Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55135 |
| ensemblid | ENSG00000141499.18 |
| hgncid | 25522 |
| symbol | WRAP53 |
| name | WD repeat containing antisense to TP53 |
| refseq_nuc | NM_001143992.2 |
| refseq_prot | NP_001137464.1 |
| ensembl_nuc | ENST00000396463.7 |
| ensembl_prot | ENSP00000379727.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 7688477 |
| end | 7703502 |
| strand | + |
| ver | v1.2 |
| region | chr17:7688477-7703502 |
| region5000 | chr17:7683477-7708502 |
| regionname0 | WRAP53_chr17_7688477_7703502 |
| regionname5000 | WRAP53_chr17_7683477_7708502 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 185 | 8 | 45 | 101 | 10 | 19 | 76 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0002 | 0/0 | 548 | 135 | 59 | 16 | 43 | 2 | 15 | 30 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0003 | 0/0 | 548 | 35 | 3 | 6 | 17 | 2 | 7 | 12 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0004 | 0/0 | 548 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0005 | 0/0 | 548 | 6 | 0 | 0 | 6 | 0 | 0 | 3 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0006 | 0/0 | 548 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0007 | 0/0 | 548 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0008 | 0/0 | 548 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0009 | 0/0 | 548 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| a0010 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | MKTLE others(543): Show |
chr17 | 7683477 | 7708502 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 184 | 8 | 45 | 100 | 10 | 19 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0001c0012 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0002 | 0/0 | 1644 | 88 | 23 | 9 | 43 | 1 | 12 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0003 | 0/0 | 1644 | 37 | 30 | 5 | 0 | 1 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0008 | 0/0 | 1644 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0009 | 0/0 | 1644 | 3 | 2 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0011 | 0/0 | 1644 | 2 | 0 | 1 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0002c0016 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0003c0004 | 0/0 | 1644 | 35 | 3 | 6 | 17 | 2 | 7 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0004c0005 | 0/0 | 1644 | 13 | 13 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0005c0006 | 0/0 | 1644 | 6 | 0 | 0 | 6 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0006c0007 | 0/0 | 1644 | 5 | 4 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0007c0010 | 0/0 | 1644 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0008c0015 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0009c0017 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 | ||
| a0010c0014 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | ATGAA others(1639): Show |
chr17 | 7683477 | 7708502 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1748 | 181 | 8 | 45 | 97 | 10 | 19 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0001c0001t0002 | 0/0 | 1748 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0001c0012t0001 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0002t0001 | 0/0 | 1748 | 88 | 23 | 9 | 43 | 1 | 12 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0003t0001 | 0/0 | 1748 | 37 | 30 | 5 | 0 | 1 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0008t0001 | 0/0 | 1748 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0009t0001 | 0/0 | 1748 | 3 | 2 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0011t0001 | 0/0 | 1748 | 2 | 0 | 1 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0013t0001 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0002c0016t0001 | 0/0 | 1748 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0003c0004t0001 | 0/0 | 1748 | 35 | 3 | 6 | 17 | 2 | 7 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0004c0005t0001 | 0/0 | 1748 | 13 | 13 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0005c0006t0001 | 0/0 | 1748 | 6 | 0 | 0 | 6 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0006c0007t0001 | 0/0 | 1748 | 5 | 4 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0007c0010t0001 | 0/0 | 1748 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0008c0015t0001 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0009c0017t0001 | 0/0 | 1748 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| a0010c0014t0001 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | AGTGC others(1743): Show |
chr17 | 7683477 | 7708502 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 1 | 16 | 1 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0002 | 0/0 | 18 | 1 | 7 | 10 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0003 | 1/0 | 13 | 2 | 5 | 0 | 3 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0001c0012t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0004 | 0/0 | 9 | 0 | 1 | 4 | 0 | 4 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0008t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0009t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0011t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0011t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0013t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0002c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0003c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0004c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0005c0006t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0005c0006t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0005c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0005c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0005c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0006c0007t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0006c0007t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0006c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0006c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0007c0010t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0008c0015t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0009c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| a0010c0014t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0137 | EUR | FIN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00438 | hp1 | a0003 | c0004 | t0001 | g0022 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00558 | hp1 | a0005 | c0006 | t0001 | g0068 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00639 | hp1 | a0006 | c0007 | t0001 | g0122 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0118 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01099 | hp1 | a0003 | c0004 | t0001 | g0226 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01168 | hp1 | a0002 | c0011 | t0001 | g0094 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01243 | hp1 | a0002 | c0009 | t0001 | g0033 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0113 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0013 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01258 | hp2 | a0003 | c0004 | t0001 | g0002 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0115 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | CLM | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01516 | hp1 | a0003 | c0004 | t0001 | g0014 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01517 | hp2 | a0003 | c0004 | t0001 | g0014 | EUR | IBS | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0229 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0138 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0014 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0101 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02080 | hp2 | a0005 | c0006 | t0001 | g0025 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0234 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02145 | hp1 | a0004 | c0005 | t0001 | g0103 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0238 | EAS | CDX | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | CDX | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0133 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02258 | hp2 | a0006 | c0007 | t0001 | g0123 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02280 | hp1 | a0006 | c0007 | t0001 | g0034 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0112 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02300 | hp2 | a0003 | c0004 | t0001 | g0014 | AMR | PEL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0136 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02523 | hp2 | a0005 | c0006 | t0001 | g0007 | EAS | KHV | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0032 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02602 | hp1 | a0003 | c0004 | t0001 | g0228 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02615 | hp1 | a0004 | c0005 | t0001 | g0104 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02615 | hp2 | a0006 | c0007 | t0001 | g0139 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0134 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0108 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0131 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02647 | hp2 | a0004 | c0005 | t0001 | g0097 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0135 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02717 | hp1 | a0006 | c0007 | t0001 | g0034 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02717 | hp2 | a0002 | c0009 | t0001 | g0033 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0119 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02809 | hp1 | a0004 | c0005 | t0001 | g0030 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02886 | hp1 | a0004 | c0005 | t0001 | g0100 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02886 | hp2 | a0002 | c0008 | t0001 | g0083 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0230 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0032 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0231 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0224 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0098 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0132 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0125 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0117 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03017 | hp1 | a0003 | c0004 | t0001 | g0148 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0099 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0128 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03130 | hp1 | a0004 | c0005 | t0001 | g0030 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0127 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0012 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0106 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03209 | hp2 | a0004 | c0005 | t0001 | g0031 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03225 | hp1 | a0008 | c0015 | t0001 | g0006 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03492 | hp2 | a0003 | c0004 | t0001 | g0225 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03516 | hp2 | a0004 | c0005 | t0001 | g0102 | AFR | ESN | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03669 | hp2 | a0002 | c0011 | t0001 | g0093 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03688 | hp2 | a0003 | c0004 | t0001 | g0232 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0241 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0223 | SAS | PJL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03831 | hp2 | a0007 | c0010 | t0001 | g0020 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03834 | hp1 | a0009 | c0017 | t0001 | g0081 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04204 | hp1 | a0007 | c0010 | t0001 | g0020 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG04228 | hp2 | a0002 | c0016 | t0001 | g0004 | SAS | STU | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0110 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18522 | hp2 | a0002 | c0008 | t0001 | g0109 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18747 | hp1 | a0003 | c0004 | t0001 | g0239 | EAS | CHB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18747 | hp2 | a0003 | c0004 | t0001 | g0149 | EAS | CHB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0105 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0096 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18959 | hp1 | a0003 | c0004 | t0001 | g0235 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18961 | hp2 | a0003 | c0004 | t0001 | g0022 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0017 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0222 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0237 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18985 | hp1 | a0003 | c0004 | t0001 | g0242 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18990 | hp1 | a0003 | c0004 | t0001 | g0153 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19002 | hp1 | a0001 | c0012 | t0001 | g0162 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19011 | hp1 | a0003 | c0004 | t0001 | g0160 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0130 | AFR | LWK | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19056 | hp2 | a0005 | c0006 | t0001 | g0010 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19060 | hp2 | a0003 | c0004 | t0001 | g0236 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19064 | hp2 | a0005 | c0006 | t0001 | g0007 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19072 | hp1 | a0003 | c0004 | t0001 | g0233 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19085 | hp2 | a0010 | c0014 | t0001 | g0054 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19087 | hp2 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19090 | hp1 | a0005 | c0006 | t0001 | g0088 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19240 | hp1 | a0002 | c0013 | t0001 | g0107 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | YRI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0114 | AFR | ASW | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0049 | EUR | TSI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20905 | hp1 | a0003 | c0004 | t0001 | g0227 | SAS | GIH | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | GIH | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0116 | AFR | ACB | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0111 | AFR | MSL | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG06807 | hp1 | a0004 | c0005 | t0001 | g0031 | AFR | USA | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | USA | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA20300 | hp2 | a0002 | c0009 | t0001 | g0124 | AFR | USA | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA21309 | hp1 | a0002 | c0008 | t0001 | g0126 | AFR | LWK | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0186 | REF | REF | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | WRAP53_chr17_7683477_7708502 | WRAP53 | chr17 | 7683477 | 7708502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:7688679 | C | T | 1 | a0004 | 13 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
missense_variant | MODERATE | c.31C>T | p.Pro11Ser | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/11 | 117/1749 | 31/1647 | 11/548 | chr17 | 7688679 | |||
| chr17:7688850 | C | G | 7 | a0002 a0004 a0005 others(4): Show |
162 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
missense_variant | MODERATE | c.202C>G | p.Arg68Gly | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/11 | 288/1749 | 202/1647 | 68/548 | chr17 | 7688850 | |||
| chr17:7688971 | A | C | 1 | a0009 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.323A>C | p.Glu108Ala | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/11 | 409/1749 | 323/1647 | 108/548 | chr17 | 7688971 | |||
| chr17:7689055 | C | G | 1 | a0005 | 6 | HG00558.hp1 HG02080.hp2 HG02523.hp2 others(3): Show |
missense_variant | MODERATE | c.407C>G | p.Pro136Arg | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/11 | 493/1749 | 407/1647 | 136/548 | chr17 | 7689055 | |||
| chr17:7702801 | G | A | 1 | a0006 | 5 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.1223G>A | p.Gly408Asp | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 9/11 | 1309/1749 | 1223/1647 | 408/548 | chr17 | 7702801 | |||
| chr17:7703353 | C | T | 1 | a0008 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1514C>T | p.Thr505Met | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 11/11 | 1600/1749 | 1514/1647 | 505/548 | chr17 | 7703353 | |||
| chr17:7703397 | G | T | 1 | a0007 | 2 | HG03831.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.1558G>T | p.Gly520Trp | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 11/11 | 1644/1749 | 1558/1647 | 520/548 | chr17 | 7703397 | |||
| chr17:7703404 | C | G | 7 | a0002 a0003 a0004 others(4): Show |
196 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(193): Show |
missense_variant | MODERATE | c.1565C>G | p.Ala522Gly | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 11/11 | 1651/1749 | 1565/1647 | 522/548 | chr17 | 7703404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:7688978 | C | T | 1 | a0001c0012 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.330C>T | p.Asn110Asn | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/11 | 416/1749 | 330/1647 | 110/548 | chr17 | 7688978 | |||
| chr17:7689242 | C | T | 7 | a0002c0002 a0002c0011 a0002c0016 others(4): Show |
100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
synonymous_variant | LOW | c.450C>T | p.Phe150Phe | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 3/11 | 536/1749 | 450/1647 | 150/548 | chr17 | 7689242 | |||
| chr17:7701507 | C | T | 1 | a0002c0016 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.780C>T | p.Phe260Phe | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 6/11 | 866/1749 | 780/1647 | 260/548 | chr17 | 7701507 | |||
| chr17:7701534 | C | T | 1 | a0002c0009 | 3 | HG01243.hp1 HG02717.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.807C>T | p.Arg269Arg | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 6/11 | 893/1749 | 807/1647 | 269/548 | chr17 | 7701534 | |||
| chr17:7701770 | C | T | 1 | a0002c0013 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.936C>T | p.Cys312Cys | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 7/11 | 1022/1749 | 936/1647 | 312/548 | chr17 | 7701770 | |||
| chr17:7703032 | T | C | 5 | a0002c0008 a0002c0009 a0002c0011 others(2): Show |
26 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(23): Show |
synonymous_variant | LOW | c.1308T>C | p.Ala436Ala | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 10/11 | 1394/1749 | 1308/1647 | 436/548 | chr17 | 7703032 | |||
| chr17:7703083 | C | T | 2 | a0002c0009 a0006c0007 |
8 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(5): Show |
synonymous_variant | LOW | c.1359C>T | p.Pro453Pro | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 10/11 | 1445/1749 | 1359/1647 | 453/548 | chr17 | 7703083 | |||
| chr17:7703321 | A | G | 1 | a0006c0007 | 5 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.1482A>G | p.Glu494Glu | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 11/11 | 1568/1749 | 1482/1647 | 494/548 | chr17 | 7703321 | |||
| chr17:7703480 | G | T | 1 | a0006c0007 | 5 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.1641G>T | p.Leu547Leu | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 11/11 | 1727/1749 | 1641/1647 | 547/548 | chr17 | 7703480 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:7688511 | C | T | 1 | a0001c0001t0002 | 3 | NA18951.hp1 NA18973.hp1 NA19005.hp1 |
5_prime_UTR_variant | MODIFIER | c.-52C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 1/11 | 138 | chr17 | 7688511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:7689094 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.431+15C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/10 | chr17 | 7689094 | |||||||
| chr17:7689164 | C | T | 24 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0003c0004t0001g0014 others(21): Show |
28 | HG00438.hp1 HG01099.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.432-60C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/10 | chr17 | 7689164 | |||||||
| chr17:7689202 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0047 |
3 | HG03831.hp1 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.432-22T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 2/10 | chr17 | 7689202 | |||||||
| chr17:7689442 | C | G | 1 | a0002c0002t0001g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.530+120C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 3/10 | chr17 | 7689442 | |||||||
| chr17:7689462 | G | A | 96 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(93): Show |
135 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.531-128G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 3/10 | chr17 | 7689462 | |||||||
| chr17:7689484 | C | T | 28 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(25): Show |
34 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.531-106C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 3/10 | chr17 | 7689484 | |||||||
| chr17:7689792 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.642+91T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7689792 | |||||||
| chr17:7689817 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0095 |
3 | HG02055.hp2 HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.642+116C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7689817 | |||||||
| chr17:7689834 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.642+133C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7689834 | |||||||
| chr17:7689846 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.642+145C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7689846 | |||||||
