Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6643 |
| ensemblid | ENSG00000205302.7 |
| hgncid | 11173 |
| symbol | SNX2 |
| name | sorting nexin 2 |
| refseq_nuc | NM_003100.4 |
| refseq_prot | NP_003091.2 |
| ensembl_nuc | ENST00000379516.7 |
| ensembl_prot | ENSP00000368831.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 122775080 |
| end | 122834543 |
| strand | + |
| ver | v1.2 |
| region | chr5:122775080-122834543 |
| region5000 | chr5:122770080-122839543 |
| regionname0 | SNX2_chr5_122775080_122834543 |
| regionname5000 | SNX2_chr5_122770080_122839543 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 519 | 370 | 92 | 68 | 160 | 14 | 34 | 127 | SNX2_chr5_122770080_122839543 | SNX2 | MAAER others(514): Show |
chr5 | 122770080 | 122839543 |
| a0002 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | MAAER others(514): Show |
chr5 | 122770080 | 122839543 |
| a0003 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | MAAER others(514): Show |
chr5 | 122770080 | 122839543 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1557 | 337 | 89 | 66 | 135 | 12 | 33 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0001c0002 | 0/0 | 1557 | 30 | 0 | 2 | 25 | 2 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0001c0005 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0001c0006 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0001c0007 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0002c0004 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 | ||
| a0003c0003 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | ATGGC others(1552): Show |
chr5 | 122770080 | 122839543 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6473 | 88 | 11 | 21 | 42 | 3 | 11 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0002 | 0/0 | 6467 | 63 | 5 | 2 | 49 | 1 | 6 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6462): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0003 | 0/0 | 6480 | 24 | 5 | 12 | 2 | 2 | 3 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6475): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0004 | 0/1 | 6479 | 24 | 1 | 9 | 7 | 2 | 4 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6474): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0005 | 0/0 | 6474 | 12 | 4 | 2 | 6 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6469): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0007 | 1/0 | 6479 | 9 | 1 | 2 | 2 | 1 | 2 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6474): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0008 | 0/0 | 6475 | 9 | 0 | 0 | 9 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6470): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0010 | 0/0 | 6464 | 7 | 7 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0011 | 0/0 | 6482 | 6 | 6 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6477): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0012 | 0/0 | 6472 | 6 | 1 | 1 | 3 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6467): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0013 | 0/0 | 6481 | 5 | 3 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6476): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0014 | 0/0 | 6494 | 5 | 4 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6489): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0015 | 0/0 | 6462 | 4 | 4 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6457): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0017 | 0/0 | 6483 | 3 | 0 | 2 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6478): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0018 | 0/0 | 6481 | 3 | 1 | 1 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6476): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0019 | 0/0 | 6481 | 3 | 2 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6476): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0020 | 0/0 | 6480 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6475): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0021 | 0/0 | 6477 | 3 | 3 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6472): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0022 | 0/0 | 6473 | 3 | 0 | 0 | 3 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0023 | 0/0 | 6469 | 3 | 3 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6464): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0025 | 0/0 | 6468 | 3 | 0 | 0 | 3 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6463): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0026 | 0/0 | 6464 | 3 | 3 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0027 | 0/0 | 6480 | 2 | 0 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6475): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0028 | 0/0 | 6477 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6472): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0029 | 0/0 | 6473 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0030 | 0/0 | 6473 | 2 | 0 | 0 | 2 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0031 | 0/0 | 6470 | 2 | 0 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6465): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0032 | 0/0 | 6464 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0033 | 0/0 | 6464 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0034 | 0/0 | 6464 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0035 | 0/0 | 6479 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6474): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0036 | 0/0 | 6486 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6481): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0037 | 0/0 | 6470 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6465): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0038 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6480): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0039 | 0/0 | 6484 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6479): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0040 | 0/0 | 6483 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6478): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0041 | 0/0 | 6483 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6478): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0042 | 0/0 | 6483 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6478): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0043 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6477): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0044 | 0/0 | 6479 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6474): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0045 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6476): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0046 | 0/0 | 6479 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6474): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0047 | 0/0 | 6481 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6476): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0048 | 0/0 | 6477 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6472): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0049 | 0/0 | 6477 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6472): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0050 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6473): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0051 | 0/0 | 6477 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6472): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0052 | 0/0 | 6476 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6471): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0053 | 0/0 | 6474 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6469): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0054 | 0/0 | 6463 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6458): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0055 | 0/0 | 6474 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6469): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0056 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0057 | 0/0 | 6473 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0058 | 0/0 | 6473 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0059 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0060 | 0/0 | 6471 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6466): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0061 | 0/0 | 6471 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6466): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0062 | 0/0 | 6471 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6466): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0065 | 0/0 | 6469 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6464): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0068 | 0/0 | 6467 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6462): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0069 | 0/0 | 6466 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6461): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0071 | 0/0 | 6465 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6460): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0072 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0001c0001t0073 | 0/0 | 6475 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6470): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0006 | 0/0 | 6470 | 12 | 0 | 0 | 11 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6465): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0009 | 0/0 | 6471 | 7 | 0 | 0 | 7 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6466): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0016 | 0/0 | 6469 | 4 | 0 | 1 | 2 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6464): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0024 | 0/0 | 6470 | 3 | 0 | 0 | 2 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6465): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0063 | 0/0 | 6472 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6467): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0064 | 0/0 | 6470 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6465): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0066 | 0/0 | 6469 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6464): Show |
chr5 | 122770080 | 122839543 |
| a0001c0002t0067 | 0/0 | 6468 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6463): Show |
chr5 | 122770080 | 122839543 |
| a0001c0005t0070 | 0/0 | 6466 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6461): Show |
chr5 | 122770080 | 122839543 |
| a0001c0006t0015 | 0/0 | 6462 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6457): Show |
chr5 | 122770080 | 122839543 |
| a0001c0007t0020 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6475): Show |
chr5 | 122770080 | 122839543 |
| a0002c0004t0033 | 0/0 | 6464 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6459): Show |
chr5 | 122770080 | 122839543 |
| a0003c0003t0001 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | GCGCA others(6468): Show |
chr5 | 122770080 | 122839543 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0011g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0012g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0013g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0014g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0014g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0015g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0017g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0017g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0017g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0018g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0018g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0019g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0019g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0021g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0021g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0022g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0022g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0022g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0023g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0023g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0023g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0025g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0025g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0026g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0026g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0027g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0027g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0028g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0028g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0029g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0029g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0030g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0030g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0031g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0031g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0032g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0032g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0033g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0034g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0034g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0035g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0036g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0037g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0038g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0039g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0040g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0041g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0042g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0043g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0044g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0045g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0046g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0047g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0048g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0049g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0050g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0051g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0052g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0053g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0054g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0055g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0056g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0057g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0058g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0059g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0060g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0061g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0062g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0065g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0068g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0069g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0071g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0072g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0001t0073g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0016g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0016g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0016g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0024g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0024g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0024g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0063g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0064g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0066g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0002t0067g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0005t0070g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0006t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0001c0007t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0002c0004t0033g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0334 | EUR | GBR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0266 | EUR | GBR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0172 | EUR | GBR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00280 | hp1 | a0001 | c0002 | t0016 | g0213 | EUR | FIN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00280 | hp2 | a0001 | c0001 | t0039 | g0142 | EUR | FIN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00323 | hp1 | a0001 | c0002 | t0024 | g0206 | EUR | FIN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0143 | EUR | FIN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0107 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00609 | hp2 | a0002 | c0004 | t0033 | g0245 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | CHS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00738 | hp1 | a0001 | c0001 | t0061 | g0255 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01069 | hp2 | a0001 | c0001 | t0027 | g0189 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01070 | hp1 | a0001 | c0001 | t0046 | g0152 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01071 | hp2 | a0001 | c0001 | t0027 | g0190 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01081 | hp1 | a0001 | c0001 | t0050 | g0182 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0262 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01168 | hp2 | a0001 | c0001 | t0031 | g0254 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01175 | hp1 | a0001 | c0002 | t0066 | g0212 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01243 | hp1 | a0001 | c0001 | t0060 | g0277 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01243 | hp2 | a0001 | c0001 | t0019 | g0217 | AMR | PUR | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0154 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0276 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01258 | hp2 | a0001 | c0001 | t0018 | g0260 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01346 | hp1 | a0001 | c0001 | t0051 | g0198 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0257 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0188 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01515 | hp2 | a0001 | c0001 | t0017 | g0258 | EUR | IBS | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0263 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01884 | hp2 | a0001 | c0001 | t0034 | g0086 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0200 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01891 | hp2 | a0001 | c0001 | t0032 | g0236 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0241 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01943 | hp2 | a0001 | c0001 | t0031 | g0256 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01978 | hp1 | a0001 | c0002 | t0016 | g0214 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01981 | hp2 | a0001 | c0001 | t0041 | g0174 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01993 | hp1 | a0001 | c0001 | t0017 | g0259 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02015 | hp1 | a0001 | c0002 | t0009 | g0238 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0250 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0195 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02071 | hp1 | a0001 | c0002 | t0024 | g0215 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0269 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02129 | hp2 | a0001 | c0001 | t0059 | g0040 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02145 | hp1 | a0001 | c0001 | t0038 | g0084 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0270 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02155 | hp1 | a0001 | c0001 | t0068 | g0312 | EAS | CDX | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CDX | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02258 | hp1 | a0001 | c0001 | t0026 | g0090 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0242 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02280 | hp1 | a0001 | c0001 | t0029 | g0283 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0202 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0272 | AMR | PEL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0239 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | KHV | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02572 | hp2 | a0001 | c0001 | t0021 | g0140 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0279 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0017 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0252 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02622 | hp2 | a0001 | c0001 | t0028 | g0145 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0201 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02683 | hp2 | a0001 | c0001 | t0049 | g0268 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02717 | hp1 | a0001 | c0001 | t0032 | g0237 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0233 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02809 | hp1 | a0001 | c0007 | t0020 | g0231 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02818 | hp1 | a0001 | c0001 | t0056 | g0092 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02818 | hp2 | a0001 | c0001 | t0019 | g0199 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02895 | hp1 | a0001 | c0001 | t0037 | g0345 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02896 | hp1 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02896 | hp2 | a0001 | c0001 | t0057 | g0093 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02965 | hp1 | a0001 | c0001 | t0062 | g0234 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0191 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02970 | hp1 | a0001 | c0001 | t0047 | g0147 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02970 | hp2 | a0001 | c0001 | t0042 | g0149 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02976 | hp2 | a0001 | c0001 | t0072 | g0088 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0196 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03041 | hp2 | a0001 | c0006 | t0015 | g0017 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03098 | hp1 | a0001 | c0001 | t0034 | g0087 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03098 | hp2 | a0001 | c0005 | t0070 | g0020 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0264 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0157 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03195 | hp1 | a0001 | c0001 | t0069 | g0290 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03195 | hp2 | a0001 | c0001 | t0023 | g0286 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03209 | hp1 | a0001 | c0001 | t0040 | g0165 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0022 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0243 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0246 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0240 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03492 | hp2 | a0001 | c0001 | t0033 | g0244 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03516 | hp2 | a0001 | c0001 | t0073 | g0129 | AFR | ESN | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0232 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0247 | AFR | GWD | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03579 | hp1 | a0001 | c0001 | t0026 | g0089 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0224 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03710 | hp2 | a0001 | c0001 | t0058 | g0006 | SAS | PJL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0271 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03834 | hp2 | a0001 | c0001 | t0054 | g0003 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0163 