Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4267 |
| ensemblid | ENSG00000002586.20 |
| hgncid | 7082 |
| symbol | CD99 |
| name | CD99 molecule (Xg blood group) |
| refseq_nuc | NM_002414.5 |
| refseq_prot | NP_002405.1 |
| ensembl_nuc | ENST00000381192.10 |
| ensembl_prot | ENSP00000370588.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2691295 |
| end | 2741309 |
| strand | + |
| ver | v1.2 |
| region | chrX:2691295-2741309 |
| region5000 | chrX:2686295-2746309 |
| regionname0 | CD99_chrX_2691295_2741309 |
| regionname5000 | CD99_chrX_2686295_2746309 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 185 | 203 | 52 | 37 | 91 | 7 | 14 | 70 | CD99_chrX_2686295_2746309 | CD99 | MARGA others(180): Show |
chrX | 2686295 | 2746309 |
| a0002 | 0/0 | 185 | 16 | 4 | 5 | 4 | 0 | 3 | 4 | CD99_chrX_2686295_2746309 | CD99 | MARGA others(180): Show |
chrX | 2686295 | 2746309 |
| a0003 | 0/0 | 185 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | MARGA others(180): Show |
chrX | 2686295 | 2746309 |
| a0004 | 0/0 | 185 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | MARGA others(180): Show |
chrX | 2686295 | 2746309 |
| a0005 | 0/0 | 185 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | MARGA others(180): Show |
chrX | 2686295 | 2746309 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 555 | 124 | 46 | 13 | 53 | 3 | 7 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0002 | 0/0 | 555 | 58 | 0 | 16 | 31 | 4 | 7 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0004 | 0/0 | 555 | 9 | 3 | 6 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0005 | 0/0 | 555 | 5 | 0 | 0 | 5 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0007 | 0/0 | 555 | 5 | 1 | 2 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0010 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0001c0012 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0002c0003 | 0/0 | 555 | 11 | 4 | 3 | 2 | 0 | 2 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0002c0006 | 0/0 | 555 | 5 | 0 | 2 | 2 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0003c0008 | 0/0 | 555 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0003c0009 | 0/0 | 555 | 2 | 0 | 2 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0004c0011 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0004c0013 | 0/0 | 555 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 | ||
| a0005c0014 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATGGC others(550): Show |
chrX | 2686295 | 2746309 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1129 | 100 | 37 | 9 | 43 | 3 | 6 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0002 | 0/0 | 1130 | 14 | 4 | 2 | 7 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1125): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0003 | 0/0 | 1129 | 3 | 0 | 2 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0005 | 0/0 | 1129 | 3 | 3 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0006 | 0/0 | 1129 | 2 | 2 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0008 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0001t0010 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0002t0001 | 0/0 | 1129 | 53 | 0 | 16 | 27 | 3 | 7 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0002t0002 | 0/0 | 1130 | 2 | 0 | 0 | 1 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1125): Show |
chrX | 2686295 | 2746309 |
| a0001c0002t0003 | 0/0 | 1129 | 2 | 0 | 0 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0002t0009 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0004t0001 | 0/0 | 1129 | 7 | 2 | 5 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0004t0002 | 0/0 | 1130 | 2 | 1 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1125): Show |
chrX | 2686295 | 2746309 |
| a0001c0005t0001 | 0/0 | 1129 | 5 | 0 | 0 | 5 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0007t0001 | 0/0 | 1129 | 4 | 1 | 1 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0007t0002 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1125): Show |
chrX | 2686295 | 2746309 |
| a0001c0010t0001 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0001c0012t0001 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0002c0003t0001 | 0/0 | 1129 | 11 | 4 | 3 | 2 | 0 | 2 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0002c0006t0001 | 0/0 | 1129 | 5 | 0 | 2 | 2 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0003c0008t0004 | 0/0 | 1129 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0003c0009t0001 | 0/0 | 1129 | 2 | 0 | 2 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0004c0011t0007 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0004c0013t0007 | 0/0 | 1129 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| a0005c0014t0001 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | ATCTG others(1124): Show |
chrX | 2686295 | 2746309 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0007t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0007t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0007t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0007t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0010t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0012t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0006t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0006t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0009t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0009t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0004c0011t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0004c0013t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0005c0014t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0048 | EUR | GBR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0189 | EUR | FIN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | FIN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00408 | hp1 | a0001 | c0002 | t0009 | g0137 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00544 | hp1 | a0001 | c0005 | t0001 | g0218 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00639 | hp1 | a0002 | c0006 | t0001 | g0016 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0200 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01168 | hp2 | a0003 | c0009 | t0001 | g0192 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01169 | hp1 | a0003 | c0009 | t0001 | g0191 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0146 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01257 | hp2 | a0001 | c0007 | t0002 | g0126 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0149 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0214 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01516 | hp2 | a0004 | c0013 | t0007 | g0019 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0081 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0210 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0155 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02004 | hp1 | a0001 | c0004 | t0002 | g0035 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02004 | hp2 | a0002 | c0006 | t0001 | g0022 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0145 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0144 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0206 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0205 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0153 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02896 | hp1 | a0003 | c0008 | t0004 | g0086 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0202 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02897 | hp2 | a0003 | c0008 | t0004 | g0087 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03486 | hp1 | a0003 | c0008 | t0004 | g0088 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03486 | hp2 | a0001 | c0012 | t0001 | g0194 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0171 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03540 | hp1 | a0004 | c0011 | t0007 | g0013 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0098 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03831 | hp1 | a0002 | c0006 | t0001 | g0028 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0216 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18906 | hp1 | a0003 | c0008 | t0004 | g0071 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18974 | hp1 | a0002 | c0006 | t0001 | g0122 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18975 | hp1 | a0001 | c0007 | t0001 | g0050 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19001 | hp2 | a0002 | c0006 | t0001 | g0111 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19002 | hp2 | a0001 | c0005 | t0001 | g0222 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19006 | hp1 | a0001 | c0005 | t0001 | g0133 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19064 | hp1 | a0001 | c0005 | t0001 | g0132 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19076 | hp2 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19077 | hp2 | a0005 | c0014 | t0001 | g0134 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19080 | hp1 | a0001 | c0007 | t0001 | g0143 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0131 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | GIH | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA21309 | hp1 | a0001 | c0010 | t0001 | g0201 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0040 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0069 | REF | REF | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0168 | REF | REF | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2691412 | C | G | 1 | a0003 | 6 | HG01168.hp2 HG01169.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.52C>G | p.Leu18Val | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/10 | 118/1129 | 52/558 | 18/185 | chrX | 2691412 | |||
| chrX:2714422 | A | G | 1 | a0005 | 1 | NA19077.hp2 | missense_variant&splice_region_variant | MODERATE | c.68A>G | p.Asp23Gly | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/10 | 134/1129 | 68/558 | 23/185 | chrX | 2714422 | |||
| chrX:2738217 | G | A | 1 | a0004 | 2 | HG01516.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.493G>A | p.Asp165Asn | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 559/1129 | 493/558 | 165/185 | chrX | 2738217 | |||
| chrX:2738220 | A | G | 2 | a0002 a0005 |
17 | HG00639.hp1 HG01496.hp1 HG01981.hp2 others(14): Show |
missense_variant | MODERATE | c.496A>G | p.Met166Val | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 562/1129 | 496/558 | 166/185 | chrX | 2738220 | |||
| chrX:2738242 | A | T | 2 | a0002 a0005 |
17 | HG00639.hp1 HG01496.hp1 HG01981.hp2 others(14): Show |
missense_variant | MODERATE | c.518A>T | p.Asn173Ile | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 584/1129 | 518/558 | 173/185 | chrX | 2738242 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2714441 | C | T | 5 | a0001c0002 a0001c0007 a0002c0006 others(2): Show |
70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
synonymous_variant | LOW | c.87C>T | p.Ser29Ser | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/10 | 153/1129 | 87/558 | 29/185 | chrX | 2714441 | |||
| chrX:2722652 | G | A | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.288G>A | p.Ala96Ala | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/10 | 354/1129 | 288/558 | 96/185 | chrX | 2722652 | |||
| chrX:2726261 | C | T | 4 | a0001c0004 a0001c0007 a0001c0010 others(1): Show |
17 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.363C>T | p.Ala121Ala | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 429/1129 | 363/558 | 121/185 | chrX | 2726261 | |||
| chrX:2726273 | C | T | 1 | a0001c0012 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.375C>T | p.Gly125Gly | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 441/1129 | 375/558 | 125/185 | chrX | 2726273 | |||
| chrX:2726282 | C | T | 1 | a0001c0005 | 5 | HG00544.hp1 NA19002.hp2 NA19006.hp1 others(2): Show |
synonymous_variant | LOW | c.384C>T | p.Pro128Pro | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 450/1129 | 384/558 | 128/185 | chrX | 2726282 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2691310 | T | A | 1 | a0003c0008t0004 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-51T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/10 | 51 | chrX | 2691310 | ||||||
| chrX:2740893 | C | A | 1 | a0001c0001t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 89 | chrX | 2740893 | ||||||
| chrX:2741113 | G | A | 2 | a0001c0001t0003 a0001c0002t0003 |
5 | HG01978.hp1 HG01981.hp1 NA18941.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 309 | chrX | 2741113 | ||||||
| chrX:2741118 | A | AC | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(1): Show |
19 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*321dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 322 | INFO_REALIGN_3_PRIME | chrX | 2741118 | |||||
| chrX:2741164 | A | T | 1 | a0001c0001t0005 | 3 | HG02976.hp1 HG03195.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*360A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 360 | chrX | 2741164 | ||||||
| chrX:2741184 | C | G | 1 | a0001c0001t0010 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 380 | chrX | 2741184 | ||||||
| chrX:2741187 | G | C | 1 | a0001c0001t0006 | 2 | HG01891.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*383G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 383 | chrX | 2741187 | ||||||
| chrX:2741191 | C | T | 2 | a0004c0011t0007 a0004c0013t0007 |
2 | HG01516.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 387 | chrX | 2741191 | ||||||
| chrX:2741194 | C | T | 1 | a0001c0002t0009 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 390 | chrX | 2741194 | ||||||
| chrX:2741203 | T | C | 1 | a0001c0001t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 399 | chrX | 2741203 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2691457 | G | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG06807.hp2 NA18906.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+30G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691457 | |||||||
| chrX:2691502 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG00438.hp2 HG00733.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+75G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691502 | |||||||
| chrX:2691510 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+83G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691510 | |||||||
| chrX:2691676 | G | T | 58 | a0001c0001t0001g0014 a0001c0001t0001g0169 a0001c0001t0001g0170 others(55): Show |
59 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+249G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691676 | |||||||
| chrX:2691708 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.67+281T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691708 | |||||||
| chrX:2691824 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67+397G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691824 | |||||||
| chrX:2691824 | G | T | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+397G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691824 | |||||||
| chrX:2691825 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67+398C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691825 | |||||||
| chrX:2691840 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+413C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691840 | |||||||
| chrX:2691886 | A | G | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.67+459A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691886 | |||||||
| chrX:2691918 | G | C | 1 | a0001c0004t0001g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.67+491G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691918 | |||||||
| chrX:2691942 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(79): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.67+515T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691942 | |||||||
| chrX:2691984 | C | T | 61 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0136 others(58): Show |
63 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.67+557C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691984 | |||||||
| chrX:2692021 | G | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0175 |
3 | HG02257.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.67+594G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692021 | |||||||
| chrX:2692120 | ACCCTCCC others(4): Show |
A | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+696_67+706delCT others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692120 | ||||||
| chrX:2692183 | C | T | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG00423.hp1 HG02080.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+756C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692183 | |||||||
| chrX:2692221 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0176 a0001c0001t0001g0178 others(11): Show |
14 | HG02080.hp1 HG02155.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+794G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692221 | |||||||
| chrX:2692243 | CATGTTAT others(12): Show |
C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+817_67+835delAT others(17): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692243 | |||||||
| chrX:2692265 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+838A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692265 | |||||||
| chrX:2692393 | G | T | 2 | a0001c0001t0002g0033 a0001c0001t0005g0034 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+966G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692393 | |||||||
| chrX:2692453 | T | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0107 others(22): Show |
25 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+1026T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692453 | |||||||
| chrX:2692470 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67+1043G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692470 | |||||||
| chrX:2692634 | C | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0169 a0001c0001t0001g0170 others(5): Show |
8 | HG01123.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1207C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692634 | |||||||
| chrX:2692668 | G | GTCCT | 70 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.67+1244_67+1247dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692668 | ||||||
| chrX:2692788 | A | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0005g0224 |
3 | HG02257.hp2 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.67+1361A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692788 | |||||||
| chrX:2692803 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+1376A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692803 | |||||||
| chrX:2692836 | G | T | 2 | a0001c0001t0002g0033 a0001c0001t0005g0034 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1409G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692836 | |||||||
| chrX:2692864 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG03195.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1437G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692864 | |||||||
| chrX:2692942 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0005g0034 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1515G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692942 | |||||||
| chrX:2693050 | G | C | 3 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0004t0002g0035 |
3 | HG01496.hp2 HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.67+1623G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693050 | |||||||
| chrX:2693111 | A | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0082 others(49): Show |
54 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.67+1684A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693111 | |||||||
| chrX:2693141 | G | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+1714G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693141 | |||||||
| chrX:2693150 | G | GTGGTT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0082 others(41): Show |
46 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+1724_67+1725ins others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | ||||||
| chrX:2693150 | G | GTGGTTT | 6 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0165 others(3): Show |
