GenBank acc. | Mutation profile | Haplotype | Inconsistency | |
---|---|---|---|---|
according to GenBank | recognized by CHD | |||
KM262649.1 | A15627G T15639A C15814T A15931- C15959T T16025C A16033G | A228 | A140 (A15627G T15639A C15814T A15931- C15959T T16025C A16033G) | assignment of a new haplotype for an assigned haplotype |
JF342817.1 | A15653G C15814T C15955T | A17 (T15620C A15627G T15639A C15814T C15955T) | new haplotype A (A15653G C15814T C15955T) | Wrong identification for a new haplotype |
JF342836.1 | A15553G T15639A C15814T A15931-) | A171 (T15639A C15814T G15848A T16025C) | A246 (A15553G T15639A C15814T A15931-) | Wrong identification for an assigned haplotype |
KJ637102.1 | C15483T A15627G T15639A C15814T C15912T | haplotype Be36_2 | A1 (C15483T A15627G T15639A C15814T C15912T) | Annotated with other haplotyping system |