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04199 | hp1 | a0001 | c0001 | t0035 | g0275 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04199 | hp2 | a0001 | c0001 | t0012 | g0116 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04204 | hp1 | a0001 | c0001 | t0044 | g0265 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0164 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | YRI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18522 | hp2 | a0001 | c0001 | t0023 | g0287 | AFR | YRI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | CHB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18747 | hp2 | a0001 | c0002 | t0006 | g0230 | EAS | CHB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0288 | AFR | YRI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18944 | hp1 | a0001 | c0002 | t0006 | g0014 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18951 | hp1 | a0001 | c0001 | t0012 | g0030 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18957 | hp1 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18960 | hp1 | a0001 | c0002 | t0006 | g0228 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0060 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18961 | hp1 | a0001 | c0001 | t0030 | g0079 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18961 | hp2 | a0001 | c0001 | t0071 | g0295 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18966 | hp1 | a0001 | c0001 | t0025 | g0317 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18967 | hp1 | a0001 | c0002 | t0063 | g0209 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18970 | hp1 | a0001 | c0001 | t0022 | g0104 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18972 | hp2 | a0001 | c0001 | t0055 | g0037 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18975 | hp2 | a0001 | c0002 | t0009 | g0208 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18977 | hp1 | a0001 | c0001 | t0022 | g0105 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18983 | hp2 | a0001 | c0002 | t0009 | g0211 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18984 | hp2 | a0001 | c0002 | t0064 | g0221 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18990 | hp1 | a0001 | c0002 | t0016 | g0207 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18992 | hp1 | a0001 | c0001 | t0030 | g0117 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18992 | hp2 | a0001 | c0001 | t0022 | g0077 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18995 | hp1 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18995 | hp2 | a0001 | c0001 | t0048 | g0033 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18998 | hp1 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19001 | hp2 | a0001 | c0002 | t0009 | g0220 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19005 | hp1 | a0001 | c0002 | t0016 | g0203 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19010 | hp2 | a0001 | c0002 | t0024 | g0204 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19011 | hp1 | a0001 | c0002 | t0006 | g0226 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19012 | hp2 | a0001 | c0002 | t0009 | g0014 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0187 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19054 | hp2 | a0001 | c0001 | t0025 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19056 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19057 | hp2 | a0001 | c0001 | t0065 | g0297 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19058 | hp2 | a0001 | c0001 | t0052 | g0046 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0227 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19072 | hp1 | a0001 | c0002 | t0006 | g0225 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19074 | hp1 | a0001 | c0002 | t0006 | g0223 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19077 | hp2 | a0001 | c0002 | t0067 | g0205 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19082 | hp1 | a0001 | c0002 | t0009 | g0219 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19082 | hp2 | a0001 | c0002 | t0009 | g0210 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0055 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19083 | hp2 | a0001 | c0001 | t0025 | g0316 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0222 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19090 | hp1 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0249 | AFR | ASW | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20129 | hp2 | a0001 | c0001 | t0029 | g0282 | AFR | ASW | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0179 | EUR | TSI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20752 | hp2 | a0001 | c0001 | t0018 | g0261 | EUR | TSI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0016 | EUR | TSI | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0251 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0274 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0235 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02559 | hp1 | a0001 | c0001 | t0043 | g0170 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG02559 | hp2 | a0001 | c0001 | t0045 | g0146 | AFR | ACB | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03471 | hp1 | a0001 | c0001 | t0028 | g0144 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0267 | AFR | USA | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | USA | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA20300 | hp2 | a0001 | c0001 | t0053 | g0021 | AFR | USA | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| NA21309 | hp2 | a0001 | c0001 | t0036 | g0082 | AFR | LWK | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0216 | REF | REF | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0278 | REF | REF | SNX2_chr5_122770080_122839543 | SNX2 | chr5 | 122770080 | 122839543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:122818975 | G | A | 1 | a0003 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1164G>A | p.Met388Ile | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/15 | 1188/6479 | 1164/1560 | 388/519 | chr5 | 122818975 | |||
| chr5:122819004 | G | A | 1 | a0002 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1193G>A | p.Arg398His | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/15 | 1217/6479 | 1193/1560 | 398/519 | chr5 | 122819004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:122803525 | C | T | 1 | a0001c0007 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.555C>T | p.Ser185Ser | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/15 | 579/6479 | 555/1560 | 185/519 | chr5 | 122803525 | |||
| chr5:122808278 | G | T | 1 | a0001c0006 | 1 | HG03041.hp2 | splice_region_variant&synonymous_variant | LOW | c.645G>T | p.Gly215Gly | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/15 | 669/6479 | 645/1560 | 215/519 | chr5 | 122808278 | |||
| chr5:122816995 | C | T | 1 | a0001c0005 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.879C>T | p.Asn293Asn | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 9/15 | 903/6479 | 879/1560 | 293/519 | chr5 | 122816995 | |||
| chr5:122829622 | C | T | 1 | a0001c0002 | 30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
synonymous_variant | LOW | c.1534C>T | p.Leu512Leu | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1558/6479 | 1534/1560 | 512/519 | chr5 | 122829622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:122829775 | T | C | 1 | a0001c0001t0035 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 127 | chr5 | 122829775 | ||||||
| chr5:122829775 | T | TAC | 4 | a0001c0001t0018 a0001c0001t0038 a0001c0001t0039 others(1): Show |
6 | HG00280.hp2 HG01258.hp2 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*162_*163dupAC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 164 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | T | TACAC | 3 | a0001c0001t0017 a0001c0001t0036 a0001c0001t0037 |
5 | HG01109.hp2 HG01515.hp2 HG01993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*160_*163dupACAC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 164 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TAC | T | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(10): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*162_*163delAC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 162 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACAC | T | 6 | a0001c0001t0008 a0001c0001t0050 a0001c0001t0051 others(3): Show |
14 | HG00544.hp2 HG01081.hp1 HG01346.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*160_*163delACAC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 160 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACAC | T | 14 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(11): Show |
121 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*158_*163delACACAC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 158 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACACA others(1): Show |
T | 3 | a0001c0001t0031 a0001c0001t0061 a0001c0001t0062 |
4 | HG00738.hp1 HG01168.hp2 HG01943.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*156_*163delACACAC others(2): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 156 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACACA others(3): Show |
T | 4 | a0001c0002t0006 a0001c0002t0009 a0001c0002t0063 others(1): Show |
21 | HG02015.hp1 HG03704.hp1 NA18747.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*154_*163delACACAC others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 154 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACACA others(5): Show |
T | 6 | a0001c0001t0023 a0001c0001t0065 a0001c0002t0016 others(3): Show |
13 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*152_*163delACACAC others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 152 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACACA others(7): Show |
T | 5 | a0001c0001t0002 a0001c0001t0025 a0001c0001t0032 others(2): Show |
70 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*150_*163delACACAC others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 150 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829775 | TACACACA others(9): Show |
T | 10 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0026 others(7): Show |
22 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*148_*163delACACAC others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 148 | INFO_REALIGN_3_PRIME | chr5 | 122829775 | |||||
| chr5:122829781 | C | T | 1 | a0001c0001t0073 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 133 | chr5 | 122829781 | ||||||
| chr5:122829849 | T | C | 1 | a0001c0001t0023 | 3 | HG03195.hp2 NA18522.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 201 | chr5 | 122829849 | ||||||
| chr5:122830133 | T | C | 14 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0023 others(11): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*485T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 485 | chr5 | 122830133 | ||||||
| chr5:122830264 | G | A | 1 | a0001c0001t0068 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*616G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 616 | chr5 | 122830264 | ||||||
| chr5:122830350 | CTTGTTTT others(3): Show |
C | 1 | a0001c0001t0054 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703_*712delTTGTTT others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 703 | chr5 | 122830350 | ||||||
| chr5:122830450 | C | T | 1 | a0001c0001t0073 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 802 | chr5 | 122830450 | ||||||
| chr5:122830468 | G | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(20): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*820G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 820 | chr5 | 122830468 | ||||||
| chr5:122830494 | T | C | 2 | a0001c0001t0033 a0002c0004t0033 |
2 | HG00609.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*846T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 846 | chr5 | 122830494 | ||||||
| chr5:122830746 | C | T | 1 | a0001c0001t0047 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1098C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1098 | chr5 | 122830746 | ||||||
| chr5:122830769 | G | A | 1 | a0001c0001t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1121 | chr5 | 122830769 | ||||||
| chr5:122831009 | C | CA | 7 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0052 others(4): Show |
30 | HG01069.hp2 HG01071.hp2 HG01099.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1385dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1386 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | C | CAA | 8 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0040 others(5): Show |
43 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1384_*1385dupAA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1386 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | C | CAAA | 12 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(9): Show |
49 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1383_*1385dupAAA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1386 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | C | CAAAA | 6 | a0001c0001t0019 a0001c0001t0038 a0001c0001t0041 others(3): Show |
8 | HG01243.hp2 HG01981.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1382_*1385dupAAAA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1386 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | CA | C | 12 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0023 others(9): Show |
86 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1385delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1385 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | CAA | C | 5 | a0001c0001t0010 a0001c0001t0033 a0001c0001t0060 others(2): Show |
11 | HG00609.hp2 HG01243.hp1 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1384_*1385delAA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1384 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831009 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0037 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373_*1385delAAAA others(9): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1373 | INFO_REALIGN_3_PRIME | chr5 | 122831009 | |||||
| chr5:122831025 | A | G | 3 | a0001c0001t0026 a0001c0001t0034 a0001c0001t0072 |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1377A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1377 | chr5 | 122831025 | ||||||
| chr5:122831121 | C | A | 2 | a0001c0001t0033 a0002c0004t0033 |
2 | HG00609.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1473C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1473 | chr5 | 122831121 | ||||||
| chr5:122831428 | G | A | 1 | a0001c0001t0046 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1780G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1780 | chr5 | 122831428 | ||||||
| chr5:122831488 | TA | T | 3 | a0001c0001t0026 a0001c0001t0034 a0001c0001t0072 |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1848delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1848 | INFO_REALIGN_3_PRIME | chr5 | 122831488 | |||||
| chr5:122831494 | A | C | 1 | a0001c0001t0034 | 2 | HG01884.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1846A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1846 | chr5 | 122831494 | ||||||
| chr5:122831511 | G | A | 1 | a0001c0001t0072 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1863G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 1863 | chr5 | 122831511 | ||||||
| chr5:122831652 | C | T | 1 | a0001c0001t0030 | 2 | NA18961.hp1 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2004 | chr5 | 122831652 | ||||||
| chr5:122831729 | T | C | 1 | a0001c0001t0055 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2081T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2081 | chr5 | 122831729 | ||||||
| chr5:122831780 | A | G | 8 | a0001c0002t0006 a0001c0002t0009 a0001c0002t0016 others(5): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2132A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2132 | chr5 | 122831780 | ||||||
| chr5:122831809 | T | C | 1 | a0001c0001t0029 | 2 | HG02280.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2161T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2161 | chr5 | 122831809 | ||||||
| chr5:122832135 | T | TGAGATCA others(7): Show |
1 | a0001c0001t0014 | 5 | HG01934.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2488_*2501dupGAGA others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2502 | INFO_REALIGN_3_PRIME | chr5 | 122832135 | |||||
| chr5:122832242 | T | G | 1 | a0001c0001t0044 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2594T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2594 | chr5 | 122832242 | ||||||
| chr5:122832385 | T | TAAG | 14 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0023 others(11): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2738_*2740dupAAG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2741 | INFO_REALIGN_3_PRIME | chr5 | 122832385 | |||||
| chr5:122832405 | G | A | 1 | a0001c0001t0073 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2757G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2757 | chr5 | 122832405 | ||||||
| chr5:122832420 | C | A | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(30): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2772C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2772 | chr5 | 122832420 | ||||||
| chr5:122832454 | C | A | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG02818.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2806C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2806 | chr5 | 122832454 | ||||||
| chr5:122832548 | TATC | T | 1 | a0001c0001t0021 | 3 | HG02280.hp2 HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2901_*2903delATC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2901 | chr5 | 122832548 | ||||||
| chr5:122832618 | C | T | 1 | a0001c0001t0057 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 2970 | chr5 | 122832618 | ||||||
| chr5:122832841 | A | G | 1 | a0001c0002t0064 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3193 | chr5 | 122832841 | ||||||
| chr5:122832875 | A | G | 1 | a0001c0001t0073 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3227A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3227 | chr5 | 122832875 | ||||||
| chr5:122833063 | A | G | 4 | a0001c0001t0011 a0001c0001t0036 a0001c0001t0038 others(1): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3415A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3415 | chr5 | 122833063 | ||||||
| chr5:122833242 | A | G | 2 | a0001c0001t0015 a0001c0006t0015 |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3594A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3594 | chr5 | 122833242 | ||||||
| chr5:122833313 | T | C | 1 | a0001c0001t0058 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3665T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3665 | chr5 | 122833313 | ||||||
| chr5:122833350 | A | T | 2 | a0001c0001t0015 a0001c0006t0015 |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3702A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3702 | chr5 | 122833350 | ||||||
| chr5:122833487 | AG | A | 2 | a0001c0001t0015 a0001c0006t0015 |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3840delG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 3840 | chr5 | 122833487 | ||||||
| chr5:122833746 | T | C | 1 | a0001c0001t0059 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4098T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4098 | chr5 | 122833746 | ||||||
| chr5:122833753 | C | A | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*4105C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4105 | chr5 | 122833753 | ||||||
| chr5:122833793 | G | A | 2 | a0001c0001t0020 a0001c0007t0020 |
3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4145G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4145 | chr5 | 122833793 | ||||||
| chr5:122833850 | C | T | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(20): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*4202C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4202 | chr5 | 122833850 | ||||||
| chr5:122834063 | T | G | 1 | a0001c0002t0066 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4415T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4415 | chr5 | 122834063 | ||||||
| chr5:122834238 | G | C | 1 | a0001c0001t0073 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4590G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4590 | chr5 | 122834238 | ||||||
| chr5:122834282 | A | G | 1 | a0001c0001t0022 | 3 | NA18970.hp1 NA18977.hp1 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4634A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4634 | chr5 | 122834282 | ||||||
| chr5:122834409 | C | T | 1 | a0001c0001t0010 | 7 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4761C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4761 | chr5 | 122834409 | ||||||
| chr5:122834426 | T | G | 2 | a0001c0001t0031 a0001c0001t0061 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4778T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4778 | chr5 | 122834426 | ||||||
| chr5:122834540 | A | G | 3 | a0001c0001t0010 a0001c0001t0033 a0002c0004t0033 |
9 | HG00609.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4892A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 15/15 | 4892 | chr5 | 122834540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:122775231 | G | T | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.108+20G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775231 | |||||||
| chr5:122775239 | G | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+28G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775239 | |||||||
| chr5:122775300 | G | T | 2 | a0001c0001t0002g0343 a0001c0001t0002g0344 |
2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.108+89G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775300 | |||||||
| chr5:122775310 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.108+99G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775310 | |||||||
| chr5:122775338 | C | T | 4 | a0001c0001t0005g0280 a0001c0001t0005g0281 a0001c0001t0029g0282 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+127C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775338 | |||||||
| chr5:122775380 | T | C | 2 | a0001c0001t0012g0022 a0001c0001t0053g0021 |
2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.108+169T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775380 | |||||||
| chr5:122775477 | T | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
69 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.108+266T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775477 | |||||||
| chr5:122775515 | G | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.108+304G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775515 | |||||||
| chr5:122775620 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0253 |
3 | HG01258.hp1 HG01346.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.108+409C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775620 | |||||||
| chr5:122775644 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.108+433T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775644 | |||||||
| chr5:122775716 | G | C | 1 | a0001c0001t0036g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108+505G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775716 | |||||||
| chr5:122775726 | C | G | 9 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(6): Show |
9 | HG00609.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+515C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775726 | |||||||
| chr5:122775947 | C | G | 5 | a0001c0001t0014g0239 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01934.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+736C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122775947 | |||||||