| chr17:7689895 | A | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.642+194A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7689895 | |||||||
| chr17:7690001 | T | C | 88 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(85): Show |
126 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.642+300T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690001 | |||||||
| chr17:7690041 | C | T | 1 | a0006c0007t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642+340C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690041 | |||||||
| chr17:7690191 | C | T | 17 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(14): Show |
21 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.642+490C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690191 | |||||||
| chr17:7690218 | G | A | 7 | a0002c0003t0001g0121 a0002c0009t0001g0033 a0002c0009t0001g0124 others(4): Show |
9 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+517G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690218 | |||||||
| chr17:7690222 | C | T | 30 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(27): Show |
36 | HG00733.hp2 HG01168.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.642+521C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690222 | |||||||
| chr17:7690233 | G | A | 11 | a0002c0003t0001g0012 a0002c0003t0001g0125 a0002c0003t0001g0127 others(8): Show |
14 | HG01167.hp1 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.642+532G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690233 | |||||||
| chr17:7690522 | A | G | 4 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0001g0137 others(1): Show |
4 | HG00323.hp2 HG01981.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+821A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690522 | |||||||
| chr17:7690571 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.642+870C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690571 | |||||||
| chr17:7690603 | T | C | 1 | a0002c0003t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.642+902T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690603 | |||||||
| chr17:7690654 | G | C | 1 | a0002c0002t0001g0048 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.642+953G>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690654 | |||||||
| chr17:7690757 | C | T | 1 | a0002c0003t0001g0134 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.642+1056C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690757 | |||||||
| chr17:7690873 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0020 others(24): Show |
51 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.642+1172C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7690873 | |||||||
| chr17:7691113 | G | A | 1 | a0003c0004t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.642+1412G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691113 | |||||||
| chr17:7691145 | G | T | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+1444G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691145 | |||||||
| chr17:7691167 | T | C | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+1466T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691167 | |||||||
| chr17:7691209 | A | AAAAC | 45 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(42): Show |
74 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.642+1542_642+1545d others(6): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691209 | A | AAAACAAA others(1): Show |
5 | a0001c0001t0001g0140 a0001c0001t0001g0219 a0002c0011t0001g0093 others(2): Show |
5 | HG02135.hp2 HG02922.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+1538_642+1545d others(10): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691209 | AAAAC | A | 44 | a0001c0001t0001g0022 a0001c0001t0001g0120 a0001c0001t0001g0195 others(41): Show |
59 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.642+1542_642+1545d others(6): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691209 | AAAACAAA others(1): Show |
A | 3 | a0001c0001t0001g0198 a0002c0002t0001g0091 a0002c0002t0001g0092 |
3 | HG04115.hp1 NA18973.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.642+1538_642+1545d others(10): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691209 | AAAACAAA others(5): Show |
A | 27 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(24): Show |
33 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.642+1534_642+1545d others(14): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691209 | AAAACAAA others(9): Show |
A | 17 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0119 others(14): Show |
20 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.642+1530_642+1545d others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691209 | ||||||
| chr17:7691221 | C | A | 1 | a0003c0004t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.642+1520C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691221 | |||||||
| chr17:7691306 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.642+1605G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691306 | |||||||
| chr17:7691390 | G | GT | 36 | a0001c0001t0001g0240 a0002c0002t0001g0006 a0002c0002t0001g0027 others(33): Show |
48 | HG00323.hp2 HG00423.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+1690dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691390 | ||||||
| chr17:7691390 | G | GTT | 4 | a0002c0002t0001g0090 a0002c0002t0001g0095 a0002c0003t0001g0133 others(1): Show |
4 | HG01981.hp2 HG02055.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+1690_642+1691i others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691390 | ||||||
| chr17:7691392 | G | GT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0159 others(5): Show |
8 | HG00735.hp2 HG01952.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+1707dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691392 | ||||||
| chr17:7691392 | G | T | 142 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0002c0002t0001g0004 others(139): Show |
188 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.642+1691G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691392 | |||||||
| chr17:7691450 | C | T | 1 | a0002c0008t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.642+1749C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691450 | |||||||
| chr17:7691451 | G | A | 1 | a0002c0003t0001g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.642+1750G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691451 | |||||||
| chr17:7691458 | C | T | 15 | a0002c0003t0001g0012 a0002c0003t0001g0125 a0002c0003t0001g0127 others(12): Show |
18 | HG00323.hp2 HG01167.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+1757C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691458 | |||||||
| chr17:7691499 | C | T | 11 | a0004c0005t0001g0030 a0004c0005t0001g0031 a0004c0005t0001g0096 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.642+1798C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691499 | |||||||
| chr17:7691670 | A | G | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+1969A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691670 | |||||||
| chr17:7691691 | A | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG00609.hp1 HG02071.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1990A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691691 | |||||||
| chr17:7691726 | C | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.642+2025C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691726 | |||||||
| chr17:7691834 | G | GT | 66 | a0001c0001t0001g0168 a0001c0001t0001g0192 a0001c0001t0001g0211 others(63): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.642+2141dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7691834 | ||||||
| chr17:7691847 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.642+2146G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691847 | |||||||
| chr17:7691922 | C | T | 12 | a0002c0003t0001g0132 a0004c0005t0001g0030 a0004c0005t0001g0031 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.642+2221C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7691922 | |||||||
| chr17:7692011 | G | A | 26 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(23): Show |
32 | HG01168.hp1 HG02055.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.642+2310G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692011 | |||||||
| chr17:7692019 | T | C | 1 | a0003c0004t0001g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.642+2318T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692019 | |||||||
| chr17:7692061 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.642+2360C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692061 | |||||||
| chr17:7692101 | A | G | 6 | a0002c0009t0001g0033 a0002c0009t0001g0124 a0006c0007t0001g0034 others(3): Show |
8 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+2400A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692101 | |||||||
| chr17:7692120 | A | G | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+2419A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692120 | |||||||
| chr17:7692216 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.642+2515A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692216 | |||||||
| chr17:7692490 | G | A | 5 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0002c0003t0001g0115 others(2): Show |
5 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+2789G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692490 | |||||||
| chr17:7692506 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.642+2805A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692506 | |||||||
| chr17:7692620 | C | CA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(101): Show |
165 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.642+2941dupA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692620 | ||||||
| chr17:7692620 | C | CAA | 15 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0047 others(12): Show |
17 | HG00609.hp1 HG01175.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.642+2940_642+2941d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692620 | ||||||
| chr17:7692620 | CA | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0210 a0002c0003t0001g0110 others(5): Show |
9 | HG00597.hp2 HG02080.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+2941delA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692620 | ||||||
| chr17:7692628 | A | T | 1 | a0002c0002t0001g0071 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.642+2927A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692628 | |||||||
| chr17:7692744 | T | G | 3 | a0003c0004t0001g0014 a0003c0004t0001g0223 a0003c0004t0001g0226 |
6 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+3043T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692744 | |||||||
