NM_001854.3:c.3708+437T>G

HGVS Expressions

  • NG_008033.1:g.192416T>G
  • NM_001854.3:c.3708+437T>G
  • NP_001845.3:p.?
  • NC_000001.11:g.102921081A>C
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
228520.3.1Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.7 from family 'FB' in the pu...
228520.3.2Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.1 from family 'FB' in the pu...
228520.3.3Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.2 from family 'FB' in the pu...
228520.3.4Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.4 from family 'FB' in the pu...
228520.3.5Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.5 from family 'FB' in the pu...
228520.3.6Oman2NAUncertain SignificanceFibrochondrogenesis 1Akawi et al. 2012 Patient III.8 from family 'FB' in the pu...
228520.3.7Oman1NAUncertain SignificanceAkawi et al. 2012 Patient III.6 with mild symptoms from fa...
228520.3.8Oman1NAUncertain SignificanceAkawi et al. 2012 Father of 228520.3.1, mild phenotype not...
228520.3.9Oman1NAUncertain SignificanceAkawi et al. 2012 Mother of 228520.3.1
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