6 | HG01884.hp1 HG01981.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1724_67+1725ins others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | ||||||
| chrX:2693158 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
49 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+1731T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693158 | |||||||
| chrX:2693204 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
103 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.67+1777A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693204 | |||||||
| chrX:2693372 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67+1945A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693372 | |||||||
| chrX:2693395 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0002g0033 a0001c0001t0005g0034 |
3 | HG02615.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67+1968A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693395 | |||||||
| chrX:2693410 | G | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0082 others(54): Show |
59 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+1983G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693410 | |||||||
| chrX:2693458 | C | G | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0082 others(51): Show |
56 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.67+2031C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693458 | |||||||
| chrX:2693594 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0170 others(3): Show |
6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2167G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693594 | |||||||
| chrX:2693659 | G | A | 1 | a0005c0014t0001g0134 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.67+2232G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693659 | |||||||
| chrX:2693670 | G | C | 3 | a0001c0001t0001g0004 a0001c0001t0002g0097 a0002c0003t0001g0005 |
3 | HG02723.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67+2243G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693670 | |||||||
| chrX:2693749 | A | T | 1 | a0002c0006t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+2322A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693749 | |||||||
| chrX:2693855 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67+2428G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693855 | |||||||
| chrX:2693947 | C | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0170 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+2520C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693947 | |||||||
| chrX:2694008 | A | G | 1 | a0004c0011t0007g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+2581A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694008 | |||||||
| chrX:2694089 | A | G | 8 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0175 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+2662A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694089 | |||||||
| chrX:2694266 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0170 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+2839T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694266 | |||||||
| chrX:2694279 | G | GT | 19 | a0001c0001t0001g0007 a0001c0001t0001g0072 a0001c0001t0001g0073 others(16): Show |
19 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+2867dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694279 | ||||||
| chrX:2694295 | A | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0170 others(1): Show |
4 | HG02080.hp2 HG02257.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2868A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694295 | |||||||
| chrX:2694482 | G | T | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+3055G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694482 | |||||||
| chrX:2694519 | AG | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(145): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.67+3095delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694519 | ||||||
| chrX:2694688 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0002g0097 |
3 | HG02622.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+3261G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694688 | |||||||
| chrX:2694753 | A | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(51): Show |
55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+3326A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694753 | |||||||
| chrX:2694908 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.67+3481T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694908 | |||||||
| chrX:2695018 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.67+3591C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695018 | |||||||
| chrX:2695064 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.67+3637C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695064 | |||||||
| chrX:2695188 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.67+3761T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695188 | |||||||
| chrX:2695191 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0005g0092 |
3 | HG02630.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+3764C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695191 | |||||||
| chrX:2695213 | C | CT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02622.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3796dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695213 | ||||||
| chrX:2695238 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
53 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.67+3811C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695238 | |||||||
| chrX:2695409 | T | G | 1 | a0001c0002t0001g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.67+3982T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695409 | |||||||
| chrX:2695521 | T | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4094T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695521 | |||||||
| chrX:2695535 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
163 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.67+4108T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695535 | |||||||
| chrX:2695552 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+4125C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695552 | |||||||
| chrX:2695554 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4127A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695554 | |||||||
| chrX:2695588 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+4161T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695588 | |||||||
| chrX:2695637 | C | CT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0038 others(17): Show |
20 | HG01891.hp1 HG01975.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+4224dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | ||||||
| chrX:2695637 | C | CTT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+4223_67+4224dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | ||||||
| chrX:2695638 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0005g0034 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+4211T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695638 | |||||||
| chrX:2695659 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.67+4232T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695659 | |||||||
| chrX:2695712 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+4285C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695712 | |||||||
| chrX:2695713 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4286G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695713 | |||||||
| chrX:2695822 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0002g0097 |
3 | HG02622.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+4395C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695822 | |||||||
| chrX:2695877 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+4450G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695877 | |||||||
| chrX:2695956 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4529A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695956 | |||||||
| chrX:2695971 | T | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4544T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695971 | |||||||
| chrX:2696022 | C | T | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+4595C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696022 | |||||||
| chrX:2696041 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+4614A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696041 | |||||||
| chrX:2696071 | G | A | 26 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0002t0001g0008 others(23): Show |
26 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+4644G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696071 | |||||||
| chrX:2696145 | G | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4718G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696145 | |||||||
| chrX:2696178 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(84): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.67+4751A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696178 | |||||||
| chrX:2696198 | G | C | 1 | a0002c0006t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+4771G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696198 | |||||||
| chrX:2696226 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(46): Show |
50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+4799T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696226 | |||||||
| chrX:2696269 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0170 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+4842C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696269 | |||||||
| chrX:2696309 | C | T | 1 | a0001c0007t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+4882C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696309 | |||||||
| chrX:2696393 | CTTTCT | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 others(2): Show |
5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4980_67+4984del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696393 | ||||||
| chrX:2696439 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
163 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.67+5012T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696439 | |||||||
| chrX:2696547 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 others(2): Show |
5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5120C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696547 | |||||||
| chrX:2696557 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5130C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696557 | |||||||
| chrX:2696558 | A | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 others(2): Show |
5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5131A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696558 | |||||||
| chrX:2696649 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+5222C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696649 | |||||||
| chrX:2696927 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0002g0084 a0001c0001t0002g0085 |
3 | HG01070.hp1 HG01071.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.67+5500T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696927 | |||||||
| chrX:2697031 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 others(2): Show |
5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5604T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697031 | |||||||
| chrX:2697142 | C | T | 1 | a0002c0003t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67+5715C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697142 | |||||||
| chrX:2697156 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 others(2): Show |
5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5729C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697156 | |||||||
| chrX:2697312 | A | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+5885A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697312 | |||||||
| chrX:2697338 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
38 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+5911C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697338 | |||||||
| chrX:2697464 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+6037C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697464 | |||||||
| chrX:2697475 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(145): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.67+6048T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697475 | |||||||
| chrX:2697482 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.67+6055A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697482 | |||||||
| chrX:2697555 | C | A | 95 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0073 others(92): Show |
97 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.67+6128C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697555 | |||||||
| chrX:2697946 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.67+6519T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697946 | |||||||
| chrX:2698185 | C | CTT | 7 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG00544.hp2 HG02080.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+6774_67+6775dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698185 | ||||||
| chrX:2698202 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0002g0097 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+6775T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698202 | |||||||
| chrX:2698217 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0001g0195 others(11): Show |
14 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+6790C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698217 | |||||||
| chrX:2698380 | G | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6953G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698380 | |||||||
| chrX:2698416 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0106 a0001c0001t0001g0158 |
3 | HG00544.hp2 HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.67+6989G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698416 | |||||||
| chrX:2698422 | G | A | 2 | a0001c0001t0001g0174 a0001c0004t0001g0171 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+6995G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698422 | |||||||
| chrX:2698475 | C | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+7048C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698475 | |||||||
| chrX:2698549 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0001g0175 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+7122C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698549 | |||||||
| chrX:2698739 | C | T | 98 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0073 others(95): Show |
100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.67+7312C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698739 | |||||||
| chrX:2698744 | C | T | 2 | a0001c0001t0001g0174 a0001c0004t0001g0171 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+7317C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698744 | |||||||
| chrX:2698770 | G | T | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+7343G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698770 | |||||||
| chrX:2698784 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+7357C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698784 | |||||||
| chrX:2698850 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+7423C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698850 | |||||||
| chrX:2698851 | A | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.67+7424A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698851 | |||||||
| chrX:2698929 | A | AT | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG00423.hp1 NA18941.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+7517dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698929 | ||||||
| chrX:2698929 | AT | A | 9 | a0001c0001t0001g0076 a0001c0001t0001g0175 a0001c0001t0001g0195 others(6): Show |
9 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+7517delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698929 | ||||||
| chrX:2698936 | T | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0091 a0001c0001t0001g0108 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+7509T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698936 | |||||||
| chrX:2698953 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.67+7526A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698953 | |||||||
| chrX:2699110 | G | GT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67+7690dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699110 | ||||||
| chrX:2699130 | CTTCTTTT others(3): Show |
C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0001g0175 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+7711_67+7720del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699130 | ||||||
| chrX:2699355 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+7928A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699355 | |||||||
| chrX:2699377 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0170 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+7950C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699377 | |||||||
| chrX:2699437 | G | C | 3 | a0001c0001t0002g0033 a0001c0001t0005g0224 a0001c0010t0001g0201 |
3 | HG02615.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+8010G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699437 | |||||||
| chrX:2699467 | C | CT | 37 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0032 others(34): Show |
37 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+8060dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699467 | ||||||
| chrX:2699470 | T | C | 1 | a0001c0002t0009g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.67+8043T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699470 | |||||||
| chrX:2699572 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67+8145G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699572 | |||||||
| chrX:2699583 | G | T | 66 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(63): Show |
68 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.67+8156G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699583 | |||||||
| chrX:2699640 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+8213A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699640 | |||||||
| chrX:2699761 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+8334G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699761 | |||||||
| chrX:2699855 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0002g0097 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8428A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699855 | |||||||
| chrX:2700047 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(3): Show |
6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8620A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700047 | |||||||
| chrX:2700153 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67+8726C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700153 | |||||||
| chrX:2700202 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67+8775T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700202 | |||||||
| chrX:2700271 | T | G | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+8844T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700271 | |||||||
| chrX:2700356 | T | C | 1 | a0001c0002t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.67+8929T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700356 | |||||||
| chrX:2700462 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+9035G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700462 | |||||||
| chrX:2700522 | ATGCATCC others(13): Show |
A | 1 | a0002c0003t0001g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.67+9113_67+9132del others(20): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700522 | ||||||
| chrX:2700561 | T | TATCC | 2 | a0002c0003t0001g0205 a0002c0003t0001g0206 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.67+9155_67+9158dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700561 | ||||||