| chr17:7692746 | C | CT | 45 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0163 others(42): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.642+3069dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692746 | ||||||
| chr17:7692746 | C | CTT | 20 | a0001c0001t0001g0164 a0001c0001t0001g0209 a0002c0003t0001g0012 others(17): Show |
24 | HG00323.hp2 HG01167.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+3068_642+3069d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692746 | ||||||
| chr17:7692746 | CT | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0193 a0002c0002t0001g0050 others(7): Show |
10 | HG02895.hp1 HG02897.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+3069delT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7692746 | ||||||
| chr17:7692807 | A | G | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+3106A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7692807 | |||||||
| chr17:7693064 | C | T | 4 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0002c0003t0001g0115 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+3363C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693064 | |||||||
| chr17:7693151 | TCTC | T | 30 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(27): Show |
36 | HG00733.hp2 HG01168.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.642+3458_642+3460d others(5): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7693151 | ||||||
| chr17:7693184 | C | CTTTTTT | 134 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0002c0002t0001g0004 others(131): Show |
182 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.642+3486_642+3491d others(8): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7693184 | ||||||
| chr17:7693209 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.642+3508A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693209 | |||||||
| chr17:7693484 | C | T | 62 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(59): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.642+3783C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693484 | |||||||
| chr17:7693485 | G | A | 62 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(59): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.642+3784G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693485 | |||||||
| chr17:7693592 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.642+3891G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693592 | |||||||
| chr17:7693675 | A | G | 108 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(105): Show |
150 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.642+3974A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693675 | |||||||
| chr17:7693737 | A | T | 78 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(75): Show |
114 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.642+4036A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693737 | |||||||
| chr17:7693738 | A | T | 8 | a0002c0003t0001g0012 a0002c0003t0001g0125 a0002c0003t0001g0127 others(5): Show |
11 | HG01167.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.642+4037A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693738 | |||||||
| chr17:7693952 | A | T | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+4251A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693952 | |||||||
| chr17:7693956 | T | C | 2 | a0002c0002t0001g0050 a0002c0002t0001g0053 |
2 | NA18970.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.642+4255T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7693956 | |||||||
| chr17:7694152 | G | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0079 |
2 | HG02523.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.642+4451G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694152 | |||||||
| chr17:7694160 | G | A | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+4459G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694160 | |||||||
| chr17:7694191 | A | T | 2 | a0002c0002t0001g0064 a0002c0002t0001g0067 |
2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.642+4490A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694191 | |||||||
| chr17:7694242 | C | CT | 35 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0040 others(32): Show |
41 | HG00438.hp1 HG01099.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.642+4560dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694242 | ||||||
| chr17:7694242 | CT | C | 44 | a0001c0001t0001g0045 a0001c0001t0001g0173 a0002c0002t0001g0048 others(41): Show |
54 | HG00323.hp2 HG00733.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.642+4560delT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694242 | ||||||
| chr17:7694242 | CTTT | C | 59 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(56): Show |
91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.642+4558_642+4560d others(5): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694242 | ||||||
| chr17:7694395 | A | C | 1 | a0002c0002t0001g0055 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.642+4694A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694395 | |||||||
| chr17:7694401 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0168 |
3 | NA18943.hp2 NA18949.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.642+4700C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694401 | |||||||
| chr17:7694471 | G | A | 4 | a0002c0003t0001g0135 a0002c0003t0001g0136 a0002c0003t0001g0137 others(1): Show |
4 | HG00323.hp2 HG01981.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+4770G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694471 | |||||||
| chr17:7694589 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.642+4888T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694589 | |||||||
| chr17:7694621 | G | A | 16 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(13): Show |
19 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+4920G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694621 | |||||||
| chr17:7694754 | C | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.642+5053C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694754 | |||||||
| chr17:7694855 | C | CT | 15 | a0001c0001t0001g0192 a0002c0003t0001g0012 a0002c0003t0001g0112 others(12): Show |
18 | HG00323.hp2 HG01167.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+5170dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694855 | ||||||
| chr17:7694855 | CT | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0147 a0001c0001t0001g0212 others(40): Show |
65 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.642+5170delT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694855 | ||||||
| chr17:7694855 | CTT | C | 29 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0015 others(26): Show |
43 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.642+5169_642+5170d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694855 | ||||||
| chr17:7694885 | C | A | 1 | a0002c0002t0001g0063 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.642+5184C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694885 | |||||||
| chr17:7694894 | C | A | 62 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(59): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.642+5193C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694894 | |||||||
| chr17:7694895 | G | T | 1 | a0006c0007t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642+5194G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694895 | |||||||
| chr17:7694900 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.642+5199C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694900 | |||||||
| chr17:7694944 | A | C | 1 | a0002c0003t0001g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.642+5243A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7694944 | |||||||
| chr17:7694959 | C | CT | 17 | a0002c0003t0001g0012 a0002c0003t0001g0125 a0002c0003t0001g0127 others(14): Show |
20 | HG00323.hp2 HG01167.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.642+5269dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7694959 | ||||||
| chr17:7695046 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0196 |
2 | HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.642+5345G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695046 | |||||||
| chr17:7695112 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0175 |
2 | NA19057.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.642+5411C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695112 | |||||||
| chr17:7695161 | T | G | 78 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(75): Show |
114 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.642+5460T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695161 | |||||||
| chr17:7695190 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.642+5489C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695190 | |||||||
| chr17:7695317 | A | G | 2 | a0004c0005t0001g0101 a0004c0005t0001g0103 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.643-5424A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695317 | |||||||
| chr17:7695424 | C | T | 27 | a0002c0002t0001g0048 a0002c0003t0001g0012 a0002c0003t0001g0125 others(24): Show |
32 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.643-5317C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695424 | |||||||
| chr17:7695443 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0045 others(11): Show |
34 | HG00408.hp2 HG00735.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.643-5298C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695443 | |||||||
| chr17:7695457 | T | C | 1 | a0003c0004t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.643-5284T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695457 | |||||||
| chr17:7695548 | A | G | 46 | a0002c0002t0001g0048 a0002c0003t0001g0011 a0002c0003t0001g0012 others(43): Show |
55 | HG00323.hp2 HG00733.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.643-5193A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695548 | |||||||
| chr17:7695549 | T | C | 46 | a0002c0002t0001g0048 a0002c0003t0001g0011 a0002c0003t0001g0012 others(43): Show |
55 | HG00323.hp2 HG00733.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.643-5192T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695549 | |||||||
| chr17:7695586 | C | T | 1 | a0003c0004t0001g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.643-5155C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695586 | |||||||
| chr17:7695643 | C | T | 13 | a0002c0011t0001g0093 a0002c0011t0001g0094 a0004c0005t0001g0030 others(10): Show |
15 | HG01168.hp1 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.643-5098C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695643 | |||||||
| chr17:7695705 | G | A | 1 | a0002c0009t0001g0033 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.643-5036G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695705 | |||||||