| chr5:122776052 | T | C | 3 | a0001c0001t0003g0083 a0001c0001t0003g0085 a0001c0001t0038g0084 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108+841T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776052 | |||||||
| chr5:122776236 | A | G | 1 | a0001c0002t0009g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.108+1025A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776236 | |||||||
| chr5:122776334 | C | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+1123C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776334 | |||||||
| chr5:122776610 | C | G | 1 | a0001c0001t0002g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.108+1399C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776610 | |||||||
| chr5:122776617 | A | G | 1 | a0001c0001t0026g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+1406A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776617 | |||||||
| chr5:122776648 | G | A | 1 | a0001c0001t0032g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.108+1437G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776648 | |||||||
| chr5:122776786 | G | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+1575G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776786 | |||||||
| chr5:122776825 | T | G | 1 | a0001c0001t0002g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.108+1614T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776825 | |||||||
| chr5:122776891 | G | C | 1 | a0001c0001t0002g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.108+1680G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776891 | |||||||
| chr5:122776990 | G | T | 1 | a0001c0001t0007g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.108+1779G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122776990 | |||||||
| chr5:122777323 | C | T | 1 | a0001c0001t0062g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.108+2112C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777323 | |||||||
| chr5:122777358 | T | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+2147T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777358 | |||||||
| chr5:122777371 | T | A | 16 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(13): Show |
16 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.108+2160T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777371 | |||||||
| chr5:122777414 | A | G | 1 | a0001c0001t0002g0341 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.108+2203A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777414 | |||||||
| chr5:122777712 | T | G | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.108+2501T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777712 | |||||||
| chr5:122777756 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.108+2545G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777756 | |||||||
| chr5:122777768 | A | G | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.108+2557A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777768 | |||||||
| chr5:122777841 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00597.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.108+2630C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777841 | |||||||
| chr5:122777977 | A | G | 4 | a0001c0001t0012g0022 a0001c0001t0029g0282 a0001c0001t0029g0283 others(1): Show |
4 | HG02280.hp1 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+2766A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777977 | |||||||
| chr5:122777980 | G | A | 114 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(111): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.108+2769G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122777980 | |||||||
| chr5:122778061 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.108+2850G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778061 | |||||||
| chr5:122778298 | C | T | 1 | a0001c0001t0002g0341 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.108+3087C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778298 | |||||||
| chr5:122778360 | C | A | 1 | a0001c0001t0001g0008 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.108+3149C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778360 | |||||||
| chr5:122778396 | T | C | 6 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0023g0286 others(3): Show |
6 | HG03195.hp1 HG03195.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+3185T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778396 | |||||||
| chr5:122778558 | G | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.108+3347G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778558 | |||||||
| chr5:122778573 | A | G | 3 | a0001c0001t0020g0232 a0001c0001t0020g0233 a0001c0007t0020g0231 |
3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.108+3362A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778573 | |||||||
| chr5:122778591 | C | A | 1 | a0001c0001t0003g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.108+3380C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778591 | |||||||
| chr5:122778641 | T | A | 3 | a0001c0001t0003g0137 a0001c0001t0003g0139 a0001c0001t0004g0138 |
3 | NA18949.hp2 NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.108+3430T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778641 | |||||||
| chr5:122778653 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.108+3442C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778653 | |||||||
| chr5:122778832 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.108+3621G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122778832 | |||||||
| chr5:122779034 | A | G | 15 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(12): Show |
16 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.108+3823A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779034 | |||||||
| chr5:122779041 | G | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+3830G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779041 | |||||||
| chr5:122779228 | A | T | 2 | a0001c0001t0012g0022 a0001c0001t0053g0021 |
2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.108+4017A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779228 | |||||||
| chr5:122779231 | G | C | 6 | a0001c0001t0007g0257 a0001c0001t0017g0258 a0001c0001t0017g0259 others(3): Show |
6 | HG01109.hp2 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+4020G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779231 | |||||||
| chr5:122779434 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.108+4223C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779434 | |||||||
| chr5:122779558 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.108+4347A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779558 | |||||||
| chr5:122779779 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+4568G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779779 | |||||||
| chr5:122779827 | A | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+4616A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779827 | |||||||
| chr5:122779876 | C | T | 2 | a0001c0001t0002g0289 a0001c0001t0069g0290 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.108+4665C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779876 | |||||||
| chr5:122779943 | C | T | 1 | a0001c0001t0019g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108+4732C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779943 | |||||||
| chr5:122779998 | G | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+4787G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122779998 | |||||||
| chr5:122780017 | T | A | 1 | a0001c0001t0021g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.108+4806T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780017 | |||||||
| chr5:122780158 | G | C | 1 | a0001c0001t0002g0291 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.108+4947G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780158 | |||||||
| chr5:122780224 | A | G | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+5013A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780224 | |||||||
| chr5:122780261 | C | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+5050C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780261 | |||||||
| chr5:122780394 | G | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.108+5183G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780394 | |||||||
| chr5:122780478 | CTT | C | 3 | a0001c0001t0020g0232 a0001c0001t0020g0233 a0001c0007t0020g0231 |
3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.108+5270_108+5271d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122780478 | ||||||
| chr5:122780537 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.108+5326A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780537 | |||||||
| chr5:122780571 | C | CT | 4 | a0001c0001t0001g0080 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG01168.hp1 HG01496.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+5364dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122780571 | ||||||
| chr5:122780574 | TTC | T | 18 | a0001c0001t0003g0085 a0001c0001t0021g0201 a0001c0001t0021g0202 others(15): Show |
18 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.108+5365_108+5366d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122780574 | ||||||
| chr5:122780575 | TC | T | 59 | a0001c0001t0001g0074 a0001c0001t0001g0099 a0001c0001t0003g0012 others(56): Show |
60 | HG00609.hp2 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.108+5365delC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780575 | |||||||
| chr5:122780576 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.108+5365C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122780576 | |||||||
| chr5:122780576 | CT | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(70): Show |
82 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.108+5378delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122780576 | ||||||
| chr5:122781011 | G | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.108+5800G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781011 | |||||||
| chr5:122781044 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.108+5833G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781044 | |||||||
| chr5:122781108 | A | G | 59 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.108+5897A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781108 | |||||||
| chr5:122781301 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+6090A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781301 | |||||||
| chr5:122781335 | A | G | 3 | a0001c0001t0005g0280 a0001c0001t0005g0281 a0001c0001t0011g0200 |
3 | HG01891.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.108+6124A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781335 | |||||||
| chr5:122781515 | G | A | 101 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(98): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.108+6304G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781515 | |||||||
| chr5:122781907 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+6696T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122781907 | |||||||
| chr5:122782184 | C | T | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+6973C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782184 | |||||||
| chr5:122782269 | G | A | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.108+7058G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782269 | |||||||
| chr5:122782294 | G | A | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.108+7083G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782294 | |||||||
| chr5:122782319 | A | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+7108A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782319 | |||||||
| chr5:122782527 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+7316T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782527 | |||||||
| chr5:122782530 | C | T | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.108+7319C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782530 | |||||||
| chr5:122782534 | C | T | 2 | a0001c0001t0012g0022 a0001c0001t0053g0021 |
2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.108+7323C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782534 | |||||||
| chr5:122782587 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108+7376G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782587 | |||||||
| chr5:122782598 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.108+7387A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782598 | |||||||
| chr5:122782625 | C | G | 2 | a0001c0001t0005g0280 a0001c0001t0005g0281 |
2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.108+7414C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782625 | |||||||
| chr5:122782712 | T | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+7501T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782712 | |||||||
| chr5:122782770 | G | A | 2 | a0001c0001t0056g0092 a0001c0001t0057g0093 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.108+7559G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782770 | |||||||
| chr5:122782828 | C | A | 1 | a0001c0001t0002g0018 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.108+7617C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782828 | |||||||
| chr5:122782903 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+7692C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122782903 | |||||||
| chr5:122783103 | A | AT | 92 | a0001c0001t0002g0339 a0001c0001t0002g0340 a0001c0001t0002g0342 others(89): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.108+7907dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122783103 | ||||||
| chr5:122783103 | AT | A | 8 | a0001c0001t0005g0280 a0001c0001t0005g0281 a0001c0001t0012g0022 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+7907delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122783103 | ||||||
| chr5:122783103 | ATT | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
120 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.108+7906_108+7907d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122783103 | ||||||
| chr5:122783139 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+7928G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783139 | |||||||
| chr5:122783167 | G | C | 1 | a0001c0001t0005g0024 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.108+7956G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783167 | |||||||
| chr5:122783197 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+7986G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783197 | |||||||
| chr5:122783299 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+8088C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783299 | |||||||
| chr5:122783580 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.108+8369A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783580 | |||||||
| chr5:122783702 | G | A | 1 | a0001c0001t0005g0025 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+8491G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783702 | |||||||
| chr5:122783885 | C | A | 2 | a0001c0001t0034g0086 a0001c0001t0034g0087 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.108+8674C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783885 | |||||||
| chr5:122783910 | CTATT | C | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.108+8706_108+8709d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122783910 | ||||||
| chr5:122783964 | A | G | 1 | a0001c0001t0019g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.108+8753A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783964 | |||||||
| chr5:122783969 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.108+8758G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783969 | |||||||
| chr5:122783972 | C | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.108+8761C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783972 | |||||||
| chr5:122783987 | T | C | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.108+8776T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122783987 | |||||||
| chr5:122784043 | T | G | 1 | a0001c0001t0039g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.108+8832T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784043 | |||||||
| chr5:122784116 | G | C | 1 | a0001c0001t0003g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.108+8905G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784116 | |||||||
| chr5:122784140 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | NA18944.hp2 NA18948.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+8929C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784140 | |||||||
| chr5:122784182 | G | A | 6 | a0001c0001t0019g0199 a0001c0001t0019g0217 a0001c0001t0028g0144 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+8971G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784182 | |||||||
| chr5:122784211 | C | CT | 6 | a0001c0001t0020g0232 a0001c0001t0020g0233 a0001c0001t0031g0254 others(3): Show |
6 | HG00738.hp1 HG01168.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+9012dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122784211 | ||||||
| chr5:122784211 | C | T | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+9000C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784211 | |||||||
| chr5:122784316 | A | T | 1 | a0001c0001t0007g0273 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.108+9105A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784316 | |||||||
| chr5:122784496 | T | C | 1 | a0001c0001t0007g0273 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.108+9285T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784496 | |||||||
| chr5:122784621 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.108+9410C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784621 | |||||||
| chr5:122784696 | T | C | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+9485T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784696 | |||||||
| chr5:122784828 | G | A | 14 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+9617G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784828 | |||||||
| chr5:122784918 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0127 others(2): Show |
7 | HG01106.hp1 HG01261.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+9707C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122784918 | |||||||
| chr5:122785181 | T | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.108+9970T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785181 | |||||||
| chr5:122785275 | T | A | 1 | a0001c0001t0002g0018 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.109-9991T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785275 | |||||||
| chr5:122785278 | T | G | 1 | a0001c0001t0002g0292 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109-9988T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785278 | |||||||
| chr5:122785502 | TC | T | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.109-9763delC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785502 | |||||||
| chr5:122785503 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
149 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.109-9763C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785503 | |||||||
| chr5:122785529 | T | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-9737T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785529 | |||||||
| chr5:122785545 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.109-9721T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785545 | |||||||
| chr5:122785629 | C | T | 1 | a0001c0001t0026g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.109-9637C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785629 | |||||||
| chr5:122785772 | A | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-9494A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785772 | |||||||
| chr5:122785809 | C | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.109-9457C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785809 | |||||||
| chr5:122785859 | G | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
70 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.109-9407G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785859 | |||||||
| chr5:122785918 | C | T | 1 | a0001c0001t0051g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.109-9348C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122785918 | |||||||
| chr5:122786052 | G | A | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.109-9214G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786052 | |||||||
| chr5:122786064 | C | A | 1 | a0001c0001t0053g0021 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109-9202C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786064 | |||||||
| chr5:122786216 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.109-9050A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786216 | |||||||
| chr5:122786314 | A | G | 6 | a0001c0002t0006g0015 a0001c0002t0006g0225 a0001c0002t0006g0226 others(3): Show |
7 | NA18960.hp1 NA18995.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-8952A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786314 | |||||||
| chr5:122786338 | T | G | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-8928T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786338 | |||||||
| chr5:122786369 | C | T | 4 | a0001c0001t0010g0252 a0001c0001t0021g0140 a0001c0001t0021g0201 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-8897C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786369 | |||||||
| chr5:122786370 | G | A | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-8896G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786370 | |||||||
| chr5:122786464 | A | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.109-8802A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786464 | |||||||
| chr5:122786465 | T | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.109-8801T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786465 | |||||||
| chr5:122786579 | C | T | 1 | a0001c0001t0038g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109-8687C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786579 | |||||||
| chr5:122786629 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-8637C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786629 | |||||||
| chr5:122786688 | T | TA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-8567dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122786688 | ||||||
| chr5:122786724 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.109-8542C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786724 | |||||||
| chr5:122786759 | C | T | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.109-8507C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786759 | |||||||
| chr5:122786999 | A | T | 1 | a0001c0001t0002g0338 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109-8267A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122786999 | |||||||
| chr5:122787120 | C | T | 4 | a0001c0001t0019g0199 a0001c0001t0019g0217 a0001c0001t0045g0146 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-8146C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787120 | |||||||
| chr5:122787520 | C | G | 1 | a0001c0001t0008g0072 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.109-7746C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787520 | |||||||
| chr5:122787523 | A | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
139 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.109-7743A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787523 | |||||||
| chr5:122787604 | C | T | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.109-7662C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787604 | |||||||
| chr5:122787637 | A | G | 14 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-7629A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787637 | |||||||
