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85318:
Fanconi Anemia C Mutation Analysis, IVS4(+4)A->T and 322delG

CPT Code Information Current Value

81242-FANCC (Fanconi anemia, complementation group C) (eg, Fanconi anemia, type C) gene analysis, common variant (eg, IVS4+4A->T)


CPT Code Information Value Prior to 1/01/2013 7:02am

81242-FANCC (Fanconi anemia, complementation group C) (eg, Fanconi anemia, type C) gene analysis, common variant (eg, IVS4+4A->T)

 

Amniotic Fluid Culture for Genetic Testing

88235-Tissue culture for amniotic fluid (if appropriate)

88240-Cryopreservation (if appropriate)

 

Fibroblast Culture for Genetic Testing

88233-Tissue culture, skin, or solid tissue biopsy (if appropriate)

88240-Cryopreservation (if appropriate)

 

Maternal Cell Contamination, B

83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)

83909 x 2-Separation and identification by high-resolution technique (if appropriate)

83912-Interpretation and report (if appropriate)

 

For nonparticipating payers:

Fanconi Anemia C Mutation Analysis, IVS4(+4)A->T and 322delG

83890-Molecular isolation or extraction

83892-Enzymatic digestion

83896 x 2-Nucleic acid probe, each

83900-Amplification, target, multiplex, first 2 nucleic acid sequences

83909-Separation and identification by high-resolution technique

83912-Interpretation and report

83914 x 2-Mutation identification by enzymatic ligation or primer extension, single segment, each segment

 

Amniotic Fluid Culture for Genetic Testing

88235-Tissue culture for amniotic fluid (if appropriate)

88240-Cryopreservation (if appropriate)

 

Fibroblast Culture for Genetic Testing

88233-Tissue culture, skin, or solid tissue biopsy (if appropriate)

88240-Cryopreservation (if appropriate)

 

Maternal Cell Contamination, B

83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)

83909 x 2-Separation and identification by high-resolution technique (if appropriate)

83912-Interpretation and report (if appropriate)