Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55787 |
| ensemblid | ENSG00000086712.13 |
| hgncid | 18578 |
| symbol | TXLNG |
| name | taxilin gamma |
| refseq_nuc | NM_018360.3 |
| refseq_prot | NP_060830.2 |
| ensembl_nuc | ENST00000380122.10 |
| ensembl_prot | ENSP00000369465.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 16786466 |
| end | 16844519 |
| strand | + |
| ver | v1.2 |
| region | chrX:16786466-16844519 |
| region5000 | chrX:16781466-16849519 |
| regionname0 | TXLNG_chrX_16786466_16844519 |
| regionname5000 | TXLNG_chrX_16781466_16849519 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 528 | 258 | 61 | 51 | 107 | 11 | 26 | 84 | TXLNG_chrX_16781466_16849519 | TXLNG | MATRV others(523): Show |
chrX | 16781466 | 16849519 |
| a0002 | 0/0 | 528 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | MATRV others(523): Show |
chrX | 16781466 | 16849519 |
| a0003 | 0/0 | 528 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | MATRV others(523): Show |
chrX | 16781466 | 16849519 |
| a0004 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | MATRV others(523): Show |
chrX | 16781466 | 16849519 |
| a0005 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | MATRV others(523): Show |
chrX | 16781466 | 16849519 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1584 | 192 | 47 | 35 | 93 | 4 | 12 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0001c0002 | 1/0 | 1584 | 59 | 7 | 16 | 14 | 7 | 14 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0001c0004 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0001c0005 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0001c0006 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0002c0003 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0003c0008 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0004c0007 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 | ||
| a0005c0009 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | ATGGC others(1579): Show |
chrX | 16781466 | 16849519 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4362 | 90 | 10 | 18 | 52 | 3 | 7 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0003 | 0/0 | 4361 | 47 | 10 | 8 | 25 | 1 | 3 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0004 | 0/0 | 4363 | 18 | 2 | 4 | 11 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4358): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0005 | 0/0 | 4361 | 9 | 7 | 1 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0006 | 0/0 | 4361 | 6 | 6 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0007 | 0/0 | 4362 | 4 | 4 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0009 | 0/0 | 4337 | 3 | 2 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4332): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0011 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0012 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0013 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0014 | 0/1 | 4362 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0015 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0016 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4358): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0017 | 0/0 | 4361 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0018 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0019 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0020 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0021 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0022 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0023 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0001t0024 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0001 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0002 | 1/0 | 4362 | 51 | 2 | 15 | 13 | 6 | 14 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0008 | 0/0 | 4362 | 3 | 2 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0010 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0029 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0002t0030 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0004t0025 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0004t0026 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4380): Show |
chrX | 16781466 | 16849519 |
| a0001c0004t0027 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0001c0005t0006 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0001c0006t0002 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0002c0003t0003 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4356): Show |
chrX | 16781466 | 16849519 |
| a0002c0003t0028 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0003c0008t0002 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0004c0007t0008 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4357): Show |
chrX | 16781466 | 16849519 |
| a0005c0009t0031 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | GTTTG others(4358): Show |
chrX | 16781466 | 16849519 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0013g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0014g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0015g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0019g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0020g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0021g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0022g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0023g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0001t0024g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0001 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0029g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0002t0030g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0004t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0004t0026g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0004t0027g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0005t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0005t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0006t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0001c0006t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0002c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0002c0003t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0002c0003t0028g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0003c0008t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0004c0007t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| a0005c0009t0031g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0048 | EUR | GBR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0060 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG00741 | hp2 | a0003 | c0008 | t0002 | g0072 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01106 | hp1 | a0001 | c0001 | t0016 | g0115 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0206 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0246 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0056 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0247 | EUR | IBS | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01884 | hp1 | a0001 | c0004 | t0026 | g0016 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0208 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02055 | hp1 | a0001 | c0005 | t0006 | g0029 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02080 | hp1 | a0001 | c0001 | t0012 | g0182 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02258 | hp1 | a0002 | c0003 | t0028 | g0132 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02280 | hp1 | a0004 | c0007 | t0008 | g0046 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02293 | hp1 | a0001 | c0001 | t0015 | g0091 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02451 | hp1 | a0001 | c0005 | t0006 | g0028 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02451 | hp2 | a0005 | c0009 | t0031 | g0015 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02572 | hp1 | a0001 | c0001 | t0019 | g0088 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02886 | hp2 | a0001 | c0002 | t0008 | g0031 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02922 | hp1 | a0001 | c0001 | t0023 | g0158 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02970 | hp2 | a0001 | c0001 | t0022 | g0129 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0087 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03041 | hp2 | a0001 | c0006 | t0002 | g0032 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0034 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0161 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03486 | hp2 | a0001 | c0006 | t0002 | g0066 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | ESN | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03540 | hp1 | a0001 | c0002 | t0010 | g0051 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0192 | AFR | GWD | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0089 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03654 | hp1 | a0001 | c0001 | t0017 | g0173 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0075 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | BEB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | STU | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18906 | hp2 | a0002 | c0003 | t0003 | g0175 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18951 | hp1 | a0001 | c0002 | t0008 | g0084 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18951 | hp2 | a0001 | c0001 | t0024 | g0137 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18971 | hp1 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19009 | hp1 | a0001 | c0001 | t0021 | g0130 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19030 | hp1 | a0001 | c0004 | t0027 | g0017 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | YRI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ASW | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ASW | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA20752 | hp1 | a0001 | c0002 | t0030 | g0042 | EUR | TSI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0062 | EUR | TSI | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | GIH | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02559 | hp1 | a0001 | c0004 | t0025 | g0018 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG02559 | hp2 | a0001 | c0002 | t0010 | g0052 | AFR | ACB | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | MSL | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0090 | AFR | USA | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| NA21309 | hp2 | a0001 | c0002 | t0029 | g0004 | AFR | LWK | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0222 | REF | REF | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0152 | REF | REF | TXLNG_chrX_16781466_16849519 | TXLNG | chrX | 16781466 | 16849519 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:16786504 | A | G | 1 | a0005 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.17A>G | p.Glu6Gly | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 39/4362 | 17/1587 | 6/528 | chrX | 16786504 | |||
| chrX:16786510 | C | T | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.23C>T | p.Ala8Val | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 45/4362 | 23/1587 | 8/528 | chrX | 16786510 | |||
| chrX:16841706 | A | C | 1 | a0002 | 3 | HG02258.hp1 HG06807.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1527A>C | p.Arg509Ser | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1549/4362 | 1527/1587 | 509/528 | chrX | 16841706 | |||
| chrX:16841744 | C | T | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1565C>T | p.Pro522Leu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1587/4362 | 1565/1587 | 522/528 | chrX | 16841744 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:16786538 | A | G | 1 | a0001c0004 | 3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.51A>G | p.Glu17Glu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/10 | 73/4362 | 51/1587 | 17/528 | chrX | 16786538 | |||
| chrX:16841505 | G | A | 5 | a0001c0001 a0001c0004 a0001c0005 others(2): Show |
200 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(197): Show |
synonymous_variant | LOW | c.1326G>A | p.Gln442Gln | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1348/4362 | 1326/1587 | 442/528 | chrX | 16841505 | |||
| chrX:16841544 | G | C | 1 | a0001c0005 | 2 | HG02055.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.1365G>C | p.Leu455Leu | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1387/4362 | 1365/1587 | 455/528 | chrX | 16841544 | |||
| chrX:16841559 | C | T | 1 | a0001c0006 | 2 | HG03041.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.1380C>T | p.Ser460Ser | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1402/4362 | 1380/1587 | 460/528 | chrX | 16841559 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:16842011 | T | C | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(5): Show |
116 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*245T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 245 | chrX | 16842011 | ||||||
| chrX:16842079 | G | T | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 313 | chrX | 16842079 | ||||||
| chrX:16842130 | A | G | 1 | a0001c0001t0015 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 364 | chrX | 16842130 | ||||||
| chrX:16842150 | G | GC | 3 | a0001c0001t0004 a0001c0001t0016 a0005c0009t0031 |
20 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*395dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 396 | INFO_REALIGN_3_PRIME | chrX | 16842150 | |||||
| chrX:16842150 | GC | G | 13 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(10): Show |
74 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*395delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 395 | INFO_REALIGN_3_PRIME | chrX | 16842150 | |||||
| chrX:16842373 | C | T | 1 | a0001c0001t0024 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 607 | chrX | 16842373 | ||||||
| chrX:16842431 | G | A | 1 | a0001c0001t0017 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 665 | chrX | 16842431 | ||||||
| chrX:16842604 | A | G | 1 | a0001c0001t0011 | 2 | HG03195.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*838A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 838 | chrX | 16842604 | ||||||
| chrX:16842607 | A | C | 1 | a0001c0002t0030 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 841 | chrX | 16842607 | ||||||
| chrX:16842749 | C | T | 1 | a0001c0002t0029 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 983 | chrX | 16842749 | ||||||
| chrX:16842765 | C | T | 1 | a0001c0001t0009 | 3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 999 | chrX | 16842765 | ||||||
| chrX:16842790 | A | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
185 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1024 | chrX | 16842790 | ||||||
| chrX:16842992 | T | C | 1 | a0001c0004t0025 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1226 | chrX | 16842992 | ||||||
| chrX:16843321 | T | C | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | HG02572.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1555T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1555 | chrX | 16843321 | ||||||
| chrX:16843370 | T | C | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
192 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1604T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1604 | chrX | 16843370 | ||||||
| chrX:16843467 | C | A | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
181 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1701C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1701 | chrX | 16843467 | ||||||
| chrX:16843509 | C | T | 1 | a0001c0001t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 1743 | chrX | 16843509 | ||||||
| chrX:16843783 | C | T | 1 | a0001c0001t0013 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2017 | chrX | 16843783 | ||||||
| chrX:16843833 | A | ATTCTGTC others(16): Show |
1 | a0001c0004t0026 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2069_*2091dupTCTG others(19): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2092 | INFO_REALIGN_3_PRIME | chrX | 16843833 | |||||
| chrX:16843923 | T | C | 1 | a0005c0009t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2157T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2157 | chrX | 16843923 | ||||||
| chrX:16843978 | G | A | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
187 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*2212G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2212 | chrX | 16843978 | ||||||
| chrX:16844063 | TTGCACCA others(18): Show |
T | 1 | a0001c0001t0009 | 3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2299_*2323delGCAC others(21): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2299 | INFO_REALIGN_3_PRIME | chrX | 16844063 | |||||
| chrX:16844104 | C | T | 1 | a0001c0001t0021 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2338 | chrX | 16844104 | ||||||
| chrX:16844392 | T | C | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0002t0010 others(1): Show |
14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2626T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2626 | chrX | 16844392 | ||||||
| chrX:16844486 | G | A | 1 | a0001c0001t0020 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 10/10 | 2720 | chrX | 16844486 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:16786606 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.102+17C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16786606 | |||||||
| chrX:16786705 | G | A | 1 | a0005c0009t0031g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.102+116G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16786705 | |||||||
| chrX:16787313 | C | T | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+724C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787313 | |||||||
| chrX:16787315 | G | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+726G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787315 | |||||||
