The UMD-FBN1 mutations database
Record ID: 2191

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation statusVariation class
c.2534G>Ap.Cys845TyrHeterozygousMutation

wt codonwt aamutant codonmutant aamutational eventmutation type
TGCCysTACTyrG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
cb EGF-like #09 Disulfide bonds 832-845 (C6)NoNo

Mutation impact


At the mRNA levelOn restriction map
NANew restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.670.00 (pathogenous)100 (Pathogenous)

Patient and sample data


Sample IDPatient statusGenderTransmissionAge of onsetAge of deathGeographic origin
FRA04DIJ F0002 I0001ProbandMaleNAFRANCE

Phenotypic groupDisease
NAMarfanoid Syndrome

Clinical data


SymptomSeverityAge
C-Cardiac malformation54
C-Mitral valve prolapse54
O-Ectopia lentissurgery54
S-Arachnodactyly (M)54
S-Crowding teeth (m)54
S-High arched palate54
S-Pectus excavatum moderate (m)(1)54
S-Scoliosis > 20° (M)(1)54

Reference


Reference IDPubMed IDReference
25623506379
Callier P, Aral B, Hanna N, Lambert S, Dindy H, Ragon C, Payet M, Collod-Beroud G, Carmignac V, Delrue M, Goizet C, Philip N, Busa T, Dulac Y, Missotte I, Sznajer Y, Toutain A, Francannet C, Megarbane A, Julia S, Edouard T, Sarda P, Amiel J, Lyonnet S, Cormier-Daire V, Gilbert B, Jacquette A, Heron D, Collignon P, Lacombe D, Morice-Picard F, Jouk P, Cusin V, Willems M, Sarrazin E, Amarof K, Coubes C, Addor M, Journel H, Colin E, Khau Van Kien P, Baumann C, Leheup B, Martin-Coignard D, Doco-Fenzy M, Goldenberg A, Plessis G, Thevenon J, Pasquier L, Odent S, Vabres P, Huet F, Marle N, Mosca-Boidron A, Mugneret F, Gauthier S, Binquet C, Thauvin-Robinet C, Jondeau G, Boileau C, Faivre L. "Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability". Clin Genet. 2013 Dec;84(6):507-21.