ClinVar Miner

List of variants in gene TMEM126A reported as likely benign for not provided

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_032273.4(TMEM126A):c.281-260G>A rs189238212 0.00434
NC_000011.10:g.85656581A>G rs568835348 0.00278
NM_032273.4(TMEM126A):c.314G>A (p.Arg105Gln) rs146573578 0.00247
NM_032273.4(TMEM126A):c.562T>A (p.Ser188Thr) rs34397695 0.00240
NM_032273.4(TMEM126A):c.154A>G (p.Ser52Gly) rs140047528 0.00239
NM_032273.4(TMEM126A):c.96T>G (p.Leu32=) rs36100288 0.00220
NM_032273.4(TMEM126A):c.191G>A (p.Arg64His) rs11556797 0.00161
NM_032273.4(TMEM126A):c.492G>A (p.Leu164=) rs140123526 0.00016
NM_032273.4(TMEM126A):c.87-17T>A rs147312342 0.00014
NM_032273.4(TMEM126A):c.372T>C (p.Pro124=) rs374493425 0.00008
NM_032273.4(TMEM126A):c.234A>G (p.Thr78=) rs371334632 0.00006
NM_032273.4(TMEM126A):c.271T>C (p.Leu91=) rs1042977900 0.00005
NM_032273.4(TMEM126A):c.402A>G (p.Gln134=) rs375711712 0.00005
NM_032273.4(TMEM126A):c.531A>G (p.Gln177=) rs369467944 0.00004
NM_032273.4(TMEM126A):c.87-9C>T rs369708298 0.00004
NM_032273.4(TMEM126A):c.87-19T>G rs778679518 0.00003
NM_032273.4(TMEM126A):c.172T>C (p.Leu58=) rs1328441511 0.00002
NM_032273.4(TMEM126A):c.280+12T>C rs904221195 0.00002
NM_032273.4(TMEM126A):c.281-19T>C rs781058291 0.00002
NM_032273.4(TMEM126A):c.240C>T (p.Asp80=) rs532521030 0.00001
NM_032273.4(TMEM126A):c.280+8C>A rs765042337 0.00001
NM_032273.4(TMEM126A):c.281-13A>C rs750201466 0.00001
NM_032273.4(TMEM126A):c.286T>C (p.Leu96=) rs779706678 0.00001
NM_032273.4(TMEM126A):c.354T>C (p.Pro118=) rs767466864 0.00001
NM_032273.4(TMEM126A):c.361T>C (p.Leu121=) rs750349230 0.00001
NM_032273.4(TMEM126A):c.385C>G (p.Leu129Val) rs546358774 0.00001
NM_032273.4(TMEM126A):c.108G>A (p.Ser36=)
NM_032273.4(TMEM126A):c.195A>T (p.Ile65=) rs768104829
NM_032273.4(TMEM126A):c.216A>G (p.Ala72=)
NM_032273.4(TMEM126A):c.280+17T>C
NM_032273.4(TMEM126A):c.281-10T>G rs2153313647
NM_032273.4(TMEM126A):c.281-12T>C rs2153313645
NM_032273.4(TMEM126A):c.281-6dup rs1263938348
NM_032273.4(TMEM126A):c.281-7_281-6del
NM_032273.4(TMEM126A):c.306C>G (p.Thr102=) rs1234858273
NM_032273.4(TMEM126A):c.315G>C (p.Arg105=) rs2153313666
NM_032273.4(TMEM126A):c.333T>C (p.Leu111=)
NM_032273.4(TMEM126A):c.351C>T (p.Tyr117=)
NM_032273.4(TMEM126A):c.395+11A>C
NM_032273.4(TMEM126A):c.395+11A>G
NM_032273.4(TMEM126A):c.395+9_395+10delinsCG rs2153313732
NM_032273.4(TMEM126A):c.396-18C>A
NM_032273.4(TMEM126A):c.396-4dup
NM_032273.4(TMEM126A):c.426G>T (p.Gly142=) rs2082539720
NM_032273.4(TMEM126A):c.480A>G (p.Leu160=) rs2082540485
NM_032273.4(TMEM126A):c.552C>T (p.Ala184=) rs2153314027
NM_032273.4(TMEM126A):c.573C>A (p.Gly191=)
NM_032273.4(TMEM126A):c.63T>C (p.Ile21=) rs2153312375
NM_032273.4(TMEM126A):c.69G>A (p.Gln23=) rs2082489677
NM_032273.4(TMEM126A):c.86+11T>C
NM_032273.4(TMEM126A):c.86+13_86+15del rs772468832
NM_032273.4(TMEM126A):c.87-19T>A
NM_032273.4(TMEM126A):c.87-19T>C rs778679518
NM_032273.4(TMEM126A):c.87-20C>A

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