| chr5:122787828 | C | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.109-7438C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787828 | |||||||
| chr5:122787885 | T | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
8 | NA18939.hp1 NA18944.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-7381T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787885 | |||||||
| chr5:122787912 | A | G | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.109-7354A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787912 | |||||||
| chr5:122787914 | C | G | 14 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-7352C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122787914 | |||||||
| chr5:122788172 | A | G | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.109-7094A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788172 | |||||||
| chr5:122788184 | A | G | 7 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-7082A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788184 | |||||||
| chr5:122788219 | T | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-7047T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788219 | |||||||
| chr5:122788244 | C | T | 1 | a0001c0001t0031g0256 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.109-7022C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788244 | |||||||
| chr5:122788278 | C | T | 3 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 |
3 | HG02055.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.109-6988C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788278 | |||||||
| chr5:122788360 | A | G | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-6906A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788360 | |||||||
| chr5:122788517 | G | T | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-6749G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788517 | |||||||
| chr5:122788622 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.109-6644A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788622 | |||||||
| chr5:122788740 | TTTTC | T | 13 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.109-6519_109-6516d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122788740 | ||||||
| chr5:122788767 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0012g0030 |
3 | HG00673.hp1 NA18951.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.109-6499T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788767 | |||||||
| chr5:122788869 | A | G | 7 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-6397A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788869 | |||||||
| chr5:122788927 | G | C | 1 | a0001c0001t0045g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.109-6339G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788927 | |||||||
| chr5:122788929 | C | T | 116 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(113): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.109-6337C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122788929 | |||||||
| chr5:122789071 | T | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-6195T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789071 | |||||||
| chr5:122789090 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.109-6176G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789090 | |||||||
| chr5:122789097 | A | G | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.109-6169A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789097 | |||||||
| chr5:122789284 | G | C | 1 | a0001c0001t0053g0021 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109-5982G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789284 | |||||||
| chr5:122789413 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.109-5853C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789413 | |||||||
| chr5:122789442 | T | TAC | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.109-5804_109-5803d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789442 | ||||||
| chr5:122789442 | T | TACAC | 6 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0130 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-5806_109-5803d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789442 | ||||||
| chr5:122789442 | TAC | T | 5 | a0001c0001t0002g0333 a0001c0001t0002g0334 a0001c0001t0020g0232 others(2): Show |
5 | HG00099.hp1 HG02040.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-5804_109-5803d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789442 | ||||||
| chr5:122789448 | C | CACACACA others(1): Show |
4 | a0001c0001t0014g0240 a0001c0001t0014g0241 a0001c0001t0014g0242 others(1): Show |
4 | HG01934.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-5811_109-5810i others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789448 | ||||||
| chr5:122789456 | CACACACA others(1): Show |
C | 5 | a0001c0001t0003g0085 a0001c0001t0003g0137 a0001c0001t0019g0199 others(2): Show |
5 | HG01243.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-5802_109-5795d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789456 | ||||||
| chr5:122789458 | CACACAG | C | 64 | a0001c0001t0003g0083 a0001c0001t0003g0136 a0001c0001t0003g0139 others(61): Show |
66 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.109-5802_109-5797d others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789458 | ||||||
| chr5:122789460 | C | G | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.109-5806C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789460 | |||||||
| chr5:122789460 | CACAG | C | 8 | a0001c0001t0003g0012 a0001c0001t0003g0143 a0001c0001t0003g0158 others(5): Show |
9 | HG00140.hp1 HG00323.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-5802_109-5799d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789460 | ||||||
| chr5:122789464 | G | C | 6 | a0001c0001t0014g0239 a0001c0001t0014g0240 a0001c0001t0014g0241 others(3): Show |
6 | HG01934.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-5802G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789464 | |||||||
| chr5:122789469 | A | G | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.109-5797A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789469 | |||||||
| chr5:122789470 | C | G | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.109-5796C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789470 | |||||||
| chr5:122789473 | G | A | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.109-5793G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789473 | |||||||
| chr5:122789474 | G | C | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.109-5792G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789474 | |||||||
| chr5:122789474 | G | GAC | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
124 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.109-5763_109-5762d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACAC | 58 | a0001c0001t0001g0076 a0001c0001t0001g0098 a0001c0001t0001g0099 others(55): Show |
65 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.109-5765_109-5762d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACAC | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
10 | HG00639.hp1 HG02071.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-5767_109-5762d others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACACA others(1): Show |
3 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0002g0338 |
3 | HG01074.hp2 NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.109-5769_109-5762d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACACA others(7): Show |
6 | a0001c0002t0006g0014 a0001c0002t0006g0222 a0001c0002t0006g0223 others(3): Show |
6 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-5775_109-5762d others(16): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACACA others(9): Show |
6 | a0001c0002t0006g0015 a0001c0002t0006g0227 a0001c0002t0006g0228 others(3): Show |
7 | NA18960.hp1 NA18984.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-5777_109-5762d others(18): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACACA others(11): Show |
2 | a0001c0002t0006g0226 a0001c0002t0009g0219 |
2 | NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.109-5779_109-5762d others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | G | GACACACA others(15): Show |
1 | a0001c0002t0006g0225 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.109-5783_109-5762d others(24): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | GAC | G | 19 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0007g0272 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.109-5763_109-5762d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | GACAC | G | 4 | a0001c0001t0015g0017 a0001c0001t0015g0264 a0001c0001t0015g0274 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-5765_109-5762d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789474 | GACACACA others(3): Show |
G | 3 | a0001c0001t0020g0232 a0001c0001t0020g0233 a0001c0007t0020g0231 |
3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.109-5771_109-5762d others(12): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122789474 | ||||||
| chr5:122789482 | C | CGG | 5 | a0001c0001t0014g0239 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01934.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-5784_109-5783i others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789482 | |||||||
| chr5:122789483 | A | G | 79 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(76): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.109-5783A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789483 | |||||||
| chr5:122789484 | C | G | 79 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(76): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.109-5782C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789484 | |||||||
| chr5:122789768 | G | C | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-5498G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789768 | |||||||
| chr5:122789860 | T | C | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-5406T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789860 | |||||||
| chr5:122789963 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.109-5303C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122789963 | |||||||
| chr5:122790057 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109-5209G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790057 | |||||||
| chr5:122790205 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-5061G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790205 | |||||||
| chr5:122790233 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
126 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.109-5033T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790233 | |||||||
| chr5:122790356 | G | C | 1 | a0001c0001t0005g0026 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.109-4910G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790356 | |||||||
| chr5:122790532 | A | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-4734A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790532 | |||||||
| chr5:122790535 | A | T | 1 | a0001c0001t0002g0327 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.109-4731A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790535 | |||||||
| chr5:122790629 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-4637A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790629 | |||||||
| chr5:122790675 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-4591C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790675 | |||||||
| chr5:122790718 | G | C | 12 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(9): Show |
13 | NA18747.hp2 NA18944.hp1 NA18960.hp1 others(10): Show |
intron_variant | MODIFIER | c.109-4548G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790718 | |||||||
| chr5:122790779 | T | C | 2 | a0001c0001t0011g0148 a0001c0001t0042g0149 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.109-4487T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790779 | |||||||
| chr5:122790873 | T | C | 2 | a0001c0001t0011g0148 a0001c0001t0042g0149 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.109-4393T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790873 | |||||||
| chr5:122790934 | G | T | 2 | a0001c0001t0031g0256 a0001c0001t0061g0255 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.109-4332G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790934 | |||||||
| chr5:122790940 | G | C | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-4326G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122790940 | |||||||
| chr5:122791062 | A | G | 8 | a0001c0001t0011g0013 a0001c0001t0011g0148 a0001c0001t0011g0195 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-4204A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791062 | |||||||
| chr5:122791119 | A | AT | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
131 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.109-4125dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122791119 | ||||||
| chr5:122791119 | A | ATT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0063 others(14): Show |
17 | HG01123.hp1 HG01928.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.109-4126_109-4125d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122791119 | ||||||
| chr5:122791119 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.109-4147A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791119 | |||||||
| chr5:122791119 | ATTTTTTT | A | 6 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-4131_109-4125d others(9): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122791119 | ||||||
| chr5:122791119 | ATTTTTTT others(1): Show |
A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.109-4132_109-4125d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122791119 | ||||||
| chr5:122791153 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.109-4113T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791153 | |||||||
| chr5:122791209 | T | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.109-4057T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791209 | |||||||
| chr5:122791230 | T | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.109-4036T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791230 | |||||||
| chr5:122791285 | G | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.109-3981G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791285 | |||||||
| chr5:122791375 | G | A | 2 | a0001c0001t0002g0289 a0001c0001t0069g0290 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.109-3891G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791375 | |||||||
| chr5:122791388 | T | G | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-3878T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791388 | |||||||
| chr5:122791571 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.109-3695T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791571 | |||||||
| chr5:122791572 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.109-3694G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791572 | |||||||
| chr5:122791625 | C | T | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.109-3641C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791625 | |||||||
| chr5:122791715 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.109-3551C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791715 | |||||||
| chr5:122791717 | C | T | 1 | a0001c0001t0012g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.109-3549C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791717 | |||||||
| chr5:122791853 | T | A | 1 | a0001c0001t0044g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.109-3413T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791853 | |||||||
| chr5:122791893 | G | A | 7 | a0001c0001t0003g0141 a0001c0001t0003g0218 a0001c0001t0004g0016 others(4): Show |
8 | HG01070.hp1 HG01074.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-3373G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791893 | |||||||
| chr5:122791958 | C | G | 2 | a0001c0001t0034g0086 a0001c0001t0034g0087 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.109-3308C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791958 | |||||||
| chr5:122791978 | A | G | 1 | a0001c0001t0002g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.109-3288A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122791978 | |||||||
| chr5:122792108 | G | T | 1 | a0001c0001t0007g0257 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.109-3158G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792108 | |||||||
| chr5:122792348 | C | G | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-2918C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792348 | |||||||
| chr5:122792512 | G | A | 8 | a0001c0001t0011g0013 a0001c0001t0011g0148 a0001c0001t0011g0195 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-2754G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792512 | |||||||
| chr5:122792522 | G | A | 8 | a0001c0001t0011g0013 a0001c0001t0011g0148 a0001c0001t0011g0195 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-2744G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792522 | |||||||
| chr5:122792526 | G | A | 14 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-2740G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792526 | |||||||
| chr5:122792572 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.109-2694G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792572 | |||||||
| chr5:122792597 | C | CA | 36 | a0001c0001t0001g0070 a0001c0001t0001g0091 a0001c0001t0001g0103 others(33): Show |
37 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.109-2653dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122792597 | ||||||
| chr5:122792597 | C | CAA | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
126 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.109-2654_109-2653d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122792597 | ||||||
| chr5:122792597 | CA | C | 21 | a0001c0001t0002g0325 a0001c0001t0004g0153 a0001c0001t0010g0246 others(18): Show |
21 | HG01074.hp1 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.109-2653delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122792597 | ||||||
| chr5:122792687 | A | G | 1 | a0001c0001t0061g0255 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.109-2579A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792687 | |||||||
| chr5:122792700 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-2566A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792700 | |||||||
| chr5:122792703 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.109-2563G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792703 | |||||||
| chr5:122792704 | G | A | 87 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(84): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.109-2562G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792704 | |||||||
| chr5:122792712 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.109-2554A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792712 | |||||||
| chr5:122792748 | A | C | 1 | a0001c0001t0003g0137 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.109-2518A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122792748 | |||||||
| chr5:122793016 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.109-2250T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793016 | |||||||
| chr5:122793085 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.109-2181A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793085 | |||||||
| chr5:122793095 | C | G | 1 | a0001c0001t0002g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.109-2171C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793095 | |||||||
| chr5:122793443 | C | T | 1 | a0001c0001t0007g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.109-1823C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793443 | |||||||
| chr5:122793498 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.109-1768G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793498 | |||||||
| chr5:122793538 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.109-1728G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793538 | |||||||
| chr5:122793643 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.109-1623C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793643 | |||||||
| chr5:122793685 | G | A | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-1581G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793685 | |||||||
| chr5:122793719 | G | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.109-1547G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793719 | |||||||
| chr5:122793782 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-1484A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793782 | |||||||
| chr5:122793795 | C | T | 2 | a0001c0001t0023g0287 a0001c0001t0023g0288 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.109-1471C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793795 | |||||||
| chr5:122793800 | C | A | 1 | a0001c0001t0013g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.109-1466C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793800 | |||||||
| chr5:122793803 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-1463C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793803 | |||||||
| chr5:122793840 | G | C | 7 | a0001c0001t0002g0296 a0001c0001t0002g0299 a0001c0001t0002g0300 others(4): Show |
7 | HG02040.hp2 NA18953.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-1426G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793840 | |||||||
| chr5:122793910 | T | TC | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.109-1350dupC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122793910 | ||||||
| chr5:122793917 | A | C | 80 | a0001c0001t0001g0051 a0001c0001t0002g0001 a0001c0001t0002g0018 others(77): Show |
88 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.109-1349A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793917 | |||||||
| chr5:122793918 | A | C | 5 | a0001c0001t0001g0051 a0001c0001t0002g0324 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG03098.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-1348A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122793918 | |||||||
| chr5:122794129 | G | A | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.109-1137G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794129 | |||||||
| chr5:122794144 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.109-1122C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794144 | |||||||
| chr5:122794217 | A | G | 29 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.109-1049A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794217 | |||||||
| chr5:122794261 | A | G | 87 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(84): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.109-1005A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794261 | |||||||
| chr5:122794327 | C | CA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.109-931dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 122794327 | ||||||
| chr5:122794493 | C | T | 1 | a0001c0001t0036g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-773C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794493 | |||||||
| chr5:122794630 | G | A | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-636G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794630 | |||||||
| chr5:122794781 | G | A | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-485G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794781 | |||||||
| chr5:122794940 | T | C | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-326T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794940 | |||||||
| chr5:122794982 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0002g0322 a0001c0001t0002g0327 |
3 | HG00735.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.109-284C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794982 | |||||||
