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83706:
MSH6 Known Mutation

CPT Code Information Current Value

81299-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; known familial variants

81300-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; duplication/deletion variants (if appropriate)


CPT Code Information Value Prior to 12/14/2012 10:03am

81299-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; known familial variants

81300-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; duplication/deletion variants (if appropriate)

 

For nonparticipating payers:

MSH6 Known Mutation

83891-Isolation or extraction of highly purified nucleic acid

83912-Interpretation and report

 

DNA Sequence, Follow-up Analysis

83898-Amplification, target, each nucleic acid sequence (if appropriate)

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

 

hMSH6 Large Deletion/Duplication

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

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

83914 x 10-Mutation identification by enzymatic ligation or primer extension, single segment, each segment (if appropriate)