| chrX:16787378 | CCT | C | 63 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0181 others(60): Show |
65 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.102+792_102+793del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16787378 | ||||||
| chrX:16787380 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+791T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787380 | |||||||
| chrX:16787381 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.102+792C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787381 | |||||||
| chrX:16787481 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+892C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787481 | |||||||
| chrX:16787575 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.102+986A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16787575 | |||||||
| chrX:16788056 | G | A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+1467G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788056 | |||||||
| chrX:16788346 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.102+1757A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788346 | |||||||
| chrX:16788539 | G | A | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+1950G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16788539 | |||||||
| chrX:16788667 | G | GT | 24 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
24 | HG01175.hp1 HG01175.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+2096dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | ||||||
| chrX:16788667 | G | GTTTT | 49 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0006g0053 others(46): Show |
53 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.102+2093_102+2096d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | ||||||
| chrX:16788667 | G | GTTTTT | 24 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(21): Show |
26 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.102+2092_102+2096d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | ||||||
| chrX:16788667 | G | GTTTTTT | 7 | a0001c0001t0005g0026 a0001c0001t0006g0081 a0001c0001t0007g0079 others(4): Show |
7 | HG02293.hp2 HG03453.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+2091_102+2096d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16788667 | ||||||
| chrX:16789205 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+2616T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789205 | |||||||
| chrX:16789446 | AT | A | 4 | a0001c0001t0007g0027 a0001c0001t0007g0064 a0001c0001t0007g0079 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2859delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789446 | ||||||
| chrX:16789477 | C | G | 69 | a0001c0001t0001g0033 a0001c0001t0006g0053 a0001c0001t0006g0054 others(66): Show |
75 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.102+2888C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789477 | |||||||
| chrX:16789533 | C | A | 3 | a0001c0001t0006g0065 a0001c0005t0006g0028 a0001c0005t0006g0029 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.102+2944C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789533 | |||||||
| chrX:16789658 | T | TATGTAGA others(6): Show |
1 | a0001c0001t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+3070_102+3082d others(15): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16789658 | ||||||
| chrX:16789907 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+3318G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16789907 | |||||||
| chrX:16790040 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+3451T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790040 | |||||||
| chrX:16790105 | C | T | 1 | a0001c0002t0002g0063 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.102+3516C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790105 | |||||||
| chrX:16790314 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102+3725C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790314 | |||||||
| chrX:16790506 | C | G | 2 | a0001c0002t0002g0061 a0001c0002t0002g0062 |
2 | HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.102+3917C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790506 | |||||||
| chrX:16790550 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.102+3961G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790550 | |||||||
| chrX:16790952 | G | A | 2 | a0001c0001t0018g0087 a0001c0001t0019g0088 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.102+4363G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790952 | |||||||
| chrX:16790984 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102+4395C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16790984 | |||||||
| chrX:16791370 | GAAGTA | G | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+4791_102+4795d others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16791370 | ||||||
| chrX:16791409 | T | A | 1 | a0001c0001t0011g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102+4820T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791409 | |||||||
| chrX:16791423 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.102+4834C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791423 | |||||||
| chrX:16791466 | A | T | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+4877A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791466 | |||||||
| chrX:16791674 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+5085T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16791674 | |||||||
| chrX:16792372 | C | G | 1 | a0001c0002t0002g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.102+5783C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792372 | |||||||
| chrX:16792428 | TG | T | 3 | a0001c0002t0002g0060 a0001c0002t0002g0075 a0001c0002t0002g0076 |
3 | HG00323.hp1 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.102+5840delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792428 | |||||||
| chrX:16792747 | C | T | 11 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0057 others(8): Show |
13 | HG01943.hp1 HG01975.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+6158C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16792747 | |||||||
| chrX:16793112 | A | T | 2 | a0001c0002t0002g0055 a0001c0002t0002g0056 |
2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.102+6523A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793112 | |||||||
| chrX:16793113 | G | A | 54 | a0001c0001t0001g0033 a0001c0002t0002g0001 a0001c0002t0002g0003 others(51): Show |
60 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.102+6524G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793113 | |||||||
| chrX:16793713 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+7124C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793713 | |||||||
| chrX:16793734 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102+7145C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793734 | |||||||
| chrX:16793770 | A | G | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.102+7181A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793770 | |||||||
| chrX:16793989 | T | G | 1 | a0001c0001t0001g0181 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+7400T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16793989 | |||||||
| chrX:16794043 | C | T | 55 | a0001c0001t0001g0033 a0001c0002t0002g0001 a0001c0002t0002g0003 others(52): Show |
61 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.102+7454C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794043 | |||||||
| chrX:16794090 | T | A | 1 | a0001c0001t0005g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102+7501T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794090 | |||||||
| chrX:16794273 | A | C | 1 | a0001c0001t0003g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.102+7684A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794273 | |||||||
| chrX:16794481 | T | G | 1 | a0002c0003t0003g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.102+7892T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794481 | |||||||
| chrX:16794536 | ACTT | A | 69 | a0001c0001t0001g0033 a0001c0001t0006g0053 a0001c0001t0006g0054 others(66): Show |
75 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.102+7951_102+7953d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16794536 | ||||||
| chrX:16794659 | T | G | 194 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(191): Show |
203 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.102+8070T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794659 | |||||||
| chrX:16794865 | T | A | 1 | a0001c0002t0002g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102+8276T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794865 | |||||||
| chrX:16794896 | T | C | 1 | a0001c0001t0012g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.102+8307T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794896 | |||||||