| chr5:122794987 | C | T | 2 | a0001c0001t0023g0287 a0001c0001t0023g0288 |
2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.109-279C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122794987 | |||||||
| chr5:122795079 | A | G | 4 | a0001c0001t0013g0188 a0001c0001t0013g0191 a0001c0001t0027g0189 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-187A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122795079 | |||||||
| chr5:122795223 | T | G | 7 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-43T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | chr5 | 122795223 | |||||||
| chr5:122795387 | A | G | 116 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(113): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
splice_region_variant&intron_variant | LOW | c.226+4A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795387 | |||||||
| chr5:122795528 | G | A | 2 | a0001c0001t0012g0022 a0001c0001t0053g0021 |
2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226+145G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795528 | |||||||
| chr5:122795580 | T | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226+197T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795580 | |||||||
| chr5:122795658 | A | G | 29 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.226+275A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795658 | |||||||
| chr5:122795713 | T | C | 1 | a0001c0001t0007g0266 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.226+330T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795713 | |||||||
| chr5:122795816 | C | T | 58 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0284 others(55): Show |
65 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.226+433C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795816 | |||||||
| chr5:122795831 | T | A | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.226+448T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122795831 | |||||||
| chr5:122796028 | T | C | 3 | a0001c0001t0002g0292 a0001c0001t0002g0335 a0001c0001t0002g0336 |
3 | HG03017.hp2 NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.226+645T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796028 | |||||||
| chr5:122796358 | C | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.226+975C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796358 | |||||||
| chr5:122796364 | A | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.226+981A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796364 | |||||||
| chr5:122796372 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.226+989C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796372 | |||||||
| chr5:122796429 | T | C | 27 | a0001c0002t0006g0015 a0001c0002t0006g0222 a0001c0002t0006g0223 others(24): Show |
28 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.226+1046T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796429 | |||||||
| chr5:122796473 | C | CTT | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.226+1092_226+1093d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122796473 | ||||||
| chr5:122796646 | A | G | 4 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(1): Show |
4 | HG00438.hp1 HG02155.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1263A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796646 | |||||||
| chr5:122796759 | T | C | 1 | a0001c0001t0005g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.226+1376T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796759 | |||||||
| chr5:122796824 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.226+1441G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796824 | |||||||
| chr5:122796868 | C | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.226+1485C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796868 | |||||||
| chr5:122796874 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.226+1491G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122796874 | |||||||
| chr5:122797030 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.226+1647T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797030 | |||||||
| chr5:122797042 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.226+1659C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797042 | |||||||
| chr5:122797071 | A | G | 7 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+1688A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797071 | |||||||
| chr5:122797146 | T | G | 1 | a0001c0001t0003g0155 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.226+1763T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797146 | |||||||
| chr5:122797207 | C | T | 14 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.226+1824C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797207 | |||||||
| chr5:122797262 | AGTCTATA others(11): Show |
A | 1 | a0001c0001t0005g0025 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.226+1881_226+1898d others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122797262 | ||||||
| chr5:122797466 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.226+2083C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797466 | |||||||
| chr5:122797472 | A | AT | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.226+2094dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122797472 | ||||||
| chr5:122797485 | T | C | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.226+2102T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797485 | |||||||
| chr5:122797498 | C | T | 4 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | NA18949.hp1 NA18965.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2115C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797498 | |||||||
| chr5:122797593 | A | G | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.227-2099A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797593 | |||||||
| chr5:122797715 | C | T | 2 | a0001c0001t0003g0083 a0001c0001t0003g0085 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.227-1977C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797715 | |||||||
| chr5:122797754 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.227-1938A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797754 | |||||||
| chr5:122797875 | A | ATT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.227-1816_227-1815d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122797875 | ||||||
| chr5:122797924 | C | T | 1 | a0001c0001t0013g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.227-1768C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797924 | |||||||
| chr5:122797947 | A | G | 2 | a0001c0001t0005g0280 a0001c0001t0005g0281 |
2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.227-1745A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122797947 | |||||||
| chr5:122798042 | C | A | 2 | a0001c0001t0003g0083 a0001c0001t0003g0085 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.227-1650C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122798042 | |||||||
| chr5:122798162 | C | CT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
131 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.227-1521dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122798162 | ||||||
| chr5:122798334 | C | T | 119 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(116): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.227-1358C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122798334 | |||||||
| chr5:122798486 | A | T | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.227-1206A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122798486 | |||||||
| chr5:122798740 | A | C | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-952A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122798740 | |||||||
| chr5:122798956 | T | A | 119 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(116): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.227-736T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122798956 | |||||||
| chr5:122799014 | A | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.227-678A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799014 | |||||||
| chr5:122799089 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.227-603G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799089 | |||||||
| chr5:122799105 | T | TAGTATTA others(2754): Show |
1 | a0001c0001t0002g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.227-572_227-571ins others(2761): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 122799105 | ||||||
| chr5:122799158 | A | C | 1 | a0001c0001t0002g0332 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.227-534A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799158 | |||||||
| chr5:122799397 | A | G | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-295A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799397 | |||||||
| chr5:122799487 | C | G | 29 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.227-205C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799487 | |||||||
| chr5:122799493 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.227-199T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799493 | |||||||
| chr5:122799635 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.227-57G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799635 | |||||||
| chr5:122799663 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0012g0060 |
3 | NA18960.hp2 NA18966.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.227-29C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 2/14 | chr5 | 122799663 | |||||||
| chr5:122799866 | A | G | 4 | a0001c0001t0002g0296 a0001c0001t0002g0300 a0001c0001t0002g0301 others(1): Show |
4 | NA18953.hp1 NA18987.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+11A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122799866 | |||||||
| chr5:122799883 | A | G | 5 | a0001c0001t0014g0239 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01934.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+28A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122799883 | |||||||
| chr5:122799924 | C | G | 1 | a0001c0001t0010g0252 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.390+69C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122799924 | |||||||
| chr5:122800233 | G | C | 1 | a0001c0001t0032g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390+378G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800233 | |||||||
| chr5:122800380 | G | A | 1 | a0001c0001t0008g0035 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.390+525G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800380 | |||||||
| chr5:122800521 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0063 |
4 | HG01081.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+666A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800521 | |||||||
| chr5:122800558 | G | A | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+703G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800558 | |||||||
| chr5:122800617 | G | T | 3 | a0001c0002t0016g0213 a0001c0002t0016g0214 a0001c0002t0066g0212 |
3 | HG00280.hp1 HG01175.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.390+762G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800617 | |||||||
| chr5:122800807 | ATAGTGT | A | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.390+956_390+961del others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122800807 | ||||||
| chr5:122800964 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.391-905G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122800964 | |||||||
| chr5:122800982 | C | CT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.391-885dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122800982 | ||||||
| chr5:122801022 | C | T | 1 | a0001c0001t0007g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.391-847C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801022 | |||||||
| chr5:122801023 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.391-846G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801023 | |||||||
| chr5:122801062 | TGATACTA others(162): Show |
T | 1 | a0001c0001t0001g0076 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.391-803_391-635del | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801062 | ||||||
| chr5:122801082 | A | T | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.391-787A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801082 | |||||||
| chr5:122801136 | C | G | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.391-733C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801136 | |||||||
| chr5:122801140 | C | T | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.391-729C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801140 | |||||||
| chr5:122801239 | T | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.391-630T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801239 | |||||||
| chr5:122801605 | T | TA | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
137 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.391-244dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801605 | ||||||
| chr5:122801605 | TA | T | 99 | a0001c0001t0002g0302 a0001c0001t0002g0331 a0001c0001t0003g0012 others(96): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.391-244delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801605 | ||||||
| chr5:122801605 | TAA | T | 6 | a0001c0001t0003g0085 a0001c0001t0003g0141 a0001c0001t0004g0186 others(3): Show |
6 | HG01169.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-245_391-244del others(2): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801605 | ||||||
| chr5:122801652 | C | CGT | 24 | a0001c0001t0002g0293 a0001c0001t0002g0304 a0001c0001t0002g0322 others(21): Show |
24 | HG00099.hp1 HG00738.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.391-180_391-179dup others(2): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGT | 4 | a0001c0001t0002g0285 a0001c0002t0016g0203 a0001c0002t0016g0214 others(1): Show |
4 | HG01978.hp1 HG03098.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-182_391-179dup others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGT | 19 | a0001c0001t0003g0136 a0001c0001t0003g0155 a0001c0001t0003g0179 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.391-184_391-179dup others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(1): Show |
36 | a0001c0001t0003g0012 a0001c0001t0003g0085 a0001c0001t0003g0139 others(33): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.391-186_391-179dup others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(3): Show |
35 | a0001c0001t0003g0137 a0001c0001t0003g0158 a0001c0001t0003g0161 others(32): Show |
36 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.391-188_391-179dup others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(5): Show |
15 | a0001c0001t0004g0150 a0001c0001t0010g0246 a0001c0001t0010g0250 others(12): Show |
15 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.391-190_391-179dup others(12): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(7): Show |
14 | a0001c0001t0010g0249 a0001c0001t0011g0013 a0001c0001t0011g0195 others(11): Show |
15 | HG01496.hp2 HG01891.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.391-192_391-179dup others(14): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(9): Show |
3 | a0001c0001t0003g0083 a0001c0001t0028g0144 a0001c0001t0042g0149 |
3 | HG02970.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.391-194_391-179dup others(16): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0011g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.391-198_391-179dup others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | CGT | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
100 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.391-180_391-179del others(2): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801652 | CGTGT | C | 3 | a0001c0001t0001g0045 a0001c0001t0029g0282 a0001c0001t0029g0283 |
3 | HG02280.hp1 HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.391-182_391-179del others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 122801652 | ||||||
| chr5:122801690 | T | TGTGTGTG others(2): Show |
3 | a0001c0001t0003g0184 a0001c0001t0003g0218 a0001c0001t0004g0151 |
3 | HG01106.hp2 HG01261.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.391-179_391-178ins others(9): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801690 | |||||||
| chr5:122801690 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0038g0084 a0001c0001t0047g0147 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-179_391-178ins others(13): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801690 | |||||||
| chr5:122801690 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0021g0202 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.391-179_391-178ins others(15): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 3/14 | chr5 | 122801690 | |||||||
| chr5:122802013 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.458-68A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 4/14 | chr5 | 122802013 | |||||||
| chr5:122802214 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.501+90G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802214 | |||||||
| chr5:122802267 | G | A | 6 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0023g0286 others(3): Show |
6 | HG03195.hp1 HG03195.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+143G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802267 | |||||||
| chr5:122802300 | G | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.501+176G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802300 | |||||||
| chr5:122802340 | T | C | 4 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0274 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+216T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802340 | |||||||
| chr5:122802450 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.501+326T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802450 | |||||||
| chr5:122802464 | T | C | 1 | a0001c0001t0011g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.501+340T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802464 | |||||||
| chr5:122802653 | G | A | 1 | a0001c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.501+529G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802653 | |||||||
| chr5:122802671 | G | A | 1 | a0001c0001t0005g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.501+547G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802671 | |||||||
| chr5:122802694 | C | T | 2 | a0001c0001t0033g0244 a0002c0004t0033g0245 |
2 | HG00609.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.501+570C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802694 | |||||||
| chr5:122802710 | G | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.501+586G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122802710 | |||||||
| chr5:122803094 | T | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0195 a0001c0001t0036g0082 |
4 | HG02055.hp2 HG03453.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-378T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122803094 | |||||||
| chr5:122803122 | T | G | 29 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.502-350T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122803122 | |||||||
| chr5:122803220 | A | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.502-252A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122803220 | |||||||
| chr5:122803222 | C | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.502-250C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | chr5 | 122803222 | |||||||
| chr5:122803313 | GT | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.502-149delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 122803313 | ||||||
| chr5:122803745 | T | A | 1 | a0001c0001t0046g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.643+132T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122803745 | |||||||
| chr5:122803861 | G | A | 2 | a0001c0001t0008g0054 a0001c0001t0008g0072 |
2 | NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.643+248G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122803861 | |||||||
| chr5:122803897 | G | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643+284G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122803897 | |||||||
| chr5:122803990 | G | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.643+377G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122803990 | |||||||
| chr5:122804010 | G | A | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.643+397G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804010 | |||||||
| chr5:122804022 | C | A | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.643+409C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804022 | |||||||
| chr5:122804032 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.643+419G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804032 | |||||||
| chr5:122804096 | G | A | 1 | a0001c0001t0002g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.643+483G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804096 | |||||||
| chr5:122804124 | C | CA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.643+521dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122804124 | ||||||
| chr5:122804201 | A | G | 1 | a0001c0001t0028g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.643+588A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804201 | |||||||
| chr5:122804251 | A | G | 3 | a0001c0001t0023g0286 a0001c0001t0023g0287 a0001c0001t0023g0288 |
3 | HG03195.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.643+638A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804251 | |||||||
| chr5:122804320 | C | G | 2 | a0001c0001t0002g0335 a0001c0001t0002g0336 |
2 | NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.643+707C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804320 | |||||||
| chr5:122804332 | C | T | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.643+719C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804332 | |||||||
| chr5:122804365 | C | CT | 21 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0004g0163 others(18): Show |
22 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.643+770dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122804365 | ||||||
| chr5:122804365 | CT | C | 6 | a0001c0001t0002g0298 a0001c0001t0002g0306 a0001c0001t0002g0307 others(3): Show |
6 | HG00597.hp1 HG00738.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.643+770delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122804365 | ||||||
| chr5:122804500 | G | A | 1 | a0001c0001t0002g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.643+887G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804500 | |||||||
| chr5:122804582 | T | C | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.643+969T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804582 | |||||||
| chr5:122804583 | G | T | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.643+970G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804583 | |||||||
| chr5:122804622 | G | A | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.643+1009G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804622 | |||||||
| chr5:122804628 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.643+1015A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804628 | |||||||
| chr5:122804987 | T | C | 1 | a0001c0002t0009g0220 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.643+1374T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122804987 | |||||||
| chr5:122805042 | G | A | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.643+1429G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805042 | |||||||
| chr5:122805090 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.643+1477G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805090 | |||||||
| chr5:122805134 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.643+1521T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805134 | |||||||