| chr17:7695799 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.643-4942C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695799 | |||||||
| chr17:7695849 | T | C | 8 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(5): Show |
12 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.643-4892T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695849 | |||||||
| chr17:7695942 | C | G | 73 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(70): Show |
109 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.643-4799C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7695942 | |||||||
| chr17:7696045 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.643-4696A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696045 | |||||||
| chr17:7696129 | G | A | 1 | a0002c0003t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.643-4612G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696129 | |||||||
| chr17:7696290 | A | AT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(121): Show |
185 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.643-4425dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7696290 | ||||||
| chr17:7696290 | A | ATT | 61 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0040 others(58): Show |
83 | HG00323.hp2 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.643-4426_643-4425d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7696290 | ||||||
| chr17:7696290 | A | ATTT | 13 | a0001c0001t0001g0155 a0001c0001t0001g0181 a0001c0001t0001g0240 others(10): Show |
16 | HG00438.hp2 HG01884.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-4427_643-4425d others(5): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7696290 | ||||||
| chr17:7696290 | A | T | 1 | a0003c0004t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.643-4451A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696290 | |||||||
| chr17:7696290 | ATTTTTTT others(3): Show |
A | 2 | a0003c0004t0001g0232 a0003c0004t0001g0241 |
2 | HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.643-4434_643-4425d others(12): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7696290 | ||||||
| chr17:7696347 | G | A | 62 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(59): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.643-4394G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696347 | |||||||
| chr17:7696453 | C | T | 11 | a0004c0005t0001g0030 a0004c0005t0001g0031 a0004c0005t0001g0096 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.643-4288C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696453 | |||||||
| chr17:7696533 | T | C | 140 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0002c0002t0001g0004 others(137): Show |
188 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.643-4208T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696533 | |||||||
| chr17:7696541 | G | A | 75 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(72): Show |
110 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.643-4200G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696541 | |||||||
| chr17:7696688 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.643-4053G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696688 | |||||||
| chr17:7696808 | ACAG | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0020 others(23): Show |
50 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.643-3929_643-3927d others(5): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7696808 | ||||||
| chr17:7696965 | C | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-3776C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7696965 | |||||||
| chr17:7697190 | A | G | 19 | a0002c0003t0001g0121 a0002c0008t0001g0083 a0002c0009t0001g0033 others(16): Show |
23 | HG00639.hp1 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.643-3551A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697190 | |||||||
| chr17:7697276 | G | A | 1 | a0003c0004t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.643-3465G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697276 | |||||||
| chr17:7697313 | C | G | 1 | a0003c0004t0001g0224 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.643-3428C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697313 | |||||||
| chr17:7697320 | C | CA | 70 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0168 others(67): Show |
103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.643-3408dupA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7697320 | ||||||
| chr17:7697362 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-3379G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697362 | |||||||
| chr17:7697389 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.643-3352G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697389 | |||||||
| chr17:7697423 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0183 |
2 | NA18991.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.643-3318C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697423 | |||||||
| chr17:7697608 | A | G | 139 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0002c0002t0001g0004 others(136): Show |
187 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.643-3133A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697608 | |||||||
| chr17:7697615 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.643-3126T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697615 | |||||||
| chr17:7697648 | G | A | 1 | a0002c0008t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.643-3093G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697648 | |||||||
| chr17:7697710 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.643-3031C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7697710 | |||||||
| chr17:7697870 | C | CTT | 112 | a0001c0001t0001g0022 a0002c0002t0001g0004 a0002c0002t0001g0006 others(109): Show |
156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.643-2858_643-2857d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7697870 | ||||||
| chr17:7697870 | C | CTTT | 23 | a0001c0001t0001g0240 a0002c0002t0001g0095 a0002c0003t0001g0121 others(20): Show |
27 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.643-2859_643-2857d others(5): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7697870 | ||||||
| chr17:7698155 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.643-2586A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698155 | |||||||
| chr17:7698381 | TGTTTCCA others(24): Show |
T | 1 | a0004c0005t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-2358_643-2328d others(33): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7698381 | ||||||
| chr17:7698453 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.643-2288C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698453 | |||||||
| chr17:7698677 | C | G | 2 | a0002c0002t0001g0084 a0002c0002t0001g0087 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.643-2064C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698677 | |||||||
| chr17:7698703 | C | T | 4 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0002c0003t0001g0115 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-2038C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698703 | |||||||
| chr17:7698705 | T | C | 2 | a0003c0004t0001g0234 a0003c0004t0001g0236 |
2 | HG02132.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.643-2036T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698705 | |||||||
| chr17:7698734 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.643-2007G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698734 | |||||||
| chr17:7698751 | C | T | 1 | a0002c0002t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.643-1990C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698751 | |||||||
| chr17:7698855 | G | A | 1 | a0002c0008t0001g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.643-1886G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7698855 | |||||||
| chr17:7698875 | A | AAAAT | 9 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0177 others(6): Show |
10 | HG00642.hp2 HG01099.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-1835_643-1832d others(6): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7698875 | ||||||
| chr17:7698875 | AAAAT | A | 136 | a0001c0001t0001g0022 a0001c0001t0001g0240 a0002c0002t0001g0004 others(133): Show |
184 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.643-1835_643-1832d others(6): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7698875 | ||||||
| chr17:7699109 | G | GT | 18 | a0001c0001t0001g0207 a0002c0003t0001g0011 a0002c0003t0001g0032 others(15): Show |
22 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.643-1624dupT | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699109 | ||||||
| chr17:7699117 | T | C | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-1624T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699117 | |||||||
| chr17:7699120 | C | T | 3 | a0006c0007t0001g0034 a0006c0007t0001g0122 a0006c0007t0001g0123 |
4 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1621C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699120 | |||||||
| chr17:7699200 | A | T | 1 | a0002c0003t0001g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.643-1541A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699200 | |||||||
| chr17:7699227 | C | G | 1 | a0002c0003t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.643-1514C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699227 | |||||||
| chr17:7699325 | A | G | 21 | a0002c0003t0001g0121 a0002c0008t0001g0083 a0002c0009t0001g0033 others(18): Show |
25 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.643-1416A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699325 | |||||||
| chr17:7699343 | C | T | 4 | a0002c0003t0001g0113 a0002c0003t0001g0114 a0002c0003t0001g0115 others(1): Show |
4 | HG00733.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1398C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699343 | |||||||
| chr17:7699426 | TA | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0180 a0001c0001t0001g0182 others(9): Show |
14 | HG00609.hp2 HG02027.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.643-1303delA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699426 | ||||||
| chr17:7699435 | A | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-1306A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699435 | |||||||
| chr17:7699436 | AAATTTAT others(12): Show |
A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0175 |
2 | NA19057.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.643-1303_643-1285d others(21): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699436 | ||||||
| chr17:7699437 | AATTTATA others(11): Show |
A | 2 | a0001c0001t0001g0164 a0003c0004t0001g0148 |
2 | HG03017.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.643-1265_643-1248d others(20): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699437 | ||||||