| chrX:16794979 | A | T | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+8390A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16794979 | |||||||
| chrX:16795004 | G | A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+8415G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795004 | |||||||
| chrX:16795005 | C | T | 70 | a0001c0001t0001g0033 a0001c0001t0006g0053 a0001c0001t0006g0054 others(67): Show |
76 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.102+8416C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795005 | |||||||
| chrX:16795073 | C | A | 3 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0179 |
3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.102+8484C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795073 | |||||||
| chrX:16795201 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+8612T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795201 | |||||||
| chrX:16795208 | C | T | 6 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(3): Show |
6 | HG02071.hp1 HG02080.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+8619C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795208 | |||||||
| chrX:16795212 | G | A | 1 | a0001c0001t0015g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.102+8623G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795212 | |||||||
| chrX:16795234 | G | A | 1 | a0001c0001t0003g0127 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.102+8645G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795234 | |||||||
| chrX:16795368 | T | C | 1 | a0001c0001t0006g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.102+8779T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795368 | |||||||
| chrX:16795538 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.102+8949C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16795538 | |||||||
| chrX:16796094 | A | G | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+9505A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796094 | |||||||
| chrX:16796116 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.102+9527A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796116 | |||||||
| chrX:16796323 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+9734T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796323 | |||||||
| chrX:16796473 | A | G | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0063 |
3 | NA18952.hp1 NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.102+9884A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796473 | |||||||
| chrX:16796850 | C | T | 14 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(11): Show |
14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+10261C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16796850 | |||||||
| chrX:16797079 | T | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+10490T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797079 | |||||||
| chrX:16797281 | C | CA | 6 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0004g0092 others(3): Show |
6 | HG02071.hp1 HG02922.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+10708dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | ||||||
| chrX:16797281 | CA | C | 80 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0124 others(77): Show |
86 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+10708delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | ||||||
| chrX:16797281 | CAA | C | 6 | a0001c0001t0005g0025 a0001c0002t0002g0048 a0001c0002t0002g0059 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+10707_102+1070 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16797281 | ||||||
| chrX:16797462 | G | C | 5 | a0001c0001t0001g0033 a0001c0002t0008g0031 a0001c0002t0008g0034 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.102+10873G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797462 | |||||||
| chrX:16797845 | T | A | 2 | a0001c0001t0011g0089 a0001c0001t0011g0161 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+11256T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797845 | |||||||
| chrX:16797904 | A | G | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+11315A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16797904 | |||||||
| chrX:16798071 | G | C | 1 | a0001c0001t0003g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.102+11482G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798071 | |||||||
| chrX:16798105 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.102+11516G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798105 | |||||||
| chrX:16798155 | T | C | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+11566T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798155 | |||||||
| chrX:16798245 | C | A | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.102+11656C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798245 | |||||||
| chrX:16798383 | T | A | 1 | a0001c0001t0022g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102+11794T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798383 | |||||||
| chrX:16798432 | A | G | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+11843A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798432 | |||||||
| chrX:16798536 | T | G | 2 | a0001c0002t0002g0035 a0001c0002t0002g0067 |
2 | HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.102+11947T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798536 | |||||||
| chrX:16798583 | G | GT | 20 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0180 others(17): Show |
21 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+12009dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16798583 | ||||||
| chrX:16798800 | A | C | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+12211A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16798800 | |||||||
| chrX:16799134 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+12545T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799134 | |||||||
| chrX:16799493 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.102+12904C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799493 | |||||||
| chrX:16799639 | C | T | 3 | a0001c0001t0004g0007 a0001c0001t0004g0092 a0001c0001t0004g0170 |
4 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+13050C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799639 | |||||||
| chrX:16799681 | G | C | 2 | a0001c0001t0003g0127 a0001c0001t0021g0130 |
2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.102+13092G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799681 | |||||||
| chrX:16799764 | C | G | 1 | a0001c0001t0006g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102+13175C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799764 | |||||||
| chrX:16799793 | G | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.102+13204G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799793 | |||||||
| chrX:16799973 | A | G | 2 | a0001c0001t0006g0053 a0001c0001t0006g0054 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102+13384A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16799973 | |||||||
| chrX:16800152 | C | T | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+13563C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800152 | |||||||
| chrX:16800284 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.102+13695T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800284 | |||||||
| chrX:16800539 | A | G | 1 | a0001c0002t0008g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102+13950A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800539 | |||||||
| chrX:16800562 | C | CT | 5 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0240 others(2): Show |
5 | HG01175.hp1 NA18940.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+13993dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16800562 | ||||||
| chrX:16800562 | CT | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0185 a0001c0001t0001g0227 others(8): Show |
11 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.102+13993delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16800562 | ||||||
| chrX:16800648 | T | C | 1 | a0001c0002t0002g0038 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.102+14059T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16800648 | |||||||
| chrX:16801112 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+14523G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801112 | |||||||
| chrX:16801178 | G | A | 1 | a0001c0001t0017g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102+14589G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801178 | |||||||
| chrX:16801347 | GGCTAATT others(8151): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102+14793_103-9035 others(3): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801347 | ||||||
| chrX:16801435 | C | T | 1 | a0001c0001t0023g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102+14846C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801435 | |||||||
