11568531 0.00670
NM_139319.3(SLC17A8):c.23C>T (p.Thr8Ile) rs45610843 0.00512
NM_139319.3(SLC17A8):c.171G>A (p.Thr57=) rs11110359 0.00452
NM_139319.3(SLC17A8):c.102-24C>A rs148710845 0.00385
NM_139319.3(SLC17A8):c.1425+23T>C rs139883070 0.00380
NM_139319.3(SLC17A8):c.354+16T>C rs77707755 0.00380
NM_139319.3(SLC17A8):c.336T>C (p.Asp112=) rs11568546 0.00265
NM_139319.3(SLC17A8):c.858T>C (p.Tyr286=) rs148882860 0.00261
NM_139319.3(SLC17A8):c.1120G>T (p.Ala374Ser) rs138307707 0.00078
NM_139319.3(SLC17A8):c.723G>A (p.Leu241=) rs11568545 0.00019
NM_139319.3(SLC17A8):c.15A>G (p.Ala5=) rs540525737 0.00007
NM_139319.3(SLC17A8):c.102-310A>G rs943403
NM_139319.3(SLC17A8):c.1187-127dup rs138819500
NM_139319.3(SLC17A8):c.1187-159del rs57500563
NM_139319.3(SLC17A8):c.1187-159dup rs57500563
NM_139319.3(SLC17A8):c.1298-14dup rs730880358
NM_139319.3(SLC17A8):c.1298-17T>A
NM_139319.3(SLC17A8):c.354+177CATCTCAG[4] rs59620980
NM_139319.3(SLC17A8):c.474-3dup rs757414143
NM_139319.3(SLC17A8):c.589-256T>C rs7960935
NM_139319.3(SLC17A8):c.763+58A>G rs11568544

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