ClinVar Miner

List of variants in gene LRRC39 reported as uncertain significance by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_144620.4(LRRC39):c.625A>C (p.Asn209His) rs145422779 0.00031
NM_144620.4(LRRC39):c.230C>T (p.Ser77Phe) rs201723295 0.00026
NM_144620.4(LRRC39):c.200T>C (p.Ile67Thr) rs752977918 0.00021
NM_144620.4(LRRC39):c.510A>T (p.Gln170His) rs199927631 0.00021
NM_144620.4(LRRC39):c.706T>A (p.Cys236Ser) rs148005305 0.00015
NM_144620.4(LRRC39):c.782C>A (p.Pro261Gln) rs147649568 0.00015
NM_144620.4(LRRC39):c.326T>C (p.Ile109Thr) rs780755554 0.00012
NM_144620.4(LRRC39):c.677C>T (p.Thr226Met) rs149823600 0.00008
NM_144620.4(LRRC39):c.789C>G (p.Cys263Trp) rs528764115 0.00008
NM_144620.4(LRRC39):c.602T>C (p.Leu201Pro) rs140341572 0.00007
NM_144620.4(LRRC39):c.892C>T (p.Arg298Trp) rs765807301 0.00007
NM_144620.4(LRRC39):c.419A>C (p.Lys140Thr) rs868076216 0.00003
NM_144620.4(LRRC39):c.494T>C (p.Ile165Thr) rs144639407 0.00003
NM_144620.4(LRRC39):c.187G>A (p.Val63Ile) rs763730162 0.00002
NM_144620.4(LRRC39):c.348C>G (p.Asn116Lys) rs762111111 0.00001
NM_144620.4(LRRC39):c.149C>T (p.Thr50Ile)
NM_144620.4(LRRC39):c.22A>C (p.Thr8Pro) rs770055758
NM_144620.4(LRRC39):c.22A>G (p.Thr8Ala)
NM_144620.4(LRRC39):c.268C>G (p.Leu90Val)
NM_144620.4(LRRC39):c.29C>T (p.Ala10Val)
NM_144620.4(LRRC39):c.367C>A (p.Pro123Thr)
NM_144620.4(LRRC39):c.410G>A (p.Ser137Asn)
NM_144620.4(LRRC39):c.437A>G (p.Lys146Arg)
NM_144620.4(LRRC39):c.512A>C (p.Glu171Ala) rs2523936365
NM_144620.4(LRRC39):c.553A>G (p.Met185Val) rs978856356
NM_144620.4(LRRC39):c.695A>G (p.Asn232Ser) rs2523925079
NM_144620.4(LRRC39):c.839T>C (p.Leu280Pro) rs2523913121
NM_144620.4(LRRC39):c.879T>A (p.Asp293Glu)
NM_144620.4(LRRC39):c.947G>T (p.Arg316Ile)

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