ClinVar Miner

List of variants in gene RHOBTB1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_014836.5(RHOBTB1):c.545G>T (p.Gly182Val) rs142844286 0.00015
NM_014836.5(RHOBTB1):c.1234C>T (p.Arg412Trp) rs149990776 0.00010
NM_014836.5(RHOBTB1):c.1276A>G (p.Lys426Glu) rs528236520 0.00003
NM_014836.5(RHOBTB1):c.524G>A (p.Arg175Gln) rs1157759221 0.00003
NM_014836.5(RHOBTB1):c.934G>A (p.Glu312Lys) rs370757581 0.00003
NM_014836.5(RHOBTB1):c.403G>A (p.Val135Ile) rs139627798 0.00002
NM_014836.5(RHOBTB1):c.1258A>G (p.Thr420Ala) rs140431485 0.00001
NM_014836.5(RHOBTB1):c.1358T>C (p.Met453Thr) rs772524250 0.00001
NM_014836.5(RHOBTB1):c.1394A>C (p.Lys465Thr) rs1043963546 0.00001
NM_014836.5(RHOBTB1):c.1498A>G (p.Lys500Glu) rs200154803 0.00001
NM_014836.5(RHOBTB1):c.1588A>T (p.Asn530Tyr) rs749420885 0.00001
NM_014836.5(RHOBTB1):c.1606A>G (p.Met536Val) rs771864912 0.00001
NM_014836.5(RHOBTB1):c.1798T>C (p.Tyr600His) rs376819942 0.00001
NM_014836.5(RHOBTB1):c.1830C>A (p.His610Gln) rs767758396 0.00001
NM_014836.5(RHOBTB1):c.716C>T (p.Pro239Leu) rs756288413 0.00001
NM_014836.5(RHOBTB1):c.1084G>A (p.Glu362Lys)
NM_014836.5(RHOBTB1):c.1117G>C (p.Gly373Arg) rs200381691
NM_014836.5(RHOBTB1):c.1201A>G (p.Arg401Gly)
NM_014836.5(RHOBTB1):c.122C>T (p.Thr41Met)
NM_014836.5(RHOBTB1):c.1285G>A (p.Asp429Asn)
NM_014836.5(RHOBTB1):c.1520G>T (p.Cys507Phe)
NM_014836.5(RHOBTB1):c.1556T>C (p.Val519Ala)
NM_014836.5(RHOBTB1):c.1597A>G (p.Lys533Glu)
NM_014836.5(RHOBTB1):c.1599G>T (p.Lys533Asn)
NM_014836.5(RHOBTB1):c.1823A>G (p.Asn608Ser)
NM_014836.5(RHOBTB1):c.1895G>T (p.Arg632Leu)
NM_014836.5(RHOBTB1):c.1943G>A (p.Arg648Gln)
NM_014836.5(RHOBTB1):c.1994G>A (p.Arg665His) rs143799442
NM_014836.5(RHOBTB1):c.2008C>G (p.Arg670Gly) rs148931110
NM_014836.5(RHOBTB1):c.2024T>C (p.Ile675Thr)
NM_014836.5(RHOBTB1):c.2041C>T (p.Arg681Cys)
NM_014836.5(RHOBTB1):c.2048G>C (p.Arg683Thr) rs2080778322
NM_014836.5(RHOBTB1):c.34G>A (p.Val12Ile)
NM_014836.5(RHOBTB1):c.43A>C (p.Ile15Leu) rs2540242175
NM_014836.5(RHOBTB1):c.487A>G (p.Ile163Val)
NM_014836.5(RHOBTB1):c.53T>C (p.Val18Ala) rs764689756
NM_014836.5(RHOBTB1):c.674A>G (p.Gln225Arg)
NM_014836.5(RHOBTB1):c.712G>T (p.Ala238Ser)
NM_014836.5(RHOBTB1):c.731A>G (p.Lys244Arg)
NM_014836.5(RHOBTB1):c.967C>T (p.Arg323Trp)

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