| chrX:2700643 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+9216C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700643 | |||||||
| chrX:2700784 | A | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+9357A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700784 | |||||||
| chrX:2700797 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0038 others(13): Show |
16 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+9370T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700797 | |||||||
| chrX:2701207 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+9780G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701207 | |||||||
| chrX:2701245 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+9818A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701245 | |||||||
| chrX:2701291 | C | G | 1 | a0002c0003t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+9864C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701291 | |||||||
| chrX:2701298 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9871A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701298 | |||||||
| chrX:2701381 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0038 others(13): Show |
16 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+9954T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701381 | |||||||
| chrX:2701430 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+10003G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701430 | |||||||
| chrX:2701436 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.67+10009T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701436 | |||||||
| chrX:2701483 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+10056A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701483 | |||||||
| chrX:2701585 | GCCT | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10160_67+10162d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2701585 | ||||||
| chrX:2701589 | C | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10162C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701589 | |||||||
| chrX:2701590 | T | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10163T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701590 | |||||||
| chrX:2701613 | T | G | 99 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0073 others(96): Show |
101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.67+10186T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701613 | |||||||
| chrX:2701721 | C | T | 3 | a0003c0008t0004g0086 a0003c0008t0004g0087 a0003c0008t0004g0088 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10294C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701721 | |||||||
| chrX:2702007 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.67+10580A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702007 | |||||||
| chrX:2702051 | TA | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+10626delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2702051 | ||||||
| chrX:2702130 | A | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10703A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702130 | |||||||
| chrX:2702174 | C | T | 3 | a0001c0001t0001g0203 a0001c0002t0001g0124 a0001c0012t0001g0194 |
3 | HG02809.hp2 HG03486.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.67+10747C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702174 | |||||||
| chrX:2702187 | G | C | 3 | a0003c0008t0004g0086 a0003c0008t0004g0087 a0003c0008t0004g0088 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10760G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702187 | |||||||
| chrX:2702284 | A | G | 3 | a0003c0008t0004g0086 a0003c0008t0004g0087 a0003c0008t0004g0088 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10857A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702284 | |||||||
| chrX:2702294 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67+10867C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702294 | |||||||
| chrX:2702426 | CAAT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0038 others(10): Show |
13 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+11000_67+11002d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702426 | |||||||
| chrX:2702449 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11022G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702449 | |||||||
| chrX:2702469 | T | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.67+11042T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702469 | |||||||
| chrX:2702499 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.67+11072C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702499 | |||||||
| chrX:2702595 | C | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11168C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702595 | |||||||
| chrX:2702620 | T | C | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+11193T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702620 | |||||||
| chrX:2702764 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67+11337C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702764 | |||||||
| chrX:2702779 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0183 |
3 | NA18939.hp1 NA18998.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.67+11352A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702779 | |||||||
| chrX:2702781 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0070 others(17): Show |
20 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11354T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702781 | |||||||
| chrX:2702816 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0183 |
3 | NA18939.hp1 NA18998.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.67+11389C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702816 | |||||||
| chrX:2702818 | T | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0070 others(17): Show |
20 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11391T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702818 | |||||||
| chrX:2702977 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-11445C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702977 | |||||||
| chrX:2703035 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG01891.hp2 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.68-11387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703035 | |||||||
| chrX:2703063 | A | G | 2 | a0002c0003t0001g0205 a0002c0003t0001g0206 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.68-11359A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703063 | |||||||
| chrX:2703069 | G | C | 6 | a0001c0001t0001g0108 a0001c0001t0002g0100 a0001c0001t0002g0101 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-11353G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703069 | |||||||
| chrX:2703078 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0002g0097 others(2): Show |
5 | HG02622.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-11344C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703078 | |||||||
| chrX:2703079 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.68-11343A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703079 | |||||||
| chrX:2703106 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-11316T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703106 | |||||||
| chrX:2703245 | G | A | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.68-11177G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703245 | |||||||
| chrX:2703287 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.68-11135G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703287 | |||||||
| chrX:2703371 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.68-11051G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703371 | |||||||
| chrX:2703417 | G | A | 130 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0042 others(127): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.68-11005G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703417 | |||||||
| chrX:2703444 | A | G | 1 | a0001c0004t0001g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-10978A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703444 | |||||||
| chrX:2703524 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0170 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.68-10898C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703524 | |||||||
| chrX:2703587 | TAAC | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0102 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-10832_68-10830d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703587 | ||||||
| chrX:2703602 | T | TTG | 4 | a0001c0001t0001g0195 a0001c0001t0006g0199 a0003c0009t0001g0191 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10819_68-10818i others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703602 | ||||||
| chrX:2703603 | TAA | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0002c0003t0001g0005 |
3 | HG01070.hp1 HG01071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-10818_68-10817d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703603 | |||||||
| chrX:2703604 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10818A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703604 | |||||||
| chrX:2703605 | A | AGT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0059 others(46): Show |
50 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.68-10772_68-10771d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGT | 14 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0064 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-10774_68-10771d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGTGT | 4 | a0001c0001t0001g0094 a0001c0002t0001g0112 a0001c0007t0001g0143 others(1): Show |
4 | HG02630.hp2 NA19077.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10776_68-10771d others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0073 a0001c0002t0001g0154 a0001c0002t0001g0157 |
3 | HG02165.hp2 NA19084.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.68-10778_68-10771d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGTGTG others(3): Show |
8 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0005g0092 others(5): Show |
10 | HG01884.hp2 NA18965.hp1 NA18972.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-10780_68-10771d others(12): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0075 a0001c0001t0001g0136 a0001c0001t0001g0138 others(1): Show |
4 | HG02559.hp1 NA18985.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10782_68-10771d others(14): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-10784_68-10771d others(16): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10817A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703605 | |||||||
| chrX:2703605 | AGT | A | 18 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0054 others(15): Show |
18 | HG00558.hp1 HG00735.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-10772_68-10771d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | AGTGT | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-10774_68-10771d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | AGTGTGT | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0070 a0001c0001t0001g0099 others(5): Show |
8 | HG00544.hp2 HG01123.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-10776_68-10771d others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-10780_68-10771d others(12): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0211 |
2 | HG06807.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.68-10782_68-10771d others(14): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703605 | AGTGTGTG others(17): Show |
A | 4 | a0001c0001t0002g0100 a0003c0008t0004g0086 a0003c0008t0004g0087 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10794_68-10771d others(26): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | ||||||
| chrX:2703663 | C | A | 1 | a0001c0001t0002g0187 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.68-10759C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703663 | |||||||
| chrX:2703829 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10593C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703829 | |||||||
| chrX:2703896 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0095 others(5): Show |
8 | HG02622.hp2 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10526G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703896 | |||||||
| chrX:2704041 | T | C | 99 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(96): Show |
101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-10381T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704041 | |||||||
| chrX:2704165 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.68-10257A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704165 | |||||||
| chrX:2704219 | G | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(125): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.68-10203G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704219 | |||||||
| chrX:2704377 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-10045C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704377 | |||||||
| chrX:2704396 | G | GCAGTTTA others(2): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10023_68-10015d others(11): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704396 | ||||||
| chrX:2704415 | A | C | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-10007A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704415 | |||||||
| chrX:2704606 | C | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.68-9816C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704606 | |||||||
| chrX:2704624 | T | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(128): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.68-9798T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704624 | |||||||
| chrX:2704750 | G | C | 1 | a0001c0001t0005g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-9672G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704750 | |||||||
| chrX:2704904 | G | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0005g0034 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-9518G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704904 | |||||||
| chrX:2704936 | A | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0038 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-9486A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704936 | |||||||
| chrX:2705002 | A | G | 43 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0108 others(40): Show |
43 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.68-9420A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705002 | |||||||
| chrX:2705052 | C | T | 1 | a0001c0005t0001g0218 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68-9370C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705052 | |||||||
| chrX:2705069 | A | G | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-9353A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705069 | |||||||
| chrX:2705112 | G | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0042 others(84): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.68-9310G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705112 | |||||||
| chrX:2705152 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0170 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.68-9270C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705152 | |||||||
| chrX:2705228 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-9194G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705228 | |||||||
| chrX:2705314 | G | A | 1 | a0002c0006t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-9108G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705314 | |||||||
| chrX:2705382 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.68-9040A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705382 | |||||||
| chrX:2705504 | C | T | 98 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0073 others(95): Show |
100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.68-8918C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705504 | |||||||
| chrX:2705669 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8753C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705669 | |||||||
| chrX:2705731 | T | C | 1 | a0001c0010t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-8691T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705731 | |||||||
| chrX:2705906 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8516G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705906 | |||||||
| chrX:2706040 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-8382C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706040 | |||||||
| chrX:2706063 | G | GA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0091 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-8346dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | ||||||
| chrX:2706063 | G | GAA | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(121): Show |
127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.68-8347_68-8346dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | ||||||
| chrX:2706079 | G | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0102 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-8343G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706079 | |||||||
| chrX:2706097 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-8325C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706097 | |||||||
| chrX:2706145 | T | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(123): Show |
129 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.68-8277T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706145 | |||||||
| chrX:2706156 | G | C | 1 | a0001c0002t0001g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.68-8266G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706156 | |||||||
| chrX:2706183 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8239C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706183 | |||||||
| chrX:2706354 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
179 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-8068T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706354 | |||||||
| chrX:2706368 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.68-8054G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706368 | |||||||
| chrX:2706426 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.68-7996A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706426 | |||||||
| chrX:2706483 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-7939C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706483 | |||||||
| chrX:2706666 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7756G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706666 | |||||||
| chrX:2706731 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(4): Show |
7 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-7691G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706731 | |||||||
| chrX:2706770 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.68-7652T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706770 | |||||||
| chrX:2706816 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-7606T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706816 | |||||||
| chrX:2706829 | A | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-7593A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706829 | |||||||
| chrX:2706888 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-7534T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706888 | |||||||
| chrX:2706889 | C | T | 2 | a0001c0001t0001g0065 a0004c0011t0007g0013 |
2 | HG01071.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.68-7533C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706889 | |||||||
| chrX:2706890 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-7532G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706890 | |||||||
| chrX:2707055 | C | T | 2 | a0001c0002t0001g0123 a0002c0006t0001g0122 |
2 | NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.68-7367C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707055 | |||||||
| chrX:2707056 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(4): Show |
7 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-7366G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707056 | |||||||
