ClinVar Miner

List of variants in gene TG reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.3082A>G (p.Met1028Val) rs853326 0.60247
NM_003235.5(TG):c.2334T>C (p.Pro778=) rs2069550 0.59900
NM_003235.5(TG):c.7589G>A (p.Arg2530Gln) rs1133076 0.56572
NM_003235.5(TG):c.4506T>C (p.Ala1502=) rs853304 0.55069
NM_003235.5(TG):c.7920C>T (p.Tyr2640=) rs2294024 0.49806
NM_003235.5(TG):c.3935A>G (p.Asp1312Gly) rs2069556 0.47427
NM_003235.5(TG):c.5512G>A (p.Asp1838Asn) rs2069561 0.39534
NM_003235.5(TG):c.5995C>T (p.Arg1999Trp) rs2076740 0.37641
NM_003235.5(TG):c.5921T>C (p.Met1974Thr) rs56230101 0.13536
NM_003235.5(TG):c.5119C>T (p.Pro1707Ser) rs61744678 0.07252
NM_003235.5(TG):c.5234-10T>C rs4736614 0.06877
NM_003235.5(TG):c.5549-9C>A rs77157347 0.05272
NM_003235.5(TG):c.5862A>G (p.Lys1954=) rs16904799 0.05269
NM_003235.5(TG):c.3217+11A>C rs79594547 0.04535
NM_003235.5(TG):c.7578T>A (p.Phe2526Leu) rs12114109 0.03807
NM_003235.5(TG):c.6984C>G (p.Leu2328=) rs61745590 0.02022
NM_003235.5(TG):c.3494A>G (p.Tyr1165Cys) rs61746583 0.01329
NM_003235.5(TG):c.3906G>A (p.Pro1302=) rs2294003 0.00435
NM_003235.5(TG):c.2200T>G (p.Ser734Ala) rs180223
NM_003235.5(TG):c.7847A>G (p.Asn2616Ser) rs10091530

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