| chr17:7699437 | AATTTATA others(29): Show |
A | 2 | a0003c0004t0001g0238 a0004c0005t0001g0096 |
2 | HG02155.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.643-1283_643-1248d others(38): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699437 | ||||||
| chr17:7699437 | AATTTATA others(55): Show |
A | 1 | a0003c0004t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.643-1283_643-1222d others(64): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699437 | ||||||
| chr17:7699438 | ATTTATAT others(48): Show |
A | 1 | a0002c0002t0001g0058 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.643-1302_643-1248d others(57): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699438 | |||||||
| chr17:7699440 | T | G | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-1301T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699440 | |||||||
| chr17:7699440 | T | TTA | 4 | a0001c0001t0001g0044 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG00609.hp1 HG02071.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-1285_643-1284d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699440 | TTATATAT others(31): Show |
T | 1 | a0002c0009t0001g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.643-1283_643-1246d others(40): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699440 | TTATATAT others(33): Show |
T | 3 | a0002c0009t0001g0033 a0004c0005t0001g0031 a0004c0005t0001g0101 |
3 | HG01243.hp1 HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.643-1283_643-1244d others(42): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699440 | TTATATAT others(35): Show |
T | 2 | a0004c0005t0001g0030 a0004c0005t0001g0097 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.643-1283_643-1242d others(44): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699440 | TTATATAT others(37): Show |
T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0003t0001g0138 |
3 | HG01257.hp1 HG01981.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.643-1265_643-1222d others(46): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699440 | TTATATAT others(57): Show |
T | 1 | a0006c0007t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.643-1264_643-1201d others(66): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699440 | ||||||
| chr17:7699442 | ATATATAT others(27): Show |
A | 1 | a0002c0002t0001g0092 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.643-1283_643-1250d others(36): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699442 | ||||||
| chr17:7699442 | ATATATAT others(53): Show |
A | 3 | a0002c0002t0001g0091 a0002c0003t0001g0105 a0004c0005t0001g0104 |
3 | HG02615.hp1 NA18906.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.643-1283_643-1224d others(62): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699442 | ||||||
| chr17:7699444 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0205 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.643-1283_643-1270d others(16): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699444 | ||||||
| chr17:7699444 | ATATATAT others(51): Show |
A | 7 | a0002c0002t0001g0009 a0002c0002t0001g0024 a0002c0003t0001g0011 others(4): Show |
7 | HG00673.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-1283_643-1226d others(60): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699444 | ||||||
| chr17:7699446 | ATATATAT others(49): Show |
A | 7 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0053 others(4): Show |
7 | HG00544.hp1 HG02015.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-1283_643-1228d others(58): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699446 | ||||||
| chr17:7699448 | A | ATATATAT others(577): Show |
1 | a0002c0011t0001g0093 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.643-1286_643-1285i others(586): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699448 | ||||||
| chr17:7699448 | A | ATATATAT others(599): Show |
1 | a0002c0011t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.643-1286_643-1285i others(608): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699448 | ||||||
| chr17:7699448 | A | G | 1 | a0004c0005t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-1293A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699448 | |||||||
| chr17:7699448 | ATATATAT others(47): Show |
A | 7 | a0002c0002t0001g0079 a0002c0003t0001g0011 a0002c0003t0001g0032 others(4): Show |
9 | HG02280.hp2 HG02523.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.643-1283_643-1230d others(56): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699448 | ||||||
| chr17:7699450 | A | G | 6 | a0004c0005t0001g0030 a0004c0005t0001g0031 a0004c0005t0001g0098 others(3): Show |
6 | HG02809.hp1 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-1291A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699450 | |||||||
| chr17:7699450 | ATATATAT others(65): Show |
A | 1 | a0002c0002t0001g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.643-1283_643-1212d others(74): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699450 | ||||||
| chr17:7699452 | ATATATTT others(43): Show |
A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0074 |
2 | HG00423.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.643-1283_643-1234d others(52): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699452 | ||||||
| chr17:7699454 | ATATTTAT others(41): Show |
A | 4 | a0002c0009t0001g0124 a0004c0005t0001g0030 a0004c0005t0001g0031 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1283_643-1236d others(50): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699454 | ||||||
| chr17:7699456 | ATTTATAT others(13): Show |
A | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.643-1283_643-1264d others(22): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699456 | ||||||
| chr17:7699456 | ATTTATAT others(39): Show |
A | 4 | a0002c0013t0001g0107 a0004c0005t0001g0098 a0004c0005t0001g0099 others(1): Show |
4 | HG02922.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1283_643-1238d others(48): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699456 | ||||||
| chr17:7699456 | ATTTATAT others(46): Show |
A | 1 | a0002c0002t0001g0050 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.643-1284_643-1232d others(55): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699456 | |||||||
| chr17:7699457 | TTTATATA others(26): Show |
T | 1 | a0002c0002t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.643-1282_643-1250d others(35): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699457 | ||||||
| chr17:7699457 | TTTATATA others(30): Show |
T | 1 | a0002c0002t0001g0006 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.643-1282_643-1246d others(39): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699457 | ||||||
| chr17:7699458 | T | A | 3 | a0002c0002t0001g0008 a0002c0003t0001g0114 a0004c0005t0001g0103 |
3 | HG01928.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.643-1283T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699458 | |||||||
| chr17:7699458 | TTA | T | 3 | a0001c0001t0001g0003 a0002c0003t0001g0115 a0002c0003t0001g0118 |
3 | HG00733.hp2 HG01358.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.643-1267_643-1266d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699458 | TTATATAT others(13): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0039 others(6): Show |
12 | HG00408.hp1 HG00735.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.643-1265_643-1246d others(22): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699458 | TTATATAT others(15): Show |
T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(34): Show |
54 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.643-1265_643-1244d others(24): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699458 | TTATATAT others(17): Show |
T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(10): Show |
16 | HG00280.hp2 HG00642.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-1265_643-1242d others(26): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699458 | TTATATAT others(21): Show |
T | 1 | a0002c0002t0001g0048 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-1267_643-1240d others(30): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699458 | TTATATAT others(39): Show |
T | 1 | a0003c0004t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.643-1247_643-1202d others(48): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699458 | ||||||
| chr17:7699460 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0001g0041 a0001c0001t0002g0037 |
2 | NA18951.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.643-1265_643-1250d others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699460 | ||||||
| chr17:7699460 | ATATATAT others(28): Show |
A | 1 | a0004c0005t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-1280_643-1246d others(37): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699460 | |||||||
| chr17:7699460 | ATATATAT others(35): Show |
A | 25 | a0001c0001t0001g0240 a0002c0002t0001g0004 a0002c0002t0001g0006 others(22): Show |
28 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.643-1265_643-1224d others(44): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699460 | ||||||
| chr17:7699460 | ATATATAT others(55): Show |
A | 1 | a0002c0003t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.643-1265_643-1204d others(64): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699460 | ||||||
| chr17:7699462 | ATATATAT others(33): Show |
A | 17 | a0001c0001t0001g0022 a0002c0002t0001g0007 a0002c0002t0001g0008 others(14): Show |
18 | HG02132.hp1 HG02155.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.643-1265_643-1226d others(42): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699462 | ||||||
| chr17:7699464 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0044 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.643-1266_643-1265i others(20): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699464 | ||||||
| chr17:7699464 | ATATATAT others(5): Show |
A | 1 | a0002c0003t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.643-1265_643-1254d others(14): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699464 | ||||||
| chr17:7699464 | ATATATAT others(31): Show |
A | 21 | a0001c0001t0001g0191 a0002c0002t0001g0004 a0002c0002t0001g0008 others(18): Show |
24 | HG00621.hp1 HG01099.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-1265_643-1228d others(40): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699464 | ||||||
| chr17:7699466 | ATATATAT others(29): Show |
A | 25 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0007 others(22): Show |
28 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.643-1265_643-1230d others(38): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699466 | ||||||
| chr17:7699468 | ATATATAT others(27): Show |
A | 14 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0010 others(11): Show |