| chrX:2707174 | A | G | 4 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0002g0025 others(1): Show |
4 | HG00733.hp2 HG00735.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-7248A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707174 | |||||||
| chrX:2707244 | C | T | 6 | a0001c0002t0001g0135 a0001c0002t0001g0150 a0001c0002t0001g0154 others(3): Show |
6 | NA18977.hp1 NA18981.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7178C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707244 | |||||||
| chrX:2707329 | C | CAAAAG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(62): Show |
65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.68-7073_68-7069dup others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | ||||||
| chrX:2707329 | C | CAAAAGAA others(3): Show |
34 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(31): Show |
34 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.68-7078_68-7069dup others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | ||||||
| chrX:2707329 | CAAAAG | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(45): Show |
50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-7073_68-7069del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | ||||||
| chrX:2707329 | CAAAAGAA others(3): Show |
C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-7078_68-7069del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | ||||||
| chrX:2707349 | G | GAAAAGAA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0051 |
3 | HG01516.hp1 HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.68-7069_68-7068ins others(7): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707349 | ||||||
| chrX:2707378 | A | G | 1 | a0001c0010t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-7044A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707378 | |||||||
| chrX:2707402 | C | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.68-7020C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707402 | |||||||
| chrX:2707403 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.68-7019C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707403 | |||||||
| chrX:2707443 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-6979G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707443 | |||||||
| chrX:2707502 | G | GT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(3): Show |
6 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-6914dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707502 | ||||||
| chrX:2707679 | T | C | 6 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0100 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-6743T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707679 | |||||||
| chrX:2707725 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(57): Show |
62 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-6697G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707725 | |||||||
| chrX:2707881 | G | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(51): Show |
56 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-6541G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707881 | |||||||
| chrX:2707888 | T | C | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-6534T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707888 | |||||||
| chrX:2707984 | G | C | 1 | a0002c0006t0001g0016 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.68-6438G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707984 | |||||||
| chrX:2708102 | TACACCTG others(20): Show |
T | 3 | a0001c0001t0001g0107 a0001c0004t0001g0153 a0001c0004t0002g0081 |
3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-6301_68-6275del others(27): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2708102 | ||||||
| chrX:2708119 | C | T | 2 | a0001c0001t0001g0175 a0001c0010t0001g0201 |
2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68-6303C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708119 | |||||||
| chrX:2708121 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.68-6301T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708121 | |||||||
| chrX:2708187 | A | G | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-6235A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708187 | |||||||
| chrX:2708301 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-6121A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708301 | |||||||
| chrX:2708397 | A | G | 1 | a0001c0010t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-6025A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708397 | |||||||
| chrX:2708497 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0193 |
2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-5925A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708497 | |||||||
| chrX:2708661 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
178 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.68-5761A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708661 | |||||||
| chrX:2708812 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0002c0003t0001g0098 others(1): Show |
4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-5610C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708812 | |||||||
| chrX:2708819 | C | T | 3 | a0001c0001t0001g0107 a0001c0004t0001g0153 a0001c0004t0002g0081 |
3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-5603C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708819 | |||||||
| chrX:2708881 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.68-5541G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708881 | |||||||
| chrX:2708933 | C | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(45): Show |
50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-5489C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708933 | |||||||
| chrX:2708934 | A | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(45): Show |
50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-5488A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708934 | |||||||
| chrX:2709126 | G | A | 5 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(2): Show |
5 | HG02683.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-5296G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709126 | |||||||
| chrX:2709203 | A | ACATGCAT others(24): Show |
31 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-5205_68-5175dup others(31): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709203 | ||||||
| chrX:2709280 | G | A | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-5142G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709280 | |||||||
| chrX:2709310 | GCA | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-5109_68-5108del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709310 | ||||||
| chrX:2709546 | C | CAT | 4 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0001g0203 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4871_68-4870dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709546 | ||||||
| chrX:2709578 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-4844A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709578 | |||||||
| chrX:2709600 | GCA | G | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0172 others(3): Show |
6 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4816_68-4815del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709600 | ||||||
| chrX:2709608 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68-4814G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709608 | |||||||
| chrX:2709619 | G | C | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-4803G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709619 | |||||||
| chrX:2709642 | C | T | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-4780C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709642 | |||||||
| chrX:2709650 | T | G | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.68-4772T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709650 | |||||||
| chrX:2709663 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.68-4759T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709663 | |||||||
| chrX:2709669 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0138 |
2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.68-4753T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709669 | |||||||
| chrX:2709697 | A | AACATAGA others(15): Show |
40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
41 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.68-4714_68-4693dup others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709697 | ||||||
| chrX:2709708 | A | ACACATGC others(15): Show |
1 | a0001c0001t0002g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-4693_68-4672dup others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709708 | ||||||
| chrX:2709708 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4714A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709708 | |||||||
| chrX:2709708 | ACACATGC others(15): Show |
A | 1 | a0001c0002t0001g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.68-4693_68-4672del others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709708 | ||||||
| chrX:2709730 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4692G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709730 | |||||||
| chrX:2709746 | A | G | 1 | a0001c0010t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-4676A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709746 | |||||||
| chrX:2709788 | C | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.68-4634C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709788 | |||||||
| chrX:2709865 | A | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4557A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709865 | |||||||
| chrX:2709902 | G | C | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-4520G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709902 | |||||||
| chrX:2709944 | A | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0091 a0001c0001t0001g0193 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-4478A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709944 | |||||||
| chrX:2710018 | C | T | 2 | a0001c0001t0001g0175 a0001c0012t0001g0194 |
2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.68-4404C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710018 | |||||||
| chrX:2710050 | G | A | 1 | a0002c0003t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.68-4372G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710050 | |||||||
| chrX:2710088 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-4334A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710088 | |||||||
| chrX:2710110 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-4312C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710110 | |||||||
| chrX:2710160 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): Show |
55 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.68-4262A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710160 | |||||||
| chrX:2710165 | G | A | 2 | a0003c0009t0001g0191 a0003c0009t0001g0192 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.68-4257G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710165 | |||||||
| chrX:2710175 | T | TC | 174 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.68-4246dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710175 | ||||||
| chrX:2710265 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4157C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710265 | |||||||
| chrX:2710281 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0051 |
4 | HG01516.hp1 HG01517.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4141A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710281 | |||||||
| chrX:2710305 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-4117T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710305 | |||||||
| chrX:2710375 | A | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.68-4047A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710375 | |||||||
| chrX:2710415 | G | A | 1 | a0002c0003t0001g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.68-4007G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710415 | |||||||
| chrX:2710438 | G | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-3984G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710438 | |||||||
| chrX:2710442 | A | G | 3 | a0001c0001t0001g0107 a0001c0004t0001g0153 a0001c0004t0002g0081 |
3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3980A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710442 | |||||||
| chrX:2710492 | GTACTT | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(45): Show |
50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-3923_68-3919del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710492 | ||||||
| chrX:2710503 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68-3919T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710503 | |||||||
| chrX:2710514 | G | GTTT | 11 | a0001c0001t0001g0107 a0001c0001t0001g0169 a0001c0001t0001g0175 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-3901_68-3899dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | ||||||
| chrX:2710514 | G | GTTTT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-3902_68-3899dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | ||||||
| chrX:2710735 | C | T | 3 | a0001c0001t0001g0107 a0001c0004t0001g0153 a0001c0004t0002g0081 |
3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3687C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710735 | |||||||
| chrX:2710768 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0006g0199 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-3654A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710768 | |||||||
| chrX:2710774 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-3648G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710774 | |||||||
| chrX:2710867 | C | CT | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(132): Show |
138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.68-3534dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | ||||||
| chrX:2710867 | C | CTT | 15 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0161 others(12): Show |
15 | HG00408.hp2 HG00741.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-3535_68-3534dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | ||||||
| chrX:2710907 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-3515G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710907 | |||||||
| chrX:2710950 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(99): Show |
105 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.68-3472A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710950 | |||||||
| chrX:2711037 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.68-3385A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711037 | |||||||
| chrX:2711042 | T | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0002g0084 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-3380T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711042 | |||||||
| chrX:2711061 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(8): Show |
11 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-3361C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711061 | |||||||
| chrX:2711134 | G | A | 2 | a0001c0002t0001g0017 a0001c0007t0001g0200 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.68-3288G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711134 | |||||||
| chrX:2711146 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-3276C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711146 | |||||||
| chrX:2711249 | A | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02165.hp1 NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.68-3173A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711249 | |||||||
| chrX:2711259 | T | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-3163T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711259 | |||||||
| chrX:2711410 | TA | T | 3 | a0001c0001t0001g0002 a0001c0001t0002g0084 a0001c0001t0002g0085 |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3011delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711410 | |||||||
| chrX:2711411 | AT | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
46 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.68-3009delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711411 | ||||||
| chrX:2711412 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0002g0084 a0001c0001t0002g0085 |
4 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3010T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | |||||||
| chrX:2711412 | T | TA | 4 | a0001c0001t0001g0053 a0001c0001t0001g0220 a0001c0001t0002g0033 others(1): Show |
4 | HG02109.hp2 HG02155.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-3010_68-3009ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | |||||||
| chrX:2711412 | T | TATA | 2 | a0001c0004t0001g0153 a0001c0004t0002g0081 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3010_68-3009ins others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | |||||||
| chrX:2711414 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68-3008A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711414 | |||||||
| chrX:2711435 | ATGTG | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0072 others(45): Show |
50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-2983_68-2980del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711435 | ||||||
| chrX:2711441 | G | GTA | 13 | a0001c0001t0001g0070 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-2969_68-2968dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711441 | ||||||
| chrX:2711470 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0188 |
3 | HG02155.hp1 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.68-2952G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711470 | |||||||
| chrX:2711471 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0188 |
3 | HG02155.hp1 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.68-2951G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711471 | |||||||
| chrX:2711753 | AGGTTGGC others(10): Show |
A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-2666_68-2650del others(17): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711753 | ||||||
| chrX:2711766 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0006g0223 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-2656G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711766 | |||||||
| chrX:2711767 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.68-2655C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711767 | |||||||
| chrX:2711836 | T | A | 1 | a0001c0001t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.68-2586T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711836 | |||||||
| chrX:2711837 | C | G | 1 | a0001c0001t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.68-2585C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711837 | |||||||
| chrX:2711915 | G | A | 1 | a0003c0008t0004g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.68-2507G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711915 | |||||||
| chrX:2711999 | C | T | 3 | a0001c0005t0001g0131 a0001c0005t0001g0132 a0001c0005t0001g0133 |
3 | NA19006.hp1 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.68-2423C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711999 | |||||||
| chrX:2712013 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-2409G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712013 | |||||||
| chrX:2712068 | G | T | 3 | a0001c0001t0001g0107 a0001c0004t0001g0153 a0001c0004t0002g0081 |
3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-2354G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712068 | |||||||
| chrX:2712107 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-2315G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712107 | |||||||
| chrX:2712203 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-2219C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712203 | |||||||
| chrX:2712340 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
41 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.68-2082G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712340 | |||||||