| chr5:122805178 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.643+1565C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805178 | |||||||
| chr5:122805226 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643+1613G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805226 | |||||||
| chr5:122805290 | C | CAA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
109 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.643+1693_643+1694d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122805290 | ||||||
| chr5:122805290 | C | CAAA | 21 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0058 others(18): Show |
21 | HG00438.hp2 HG02074.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.643+1692_643+1694d others(5): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122805290 | ||||||
| chr5:122805290 | CA | C | 6 | a0001c0001t0004g0194 a0001c0001t0012g0276 a0001c0001t0032g0236 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.643+1694delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122805290 | ||||||
| chr5:122805323 | A | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.643+1710A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805323 | |||||||
| chr5:122805419 | T | A | 3 | a0001c0001t0022g0077 a0001c0001t0022g0104 a0001c0001t0022g0105 |
3 | NA18970.hp1 NA18977.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.643+1806T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805419 | |||||||
| chr5:122805503 | A | G | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.643+1890A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805503 | |||||||
| chr5:122805504 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.643+1891C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805504 | |||||||
| chr5:122805505 | A | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643+1892A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805505 | |||||||
| chr5:122805541 | T | C | 6 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0023g0286 others(3): Show |
6 | HG03195.hp1 HG03195.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.643+1928T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805541 | |||||||
| chr5:122805589 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643+1976C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805589 | |||||||
| chr5:122805661 | A | G | 1 | a0001c0001t0026g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.643+2048A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805661 | |||||||
| chr5:122805760 | A | G | 1 | a0001c0002t0067g0205 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.643+2147A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805760 | |||||||
| chr5:122805764 | G | A | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.643+2151G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805764 | |||||||
| chr5:122805814 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.643+2201T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805814 | |||||||
| chr5:122805883 | C | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.643+2270C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805883 | |||||||
| chr5:122805938 | G | A | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.643+2325G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122805938 | |||||||
| chr5:122806012 | G | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.644-2265G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806012 | |||||||
| chr5:122806027 | G | A | 1 | a0001c0001t0007g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.644-2250G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806027 | |||||||
| chr5:122806094 | A | ATG | 75 | a0001c0001t0003g0012 a0001c0001t0003g0136 a0001c0001t0003g0137 others(72): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.644-2166_644-2165d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806094 | ||||||
| chr5:122806094 | A | ATGTG | 14 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(11): Show |
15 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(12): Show |
intron_variant | MODIFIER | c.644-2168_644-2165d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806094 | ||||||
| chr5:122806103 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0008g0039 a0001c0001t0052g0046 |
2 | NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.644-2167_644-2166i others(12): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806103 | ||||||
| chr5:122806109 | T | C | 16 | a0001c0001t0032g0236 a0001c0001t0032g0237 a0001c0002t0009g0208 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.644-2168T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806109 | |||||||
| chr5:122806111 | T | C | 1 | a0001c0001t0044g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.644-2166T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806111 | |||||||
| chr5:122806113 | C | CGTGTGTG others(3): Show |
121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
129 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.644-2156_644-2155i others(12): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806113 | ||||||
| chr5:122806113 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.644-2156_644-2155i others(14): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806113 | ||||||
| chr5:122806113 | C | T | 4 | a0001c0001t0008g0039 a0001c0001t0037g0345 a0001c0001t0052g0046 others(1): Show |
4 | HG02895.hp1 HG03516.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.644-2164C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806113 | |||||||
| chr5:122806115 | T | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(66): Show |
77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.644-2162T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806115 | |||||||
| chr5:122806120 | G | GTGTGTGT others(29): Show |
1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-2156_644-2155i others(38): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806120 | ||||||
| chr5:122806122 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-2155A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806122 | |||||||
| chr5:122806124 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0063 |
4 | HG01081.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.644-2153A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806124 | |||||||
| chr5:122806129 | T | C | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-2148T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806129 | |||||||
| chr5:122806129 | T | TAC | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-2143_644-2142d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806129 | ||||||
| chr5:122806132 | A | ACATG | 7 | a0001c0001t0013g0157 a0001c0001t0013g0187 a0001c0001t0013g0188 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-2143_644-2142i others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806132 | ||||||
| chr5:122806132 | A | G | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.644-2145A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806132 | |||||||
| chr5:122806135 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.644-2142C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806135 | |||||||
| chr5:122806138 | G | A | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-2139G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806138 | |||||||
| chr5:122806139 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-2138C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806139 | |||||||
| chr5:122806140 | G | A | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-2137G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806140 | |||||||
| chr5:122806140 | G | GCAGCGCG others(16): Show |
1 | a0001c0001t0042g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.644-2136_644-2135i others(25): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806140 | ||||||
| chr5:122806140 | G | GCTGCGCG others(20): Show |
1 | a0001c0001t0003g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.644-2136_644-2135i others(29): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806140 | ||||||
| chr5:122806142 | G | A | 8 | a0001c0001t0003g0141 a0001c0001t0015g0017 a0001c0001t0015g0263 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.644-2135G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806142 | |||||||
| chr5:122806142 | G | GCA | 3 | a0001c0001t0034g0086 a0001c0001t0034g0087 a0001c0005t0070g0020 |
3 | HG01884.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.644-2110_644-2109d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACA | 4 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(1): Show |
4 | HG02258.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.644-2112_644-2109d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACACGC others(19): Show |
1 | a0001c0002t0066g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.644-2130_644-2129i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACACGC others(21): Show |
2 | a0001c0002t0016g0213 a0001c0002t0016g0214 |
2 | HG00280.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.644-2130_644-2129i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACGCAC others(19): Show |
1 | a0001c0001t0014g0241 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.644-2132_644-2131i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACGCGC others(11): Show |
1 | a0001c0001t0013g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.644-2132_644-2131i others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACGCGC others(19): Show |
1 | a0001c0001t0040g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.644-2132_644-2131i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCACGCGC others(21): Show |
1 | a0001c0001t0013g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.644-2132_644-2131i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCACGC others(19): Show |
2 | a0001c0001t0011g0196 a0001c0001t0011g0200 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(17): Show |
1 | a0001c0001t0046g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(26): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(19): Show |
1 | a0001c0001t0004g0253 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(17): Show |
1 | a0001c0007t0020g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(26): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(19): Show |
4 | a0001c0001t0004g0016 a0001c0001t0014g0239 a0001c0001t0014g0240 others(1): Show |
5 | HG01346.hp2 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(21): Show |
5 | a0001c0001t0003g0083 a0001c0001t0004g0151 a0001c0001t0004g0153 others(2): Show |
5 | HG01074.hp1 HG01106.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(23): Show |
3 | a0001c0001t0003g0179 a0001c0001t0003g0218 a0001c0001t0014g0242 |
3 | HG01261.hp1 HG02258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(9): Show |
1 | a0001c0001t0036g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(18): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(13): Show |
1 | a0001c0001t0011g0013 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(22): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(15): Show |
7 | a0001c0001t0004g0160 a0001c0001t0004g0164 a0001c0001t0019g0199 others(4): Show |
7 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(24): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(17): Show |
7 | a0001c0001t0004g0156 a0001c0001t0004g0159 a0001c0001t0004g0173 others(4): Show |
7 | HG00558.hp1 HG00738.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(26): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(19): Show |
5 | a0001c0001t0003g0085 a0001c0001t0003g0158 a0001c0001t0003g0184 others(2): Show |
5 | HG00639.hp2 HG01069.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(21): Show |
7 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0186 others(4): Show |
7 | HG00140.hp1 HG00280.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(23): Show |
9 | a0001c0001t0003g0143 a0001c0001t0003g0166 a0001c0001t0003g0167 others(6): Show |
9 | HG00323.hp2 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(25): Show |
2 | a0001c0001t0003g0012 a0001c0001t0004g0194 |
3 | HG01975.hp2 HG02300.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(34): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(19): Show |
1 | a0001c0001t0019g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(28): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(23): Show |
3 | a0001c0001t0003g0137 a0001c0001t0003g0197 a0001c0001t0004g0163 |
3 | HG03516.hp1 HG04115.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(25): Show |
1 | a0001c0001t0003g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(34): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(33): Show |
1 | a0001c0001t0041g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(42): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(25): Show |
1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(34): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(27): Show |
5 | a0001c0001t0003g0139 a0001c0001t0003g0155 a0001c0001t0003g0176 others(2): Show |
5 | HG02109.hp1 HG02273.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.644-2134_644-2133i others(36): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(29): Show |
2 | a0001c0001t0004g0138 a0001c0001t0050g0182 |
2 | HG01081.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(38): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCAC others(23): Show |
1 | a0001c0001t0003g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(15): Show |
1 | a0001c0001t0011g0195 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(24): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(23): Show |
1 | a0001c0001t0004g0162 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(25): Show |
1 | a0001c0001t0004g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(34): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(21): Show |
1 | a0001c0001t0027g0190 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(23): Show |
1 | a0001c0001t0027g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(17): Show |
1 | a0001c0001t0011g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(26): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(21): Show |
1 | a0001c0001t0013g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(30): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(25): Show |
1 | a0001c0002t0024g0206 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(34): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(29): Show |
1 | a0001c0002t0009g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(38): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(27): Show |
1 | a0001c0001t0013g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(36): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(23): Show |
1 | a0001c0002t0016g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.644-2134_644-2133i others(32): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(31): Show |
3 | a0001c0002t0016g0203 a0001c0002t0024g0215 a0001c0002t0067g0205 |
3 | HG02071.hp1 NA19005.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(40): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(35): Show |
2 | a0001c0002t0009g0208 a0001c0002t0063g0209 |
2 | NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(44): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(31): Show |
1 | a0001c0002t0009g0211 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.644-2134_644-2133i others(40): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | G | GCGCGCGC others(33): Show |
2 | a0001c0002t0009g0210 a0001c0002t0024g0204 |
2 | NA19010.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.644-2134_644-2133i others(42): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | GCA | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(96): Show |
108 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.644-2110_644-2109d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806142 | GCACACA | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
131 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.644-2114_644-2109d others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806142 | ||||||
| chr5:122806146 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.644-2131A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806146 | |||||||
| chr5:122806148 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.644-2129A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806148 | |||||||
| chr5:122806149 | C | A | 1 | a0001c0001t0003g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.644-2128C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806149 | |||||||
| chr5:122806150 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
131 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.644-2127A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806150 | |||||||
| chr5:122806169 | G | C | 84 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(81): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.644-2108G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806169 | |||||||
| chr5:122806171 | C | T | 3 | a0001c0001t0004g0172 a0001c0001t0004g0186 a0001c0001t0004g0193 |
3 | HG00140.hp1 HG01069.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.644-2106C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806171 | |||||||
| chr5:122806204 | G | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-2073G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806204 | |||||||
| chr5:122806224 | G | C | 1 | a0001c0001t0049g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.644-2053G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806224 | |||||||
| chr5:122806284 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.644-1993A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806284 | |||||||
| chr5:122806467 | G | C | 9 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(6): Show |
9 | HG00609.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.644-1810G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806467 | |||||||
| chr5:122806480 | C | T | 1 | a0001c0001t0032g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644-1797C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806480 | |||||||
| chr5:122806599 | T | TTTTA | 26 | a0001c0001t0002g0001 a0001c0001t0002g0296 a0001c0001t0002g0298 others(23): Show |
32 | HG00597.hp1 HG02040.hp2 HG02074.hp2 others(29): Show |
intron_variant | MODIFIER | c.644-1647_644-1644d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806599 | ||||||
| chr5:122806599 | TTTTA | T | 113 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(110): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.644-1647_644-1644d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806599 | ||||||
| chr5:122806599 | TTTTATTT others(1): Show |
T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-1651_644-1644d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806599 | ||||||
| chr5:122806617 | T | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.644-1660T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806617 | |||||||
| chr5:122806711 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.644-1566C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806711 | |||||||
| chr5:122806807 | C | CT | 6 | a0001c0002t0006g0015 a0001c0002t0006g0225 a0001c0002t0006g0226 others(3): Show |
7 | NA18960.hp1 NA18995.hp1 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.644-1468dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122806807 | ||||||
| chr5:122806966 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.644-1311A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122806966 | |||||||
| chr5:122807148 | C | T | 1 | a0001c0001t0039g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.644-1129C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807148 | |||||||
| chr5:122807172 | G | C | 1 | a0001c0001t0032g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.644-1105G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807172 | |||||||
| chr5:122807267 | AG | A | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.644-1009delG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807267 | |||||||
| chr5:122807455 | A | G | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.644-822A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807455 | |||||||
| chr5:122807499 | G | C | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.644-778G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807499 | |||||||
| chr5:122807709 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-568A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807709 | |||||||
| chr5:122807872 | T | C | 1 | a0001c0001t0002g0309 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.644-405T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807872 | |||||||
| chr5:122807927 | C | T | 16 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(13): Show |
16 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.644-350C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122807927 | |||||||
| chr5:122808052 | A | AT | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-221dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 122808052 | ||||||
| chr5:122808103 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.644-174G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122808103 | |||||||
| chr5:122808134 | T | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.644-143T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | chr5 | 122808134 | |||||||
| chr5:122808431 | A | T | 1 | a0001c0001t0008g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.722+76A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808431 | |||||||
| chr5:122808485 | C | G | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.722+130C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808485 | |||||||
| chr5:122808494 | A | T | 1 | a0001c0001t0002g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.722+139A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808494 | |||||||
| chr5:122808544 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.722+189G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808544 | |||||||
| chr5:122808544 | G | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.722+189G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808544 | |||||||
| chr5:122808638 | T | C | 1 | a0001c0002t0066g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.722+283T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808638 | |||||||
| chr5:122808765 | A | G | 1 | a0001c0002t0016g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.722+410A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808765 | |||||||
| chr5:122808771 | C | G | 1 | a0001c0001t0004g0171 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.722+416C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808771 | |||||||
| chr5:122808993 | C | G | 3 | a0001c0001t0031g0254 a0001c0001t0031g0256 a0001c0001t0061g0255 |
3 | HG00738.hp1 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.722+638C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122808993 | |||||||
| chr5:122809068 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.722+713A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809068 | |||||||
| chr5:122809189 | G | C | 1 | a0001c0002t0066g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.722+834G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809189 | |||||||
| chr5:122809204 | A | G | 1 | a0001c0002t0006g0222 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.722+849A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809204 | |||||||
| chr5:122809211 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.722+856G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809211 | |||||||
| chr5:122809455 | G | A | 1 | a0001c0001t0059g0040 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.722+1100G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809455 | |||||||
