F13A1 V651I - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

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F13A1 V651I

(F13A1 Val651Ile)

Short summary


Variant evidence
Computational -
Functional -
Case/Control -
Familial -
Clinical importance
Severity -
Treatability -
Penetrance -


Insufficiently evaluated not reviewed

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern


Summary of published research, and additional commentary


Allele frequency

  • T @ chr6:6152140: 4.9% (531/10758) in EVS
  • T @ chr6:6097138: 7.8% (10/128) in GET-Evidence
  • Frequency shown in summary reports: 4.9% (531/10758)









GS18526 - var-GS18526-1100-36-ASM
het T @ chr6:6097139


GS19025 - var-GS19025-1100-36-ASM
het T @ chr6:6097139


GS19649 - var-GS19649-1100-36-ASM
hom T @ chr6:6097139


Other external references

  • rs5987
    Web search results (3 hits -- see all)
  • AceView: Gene:F13A1, a comprehensive annotation of human ...
    AceView offers a comprehensive annotation of human, mouse and nematode genes reconstructed by co-alignment and clustering of all publicly available mRNAs and ESTs on ...
  • Table 3 Text
    ... coagulation factor XIII, A1 polypeptide" 187 rs5983 F13A1 2162 6 6112832 NM_000129 NP_000120 A/T L589Q minus 7593 504. WIAF-CSNP WIAF-CSNP ...
  • Abstractband
    to provide data on the role of the F13A1 gene polymorphisms for coronary artery disease ... amino-acid exchanges in subunit A gene (V34l, k351M, V401I, P565l, V651I, e652Q) ...

Other in silico analyses

  • NBLOSUM100 score = –4
  • GET-Evidence autoscore = 3

Edit history

Gene search

"GENE" or "GENE A123C":

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