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HLA Database » Rare Alleles » Rare Alleles Detector (RAD)
About RAD
The Rare Alleles Detector (RAD) has been designed to assist users in the detection of potential rare alleles found in your laboratory. The RAD tool provides a summary of those alleles that are considered to be very rare (never seen excluding the initial confirmation in IMGT/HLA), rare (seen 1, 2 and 3 times, excluding IMGT/HLA) and frequent (seen more than 3 times, excluding IMGT/HLA).
How to
1. Enter your alleles inside the box, i.e. by "copy and paste" your data from your spreasheet or any electronic source. The data (alleles) must be in this format.
- For multiple loci, please use tabs, spaces, commas[,] or semicolons[;] to separate your alleles.
- If you have your data in a text file (using our format), use the "Browse" and "Load from file" options. This will fill the text box.
2. Once you have filled the text box click on "Analyse" to start the process.
3. Use the "Reset Values" button to start a new analysis.
Tip: Click on "Load example" to see an example of the analysis.
Colour code
| Very Rare | |
| Rare | |
| Frequent | |
| Invalid name | |
| Alleles not considered due to low resolution are shown in blank |
| Individual ID | A(1) | A(2) | B(1) | B(2) | C(1) | C(2) |
|---|---|---|---|---|---|---|
| 000001 | 02:01 | 29:01 | 08:01 | 18:01 | 07:01 | 15:02 |
| 000002 | 01:01 | 02:06 | 40:02 | 50:02 | 06:02 | 07:02 |
| 000003 | 02:01 | 02:06 | 15:30 | 51:02 | 01:02 | 08:01 |
| 000004 | 02:02 | 30:01 | 42:01 | 58:02 | 06:02 | 17:01 |
| 000005 | 03:01 | 30:02 | 07:02 | 07:02 | 07:02 | 07:02 |
| 000006 | 24:03 | 30:01 | 38:01 | 39:10 | 12:03 | 12:03 |
| 000007 | 34:02 | 74:01 | 18:01 | 57:03 | 02:02 | 07:01 |
| 000008 | 02:01 | 32:01 | 44:02 | 50:01 | 05:01 | 06:02 |
| 000009 | 02:01 | 33:03 | 45:01 | 53:01 | 04:01 | 16:01 |
| 000010 | 24:02 | 24:02 | 15:01 | 15:01 | 01:02 | 03:03 |
| 000011 | 02:01 | 24:02 | 51:01 | 52:01 | 02:02 | 03:03 |
| 000012 | 02:06 | 03:01 | 15:01 | 41:01 | 01:02 | 07:01 |
| 000013 | 02:07 | 03:01 | 35:03 | 46:01 | 01:85 | 12:03 |
| 000014 | 24:02 | 66:01 | 15:03 | 35:01 | 02:10 | 03:05 |
| 000015 | 02:01 | 24:02 | 40:02 | 44:02 | 03:04 | 05:01 |
| 000016 | 11:01 | 33:03 | 40:01 | 46:01 | 01:02 | 07:02 |
| 000017 | 23:01 | 24:02 | 13:01 | 42:01 | 04:03 | 17:01 |
| 000018 | 02:01 | 03:01 | 40:02 | 51:01 | 15:02 | 15:02 |
| 000019 | 26:01 | 68:05 | 07:06 | 39:05 | 07:02 | 07:02 |
| 000020 | 02:01 | 29:02 | 45:01 | 51:01 | 06:02 | 14:02 |
| 000021 | 02:07 | 34:01 | 15:21 | 46:01 | 01:02 | 04:03 |
| 000022 | 02:01 | 24:02 | 35:02 | 51:01 | 01:02 | 07:02 |
| 000023 | 01:01 | 68:01 | 37:01 | 40:02 | 03:04 | 06:02 |
| 000024 | 02:01 | 23:01 | 07:02 | 08:01 | 07:01 | 16:01 |
| 000025 | 23:01 | 66:01 | 35:01 | 58:02 | 04:01 | 06:02 |
| 000026 | 25:01 | 30:04 | 18:01 | 53:01 | 12:03 | 15:05 |
| 000027 | 23:01 | 30:04 | 45:01 | 51:01 | 06:02 | 16:01 |
| 000028 | 02:02 | 30:02 | 15:16 | 44:03 | 06:02 | 14:02 |
| 000029 | 26:01 | 29:01 | 38:01 | 38:01 | 12:03 | 12:03 |
| 000030 | 29:02 | 74:01 | 15:03 | 15:03 | 02:10 | 16:01 |
| 000031 | 02:03 | 03:01 | 07:02 | 38:02 | 07:02 | 07:02 |
| 000032 | 02:02 | 23:17 | 53:01 | 53:01 | 04:01 | 04:01 |
| 000033 | 23:01 | 80:01 | 07:06 | 35:01 | 04:01 | 07:02 |
| 33 individual(s) typed. | ||||||
Summary of results
| Very Rare (n=1) | [ C*01:85 (1) ] | |
| Rare (n=0) | [ ] | |
| Frequent (n=21) |
Allele frequency net database (AFND) 2020 update: gold-standard data classification, open access genotype data and new query tools
Gonzalez-Galarza FF, McCabe A, Santos EJ, Jones J, Takeshita LY, Ortega-Rivera ND, Del Cid-Pavon GM, Ramsbottom K, Ghattaoraya GS, Alfirevic A, Middleton D and Jones AR Nucleic Acid Research 2020, 48:D783-8.
Liverpool, U.K.
support@allelefrequencies.net