| chrX:2712406 | G | A | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-2016G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712406 | |||||||
| chrX:2712422 | GA | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.68-1992delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712422 | ||||||
| chrX:2712430 | AT | A | 2 | a0001c0001t0001g0176 a0001c0001t0010g0177 |
2 | HG02080.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.68-1991delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712430 | |||||||
| chrX:2712480 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(59): Show |
62 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-1942G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712480 | |||||||
| chrX:2712510 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-1912C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712510 | |||||||
| chrX:2712579 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
195 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.68-1843A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712579 | |||||||
| chrX:2712660 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-1762G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712660 | |||||||
| chrX:2712766 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1656C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712766 | |||||||
| chrX:2712776 | TACAC | T | 2 | a0002c0003t0001g0205 a0002c0003t0001g0206 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.68-1636_68-1633del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712776 | ||||||
| chrX:2712804 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0002g0084 a0001c0001t0002g0085 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1618C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712804 | |||||||
| chrX:2712819 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1603C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712819 | |||||||
| chrX:2712858 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-1564C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712858 | |||||||
| chrX:2712975 | TACAC | T | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-1441_68-1438del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712975 | ||||||
| chrX:2712994 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(113): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.68-1428A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712994 | |||||||
| chrX:2713009 | C | T | 10 | a0001c0001t0001g0070 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-1413C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713009 | |||||||
| chrX:2713032 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0106 |
2 | HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.68-1390A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713032 | |||||||
| chrX:2713063 | CAT | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1357_68-1356del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713063 | ||||||
| chrX:2713077 | C | T | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0112 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-1345C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713077 | |||||||
| chrX:2713085 | C | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0083 others(18): Show |
21 | HG00741.hp1 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.68-1337C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713085 | |||||||
| chrX:2713104 | CAT | C | 2 | a0002c0003t0001g0098 a0003c0008t0004g0071 |
2 | HG03669.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-1314_68-1313del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713104 | ||||||
| chrX:2713131 | TACAC | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(115): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.68-1285_68-1282del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713131 | ||||||
| chrX:2713221 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0220 a0001c0001t0006g0223 |
3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1201C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713221 | |||||||
| chrX:2713232 | A | G | 10 | a0001c0001t0001g0070 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-1190A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713232 | |||||||
| chrX:2713315 | AAC | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.68-1102_68-1101del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713315 | ||||||
| chrX:2713339 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-1083A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713339 | |||||||
| chrX:2713400 | CACAT | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(114): Show |
120 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.68-1017_68-1014del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713400 | ||||||
| chrX:2713459 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(115): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.68-963T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713459 | |||||||
| chrX:2713682 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-740G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713682 | |||||||
| chrX:2713844 | A | G | 1 | a0001c0002t0001g0021 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68-578A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713844 | |||||||
| chrX:2714148 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(90): Show |
96 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.68-274A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2714148 | |||||||
| chrX:2714231 | A | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(97): Show |
101 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.68-191A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2714231 | |||||||
| chrX:2714293 | T | TGTAAATT others(2452): Show |
1 | a0001c0001t0006g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68-117_68-116insTT others(2457): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2714293 | ||||||
| chrX:2714293 | T | TGTAAATT others(2452): Show |
1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-117_68-116insTT others(2457): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2714293 | ||||||
| chrX:2714483 | C | T | 1 | a0001c0004t0002g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+29C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714483 | |||||||
| chrX:2714560 | A | G | 1 | a0001c0004t0001g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.100+106A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714560 | |||||||
| chrX:2714781 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(93): Show |
97 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.100+327G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714781 | |||||||
| chrX:2715035 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.100+581T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715035 | |||||||
| chrX:2715066 | A | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0038 others(60): Show |
63 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.100+612A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715066 | |||||||
| chrX:2715091 | G | A | 2 | a0001c0001t0001g0170 a0001c0010t0001g0201 |
2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+637G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715091 | |||||||
| chrX:2715094 | G | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0030 others(56): Show |
59 | HG00741.hp1 HG01175.hp2 HG01346.hp2 others(56): Show |
intron_variant | MODIFIER | c.100+640G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715094 | |||||||
| chrX:2715198 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.100+744C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715198 | |||||||
| chrX:2715210 | C | CT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0078 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.100+757dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715210 | ||||||
| chrX:2715212 | A | G | 22 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0067 others(19): Show |
23 | HG00544.hp1 HG00558.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+758A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715212 | |||||||
| chrX:2715227 | TTGTCATC others(23): Show |
T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100+776_100+805del others(30): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715227 | ||||||
| chrX:2715253 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(60): Show |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.100+799G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715253 | |||||||
| chrX:2715412 | G | A | 1 | a0001c0004t0002g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+958G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715412 | |||||||
| chrX:2715433 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
83 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.100+979A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715433 | |||||||
| chrX:2715566 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
118 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+1112A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715566 | |||||||
| chrX:2715583 | C | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
118 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+1129C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715583 | |||||||
| chrX:2715601 | G | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
13 | HG00741.hp1 HG02109.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.100+1147G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715601 | |||||||
| chrX:2715628 | AC | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0195 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1176delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715628 | ||||||
| chrX:2715648 | A | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0073 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+1194A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715648 | |||||||
| chrX:2715670 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0073 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+1216G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715670 | |||||||
| chrX:2715731 | C | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0001g0160 others(9): Show |
12 | HG01175.hp2 HG01346.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+1277C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715731 | |||||||
| chrX:2715760 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.100+1306T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715760 | |||||||
| chrX:2715763 | C | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.100+1309C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715763 | |||||||
| chrX:2715763 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0220 others(2): Show |
5 | HG00741.hp1 HG02109.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+1309C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715763 | |||||||
| chrX:2715792 | G | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
112 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.100+1338G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715792 | |||||||
| chrX:2715939 | A | G | 69 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0062 others(66): Show |
70 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.100+1485A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715939 | |||||||
| chrX:2716016 | A | AT | 5 | a0001c0001t0001g0188 a0001c0002t0001g0130 a0001c0004t0001g0171 others(2): Show |
5 | HG01981.hp2 HG02293.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-1571dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716016 | ||||||
| chrX:2716016 | AT | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-1571delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716016 | ||||||
| chrX:2716254 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.101-1351T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716254 | |||||||
| chrX:2716297 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-1308A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716297 | |||||||
| chrX:2716310 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.101-1295C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716310 | |||||||
| chrX:2716342 | C | CA | 52 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0047 others(49): Show |
52 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.101-1263_101-1262i others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716342 | |||||||
| chrX:2716352 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | NA19002.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.101-1253T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716352 | |||||||
| chrX:2716367 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0195 others(2): Show |
5 | HG02451.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-1238C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716367 | |||||||
| chrX:2716368 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1237G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716368 | |||||||
| chrX:2716393 | G | C | 1 | a0001c0012t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-1212G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716393 | |||||||
| chrX:2716463 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-1142A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716463 | |||||||
| chrX:2716596 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-1009A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716596 | |||||||
| chrX:2716722 | C | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-883C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716722 | |||||||
| chrX:2716780 | A | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0047 others(58): Show |
62 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-825A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716780 | |||||||
| chrX:2716879 | G | A | 1 | a0001c0002t0001g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-726G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716879 | |||||||
| chrX:2717044 | C | G | 2 | a0002c0003t0001g0205 a0002c0003t0001g0206 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.101-561C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717044 | |||||||
| chrX:2717048 | G | A | 10 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-557G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717048 | |||||||
| chrX:2717084 | A | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.101-521A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717084 | |||||||
| chrX:2717087 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-518C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717087 | |||||||
| chrX:2717203 | C | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0047 others(50): Show |
54 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.101-402C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717203 | |||||||
| chrX:2717222 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.101-383C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717222 | |||||||
| chrX:2717241 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101-364G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717241 | |||||||
| chrX:2717347 | C | CA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0031 others(31): Show |
34 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.101-242dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | ||||||
| chrX:2717347 | C | CAA | 42 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0046 others(39): Show |
42 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.101-243_101-242dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | ||||||
| chrX:2717347 | C | CAAA | 17 | a0001c0001t0001g0062 a0001c0001t0001g0103 a0001c0001t0001g0106 others(14): Show |
20 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-244_101-242dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | ||||||
| chrX:2717347 | CAA | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-243_101-242del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | ||||||
| chrX:2717379 | C | T | 1 | a0004c0013t0007g0019 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.101-226C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717379 | |||||||
| chrX:2717447 | T | C | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0103 others(15): Show |
21 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.101-158T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717447 | |||||||
| chrX:2717448 | G | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.101-157G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717448 | |||||||
| chrX:2717579 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101-26C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717579 | |||||||
| chrX:2717905 | G | A | 5 | a0001c0001t0001g0190 a0001c0001t0002g0084 a0001c0001t0002g0085 others(2): Show |
5 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+253G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2717905 | |||||||
| chrX:2717937 | C | CT | 9 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0169 others(6): Show |
9 | HG00408.hp1 HG01981.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+306dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | ||||||
| chrX:2717937 | CT | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.148+306delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | ||||||
| chrX:2717937 | CTTT | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.148+304_148+306del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | ||||||
| chrX:2717996 | C | A | 2 | a0001c0001t0001g0108 a0003c0008t0004g0088 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148+344C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2717996 | |||||||
| chrX:2718034 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.148+382C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718034 | |||||||
| chrX:2718041 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.148+389A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718041 | |||||||
| chrX:2718146 | G | A | 1 | a0001c0004t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.148+494G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718146 | |||||||
| chrX:2718210 | G | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.148+558G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718210 | |||||||
| chrX:2718340 | T | C | 1 | a0001c0002t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.148+688T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718340 | |||||||
| chrX:2718351 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.148+699G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718351 | |||||||
| chrX:2718369 | C | CT | 5 | a0001c0001t0001g0011 a0001c0002t0001g0021 a0001c0002t0001g0130 others(2): Show |
5 | HG00733.hp1 HG01346.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+734dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718369 | ||||||
| chrX:2718373 | T | C | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0103 others(14): Show |
20 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+721T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718373 | |||||||
| chrX:2718494 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.148+842A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718494 | |||||||
| chrX:2718499 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.148+847G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718499 | |||||||
| chrX:2718615 | C | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(23): Show |
29 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.148+963C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718615 | |||||||
| chrX:2718681 | C | G | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-980C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718681 | |||||||
| chrX:2718739 | C | G | 2 | a0001c0001t0001g0108 a0003c0008t0004g0088 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149-922C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718739 | |||||||
| chrX:2718973 | G | A | 6 | a0001c0001t0001g0078 a0001c0001t0001g0108 a0001c0001t0002g0097 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-688G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718973 | |||||||