15 | HG00558.hp1 HG02027.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.643-1265_643-1232d others(36): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699468 | ||||||
| chr17:7699468 | ATATATAT others(47): Show |
A | 1 | a0002c0002t0001g0004 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.643-1265_643-1212d others(56): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699468 | ||||||
| chr17:7699470 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | NA18944.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.643-1266_643-1265i others(14): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699470 | ||||||
| chr17:7699470 | A | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-1271A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699470 | |||||||
| chr17:7699470 | ATATATTT others(25): Show |
A | 3 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0095 |
3 | HG02055.hp2 HG03490.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.643-1265_643-1234d others(34): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699470 | ||||||
| chr17:7699472 | ATATTTAT others(23): Show |
A | 1 | a0001c0001t0001g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-1265_643-1236d others(32): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699472 | ||||||
| chr17:7699472 | ATATTTAT others(43): Show |
A | 2 | a0003c0004t0001g0229 a0003c0004t0001g0242 |
2 | HG01978.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.643-1265_643-1216d others(52): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699472 | ||||||
| chr17:7699473 | TATTTATA others(12): Show |
T | 1 | a0002c0003t0001g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.643-1267_643-1249d others(21): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699473 | |||||||
| chr17:7699474 | A | T | 2 | a0001c0001t0001g0196 a0002c0003t0001g0113 |
2 | HG00733.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.643-1267A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699474 | |||||||
| chr17:7699474 | ATTTATAT others(21): Show |
A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0180 |
3 | HG00609.hp2 NA19089.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.643-1265_643-1238d others(30): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699474 | ||||||
| chr17:7699474 | ATTTATAT others(41): Show |
A | 1 | a0002c0003t0001g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.643-1265_643-1218d others(50): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699474 | ||||||
| chr17:7699475 | TTTATATA others(8): Show |
T | 1 | a0007c0010t0001g0020 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.643-1264_643-1250d others(17): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699475 | ||||||
| chr17:7699476 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(18): Show |
26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.643-1265T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699476 | |||||||
| chr17:7699478 | A | ATT | 2 | a0001c0001t0001g0001 a0001c0001t0001g0039 |
3 | HG03017.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.643-1262_643-1261i others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699478 | ||||||
| chr17:7699478 | A | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
7 | HG00597.hp1 HG01934.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-1263A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699478 | |||||||
| chr17:7699479 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.643-1261_643-1245d others(19): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699479 | |||||||
| chr17:7699480 | A | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(6): Show |
10 | HG00558.hp2 HG01515.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-1261A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699480 | |||||||
| chr17:7699480 | ATATATAT others(35): Show |
A | 1 | a0001c0001t0001g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.643-1243_643-1202d others(44): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699480 | ||||||
| chr17:7699482 | A | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0044 others(5): Show |
9 | HG00558.hp2 HG01168.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-1259A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699482 | |||||||
| chr17:7699482 | ATATATAT others(13): Show |
A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
9 | HG01516.hp2 HG01934.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-1221_643-1202d others(22): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699482 | ||||||
| chr17:7699482 | ATATATAT others(33): Show |
A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0199 a0001c0001t0001g0216 |
3 | HG00642.hp2 HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.643-1241_643-1202d others(42): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699482 | ||||||
| chr17:7699484 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.643-1257A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699484 | |||||||
| chr17:7699484 | ATATATAT others(11): Show |
A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0021 others(4): Show |
9 | HG00408.hp2 HG00733.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.643-1239_643-1222d others(20): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699484 | ||||||
| chr17:7699486 | A | G | 1 | a0004c0005t0001g0096 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.643-1255A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699486 | |||||||
| chr17:7699486 | ATATATAT others(9): Show |
A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(3): Show |
6 | HG01255.hp2 HG02080.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.643-1239_643-1224d others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699486 | ||||||
| chr17:7699490 | A | G | 2 | a0004c0005t0001g0031 a0004c0005t0001g0101 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.643-1251A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699490 | |||||||
| chr17:7699492 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0043 | 2 | HG01074.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.643-1240_643-1239i others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699492 | ||||||
| chr17:7699492 | A | G | 2 | a0004c0005t0001g0030 a0004c0005t0001g0097 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.643-1249A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699492 | |||||||
| chr17:7699492 | A | T | 2 | a0001c0001t0001g0205 a0002c0003t0001g0133 |
2 | HG02257.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.643-1249A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699492 | |||||||
| chr17:7699492 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0002 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.643-1239_643-1230d others(12): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699492 | ||||||
| chr17:7699494 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0003 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.643-1240_643-1239i others(16): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699494 | ||||||
| chr17:7699494 | A | T | 3 | a0002c0002t0001g0092 a0002c0011t0001g0093 a0002c0011t0001g0094 |
3 | HG01168.hp1 HG03669.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.643-1247A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699494 | |||||||
| chr17:7699494 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.643-1239_643-1212d others(30): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699494 | ||||||
| chr17:7699496 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0187 |
2 | HG01106.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.643-1240_643-1239i others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699496 | ||||||
| chr17:7699496 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0003 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.643-1240_643-1239i others(16): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699496 | ||||||
| chr17:7699496 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0003 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.643-1240_643-1239i others(14): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699496 | ||||||
| chr17:7699496 | A | ATATTTAT others(23): Show |
1 | a0002c0003t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.643-1242_643-1241i others(32): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699496 | ||||||
| chr17:7699496 | A | T | 3 | a0001c0001t0002g0037 a0002c0002t0001g0058 a0003c0004t0001g0238 |
3 | HG02155.hp1 NA18951.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.643-1245A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699496 | |||||||
| chr17:7699496 | ATATATTT others(19): Show |
A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0207 |
2 | HG02074.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.643-1239_643-1214d others(28): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699496 | ||||||
| chr17:7699498 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0003 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.643-1240_643-1239i others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699498 | ||||||
| chr17:7699498 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0120 a0001c0001t0001g0214 |
2 | HG00280.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.643-1240_643-1239i others(12): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699498 | ||||||
| chr17:7699498 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0164 others(4): Show |
7 | HG00597.hp1 HG02717.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-1243A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699498 | |||||||
| chr17:7699498 | ATATTTAT others(17): Show |
A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0045 others(3): Show |
13 | HG01106.hp2 HG01496.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.643-1239_643-1216d others(26): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699498 | ||||||
| chr17:7699500 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0003 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.643-1240_643-1239i others(18): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699500 | ||||||
| chr17:7699500 | A | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(11): Show |
19 | HG00408.hp1 HG01070.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.643-1241A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699500 | |||||||
| chr17:7699500 | ATTTATAT others(15): Show |
A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0042 others(6): Show |
12 | HG00735.hp1 HG01109.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.643-1239_643-1218d others(24): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699500 | ||||||
| chr17:7699500 | ATTTATAT others(32): Show |
A | 1 | a0002c0002t0001g0008 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.643-1239_643-1201d others(41): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699500 | ||||||
