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Molecular characterization of iranian patients with inherited coagulation factor VII deficiency


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Figure 1

The sequencing chromatogram of 64G>A in genomic DNA (upper) and cDNA (lower) of patient 4.
The sequencing chromatogram of 64G>A in genomic DNA (upper) and cDNA (lower) of patient 4.

Characteristics of the primer sets used for the polymerase chain reaction assay.

Oligo PrimersSequences (5’>3’)TmAmplicon (bp)
F71aFGAA CTT TGC CCG TCA GTC CC
F71aRCCG CCA GAA AAC CCT CCT G61258
F71bFGAC AGT GCC TGG GAT GTG G
F71bRGAG CGG TCA CTT CCT CTC GA60293
F72FGGG AAG GAT GGG CGA CGG
F72RCCA GGA AAG CGG AGT CAC CC62534
F734FTGT CCA GTG CTT ACC GTT GG
F734RAAT TTC CAA CTG GGG CTG AG59419
F75FGAT CAG TCC ACG GAG CAG G
F75RGTA GAT GTG AAG CCA CTC CC58408
F76FCTG AAT CTT TCC TAG TGG CAC G
F76RCAA AAG GCT TCA AGA CCC TCA G59235
F77FAGC AAT GTG ACT TCC ACA CC
F77RAGC CCC CAG TCT TTT ATC GT58543
F78aFCCC AGA CCC CAG ATT CAC CC
F78aRGCC TCC ACT GTC CCC CTT G62633
F78bFAGT CAC GGA AGG TGG GAG AC
F78bRGGG ATT TGG TGC CAG GAC AG61349

Characteristics of the primer sets used for the reverse transcription-polymerase chain reaction assay.

Oligo PrimersSequences (5’>3’)TmAmplicon (bp)
F7cD1FCAA CAG GCA GGG GCA GCA C
F7cD1RTCG TGG CAC CGA CAG GAG C63303
F7cD2FTGT GTG AAC GAG AAC GGC G
F7cD2RACC TTC CGT GAC TGC TGC60680
F7cD3FATG TGG TGC CCC TCT GCC
F7cD3RTGT CTC TGT CTC CCT CCC CA62591

The F7 mutation locations and corresponding nucleotide and amino acid changes in the study patients. The indicated variants in parentheses are in Human Genome Variation Society (HGVS) format

PatientExonNucleotide ChangeAmino Acid ChangeGenotypeMutationTaster2 Prediction a
Patient 18g.10648C>T (g.12728C>T) (GCG>G7G)A244V (A282V)heterozygotedisease causing score: 64
Patient 28g.10824C>A (g.12904C>A) (CCC>ACC)P303V (P341T)homozygotedisease causing score: 38
Patient 38g.10648C>T (g.12728C>T) (GCG>G7G)A244V (A282V)heterozygotedisease causing score: 64
Patient 41ag.64G>A (g.115G>A) (GTC>ATC)V(–39)I (V22I)heterozygotedisease causing score: 29
Patient 55g.7807G>C (g.9891G>C) (TGT>TCT)C91S (C129S)homozygotedisease causing score: 112
Patient 68g.10828G>A (g.12908G>A) (CGG>CAG)R304Q (R342Q)homozygotedisease causing score: 43
Patient 78g.10763C>G (g.12843C>G) (AGC>AGG)S282R (S320R) compounddisease causing score: 110
8g.10960A>G (g.13040A>G) (CAT>CGT)H348R (H386R)heterozygotedisease causing score: 29
Patient 88g.10828G>A (g.12908G>A) (CGG>CAG)R304Q (R342Q) compounddisease causing score: 43
Intron 7g.9733A>G (IVS7+7A>G)heterozygotedisease causing score: –

Patient characteristics, symptoms and plasma FVII coagulation activity (FVII:C).

PatientSex-AgeConsanguinityFVII:C (IU/dL)Hemorrhagic Symptoms
Patient 1M-22no18.0%gastrointestinal bleeding, epistaxis, oral cavity bleeding, cutaneous symptoms
Patient 2M-34yes7.0%hemarthrosis, epistaxis, oral cavity bleeding, cutaneous symptoms
Patient 3F-32no33.0%menorrhagia, epistaxis, oral cavity bleeding, cutaneous symptoms
Patient 4M-54no29.0%asymptomatic
Patient 5M-20NA2.0%cutaneous symptoms, epistaxis, oral cavity bleeding
Patient 6M-67yes16.0%epistaxis, oral cavity bleeding, cutaneous symptoms
Patient 7M-26no<1.0%hemathrosis, epistaxis, oral cavity bleeding, cutaneous symptoms
Patient 8M-31no25.0%gastrointestinal bleeding, epistaxis, oral cavity bleeding, cutaneous symptoms
eISSN:
1311-0160
Language:
English
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Journal Subjects:
Medicine, Basic Medical Science, other