| chr5:122809464 | C | T | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+1109C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809464 | |||||||
| chr5:122809568 | T | C | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.722+1213T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809568 | |||||||
| chr5:122809845 | G | A | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.722+1490G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809845 | |||||||
| chr5:122809911 | AGAAGTTT others(7): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.722+1558_722+1571d others(16): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122809911 | ||||||
| chr5:122809941 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+1586T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122809941 | |||||||
| chr5:122810086 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+1731C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810086 | |||||||
| chr5:122810090 | C | T | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.722+1735C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810090 | |||||||
| chr5:122810109 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.722+1754C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810109 | |||||||
| chr5:122810163 | C | T | 2 | a0001c0001t0002g0018 a0001c0002t0024g0215 |
3 | HG02071.hp1 HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.722+1808C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810163 | |||||||
| chr5:122810211 | G | A | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.722+1856G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810211 | |||||||
| chr5:122810279 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.722+1924T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810279 | |||||||
| chr5:122810325 | C | G | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+1970C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810325 | |||||||
| chr5:122810397 | AT | A | 20 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01074.hp1 HG01169.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.722+2044delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122810397 | ||||||
| chr5:122810398 | T | TA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(7): Show |
10 | HG00673.hp1 HG01106.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.722+2043_722+2044i others(3): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810398 | |||||||
| chr5:122810398 | TTAAAAAA others(3): Show |
T | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.722+2044_722+2053d others(12): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810398 | |||||||
| chr5:122810399 | T | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.722+2044T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810399 | |||||||
| chr5:122810399 | T | TA | 18 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0121 others(15): Show |
18 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+2066dupA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122810399 | ||||||
| chr5:122810399 | TA | T | 11 | a0001c0001t0002g0296 a0001c0001t0002g0302 a0001c0001t0002g0314 others(8): Show |
11 | HG00558.hp2 HG00738.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.722+2066delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122810399 | ||||||
| chr5:122810577 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+2222C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810577 | |||||||
| chr5:122810613 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.722+2258G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810613 | |||||||
| chr5:122810625 | T | G | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.722+2270T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810625 | |||||||
| chr5:122810644 | C | G | 1 | a0001c0001t0002g0294 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.722+2289C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810644 | |||||||
| chr5:122810765 | A | G | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.722+2410A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810765 | |||||||
| chr5:122810884 | A | G | 1 | a0001c0001t0029g0283 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.722+2529A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810884 | |||||||
| chr5:122810924 | G | C | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.722+2569G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810924 | |||||||
| chr5:122810993 | C | G | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+2638C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122810993 | |||||||
| chr5:122811005 | C | G | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.722+2650C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811005 | |||||||
| chr5:122811039 | CTTAAACT | C | 15 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(12): Show |
16 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.722+2691_722+2697d others(9): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811039 | ||||||
| chr5:122811136 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+2781C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811136 | |||||||
| chr5:122811202 | A | G | 6 | a0001c0001t0002g0313 a0001c0001t0002g0328 a0001c0001t0002g0329 others(3): Show |
6 | HG00673.hp2 NA18948.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+2847A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811202 | |||||||
| chr5:122811263 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.722+2908C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811263 | |||||||
| chr5:122811283 | C | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.722+2928C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811283 | |||||||
| chr5:122811543 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.722+3188A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811543 | |||||||
| chr5:122811825 | C | CTAAA | 7 | a0001c0001t0001g0045 a0001c0001t0002g0320 a0001c0001t0008g0035 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+3503_722+3506d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811825 | ||||||
| chr5:122811825 | C | CTAAATAA others(1): Show |
98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(95): Show |
102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.722+3499_722+3506d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811825 | ||||||
| chr5:122811825 | C | CTAAATAA others(5): Show |
49 | a0001c0001t0001g0114 a0001c0001t0002g0321 a0001c0001t0002g0330 others(46): Show |
50 | HG00673.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.722+3495_722+3506d others(14): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811825 | ||||||
| chr5:122811825 | C | CTAAATAA others(9): Show |
26 | a0001c0001t0003g0083 a0001c0001t0003g0136 a0001c0001t0003g0137 others(23): Show |
26 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.722+3491_722+3506d others(18): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811825 | ||||||
| chr5:122811825 | CTAAATAA others(1): Show |
C | 4 | a0001c0001t0012g0022 a0001c0001t0029g0282 a0001c0001t0029g0283 others(1): Show |
4 | HG02280.hp1 HG03209.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+3499_722+3506d others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811825 | ||||||
| chr5:122811850 | T | TAAATAAA others(1): Show |
84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
91 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.722+3502_722+3503i others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811850 | ||||||
| chr5:122811850 | T | TAAATAAA others(5): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0049 |
2 | NA18980.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.722+3496_722+3507d others(14): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122811850 | ||||||
| chr5:122811908 | A | G | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.722+3553A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811908 | |||||||
| chr5:122811993 | A | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.722+3638A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122811993 | |||||||
| chr5:122812177 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.723-3719C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812177 | |||||||
| chr5:122812194 | T | G | 9 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(6): Show |
9 | HG00609.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.723-3702T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812194 | |||||||
| chr5:122812201 | G | C | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.723-3695G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812201 | |||||||
| chr5:122812216 | C | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0102 |
3 | HG00639.hp1 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.723-3680C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812216 | |||||||
| chr5:122812240 | G | C | 1 | a0001c0001t0004g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723-3656G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812240 | |||||||
| chr5:122812267 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723-3629T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812267 | |||||||
| chr5:122812348 | CT | C | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.723-3544delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122812348 | ||||||
| chr5:122812388 | T | TAG | 331 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(328): Show |
351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.723-3507_723-3506d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122812388 | ||||||
| chr5:122812646 | G | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
122 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.723-3250G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812646 | |||||||
| chr5:122812660 | T | C | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.723-3236T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812660 | |||||||
| chr5:122812671 | T | C | 1 | a0001c0001t0059g0040 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.723-3225T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812671 | |||||||
| chr5:122812782 | C | T | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.723-3114C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812782 | |||||||
| chr5:122812841 | T | A | 1 | a0001c0001t0002g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.723-3055T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122812841 | |||||||
| chr5:122813207 | G | T | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.723-2689G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813207 | |||||||
| chr5:122813209 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.723-2687A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813209 | |||||||
| chr5:122813358 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0043 others(5): Show |
8 | HG00735.hp1 HG01099.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.723-2538A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813358 | |||||||
| chr5:122813373 | A | G | 1 | a0001c0001t0002g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-2523A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813373 | |||||||
| chr5:122813754 | A | G | 1 | a0001c0001t0002g0301 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.723-2142A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813754 | |||||||
| chr5:122813767 | C | CT | 12 | a0001c0001t0002g0298 a0001c0001t0004g0159 a0001c0001t0004g0163 others(9): Show |
12 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-2107dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122813767 | ||||||
| chr5:122813767 | CT | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0043 others(18): Show |
23 | HG00597.hp2 HG01106.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.723-2107delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122813767 | ||||||
| chr5:122813767 | CTT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
118 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.723-2108_723-2107d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122813767 | ||||||
| chr5:122813804 | C | T | 1 | a0001c0001t0036g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.723-2092C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813804 | |||||||
| chr5:122813866 | T | C | 117 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(114): Show |
121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.723-2030T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813866 | |||||||
| chr5:122813886 | G | A | 1 | a0001c0002t0024g0204 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.723-2010G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813886 | |||||||
| chr5:122813886 | G | C | 16 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(13): Show |
16 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.723-2010G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813886 | |||||||
| chr5:122813996 | A | T | 1 | a0001c0001t0002g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-1900A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122813996 | |||||||
| chr5:122814108 | G | T | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-1788G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814108 | |||||||
| chr5:122814225 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.723-1671T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814225 | |||||||
| chr5:122814239 | T | G | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.723-1657T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814239 | |||||||
| chr5:122814456 | C | A | 1 | a0001c0001t0002g0306 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.723-1440C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814456 | |||||||
| chr5:122814679 | T | C | 1 | a0001c0001t0023g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723-1217T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814679 | |||||||
| chr5:122814752 | T | TTTTTTTT others(12): Show |
1 | a0001c0001t0004g0169 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.723-1137_723-1136i others(21): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814752 | ||||||
| chr5:122814753 | T | TTTTTTTG others(10): Show |
85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.723-1137_723-1136i others(19): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814753 | T | TTTTTTTG others(9): Show |
2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.723-1137_723-1136i others(18): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814753 | T | TTTTTTTG others(10): Show |
29 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.723-1137_723-1136i others(19): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814753 | T | TTTTTTTT others(10): Show |
144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
152 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.723-1129_723-1128i others(19): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814753 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0048g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.723-1129_723-1128i others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814753 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.723-1136_723-1135i others(20): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122814753 | ||||||
| chr5:122814866 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.723-1030C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814866 | |||||||
| chr5:122814890 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.723-1006C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814890 | |||||||
| chr5:122814985 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.723-911G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814985 | |||||||
| chr5:122814995 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.723-901C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122814995 | |||||||
| chr5:122815048 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.723-848C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815048 | |||||||
| chr5:122815290 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.723-606A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815290 | |||||||
| chr5:122815388 | A | G | 15 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(12): Show |
16 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.723-508A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815388 | |||||||
| chr5:122815517 | T | C | 9 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(6): Show |
9 | HG00609.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.723-379T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815517 | |||||||
| chr5:122815646 | A | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.723-250A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815646 | |||||||
| chr5:122815786 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.723-110C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815786 | |||||||
| chr5:122815806 | T | G | 1 | a0001c0001t0002g0018 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.723-90T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815806 | |||||||
| chr5:122815810 | T | TC | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-84dupC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 122815810 | ||||||
| chr5:122815833 | C | T | 1 | a0001c0001t0068g0312 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.723-63C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | chr5 | 122815833 | |||||||
| chr5:122815983 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798+12A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122815983 | |||||||
| chr5:122816293 | GAAAGA | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.798+323_798+327del others(5): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816293 | |||||||
| chr5:122816296 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.798+325A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816296 | |||||||
| chr5:122816324 | C | A | 2 | a0001c0001t0001g0080 a0003c0003t0001g0027 |
2 | NA18939.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.798+353C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816324 | |||||||
| chr5:122816818 | G | C | 1 | a0001c0002t0016g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.799-97G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816818 | |||||||
| chr5:122816820 | G | A | 8 | a0001c0001t0011g0013 a0001c0001t0011g0148 a0001c0001t0011g0195 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-95G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816820 | |||||||
| chr5:122816820 | G | C | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.799-95G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816820 | |||||||
| chr5:122816825 | A | AG | 95 | a0001c0001t0001g0042 a0001c0001t0002g0313 a0001c0001t0002g0315 others(92): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.799-84dupG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 122816825 | ||||||
| chr5:122816826 | G | C | 1 | a0001c0001t0007g0272 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.799-89G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816826 | |||||||
| chr5:122816826 | G | GC | 28 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(25): Show |
29 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.799-89_799-88insC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 8/14 | chr5 | 122816826 | |||||||
| chr5:122817390 | A | G | 5 | a0001c0001t0013g0157 a0001c0001t0013g0188 a0001c0001t0013g0191 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+17A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817390 | |||||||
| chr5:122817526 | AT | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1006+161delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 122817526 | ||||||
| chr5:122817579 | G | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1006+206G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817579 | |||||||
| chr5:122817585 | A | G | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1006+212A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817585 | |||||||
| chr5:122817594 | T | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1006+221T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817594 | |||||||
| chr5:122817642 | A | G | 3 | a0001c0001t0004g0172 a0001c0001t0004g0186 a0001c0001t0004g0193 |
3 | HG00140.hp1 HG01069.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1006+269A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817642 | |||||||
| chr5:122817765 | T | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1006+392T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817765 | |||||||
| chr5:122817874 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1006+501C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817874 | |||||||
| chr5:122817962 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1006+589A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122817962 | |||||||
| chr5:122818069 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1006+696T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818069 | |||||||
| chr5:122818128 | G | A | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-690G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818128 | |||||||
| chr5:122818328 | G | A | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1007-490G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818328 | |||||||
| chr5:122818423 | A | G | 17 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(14): Show |
17 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1007-395A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818423 | |||||||
| chr5:122818479 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1007-339T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818479 | |||||||
| chr5:122818498 | C | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1007-320C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 10/14 | chr5 | 122818498 | |||||||
| chr5:122819040 | A | G | 15 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(12): Show |
15 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1212+17A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819040 | |||||||
| chr5:122819044 | T | C | 2 | a0001c0001t0011g0196 a0001c0001t0011g0200 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1212+21T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819044 | |||||||
| chr5:122819154 | A | G | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1212+131A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819154 | |||||||
| chr5:122819252 | C | T | 1 | a0001c0002t0024g0204 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1212+229C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819252 | |||||||
| chr5:122819262 | T | C | 1 | a0001c0001t0049g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1212+239T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819262 | |||||||
| chr5:122819452 | T | G | 2 | a0001c0001t0002g0335 a0001c0001t0002g0336 |
2 | NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1212+429T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819452 | |||||||
| chr5:122819664 | G | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1212+641G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819664 | |||||||
| chr5:122819731 | G | A | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212+708G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122819731 | |||||||
| chr5:122820364 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1212+1341C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820364 | |||||||
| chr5:122820365 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG00140.hp2 HG01515.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212+1342G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820365 | |||||||