| chrX:2719048 | A | G | 1 | a0001c0001t0002g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.149-613A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719048 | |||||||
| chrX:2719189 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.149-472T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719189 | |||||||
| chrX:2719259 | A | G | 2 | a0001c0001t0001g0108 a0003c0008t0004g0088 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149-402A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719259 | |||||||
| chrX:2719398 | T | TC | 119 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.149-259dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2719398 | ||||||
| chrX:2719466 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-195C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719466 | |||||||
| chrX:2719780 | T | A | 5 | a0001c0001t0001g0078 a0001c0001t0002g0097 a0001c0001t0002g0100 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+75T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2719780 | |||||||
| chrX:2719960 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.193+255G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2719960 | |||||||
| chrX:2720071 | T | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0030 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.194-285T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720071 | |||||||
| chrX:2720268 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.194-88G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720268 | |||||||
| chrX:2720319 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-37G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720319 | |||||||
| chrX:2720458 | G | A | 45 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0076 others(42): Show |
45 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.262+34G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720458 | |||||||
| chrX:2720620 | C | CT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(93): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.262+218dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | ||||||
| chrX:2720620 | C | CTT | 12 | a0001c0001t0001g0091 a0001c0001t0001g0103 a0001c0001t0001g0136 others(9): Show |
12 | HG02615.hp1 HG02615.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+217_262+218dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | ||||||
| chrX:2720620 | CT | C | 32 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0076 others(29): Show |
32 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.262+218delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | ||||||
| chrX:2720620 | CTT | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0078 a0001c0001t0002g0097 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+217_262+218del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | ||||||
| chrX:2720777 | G | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(68): Show |
74 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.262+353G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720777 | |||||||
| chrX:2720786 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.262+362G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720786 | |||||||
| chrX:2720986 | T | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.262+562T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720986 | |||||||
| chrX:2721067 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+643C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721067 | |||||||
| chrX:2721119 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+695G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721119 | |||||||
| chrX:2721230 | A | T | 1 | a0001c0002t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.262+806A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721230 | |||||||
| chrX:2721286 | T | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.262+862T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721286 | |||||||
| chrX:2721374 | C | T | 2 | a0001c0001t0001g0108 a0003c0008t0004g0088 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262+950C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721374 | |||||||
| chrX:2721391 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0002g0033 others(2): Show |
5 | HG01884.hp1 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+967G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721391 | |||||||
| chrX:2721577 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.263-1050C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721577 | |||||||
| chrX:2721683 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263-944A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721683 | |||||||
| chrX:2721876 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.263-751G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721876 | |||||||
| chrX:2722148 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-479C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722148 | |||||||
| chrX:2722498 | C | G | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263-129C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722498 | |||||||
| chrX:2722545 | A | C | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.263-82A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722545 | |||||||
| chrX:2722739 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0002g0033 others(2): Show |
5 | HG01884.hp1 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+65A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722739 | |||||||
| chrX:2722810 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.310+136C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722810 | |||||||
| chrX:2722869 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0169 others(3): Show |
6 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+195C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722869 | |||||||
| chrX:2722876 | C | T | 1 | a0001c0007t0001g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.310+202C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722876 | |||||||
| chrX:2722968 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.310+294G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722968 | |||||||
| chrX:2722988 | A | G | 15 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(12): Show |
15 | HG00741.hp1 HG01169.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+314A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722988 | |||||||
| chrX:2722988 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+314A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722988 | |||||||
| chrX:2723015 | T | A | 1 | a0001c0002t0001g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.311-299T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723015 | |||||||
| chrX:2723025 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.311-289T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723025 | |||||||
| chrX:2723161 | A | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0047 others(47): Show |
51 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.311-153A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723161 | |||||||
| chrX:2723211 | C | T | 2 | a0001c0001t0001g0108 a0003c0008t0004g0088 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.311-103C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723211 | |||||||
| chrX:2723245 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-69A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723245 | |||||||
| chrX:2723279 | A | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(8): Show |
11 | HG01884.hp1 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-35A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723279 | |||||||
| chrX:2723402 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.361+38C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723402 | |||||||
| chrX:2723412 | A | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+48A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723412 | |||||||
| chrX:2723465 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0002g0101 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.361+101C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723465 | |||||||
| chrX:2723532 | T | TC | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
86 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.361+173dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2723532 | ||||||
| chrX:2723561 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.361+197G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723561 | |||||||
| chrX:2723571 | C | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(18): Show |
24 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.361+207C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723571 | |||||||
| chrX:2723621 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0005g0092 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.361+257G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723621 | |||||||
| chrX:2723635 | G | A | 20 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(17): Show |
23 | HG01981.hp2 HG01993.hp2 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.361+271G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723635 | |||||||
| chrX:2723666 | C | T | 1 | a0001c0002t0002g0025 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.361+302C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723666 | |||||||
| chrX:2723781 | C | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+417C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723781 | |||||||
| chrX:2724037 | G | GGGAAGGA others(530): Show |
14 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(11): Show |
15 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.361+674_361+675ins others(537): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724037 | ||||||
| chrX:2724037 | G | GGGAAGGA others(582): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+674_361+675ins others(589): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724037 | ||||||
| chrX:2724150 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.361+786A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724150 | |||||||
| chrX:2724228 | A | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0056 others(17): Show |
21 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.361+864A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724228 | |||||||
| chrX:2724361 | G | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(13): Show |
17 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+997G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724361 | |||||||
| chrX:2724525 | C | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
85 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.361+1161C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724525 | |||||||
| chrX:2724566 | C | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(29): Show |
33 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.361+1202C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724566 | |||||||
| chrX:2724766 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+1402G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724766 | |||||||
| chrX:2724771 | C | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
84 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.361+1407C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724771 | |||||||
| chrX:2724897 | C | CA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0056 others(18): Show |
22 | HG00735.hp2 HG01993.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.362-1348dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724897 | ||||||
| chrX:2724897 | C | CAA | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0030 others(15): Show |
18 | HG01891.hp1 HG01981.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.362-1349_362-1348d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724897 | ||||||
| chrX:2724918 | C | A | 1 | a0001c0002t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.362-1342C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724918 | |||||||
| chrX:2724918 | CA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0060 others(10): Show |
13 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-1341delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724918 | |||||||
| chrX:2724991 | C | T | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362-1269C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724991 | |||||||
| chrX:2725050 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0051 others(30): Show |
34 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.362-1210A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725050 | |||||||
| chrX:2725098 | T | TA | 17 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(14): Show |
18 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.362-1147dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725098 | ||||||
| chrX:2725098 | TA | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0076 others(8): Show |
11 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-1147delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725098 | ||||||
| chrX:2725244 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.362-1016A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725244 | |||||||
| chrX:2725330 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
83 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.362-930T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725330 | |||||||
| chrX:2725444 | A | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(31): Show |
35 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.362-816A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725444 | |||||||
| chrX:2725468 | C | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0005g0034 others(1): Show |
4 | HG02896.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-792C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725468 | |||||||
| chrX:2725612 | TTTTTGTT others(3): Show |
T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(12): Show |
16 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.362-637_362-628del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725612 | ||||||
| chrX:2725652 | C | T | 13 | a0001c0004t0001g0015 a0001c0004t0001g0144 a0001c0004t0001g0145 others(10): Show |
13 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-608C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725652 | |||||||
| chrX:2725715 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0005g0034 |
3 | HG02976.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.362-545G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725715 | |||||||
| chrX:2725734 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(31): Show |
35 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.362-526C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725734 | |||||||
| chrX:2725878 | G | C | 17 | a0001c0004t0001g0015 a0001c0004t0001g0144 a0001c0004t0001g0145 others(14): Show |
17 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.362-382G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725878 | |||||||
| chrX:2725964 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG02723.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-296G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725964 | |||||||
| chrX:2725985 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362-275C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725985 | |||||||
| chrX:2726060 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.362-200G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2726060 | |||||||
| chrX:2726251 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362-9C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2726251 | |||||||
| chrX:2726475 | G | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(23): Show |
26 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.475+102G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726475 | |||||||
| chrX:2726690 | AGCC | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0193 others(24): Show |
28 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.475+320_475+322del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2726690 | ||||||
| chrX:2726693 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.475+320C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726693 | |||||||
| chrX:2726760 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.475+387T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726760 | |||||||
| chrX:2726769 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.475+396G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726769 | |||||||
| chrX:2726826 | T | TCAG | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
51 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.475+453_475+454ins others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726826 | |||||||
| chrX:2726894 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0056 others(7): Show |
10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+521G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726894 | |||||||
| chrX:2726928 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0056 others(7): Show |
10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+555G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726928 | |||||||
| chrX:2726933 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+560C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726933 | |||||||
| chrX:2726964 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+591C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726964 | |||||||
| chrX:2726998 | A | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.475+625A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726998 | |||||||
| chrX:2727019 | C | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+646C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727019 | |||||||
| chrX:2727061 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+688T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727061 | |||||||
| chrX:2727069 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+696A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727069 | |||||||
| chrX:2727131 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0203 a0001c0001t0002g0101 |
3 | HG02723.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.475+758C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727131 | |||||||
| chrX:2727257 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.475+884A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727257 | |||||||
| chrX:2727325 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.475+952G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727325 | |||||||
| chrX:2727464 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0056 others(7): Show |
10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+1091C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727464 | |||||||
| chrX:2727537 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+1164C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727537 | |||||||
| chrX:2727633 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0002g0101 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.475+1260C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727633 | |||||||
| chrX:2728111 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.475+1738G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728111 | |||||||
| chrX:2728158 | T | TACCTGGT others(1): Show |
10 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0056 others(7): Show |
10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+1786_475+1793d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728158 | ||||||
| chrX:2728200 | C | CT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0108 others(9): Show |
12 | HG00733.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.475+1849dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | ||||||
| chrX:2728200 | C | CTT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+1848_475+1849d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | ||||||
