ClinVar Miner

List of variants in gene TUBB2B reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_178012.5(TUBB2B):c.1037C>T (p.Pro346Leu) rs2113818963
NM_178012.5(TUBB2B):c.1066_1070del (p.Ile356fs) rs2533617094
NM_178012.5(TUBB2B):c.1112G>T (p.Ser371Ile)
NM_178012.5(TUBB2B):c.1149G>A (p.Glu383=)
NM_178012.5(TUBB2B):c.1188C>G (p.His396Gln) rs1554126865
NM_178012.5(TUBB2B):c.123T>G (p.Asp41Glu) rs748385221
NM_178012.5(TUBB2B):c.1241A>C (p.Asn414Thr)
NM_178012.5(TUBB2B):c.1309G>C (p.Glu437Gln) rs773869730
NM_178012.5(TUBB2B):c.16C>T (p.His6Tyr)
NM_178012.5(TUBB2B):c.202C>G (p.Leu68Val) rs2113819569
NM_178012.5(TUBB2B):c.208C>T (p.Pro70Ser) rs1554126963
NM_178012.5(TUBB2B):c.244G>A (p.Gly82Ser) rs766214058
NM_178012.5(TUBB2B):c.394G>A (p.Gly132Ser) rs1554126928
NM_178012.5(TUBB2B):c.424G>A (p.Gly142Ser) rs774873878
NM_178012.5(TUBB2B):c.436G>T (p.Gly146Trp) rs2113819270
NM_178012.5(TUBB2B):c.43C>A (p.Gln15Lys) rs1085307566
NM_178012.5(TUBB2B):c.452T>C (p.Leu151Pro) rs2533617601
NM_178012.5(TUBB2B):c.616G>T (p.Ala206Ser)
NM_178012.5(TUBB2B):c.637C>T (p.Arg213Cys) rs2533617471
NM_178012.5(TUBB2B):c.638G>A (p.Arg213His)
NM_178012.5(TUBB2B):c.656C>T (p.Thr219Ile) rs2533617455
NM_178012.5(TUBB2B):c.670del (p.Asp224fs) rs1271392248
NM_178012.5(TUBB2B):c.761C>A (p.Ala254Glu) rs1757274660
NM_178012.5(TUBB2B):c.761C>T (p.Ala254Val)
NM_178012.5(TUBB2B):c.763G>A (p.Val255Met)
NM_178012.5(TUBB2B):c.797T>C (p.Phe266Ser)
NM_178012.5(TUBB2B):c.830G>A (p.Gly277Asp)
NM_178012.5(TUBB2B):c.914C>T (p.Pro305Leu)
NM_178012.5(TUBB2B):c.952C>G (p.Arg318Gly) rs2113819009
NM_178012.5(TUBB2B):c.976G>C (p.Val326Leu)

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