| chrX:16801437 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102+14848C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801437 | |||||||
| chrX:16801619 | A | T | 2 | a0001c0006t0002g0032 a0001c0006t0002g0066 |
2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.102+15030A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801619 | |||||||
| chrX:16801628 | CA | C | 14 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0065 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+15041delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801628 | ||||||
| chrX:16801842 | A | G | 207 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(204): Show |
216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.102+15253A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801842 | |||||||
| chrX:16801950 | CT | C | 163 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(160): Show |
172 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.102+15382delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801950 | ||||||
| chrX:16801950 | CTT | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0101 others(21): Show |
24 | HG00323.hp1 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+15381_102+1538 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16801950 | ||||||
| chrX:16801955 | T | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0156 others(1): Show |
5 | HG00639.hp2 HG01081.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+15366T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16801955 | |||||||
| chrX:16802056 | C | T | 4 | a0001c0001t0007g0027 a0001c0001t0007g0064 a0001c0001t0007g0079 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+15467C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802056 | |||||||
| chrX:16802254 | C | CT | 43 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0226 others(40): Show |
43 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.102+15680dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802254 | ||||||
| chrX:16802254 | C | CTT | 40 | a0001c0001t0006g0081 a0001c0002t0002g0001 a0001c0002t0002g0003 others(37): Show |
46 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.102+15679_102+1568 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802254 | ||||||
| chrX:16802339 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.102+15750C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802339 | |||||||
| chrX:16802407 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+15818T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802407 | |||||||
| chrX:16802447 | C | T | 3 | a0001c0001t0006g0065 a0001c0005t0006g0028 a0001c0005t0006g0029 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.102+15858C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802447 | |||||||
| chrX:16802521 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.102+15932T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802521 | |||||||
| chrX:16802547 | C | T | 14 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0065 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+15958C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802547 | |||||||
| chrX:16802821 | C | CT | 7 | a0001c0001t0001g0106 a0001c0001t0001g0171 a0001c0001t0001g0239 others(4): Show |
7 | HG01981.hp1 HG02572.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-15736dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802821 | ||||||
| chrX:16802821 | CT | C | 82 | a0001c0001t0001g0033 a0001c0001t0001g0211 a0001c0001t0001g0230 others(79): Show |
88 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.103-15736delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16802821 | ||||||
| chrX:16802825 | T | C | 1 | a0001c0001t0003g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.103-15749T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16802825 | |||||||
| chrX:16803008 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-15566T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803008 | |||||||
| chrX:16803056 | G | T | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-15518G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803056 | |||||||
| chrX:16803162 | C | G | 1 | a0001c0001t0003g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15412C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803162 | |||||||
| chrX:16803164 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.103-15410C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803164 | |||||||
| chrX:16803242 | A | G | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-15332A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803242 | |||||||
| chrX:16803318 | A | G | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-15256A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803318 | |||||||
| chrX:16803354 | A | AT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0241 a0001c0001t0003g0012 others(2): Show |
5 | HG00544.hp2 HG02280.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-15202dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803354 | ||||||
| chrX:16803354 | AT | A | 12 | a0001c0001t0001g0211 a0001c0001t0003g0009 a0001c0001t0005g0021 others(9): Show |
12 | HG00738.hp1 HG01081.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-15202delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16803354 | ||||||
| chrX:16803499 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.103-15075C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803499 | |||||||
| chrX:16803586 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-14988A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803586 | |||||||
| chrX:16803589 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-14985C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803589 | |||||||
| chrX:16803608 | G | C | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-14966G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803608 | |||||||
| chrX:16803725 | G | A | 1 | a0001c0002t0002g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.103-14849G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803725 | |||||||
| chrX:16803808 | T | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-14766T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803808 | |||||||
| chrX:16803901 | G | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0176 |
2 | NA18953.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.103-14673G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16803901 | |||||||
| chrX:16804026 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.103-14548C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804026 | |||||||
| chrX:16804166 | G | A | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-14408G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804166 | |||||||
| chrX:16804196 | T | C | 1 | a0001c0001t0007g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-14378T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804196 | |||||||
| chrX:16804562 | C | A | 1 | a0001c0001t0019g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.103-14012C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804562 | |||||||
| chrX:16804727 | T | A | 1 | a0005c0009t0031g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.103-13847T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804727 | |||||||
| chrX:16804803 | G | A | 1 | a0003c0008t0002g0072 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.103-13771G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804803 | |||||||
| chrX:16804897 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-13677G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804897 | |||||||
| chrX:16804971 | A | AC | 67 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0101 others(64): Show |
69 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.103-13591dupC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | ||||||
| chrX:16804971 | A | ACC | 16 | a0001c0001t0001g0112 a0001c0001t0001g0210 a0001c0001t0001g0225 others(13): Show |
16 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.103-13592_103-1359 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | ||||||
| chrX:16804971 | AC | A | 19 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(16): Show |
23 | HG01074.hp1 HG01123.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.103-13591delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804971 | ||||||
| chrX:16804974 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-13600C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804974 | |||||||
| chrX:16804975 | C | G | 1 | a0001c0002t0002g0005 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.103-13599C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804975 | |||||||
| chrX:16804976 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.103-13598C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804976 | |||||||
| chrX:16804978 | C | G | 1 | a0001c0001t0003g0148 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.103-13596C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804978 | |||||||