| chrX:2728200 | CT | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0072 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.475+1849delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | ||||||
| chrX:2728200 | CTTT | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0058 others(6): Show |
9 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.475+1847_475+1849d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | ||||||
| chrX:2728205 | T | TC | 3 | a0001c0001t0001g0067 a0001c0001t0010g0177 a0001c0002t0001g0166 |
3 | HG03704.hp1 HG03927.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.475+1832_475+1833i others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728205 | |||||||
| chrX:2728206 | T | C | 46 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(43): Show |
48 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.475+1833T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728206 | |||||||
| chrX:2728207 | T | C | 1 | a0001c0002t0003g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.475+1834T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728207 | |||||||
| chrX:2728270 | T | A | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475+1897T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728270 | |||||||
| chrX:2728392 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0169 a0001c0004t0001g0015 others(17): Show |
21 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.475+2019C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728392 | |||||||
| chrX:2728416 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+2043G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728416 | |||||||
| chrX:2728485 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0002t0001g0021 others(2): Show |
5 | HG01346.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+2112C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728485 | |||||||
| chrX:2728486 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+2113G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728486 | |||||||
| chrX:2728577 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.475+2204C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728577 | |||||||
| chrX:2728625 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.475+2252C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728625 | |||||||
| chrX:2728780 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.475+2407G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728780 | |||||||
| chrX:2728834 | C | CT | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(24): Show |
27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.475+2481dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | ||||||
| chrX:2728834 | C | CTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(10): Show |
13 | HG01346.hp1 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.475+2480_475+2481d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | ||||||
| chrX:2728834 | CT | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0076 others(30): Show |
34 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.475+2481delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | ||||||
| chrX:2728859 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.475+2486C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728859 | |||||||
| chrX:2728916 | A | AACCTCC | 81 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
82 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.475+2548_475+2549i others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728916 | ||||||
| chrX:2728924 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.475+2551G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728924 | |||||||
| chrX:2729380 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0058 others(15): Show |
18 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.475+3007T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729380 | |||||||
| chrX:2729396 | C | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.475+3023C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729396 | |||||||
| chrX:2729440 | TA | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.475+3069delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2729440 | ||||||
| chrX:2729453 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475+3080A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729453 | |||||||
| chrX:2729462 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0193 a0001c0001t0005g0034 |
3 | HG02976.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.475+3089C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729462 | |||||||
| chrX:2729608 | C | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
105 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.475+3235C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729608 | |||||||
| chrX:2729629 | A | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.475+3256A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729629 | |||||||
| chrX:2729635 | T | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+3262T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729635 | |||||||
| chrX:2729732 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.475+3359G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729732 | |||||||
| chrX:2729838 | T | C | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475+3465T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729838 | |||||||
| chrX:2729850 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.475+3477T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729850 | |||||||
| chrX:2729989 | C | G | 2 | a0001c0004t0002g0081 a0001c0010t0001g0201 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+3616C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729989 | |||||||
| chrX:2730014 | C | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0160 others(6): Show |
9 | HG00741.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+3641C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730014 | |||||||
| chrX:2730023 | G | A | 1 | a0002c0003t0001g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.475+3650G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730023 | |||||||
| chrX:2730054 | C | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
153 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.475+3681C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730054 | |||||||
| chrX:2730144 | A | G | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.475+3771A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730144 | |||||||
| chrX:2730175 | CT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0026 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.475+3817delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730175 | ||||||
| chrX:2730175 | CTT | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(74): Show |
78 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.475+3816_475+3817d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730175 | ||||||
| chrX:2730266 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+3893G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730266 | |||||||
| chrX:2730277 | ACT | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0046 others(20): Show |
23 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.475+3908_475+3909d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730277 | ||||||
| chrX:2730339 | A | AT | 34 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0042 others(31): Show |
34 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.475+3971dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730339 | ||||||
| chrX:2730362 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.475+3989C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730362 | |||||||
| chrX:2730406 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+4033T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730406 | |||||||
| chrX:2730461 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.475+4088C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730461 | |||||||
| chrX:2730490 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+4117A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730490 | |||||||
| chrX:2730547 | A | C | 17 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0172 others(14): Show |
17 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.475+4174A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730547 | |||||||
| chrX:2730604 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.475+4231C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730604 | |||||||
| chrX:2730830 | C | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0002t0001g0018 others(6): Show |
10 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+4457C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730830 | |||||||
| chrX:2730929 | C | CA | 10 | a0001c0001t0001g0080 a0001c0001t0001g0094 a0001c0001t0001g0107 others(7): Show |
10 | HG01081.hp1 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+4575dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | ||||||
| chrX:2730929 | C | CAA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(7): Show |
10 | HG00741.hp1 HG01516.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+4574_475+4575d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | ||||||
| chrX:2730929 | CA | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0026 others(79): Show |
82 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.475+4575delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | ||||||
| chrX:2730929 | CAA | C | 36 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0104 others(33): Show |
37 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.475+4574_475+4575d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | ||||||
| chrX:2730953 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.475+4580A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730953 | |||||||
| chrX:2731016 | C | T | 50 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0042 others(47): Show |
50 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.475+4643C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731016 | |||||||
| chrX:2731221 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.475+4848C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731221 | |||||||
| chrX:2731325 | T | C | 23 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
23 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.475+4952T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731325 | |||||||
| chrX:2731327 | C | T | 20 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.475+4954C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731327 | |||||||
| chrX:2731361 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0160 others(6): Show |
9 | HG00741.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+4988G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731361 | |||||||
| chrX:2731444 | G | A | 1 | a0002c0006t0001g0122 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.475+5071G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731444 | |||||||
| chrX:2731475 | A | G | 4 | a0002c0003t0001g0003 a0002c0003t0001g0155 a0002c0003t0001g0210 others(1): Show |
5 | HG01981.hp2 HG01993.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+5102A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731475 | |||||||
| chrX:2731547 | C | T | 2 | a0001c0004t0002g0081 a0001c0010t0001g0201 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+5174C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731547 | |||||||
| chrX:2731561 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.475+5188C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731561 | |||||||
| chrX:2731612 | A | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
118 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.475+5239A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731612 | |||||||
| chrX:2731754 | C | T | 3 | a0001c0001t0002g0101 a0001c0004t0002g0081 a0001c0010t0001g0201 |
3 | HG01884.hp1 HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+5381C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731754 | |||||||
| chrX:2731791 | C | T | 106 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0031 others(103): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.475+5418C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731791 | |||||||
| chrX:2731920 | G | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.475+5547G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731920 | |||||||
| chrX:2731970 | T | TA | 53 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0032 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.475+5610dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731970 | ||||||
| chrX:2731970 | T | TAA | 20 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.475+5609_475+5610d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731970 | ||||||
| chrX:2732080 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0083 others(12): Show |
15 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.475+5707A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732080 | |||||||
| chrX:2732183 | A | C | 1 | a0001c0001t0006g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475+5810A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732183 | |||||||
| chrX:2732197 | A | C | 2 | a0001c0001t0001g0057 a0001c0004t0001g0149 |
2 | HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.475+5824A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732197 | |||||||
| chrX:2732242 | C | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0031 others(51): Show |
54 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.475+5869C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732242 | |||||||
| chrX:2732269 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.475+5896A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732269 | |||||||
| chrX:2732298 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0108 a0001c0001t0006g0199 |
3 | HG01891.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.476-5902C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732298 | |||||||
| chrX:2732442 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.476-5758C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732442 | |||||||
| chrX:2732506 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-5694C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732506 | |||||||
| chrX:2732523 | T | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(84): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.476-5677T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732523 | |||||||
| chrX:2732555 | A | C | 1 | a0001c0002t0001g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.476-5645A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732555 | |||||||
| chrX:2732562 | C | CCT | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(49): Show |
53 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.476-5627_476-5626d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732562 | ||||||
| chrX:2732571 | C | CTT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0172 others(13): Show |
17 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.476-5628_476-5627i others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732571 | ||||||
| chrX:2732571 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0072 others(22): Show |
25 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.476-5629C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732571 | |||||||
| chrX:2732619 | CCTT | C | 27 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0001g0056 others(24): Show |
29 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-5574_476-5572d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732619 | ||||||
| chrX:2732675 | T | C | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5525T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732675 | |||||||
| chrX:2732676 | C | T | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5524C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732676 | |||||||
| chrX:2732721 | T | TCTTTCCT others(60): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0072 others(12): Show |
15 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-5457_476-5391d others(69): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732721 | ||||||
| chrX:2732768 | T | TC | 15 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0094 others(12): Show |
16 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.476-5428dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732768 | ||||||
| chrX:2732773 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-5427T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732773 | |||||||
| chrX:2732801 | CCTTT | C | 3 | a0001c0002t0001g0113 a0001c0002t0001g0154 a0001c0002t0001g0157 |
3 | HG02165.hp2 NA19084.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.476-5394_476-5391d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732801 | ||||||
| chrX:2732851 | G | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
157 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.476-5349G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732851 | |||||||
| chrX:2732869 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.476-5331T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732869 | |||||||
| chrX:2732902 | CTTCTTTC others(6): Show |
C | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.476-5296_476-5284d others(15): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732902 | ||||||
| chrX:2732938 | T | C | 1 | a0001c0002t0002g0025 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.476-5262T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732938 | |||||||
| chrX:2733059 | C | CCT | 47 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.476-5138_476-5137d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2733059 | ||||||
| chrX:2733072 | T | C | 1 | a0001c0004t0001g0153 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.476-5128T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733072 | |||||||
| chrX:2733085 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
41 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.476-5115C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733085 | |||||||
| chrX:2733149 | CTCTG | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(32): Show |
36 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.476-5047_476-5044d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2733149 | ||||||
| chrX:2733223 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-4977T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733223 | |||||||
| chrX:2733336 | G | T | 3 | a0001c0001t0006g0223 a0001c0004t0001g0153 a0003c0008t0004g0071 |
3 | HG02818.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4864G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733336 | |||||||
| chrX:2733476 | C | G | 1 | a0002c0006t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.476-4724C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733476 | |||||||
| chrX:2733484 | G | A | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-4716G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733484 | |||||||
| chrX:2733497 | C | T | 1 | a0002c0006t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.476-4703C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733497 | |||||||
| chrX:2733525 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
19 | HG00099.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.476-4675C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733525 | |||||||
| chrX:2733688 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4512T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733688 | |||||||
| chrX:2733706 | T | G | 2 | a0001c0001t0001g0220 a0003c0008t0004g0071 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.476-4494T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733706 | |||||||
| chrX:2733798 | G | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0031 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.476-4402G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733798 | |||||||
| chrX:2733846 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4354T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733846 | |||||||
