Phenotype: Medullary thyroid carcinoma


OMIM: 155240
Inheritance: Autosomal dominant
Classification: Neoplasms

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RET || c.1852T>C

Gene/Locus:    RET
Dna Change:    c.1852T>C
Protein Change:    p.Cys618Arg
Mutation Type:    Substitution
Mutation Effect:    Missense
Location:    exon10
Transcript:    NM_020630.4

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
CyprusNANA1 patient/1 familyNANeocleous V et al., 2011Neocleous V, Skordis N, Portides G, Efstathiou E, Costi C, Ioannou N, Pantzaris M, Anastasiadou V, Deltas C, Phylactou LA, . RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2.. J. Endocrinol. Invest.. 2011; 34(10):764-9

References

Neocleous V, Skordis N, Portides G, Efstathiou E, Costi C, Ioannou N, Pantzaris M, Anastasiadou V, Deltas C, Phylactou LA, RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2.J. Endocrinol. Invest.. 2011; 34(10):764-9