| chrX:16804979 | C | G | 1 | a0001c0002t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.103-13595C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804979 | |||||||
| chrX:16804982 | C | G | 1 | a0001c0002t0002g0062 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13592C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804982 | |||||||
| chrX:16804983 | CG | C | 13 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0120 others(10): Show |
13 | HG00733.hp2 HG01071.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.103-13590delG | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804983 | |||||||
| chrX:16804984 | G | C | 150 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(147): Show |
155 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.103-13590G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804984 | |||||||
| chrX:16804984 | G | T | 1 | a0001c0002t0002g0062 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13590G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804984 | |||||||
| chrX:16804985 | C | CCG | 5 | a0001c0001t0001g0098 a0001c0001t0001g0169 a0001c0001t0001g0196 others(2): Show |
5 | HG00673.hp1 HG01175.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-13589_103-1358 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | C | CCGCTTT | 3 | a0001c0001t0005g0019 a0001c0001t0005g0024 a0001c0001t0005g0026 |
3 | HG02622.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.103-13589_103-1358 others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | C | CG | 10 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0012 others(7): Show |
12 | HG00544.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-13589_103-1358 others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | C | CGCT | 3 | a0001c0001t0006g0053 a0001c0001t0006g0244 a0001c0002t0010g0051 |
3 | HG02970.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-13589_103-1358 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | C | CT | 9 | a0001c0001t0006g0054 a0001c0001t0006g0065 a0001c0001t0006g0245 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-13567dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | ||||||
| chrX:16804985 | C | CTT | 5 | a0001c0001t0006g0081 a0001c0004t0025g0018 a0001c0004t0026g0016 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-13568_103-1356 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | ||||||
| chrX:16804985 | C | G | 29 | a0001c0001t0001g0145 a0001c0001t0003g0002 a0001c0001t0003g0008 others(26): Show |
29 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.103-13589C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | C | T | 1 | a0001c0002t0002g0062 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.103-13589C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804985 | |||||||
| chrX:16804985 | CT | C | 15 | a0001c0001t0001g0134 a0001c0001t0003g0002 a0001c0001t0003g0136 others(12): Show |
15 | HG00280.hp1 HG00735.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-13567delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16804985 | ||||||
| chrX:16804986 | T | C | 47 | a0001c0001t0001g0098 a0001c0001t0001g0145 a0001c0001t0001g0169 others(44): Show |
50 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.103-13588T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804986 | |||||||
| chrX:16804986 | T | G | 105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(102): Show |
107 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.103-13588T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804986 | |||||||
| chrX:16804987 | T | C | 105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(102): Show |
107 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.103-13587T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804987 | |||||||
| chrX:16804987 | T | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0209 a0001c0001t0012g0182 |
3 | HG02080.hp1 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.103-13587T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804987 | |||||||
| chrX:16804988 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0209 a0001c0001t0012g0182 |
3 | HG02080.hp1 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.103-13586T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804988 | |||||||
| chrX:16804989 | T | G | 1 | a0001c0001t0004g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.103-13585T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16804989 | |||||||
| chrX:16805007 | T | TTTTTG | 8 | a0001c0001t0001g0033 a0001c0002t0002g0044 a0001c0002t0002g0075 others(5): Show |
8 | HG01243.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(9): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTG | 8 | a0001c0002t0002g0037 a0001c0002t0002g0043 a0001c0002t0002g0048 others(5): Show |
8 | HG00140.hp1 HG00323.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(1): Show |
25 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0005 others(22): Show |
29 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(2): Show |
6 | a0001c0002t0002g0041 a0001c0002t0002g0049 a0001c0002t0002g0058 others(3): Show |
6 | HG01074.hp1 HG02027.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-13567_103-1356 others(13): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(3): Show |
2 | a0001c0002t0002g0045 a0001c0002t0002g0050 |
2 | HG01433.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.103-13567_103-1356 others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(4): Show |
1 | a0001c0002t0002g0047 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103-13567_103-1356 others(15): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(5): Show |
1 | a0001c0002t0002g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103-13567_103-1356 others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805007 | T | TTTTTTTT others(6): Show |
1 | a0001c0002t0002g0003 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.103-13567_103-1356 others(17): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805007 | |||||||
| chrX:16805010 | G | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-13564G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805010 | |||||||
| chrX:16805059 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0123 |
3 | HG02109.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.103-13515A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805059 | |||||||
| chrX:16805152 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.103-13422T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805152 | |||||||
| chrX:16805390 | A | G | 2 | a0001c0001t0006g0053 a0001c0001t0006g0054 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103-13184A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16805390 | |||||||
| chrX:16805451 | CCTT | C | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-13118_103-1311 others(7): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16805451 | ||||||
| chrX:16806231 | C | G | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-12343C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806231 | |||||||
| chrX:16806299 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-12275G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806299 | |||||||
| chrX:16806395 | G | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-12179G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806395 | |||||||
| chrX:16806615 | C | T | 1 | a0001c0001t0012g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.103-11959C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806615 | |||||||
| chrX:16806733 | C | T | 1 | a0001c0002t0008g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103-11841C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806733 | |||||||
| chrX:16806788 | G | A | 2 | a0001c0001t0004g0103 a0001c0001t0004g0163 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.103-11786G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806788 | |||||||
| chrX:16806916 | C | CA | 30 | a0001c0001t0001g0013 a0001c0001t0001g0106 a0001c0001t0001g0165 others(27): Show |
31 | HG00280.hp1 HG01123.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.103-11636dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | ||||||
| chrX:16806916 | CA | C | 7 | a0001c0001t0001g0209 a0001c0001t0003g0009 a0001c0001t0003g0149 others(4): Show |
7 | HG01099.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-11636delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | ||||||
| chrX:16806916 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0190 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.103-11645_103-1163 others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16806916 | ||||||
| chrX:16806945 | G | A | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-11629G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806945 | |||||||