| chrX:2733850 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4350C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733850 | |||||||
| chrX:2733887 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4313A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733887 | |||||||
| chrX:2733922 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.476-4278A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733922 | |||||||
| chrX:2733961 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0006g0223 a0002c0003t0001g0155 others(1): Show |
4 | HG01981.hp2 HG01993.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-4239G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733961 | |||||||
| chrX:2734065 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-4135C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734065 | |||||||
| chrX:2734374 | T | G | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-3826T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734374 | |||||||
| chrX:2734398 | C | G | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-3802C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734398 | |||||||
| chrX:2734538 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-3662T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734538 | |||||||
| chrX:2734620 | CT | C | 12 | a0001c0001t0001g0108 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
12 | HG01891.hp2 HG06807.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.476-3569delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734620 | ||||||
| chrX:2734704 | CT | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-3488delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734704 | ||||||
| chrX:2734729 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-3471C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734729 | |||||||
| chrX:2734956 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-3244G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734956 | |||||||
| chrX:2735057 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.476-3143T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735057 | |||||||
| chrX:2735210 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0006g0223 |
2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-2990C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735210 | |||||||
| chrX:2735382 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.476-2818C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735382 | |||||||
| chrX:2735390 | G | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0003c0008t0004g0086 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-2810G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735390 | |||||||
| chrX:2735511 | C | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.476-2689C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735511 | |||||||
| chrX:2735533 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.476-2667C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735533 | |||||||
| chrX:2735690 | G | A | 5 | a0001c0001t0002g0100 a0001c0001t0002g0105 a0001c0001t0002g0186 others(2): Show |
5 | HG01891.hp2 NA18941.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-2510G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735690 | |||||||
| chrX:2735848 | T | C | 6 | a0001c0001t0001g0108 a0001c0001t0006g0223 a0002c0003t0001g0005 others(3): Show |
6 | HG02004.hp2 HG02896.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-2352T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735848 | |||||||
| chrX:2735872 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
94 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.476-2328G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735872 | |||||||
| chrX:2735930 | C | T | 3 | a0001c0001t0001g0099 a0001c0002t0001g0128 a0001c0002t0001g0129 |
3 | HG01123.hp1 HG01123.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.476-2270C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735930 | |||||||
| chrX:2735985 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.476-2215G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735985 | |||||||
| chrX:2736018 | T | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0175 a0001c0001t0002g0084 others(5): Show |
8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-2182T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736018 | |||||||
| chrX:2736058 | T | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0175 a0001c0001t0002g0084 others(5): Show |
8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-2142T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736058 | |||||||
| chrX:2736150 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0092 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.476-2050C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736150 | |||||||
| chrX:2736159 | G | A | 2 | a0001c0001t0001g0090 a0001c0010t0001g0201 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.476-2041G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736159 | |||||||
| chrX:2736167 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2033G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736167 | |||||||
| chrX:2736168 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2032T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736168 | |||||||
| chrX:2736196 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2004T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736196 | |||||||
| chrX:2736201 | CA | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(14): Show |
17 | HG01891.hp2 HG02004.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.476-1983delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736201 | ||||||
| chrX:2736214 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.476-1986A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736214 | |||||||
| chrX:2736239 | G | A | 1 | a0001c0002t0001g0142 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.476-1961G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736239 | |||||||
| chrX:2736247 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0051 |
2 | HG00733.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.476-1953A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736247 | |||||||
| chrX:2736257 | C | T | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-1943C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736257 | |||||||
| chrX:2736332 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.476-1868C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736332 | |||||||
| chrX:2736355 | CTTCT | C | 2 | a0001c0001t0001g0065 a0001c0002t0001g0048 |
2 | HG00099.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.476-1844_476-1841d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736355 | |||||||
| chrX:2736419 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.476-1781A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736419 | |||||||
| chrX:2736427 | A | G | 18 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.476-1773A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736427 | |||||||
| chrX:2736459 | T | G | 1 | a0001c0001t0006g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-1741T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736459 | |||||||
| chrX:2736534 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-1666G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736534 | |||||||
| chrX:2736610 | T | C | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.476-1590T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736610 | |||||||
| chrX:2736623 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.476-1577C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736623 | |||||||
| chrX:2736786 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.476-1414G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736786 | |||||||
| chrX:2736812 | G | A | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.476-1388G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736812 | |||||||
| chrX:2736813 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0001c0002t0001g0021 others(3): Show |
6 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-1387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736813 | |||||||
| chrX:2736816 | C | T | 1 | a0001c0001t0006g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.476-1384C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736816 | |||||||
| chrX:2736834 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.476-1366G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736834 | |||||||
| chrX:2736873 | T | TAATA | 18 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.476-1303_476-1300d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736873 | ||||||
| chrX:2736884 | TAAATAAA | T | 7 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0001c0002t0001g0021 others(4): Show |
7 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-1315_476-1309d others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736884 | |||||||
| chrX:2736968 | T | C | 7 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0001c0002t0001g0021 others(4): Show |
7 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-1232T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736968 | |||||||
| chrX:2736999 | C | G | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0101 |
3 | HG01070.hp1 HG01071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476-1201C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736999 | |||||||
| chrX:2737091 | T | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.476-1109T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737091 | |||||||
| chrX:2737119 | C | T | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-1081C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737119 | |||||||
| chrX:2737166 | T | C | 4 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0004c0011t0007g0013 others(1): Show |
4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-1034T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737166 | |||||||
| chrX:2737204 | G | A | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0101 |
3 | HG01070.hp1 HG01071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476-996G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737204 | |||||||
| chrX:2737241 | G | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0097 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.476-959G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737241 | |||||||
| chrX:2737282 | A | T | 11 | a0002c0003t0001g0003 a0002c0003t0001g0098 a0002c0003t0001g0155 others(8): Show |
12 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.476-918A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737282 | |||||||
| chrX:2737291 | T | C | 4 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0004c0011t0007g0013 others(1): Show |
4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-909T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737291 | |||||||
| chrX:2737310 | G | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.476-890G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737310 | |||||||
| chrX:2737322 | T | C | 2 | a0004c0011t0007g0013 a0004c0013t0007g0019 |
2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-878T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737322 | |||||||
| chrX:2737325 | A | C | 2 | a0004c0011t0007g0013 a0004c0013t0007g0019 |
2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-875A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737325 | |||||||
| chrX:2737334 | C | T | 2 | a0004c0011t0007g0013 a0004c0013t0007g0019 |
2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-866C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737334 | |||||||
| chrX:2737422 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0004c0011t0007g0013 others(1): Show |
4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-778C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737422 | |||||||
| chrX:2737564 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.476-636G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737564 | |||||||
| chrX:2737617 | C | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.476-583C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737617 | |||||||
| chrX:2737619 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.476-581C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737619 | |||||||
| chrX:2737662 | C | G | 4 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0004c0011t0007g0013 others(1): Show |
4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-538C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737662 | |||||||
| chrX:2737702 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0136 a0003c0008t0004g0071 |
3 | HG00438.hp1 NA18906.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.476-498G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737702 | |||||||
| chrX:2738046 | A | T | 1 | a0001c0002t0001g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.476-154A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2738046 | |||||||
| chrX:2738139 | T | C | 4 | a0001c0001t0001g0220 a0001c0001t0006g0223 a0004c0011t0007g0013 others(1): Show |
4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-61T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2738139 | |||||||
| chrX:2738274 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+18C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738274 | |||||||
| chrX:2738288 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.532+32C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738288 | |||||||
| chrX:2738394 | G | A | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01516.hp2 HG02109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.532+138G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738394 | |||||||
| chrX:2738559 | G | C | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.532+303G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738559 | |||||||
| chrX:2738680 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+424G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738680 | |||||||
| chrX:2738809 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.532+553C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738809 | |||||||
| chrX:2739003 | G | A | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.532+747G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739003 | |||||||
| chrX:2739018 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.532+762G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739018 | |||||||
| chrX:2739115 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.532+859G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739115 | |||||||
| chrX:2739132 | G | C | 2 | a0001c0001t0006g0199 a0001c0001t0006g0223 |
2 | HG01891.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.532+876G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739132 | |||||||
| chrX:2739195 | A | C | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+939A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739195 | |||||||
| chrX:2739313 | G | T | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1057G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739313 | |||||||
| chrX:2739337 | A | C | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1081A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739337 | |||||||
| chrX:2739445 | A | G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1189A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739445 | |||||||
| chrX:2739449 | T | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.532+1193T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739449 | |||||||
| chrX:2739460 | T | A | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(7): Show |
10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1204T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739460 | |||||||
| chrX:2739612 | A | G | 1 | a0001c0004t0002g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533-1167A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739612 | |||||||
| chrX:2739614 | TA | T | 2 | a0001c0001t0008g0012 a0001c0001t0010g0177 |
2 | NA18992.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.533-1163delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739614 | ||||||
| chrX:2739802 | G | T | 1 | a0001c0001t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-977G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739802 | |||||||
| chrX:2739816 | C | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(58): Show |
63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.533-963C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739816 | |||||||
| chrX:2739920 | T | TA | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(30): Show |
33 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-837dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | ||||||
| chrX:2739920 | T | TAA | 16 | a0001c0001t0001g0108 a0002c0003t0001g0003 a0002c0003t0001g0098 others(13): Show |
17 | HG00639.hp1 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.533-838_533-837dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | ||||||
| chrX:2739920 | T | TAAAA | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-840_533-837dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | ||||||
| chrX:2739920 | TA | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0056 others(5): Show |
9 | HG01257.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.533-837delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | ||||||
| chrX:2739961 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533-818G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739961 | |||||||
| chrX:2740095 | AAAT | A | 32 | a0001c0001t0001g0108 a0001c0001t0002g0033 a0001c0001t0002g0084 others(29): Show |
33 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.533-666_533-664del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740095 | ||||||
| chrX:2740109 | A | C | 1 | a0001c0001t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-670A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740109 | |||||||
| chrX:2740187 | G | C | 1 | a0001c0004t0001g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533-592G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740187 | |||||||
| chrX:2740192 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.533-587A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740192 | |||||||
| chrX:2740258 | G | A | 42 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(39): Show |
43 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.533-521G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740258 | |||||||
| chrX:2740275 | G | T | 42 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(39): Show |
43 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.533-504G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740275 | |||||||
| chrX:2740463 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG00735.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.533-316C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740463 | |||||||
| chrX:2740523 | C | T | 3 | a0001c0001t0005g0034 a0001c0001t0005g0092 a0001c0001t0005g0224 |
3 | HG02976.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.533-256C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740523 | |||||||
| chrX:2740579 | A | AT | 15 | a0001c0001t0002g0033 a0001c0001t0002g0084 a0001c0001t0002g0085 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-192dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740579 | ||||||
| chrX:2740657 | G | A | 10 | a0001c0001t0002g0100 a0001c0001t0002g0105 a0001c0001t0002g0183 others(7): Show |
10 | HG01257.hp2 HG01517.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-122G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740657 | |||||||
| chrX:2740742 | C | A | 15 | a0001c0001t0002g0033 a0001c0001t0002g0084 a0001c0001t0002g0085 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-37C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740742 | |||||||
| chrX:2740756 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.533-23T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740756 | |||||||
| chrX:2740759 | T | C | 15 | a0001c0001t0002g0033 a0001c0001t0002g0084 a0001c0001t0002g0085 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-20T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740759 |