| chr5:122820514 | G | A | 1 | a0001c0001t0008g0107 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1212+1491G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820514 | |||||||
| chr5:122820656 | A | C | 7 | a0001c0001t0015g0274 a0001c0001t0026g0089 a0001c0001t0026g0090 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212+1633A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820656 | |||||||
| chr5:122820713 | A | G | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1212+1690A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820713 | |||||||
| chr5:122820724 | A | G | 1 | a0001c0001t0012g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1212+1701A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820724 | |||||||
| chr5:122820928 | G | A | 2 | a0001c0001t0031g0256 a0001c0001t0061g0255 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1212+1905G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122820928 | |||||||
| chr5:122821016 | T | C | 1 | a0001c0001t0071g0295 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1212+1993T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821016 | |||||||
| chr5:122821254 | G | A | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.1212+2231G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821254 | |||||||
| chr5:122821269 | G | A | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1212+2246G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821269 | |||||||
| chr5:122821388 | T | A | 5 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0004g0172 others(2): Show |
5 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212+2365T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821388 | |||||||
| chr5:122821454 | TC | T | 3 | a0001c0001t0002g0337 a0001c0001t0012g0276 a0001c0001t0060g0277 |
3 | HG01243.hp1 HG01255.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1212+2433delC | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122821454 | ||||||
| chr5:122821455 | C | CT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(9): Show |
12 | HG00558.hp1 HG01175.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212+2432_1212+243 others(5): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821455 | |||||||
| chr5:122821456 | C | T | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
350 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.1212+2433C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821456 | |||||||
| chr5:122821471 | T | C | 2 | a0001c0001t0008g0054 a0001c0001t0008g0072 |
2 | NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1212+2448T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821471 | |||||||
| chr5:122821494 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0253 |
3 | HG01258.hp1 HG01346.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1212+2471C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821494 | |||||||
| chr5:122821547 | C | T | 1 | a0001c0005t0070g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1212+2524C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821547 | |||||||
| chr5:122821925 | AG | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1212+2903delG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821925 | |||||||
| chr5:122821947 | A | G | 3 | a0001c0001t0003g0137 a0001c0001t0003g0139 a0001c0001t0004g0138 |
3 | NA18949.hp2 NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1212+2924A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122821947 | |||||||
| chr5:122822180 | G | A | 1 | a0001c0001t0002g0327 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1212+3157G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822180 | |||||||
| chr5:122822216 | G | A | 2 | a0001c0001t0033g0244 a0002c0004t0033g0245 |
2 | HG00609.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1212+3193G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822216 | |||||||
| chr5:122822236 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1212+3213G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822236 | |||||||
| chr5:122822338 | G | A | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1212+3315G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822338 | |||||||
| chr5:122822438 | G | A | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212+3415G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822438 | |||||||
| chr5:122822469 | A | T | 15 | a0001c0002t0006g0014 a0001c0002t0006g0015 a0001c0002t0006g0222 others(12): Show |
16 | HG03704.hp1 NA18747.hp2 NA18944.hp1 others(13): Show |
intron_variant | MODIFIER | c.1212+3446A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822469 | |||||||
| chr5:122822661 | G | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(3): Show |
6 | HG02080.hp1 NA18998.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1213-3389G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122822661 | |||||||
| chr5:122823122 | G | T | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1213-2928G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823122 | |||||||
| chr5:122823169 | T | TAATG | 85 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(82): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1213-2880_1213-287 others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823169 | ||||||
| chr5:122823208 | A | C | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1213-2842A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823208 | |||||||
| chr5:122823224 | C | T | 3 | a0001c0001t0020g0232 a0001c0001t0020g0233 a0001c0007t0020g0231 |
3 | HG02723.hp2 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1213-2826C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823224 | |||||||
| chr5:122823254 | G | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
126 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1213-2796G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823254 | |||||||
| chr5:122823315 | C | G | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1213-2735C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823315 | |||||||
| chr5:122823319 | C | T | 1 | a0001c0001t0037g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1213-2731C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823319 | |||||||
| chr5:122823352 | AT | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1213-2689delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823352 | ||||||
| chr5:122823717 | G | GGT | 9 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0023g0286 others(6): Show |
9 | HG00738.hp1 HG01168.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1213-2314_1213-231 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823717 | ||||||
| chr5:122823717 | G | GGTGT | 59 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(56): Show |
67 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1213-2316_1213-231 others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823717 | ||||||
| chr5:122823717 | GGT | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
153 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.1213-2314_1213-231 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823717 | ||||||
| chr5:122823717 | GGTGT | G | 116 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(113): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1213-2316_1213-231 others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823717 | ||||||
| chr5:122823779 | C | CGT | 51 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(48): Show |
59 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1213-2240_1213-223 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823779 | C | CGTGT | 11 | a0001c0001t0002g0293 a0001c0001t0002g0304 a0001c0001t0002g0314 others(8): Show |
11 | HG00099.hp1 HG00558.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1213-2242_1213-223 others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823779 | CGT | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
141 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1213-2240_1213-223 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823779 | CGTGT | C | 19 | a0001c0001t0002g0310 a0001c0001t0002g0318 a0001c0001t0011g0013 others(16): Show |
20 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1213-2242_1213-223 others(8): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823779 | CGTGTGT | C | 101 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(98): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1213-2244_1213-223 others(10): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823779 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1213-2250_1213-223 others(16): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122823779 | ||||||
| chr5:122823808 | G | A | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213-2242G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823808 | |||||||
| chr5:122823855 | C | A | 1 | a0001c0001t0015g0264 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1213-2195C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823855 | |||||||
| chr5:122823929 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1213-2121C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823929 | |||||||
| chr5:122823994 | G | A | 1 | a0001c0001t0017g0259 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1213-2056G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122823994 | |||||||
| chr5:122824006 | C | G | 1 | a0001c0001t0062g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1213-2044C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824006 | |||||||
| chr5:122824070 | C | G | 1 | a0001c0001t0023g0288 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1213-1980C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824070 | |||||||
| chr5:122824074 | T | C | 1 | a0001c0001t0020g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1213-1976T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824074 | |||||||
| chr5:122824133 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.1213-1917T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824133 | |||||||
| chr5:122824147 | A | G | 1 | a0001c0001t0049g0268 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1213-1903A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824147 | |||||||
| chr5:122824147 | AG | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0005g0108 others(3): Show |
6 | HG00597.hp2 HG02135.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213-1902delG | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824147 | |||||||
| chr5:122824201 | CA | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
221 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1213-1831delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122824201 | ||||||
| chr5:122824201 | CAA | C | 116 | a0001c0001t0001g0132 a0001c0001t0003g0012 a0001c0001t0003g0083 others(113): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1213-1832_1213-183 others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122824201 | ||||||
| chr5:122824247 | T | G | 2 | a0001c0001t0021g0201 a0001c0001t0021g0202 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1213-1803T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824247 | |||||||
| chr5:122824292 | A | G | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1213-1758A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824292 | |||||||
| chr5:122824321 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0103 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-1729T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824321 | |||||||
| chr5:122824425 | G | A | 114 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(111): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1213-1625G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122824425 | |||||||
| chr5:122825060 | A | G | 1 | a0001c0001t0045g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1213-990A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825060 | |||||||
| chr5:122825126 | G | T | 2 | a0001c0001t0003g0083 a0001c0001t0003g0085 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1213-924G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825126 | |||||||
| chr5:122825136 | T | TTTTTTAT others(18): Show |
1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1213-913_1213-889d others(27): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 122825136 | ||||||
| chr5:122825192 | A | G | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1213-858A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825192 | |||||||
| chr5:122825260 | A | G | 2 | a0001c0001t0003g0139 a0001c0001t0004g0138 |
2 | NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1213-790A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825260 | |||||||
| chr5:122825337 | A | G | 5 | a0001c0001t0015g0017 a0001c0001t0015g0263 a0001c0001t0015g0264 others(2): Show |
5 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213-713A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825337 | |||||||
| chr5:122825388 | A | G | 6 | a0001c0001t0003g0012 a0001c0001t0003g0143 a0001c0001t0003g0158 others(3): Show |
7 | HG00323.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-662A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825388 | |||||||
| chr5:122825489 | T | G | 1 | a0001c0001t0008g0028 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1213-561T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825489 | |||||||
| chr5:122825773 | C | A | 16 | a0001c0001t0010g0246 a0001c0001t0010g0247 a0001c0001t0010g0248 others(13): Show |
16 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1213-277C>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825773 | |||||||
| chr5:122825943 | A | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1213-107A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122825943 | |||||||
| chr5:122826036 | T | G | 1 | a0001c0001t0045g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1213-14T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 11/14 | chr5 | 122826036 | |||||||
| chr5:122826266 | A | AT | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1356+79dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 122826266 | ||||||
| chr5:122826703 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1356+510T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826703 | |||||||
| chr5:122826708 | C | T | 1 | a0001c0001t0005g0025 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1356+515C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826708 | |||||||
| chr5:122826752 | A | G | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356+559A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826752 | |||||||
| chr5:122826860 | A | G | 2 | a0001c0001t0012g0276 a0001c0001t0060g0277 |
2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1357-519A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826860 | |||||||
| chr5:122826903 | T | A | 1 | a0001c0001t0002g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357-476T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826903 | |||||||
| chr5:122826915 | C | T | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1357-464C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826915 | |||||||
| chr5:122826931 | T | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1357-448T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122826931 | |||||||
| chr5:122827162 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
133 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1357-217A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122827162 | |||||||
| chr5:122827332 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1357-47A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 12/14 | chr5 | 122827332 | |||||||
| chr5:122827706 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
132 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1509+60T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122827706 | |||||||
| chr5:122827715 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1509+69G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122827715 | |||||||
| chr5:122827821 | G | GT | 9 | a0001c0001t0001g0110 a0001c0001t0002g0311 a0001c0001t0005g0024 others(6): Show |
9 | HG00738.hp1 HG01168.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+189dupT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 122827821 | ||||||
| chr5:122827821 | G | GTT | 6 | a0001c0001t0002g0285 a0001c0001t0015g0017 a0001c0001t0015g0263 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509+188_1509+189d others(4): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 122827821 | ||||||
| chr5:122827821 | GT | G | 113 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(110): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1509+189delT | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 122827821 | ||||||
| chr5:122828010 | C | G | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1509+364C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828010 | |||||||
| chr5:122828029 | TA | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
138 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1509+394delA | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 122828029 | ||||||
| chr5:122828074 | G | T | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1509+428G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828074 | |||||||
| chr5:122828107 | G | T | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.1509+461G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828107 | |||||||
| chr5:122828256 | G | C | 2 | a0001c0001t0032g0236 a0001c0001t0032g0237 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1509+610G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828256 | |||||||
| chr5:122828271 | T | C | 6 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509+625T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828271 | |||||||
| chr5:122828282 | A | C | 4 | a0001c0001t0026g0089 a0001c0001t0026g0090 a0001c0001t0026g0235 others(1): Show |
4 | HG02258.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+636A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828282 | |||||||
| chr5:122828773 | T | A | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-825T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828773 | |||||||
| chr5:122828774 | A | T | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-824A>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828774 | |||||||
| chr5:122828775 | T | A | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-823T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828775 | |||||||
| chr5:122828832 | A | G | 1 | a0001c0001t0068g0312 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1510-766A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828832 | |||||||
| chr5:122828840 | C | T | 1 | a0001c0001t0004g0171 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1510-758C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828840 | |||||||
| chr5:122828851 | G | C | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-747G>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828851 | |||||||
| chr5:122828852 | C | G | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-746C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828852 | |||||||
| chr5:122828917 | A | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.1510-681A>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122828917 | |||||||
| chr5:122829015 | A | C | 1 | a0001c0001t0073g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1510-583A>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829015 | |||||||
| chr5:122829054 | T | C | 2 | a0001c0001t0033g0244 a0002c0004t0033g0245 |
2 | HG00609.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1510-544T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829054 | |||||||
| chr5:122829065 | C | T | 14 | a0001c0002t0009g0208 a0001c0002t0009g0210 a0001c0002t0009g0211 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1510-533C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829065 | |||||||
| chr5:122829088 | G | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0019 others(62): Show |
73 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1510-510G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829088 | |||||||
| chr5:122829174 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-424T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829174 | |||||||
| chr5:122829176 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-422T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829176 | |||||||
| chr5:122829177 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-421G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829177 | |||||||
| chr5:122829185 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-413T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829185 | |||||||
| chr5:122829197 | TTTTG | T | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1510-381_1510-378d others(6): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 122829197 | ||||||
| chr5:122829202 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-396T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829202 | |||||||
| chr5:122829203 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-395T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829203 | |||||||
| chr5:122829205 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-393G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829205 | |||||||
| chr5:122829209 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-389G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829209 | |||||||
| chr5:122829212 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-386T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829212 | |||||||
| chr5:122829213 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-385G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829213 | |||||||
| chr5:122829220 | T | G | 1 | a0001c0001t0003g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1510-378T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829220 | |||||||
| chr5:122829236 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-362G>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829236 | |||||||
| chr5:122829241 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-357G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829241 | |||||||
| chr5:122829252 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-346T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829252 | |||||||
| chr5:122829261 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-337G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829261 | |||||||
| chr5:122829265 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-333T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829265 | |||||||
| chr5:122829266 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-332G>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829266 | |||||||
| chr5:122829297 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-301T>A | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829297 | |||||||
| chr5:122829308 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-290T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829308 | |||||||
| chr5:122829313 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-285T>C | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829313 | |||||||
| chr5:122829327 | C | T | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1510-271C>T | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829327 | |||||||
| chr5:122829330 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510-268C>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829330 | |||||||
| chr5:122829514 | T | G | 115 | a0001c0001t0003g0012 a0001c0001t0003g0083 a0001c0001t0003g0085 others(112): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1510-84T>G | SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 14/14 | chr5 | 122829514 |