| chr17:7699502 | T | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
44 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.643-1239T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699502 | |||||||
| chr17:7699504 | A | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(54): Show |
84 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.643-1237A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699504 | |||||||
| chr17:7699506 | A | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0146 others(2): Show |
5 | HG02451.hp2 NA18985.hp2 NA19085.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1235A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699506 | |||||||
| chr17:7699508 | A | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0180 others(1): Show |
4 | HG00609.hp2 NA19089.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1233A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699508 | |||||||
| chr17:7699510 | A | G | 1 | a0004c0005t0001g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.643-1231A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699510 | |||||||
| chr17:7699510 | A | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0163 a0001c0001t0001g0180 |
3 | HG00609.hp2 HG02071.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.643-1231A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699510 | |||||||
| chr17:7699512 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-1229A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699512 | |||||||
| chr17:7699518 | ATATT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(3): Show |
8 | HG01358.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-1219_643-1216d others(6): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699518 | ||||||
| chr17:7699519 | T | A | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-1222T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699519 | |||||||
| chr17:7699520 | A | T | 1 | a0002c0002t0001g0048 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-1221A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699520 | |||||||
| chr17:7699520 | ATT | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(29): Show |
44 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.643-1219_643-1218d others(4): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699520 | ||||||
| chr17:7699522 | T | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.643-1219T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699522 | |||||||
| chr17:7699522 | T | TTTTATAT others(25): Show |
1 | a0001c0001t0001g0044 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.643-1218_643-1217i others(34): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7699522 | ||||||
| chr17:7699525 | T | A | 1 | a0001c0001t0001g0161 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.643-1216T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699525 | |||||||
| chr17:7699525 | T | G | 2 | a0003c0004t0001g0229 a0003c0004t0001g0242 |
2 | HG01978.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.643-1216T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699525 | |||||||
| chr17:7699526 | A | G | 2 | a0003c0004t0001g0229 a0003c0004t0001g0242 |
2 | HG01978.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.643-1215A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699526 | |||||||
| chr17:7699527 | T | A | 2 | a0003c0004t0001g0229 a0003c0004t0001g0242 |
2 | HG01978.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.643-1214T>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699527 | |||||||
| chr17:7699597 | G | C | 1 | a0002c0002t0001g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.643-1144G>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699597 | |||||||
| chr17:7699673 | A | G | 11 | a0004c0005t0001g0030 a0004c0005t0001g0031 a0004c0005t0001g0096 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.643-1068A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699673 | |||||||
| chr17:7699726 | A | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(10): Show |
18 | HG00642.hp1 HG01346.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.643-1015A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699726 | |||||||
| chr17:7699810 | C | T | 1 | a0002c0002t0001g0048 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.643-931C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699810 | |||||||
| chr17:7699819 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.643-922C>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699819 | |||||||
| chr17:7699822 | T | C | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-919T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7699822 | |||||||
| chr17:7700048 | T | G | 1 | a0002c0003t0001g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.643-693T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700048 | |||||||
| chr17:7700066 | T | G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0201 a0002c0003t0001g0135 others(2): Show |
5 | HG00323.hp2 HG01106.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-675T>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700066 | |||||||
| chr17:7700067 | G | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-674G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700067 | |||||||
| chr17:7700068 | G | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.643-673G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700068 | |||||||
| chr17:7700128 | A | G | 7 | a0002c0003t0001g0121 a0002c0009t0001g0033 a0002c0009t0001g0124 others(4): Show |
9 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-613A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700128 | |||||||
| chr17:7700163 | C | T | 1 | a0002c0008t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.643-578C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700163 | |||||||
| chr17:7700372 | C | T | 4 | a0002c0002t0001g0072 a0002c0002t0001g0075 a0004c0005t0001g0031 others(1): Show |
5 | HG01884.hp2 HG02109.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-369C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700372 | |||||||
| chr17:7700485 | T | TA | 23 | a0001c0001t0001g0169 a0001c0001t0001g0207 a0002c0002t0001g0080 others(20): Show |
28 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.643-245dupA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7700485 | ||||||
| chr17:7700485 | T | TAA | 12 | a0002c0008t0001g0083 a0004c0005t0001g0030 a0004c0005t0001g0031 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.643-246_643-245dup others(2): Show |
WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7700485 | ||||||
| chr17:7700547 | T | TA | 12 | a0001c0001t0001g0152 a0004c0005t0001g0030 a0004c0005t0001g0031 others(9): Show |
14 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.643-182dupA | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 7700547 | ||||||
| chr17:7700550 | A | T | 19 | a0002c0003t0001g0012 a0002c0003t0001g0121 a0002c0003t0001g0125 others(16): Show |
24 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-191A>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700550 | |||||||
| chr17:7700628 | G | C | 11 | a0004c0005t0001g0030 a0004c0005t0001g0031 a0004c0005t0001g0096 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.643-113G>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700628 | |||||||
| chr17:7700645 | A | C | 1 | a0004c0005t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-96A>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700645 | |||||||
| chr17:7700724 | C | T | 2 | a0001c0001t0001g0017 a0003c0004t0001g0017 |
3 | NA18969.hp2 NA19084.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.643-17C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 4/10 | chr17 | 7700724 | |||||||
| chr17:7700865 | C | A | 5 | a0002c0003t0001g0121 a0006c0007t0001g0034 a0006c0007t0001g0122 others(2): Show |
6 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.731+36C>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7700865 | |||||||
| chr17:7700930 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.731+101G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7700930 | |||||||
| chr17:7700960 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0183 |
2 | NA18991.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.731+131G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7700960 | |||||||
| chr17:7700999 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.731+170G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7700999 | |||||||
| chr17:7701140 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG01074.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.731+311T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7701140 | |||||||
| chr17:7701153 | A | G | 105 | a0001c0001t0001g0022 a0002c0002t0001g0004 a0002c0002t0001g0006 others(102): Show |
146 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.732-306A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7701153 | |||||||
| chr17:7701324 | C | T | 1 | a0002c0003t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.732-135C>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7701324 | |||||||
| chr17:7701343 | G | T | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.732-116G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 5/10 | chr17 | 7701343 | |||||||
| chr17:7701847 | G | A | 1 | a0002c0003t0001g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.955+58G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 7/10 | chr17 | 7701847 | |||||||
| chr17:7702198 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956-146G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 7/10 | chr17 | 7702198 | |||||||
| chr17:7702234 | G | T | 8 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0105 others(5): Show |
12 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.956-110G>T | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 7/10 | chr17 | 7702234 | |||||||
| chr17:7702713 | G | A | 2 | a0002c0011t0001g0093 a0002c0011t0001g0094 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1165-30G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 8/10 | chr17 | 7702713 | |||||||
| chr17:7702893 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0195 |
2 | HG01515.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1268+47G>A | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 9/10 | chr17 | 7702893 | |||||||
| chr17:7702978 | T | C | 1 | a0004c0005t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1269-15T>C | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 9/10 | chr17 | 7702978 | |||||||
| chr17:7703145 | A | G | 1 | a0005c0006t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1403+18A>G | WRAP53 | ENSG00000141499.18 | transcript | ENST00000396463.7 | protein_coding | 10/10 | chr17 | 7703145 |