| chrX:16806998 | C | T | 2 | a0002c0003t0003g0175 a0002c0003t0028g0132 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.103-11576C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16806998 | |||||||
| chrX:16807690 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.103-10884A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807690 | |||||||
| chrX:16807710 | A | G | 1 | a0001c0001t0005g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.103-10864A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807710 | |||||||
| chrX:16807752 | C | A | 77 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
83 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.103-10822C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16807752 | |||||||
| chrX:16808056 | A | G | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-10518A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808056 | |||||||
| chrX:16808131 | G | A | 2 | a0001c0002t0002g0057 a0001c0002t0002g0059 |
2 | NA18947.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.103-10443G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808131 | |||||||
| chrX:16808161 | C | T | 14 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0065 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-10413C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808161 | |||||||
| chrX:16808194 | T | A | 1 | a0001c0001t0007g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-10380T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808194 | |||||||
| chrX:16808226 | C | T | 2 | a0001c0001t0006g0053 a0001c0001t0006g0054 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.103-10348C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808226 | |||||||
| chrX:16808389 | A | AT | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-10182dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16808389 | ||||||
| chrX:16808503 | G | T | 1 | a0001c0002t0029g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.103-10071G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808503 | |||||||
| chrX:16808661 | A | G | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-9913A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808661 | |||||||
| chrX:16808684 | G | A | 3 | a0001c0001t0009g0192 a0001c0001t0009g0206 a0001c0001t0009g0223 |
3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.103-9890G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808684 | |||||||
| chrX:16808990 | T | C | 1 | a0001c0001t0005g0020 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-9584T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16808990 | |||||||
| chrX:16809345 | G | GT | 16 | a0001c0001t0001g0106 a0001c0001t0001g0219 a0001c0001t0001g0220 others(13): Show |
16 | HG01070.hp1 HG01884.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.103-9213dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | ||||||
| chrX:16809345 | G | GTT | 61 | a0001c0001t0001g0033 a0001c0001t0006g0053 a0001c0001t0006g0054 others(58): Show |
67 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.103-9214_103-9213d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | ||||||
| chrX:16809345 | G | GTTT | 8 | a0001c0001t0007g0027 a0001c0001t0007g0064 a0001c0001t0007g0079 others(5): Show |
8 | HG00140.hp1 HG01192.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-9215_103-9213d others(5): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16809345 | ||||||
| chrX:16809518 | A | G | 1 | a0001c0004t0026g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103-9056A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809518 | |||||||
| chrX:16809589 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.103-8985C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809589 | |||||||
| chrX:16809637 | C | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02523.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.103-8937C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809637 | |||||||
| chrX:16809919 | G | A | 4 | a0001c0001t0007g0027 a0001c0001t0007g0064 a0001c0001t0007g0079 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-8655G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809919 | |||||||
| chrX:16809947 | G | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-8627G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16809947 | |||||||
| chrX:16810510 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.103-8064A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810510 | |||||||
| chrX:16810933 | G | T | 2 | a0001c0002t0002g0035 a0001c0002t0002g0067 |
2 | HG01346.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-7641G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810933 | |||||||
| chrX:16810996 | A | G | 2 | a0001c0001t0003g0154 a0001c0001t0005g0155 |
2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.103-7578A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16810996 | |||||||
| chrX:16811105 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.103-7469A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811105 | |||||||
| chrX:16811480 | C | A | 4 | a0001c0001t0007g0027 a0001c0001t0007g0064 a0001c0001t0007g0079 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-7094C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811480 | |||||||
| chrX:16811576 | G | C | 1 | a0001c0002t0002g0039 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.103-6998G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811576 | |||||||
| chrX:16811646 | C | CT | 8 | a0001c0001t0001g0169 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-6914dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16811646 | ||||||
| chrX:16811762 | A | G | 80 | a0001c0001t0001g0033 a0001c0001t0005g0019 a0001c0001t0005g0020 others(77): Show |
86 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.103-6812A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811762 | |||||||
| chrX:16811827 | C | T | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-6747C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16811827 | |||||||
| chrX:16812078 | A | T | 1 | a0001c0001t0003g0153 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.103-6496A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812078 | |||||||
| chrX:16812177 | CT | C | 188 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(185): Show |
197 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.103-6386delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812177 | ||||||
| chrX:16812396 | CT | C | 163 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(160): Show |
172 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.103-6163delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812396 | ||||||
| chrX:16812456 | C | T | 1 | a0004c0007t0008g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.103-6118C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812456 | |||||||
| chrX:16812550 | T | C | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(175): Show |
187 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.103-6024T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812550 | |||||||
| chrX:16812691 | C | CT | 18 | a0001c0001t0001g0033 a0001c0001t0001g0239 a0001c0001t0003g0150 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.103-5855dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | ||||||
| chrX:16812691 | CT | C | 87 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0110 others(84): Show |
93 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.103-5855delT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | ||||||
| chrX:16812691 | CTT | C | 77 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(74): Show |
80 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.103-5856_103-5855d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16812691 | ||||||
| chrX:16812892 | T | G | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(175): Show |
187 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.103-5682T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16812892 | |||||||
| chrX:16813365 | C | T | 1 | a0001c0004t0027g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-5209C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813365 | |||||||
| chrX:16813384 | G | A | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.103-5190G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813384 | |||||||
| chrX:16813414 | A | G | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(164): Show |
176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.103-5160A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813414 | |||||||
| chrX:16813601 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.103-4973T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813601 | |||||||
| chrX:16813637 | C | CA | 10 | a0001c0001t0001g0180 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
10 | HG02027.hp1 HG02056.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4920dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813637 | ||||||
