Mobile Site ›

83723:
MSH6 Mutation Screen, Blood

CPT Code Information Current Value

81298-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; full sequence analysis

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


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

81298-MSH6 (mutS homolog 6 [E. coli]) (eg, hereditary non-polyposis colorectal cancer, Lynch syndrome) gene analysis; full sequence analysis

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

 

For nonparticipating payers:

MSH6 Mutation Screen, Blood

83891-Isolation or extraction of highly purified nucleic acid

83898 x 19-Amplification, target, each nucleic acid sequence

83909 x 38-Separation and identification by high-resolution technique

83912-Interpretation and report

 

MSH6 Large Deletion/Duplication, MLPA

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

83909-Separation and identification by high-resolution technique

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