| chrX:16813637 | CA | C | 10 | a0001c0001t0001g0166 a0001c0001t0001g0205 a0001c0001t0004g0204 others(7): Show |
10 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4920delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16813637 | ||||||
| chrX:16813722 | A | G | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-4852A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813722 | |||||||
| chrX:16813808 | C | T | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-4766C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813808 | |||||||
| chrX:16813816 | G | A | 11 | a0001c0001t0001g0093 a0001c0001t0001g0111 a0001c0001t0001g0162 others(8): Show |
11 | HG00544.hp1 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-4758G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813816 | |||||||
| chrX:16813838 | G | A | 10 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(7): Show |
10 | HG01070.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-4736G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16813838 | |||||||
| chrX:16814010 | C | T | 1 | a0001c0001t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-4564C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814010 | |||||||
| chrX:16814064 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0217 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.103-4510C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814064 | |||||||
| chrX:16814540 | G | A | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.103-4034G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814540 | |||||||
| chrX:16814650 | T | A | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(164): Show |
176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.103-3924T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814650 | |||||||
| chrX:16814710 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-3864T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814710 | |||||||
| chrX:16814711 | A | T | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-3863A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814711 | |||||||
| chrX:16814792 | G | A | 3 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0179 |
3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.103-3782G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814792 | |||||||
| chrX:16814806 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0160 |
2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.103-3768G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16814806 | |||||||
| chrX:16814977 | AGCCTCAG others(11): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103-3585_103-3568d others(20): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 16814977 | ||||||
| chrX:16815637 | C | T | 1 | a0001c0001t0022g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.103-2937C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815637 | |||||||
| chrX:16815790 | G | A | 2 | a0001c0002t0002g0036 a0001c0002t0002g0068 |
2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.103-2784G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815790 | |||||||
| chrX:16815832 | T | G | 1 | a0001c0002t0002g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-2742T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815832 | |||||||
| chrX:16815940 | C | T | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-2634C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16815940 | |||||||
| chrX:16816134 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103-2440T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816134 | |||||||
| chrX:16816142 | G | C | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(164): Show |
176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.103-2432G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816142 | |||||||
| chrX:16816292 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0238 a0001c0001t0001g0242 |
3 | NA18982.hp1 NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.103-2282G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816292 | |||||||
| chrX:16816777 | T | C | 2 | a0001c0001t0011g0089 a0001c0001t0011g0161 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.103-1797T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816777 | |||||||
| chrX:16816973 | A | G | 1 | a0002c0003t0003g0175 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-1601A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16816973 | |||||||
| chrX:16817385 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.103-1189A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817385 | |||||||
| chrX:16817623 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.103-951C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817623 | |||||||
| chrX:16817719 | A | G | 2 | a0001c0002t0002g0030 a0001c0002t0002g0070 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.103-855A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16817719 | |||||||
| chrX:16818027 | T | G | 1 | a0001c0004t0026g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103-547T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818027 | |||||||
| chrX:16818144 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.103-430A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818144 | |||||||
| chrX:16818524 | A | G | 10 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0057 others(7): Show |
12 | HG01943.hp1 HG01975.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.103-50A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 1/9 | chrX | 16818524 | |||||||
| chrX:16819623 | T | C | 1 | a0001c0005t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.407-541T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 2/9 | chrX | 16819623 | |||||||
| chrX:16820415 | T | C | 12 | a0001c0001t0003g0085 a0001c0001t0003g0125 a0001c0001t0003g0126 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.498+160T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820415 | |||||||
| chrX:16820719 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.498+464C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820719 | |||||||
| chrX:16820803 | C | G | 8 | a0001c0001t0001g0166 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02074.hp1 NA18950.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.498+548C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16820803 | |||||||
| chrX:16821054 | T | C | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(164): Show |
176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.498+799T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821054 | |||||||
| chrX:16821138 | T | C | 1 | a0001c0001t0006g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+883T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821138 | |||||||
| chrX:16821138 | TTC | T | 158 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(155): Show |
166 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.498+885_498+886del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16821138 | ||||||
| chrX:16821139 | TC | T | 69 | a0001c0001t0001g0168 a0001c0001t0001g0198 a0001c0001t0001g0214 others(66): Show |
75 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.498+885delC | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821139 | |||||||
| chrX:16821140 | C | T | 1 | a0001c0001t0006g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.498+885C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821140 | |||||||
| chrX:16821268 | G | A | 3 | a0001c0001t0003g0146 a0001c0001t0003g0172 a0001c0001t0003g0177 |
3 | HG02738.hp1 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.498+1013G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821268 | |||||||
| chrX:16821326 | G | C | 6 | a0001c0001t0003g0085 a0001c0001t0003g0125 a0001c0001t0003g0126 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+1071G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821326 | |||||||
| chrX:16821341 | G | A | 1 | a0001c0001t0023g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.498+1086G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821341 | |||||||
| chrX:16821377 | G | T | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.498+1122G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821377 | |||||||
| chrX:16821382 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0016g0115 |
2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.498+1127G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821382 | |||||||
| chrX:16821404 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.498+1149T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821404 | |||||||
| chrX:16821718 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0217 a0001c0002t0002g0060 others(1): Show |
4 | HG00323.hp1 HG03927.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1463C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821718 | |||||||
| chrX:16821726 | C | T | 4 | a0001c0001t0003g0010 a0001c0001t0003g0127 a0001c0001t0003g0133 others(1): Show |
5 | NA18956.hp1 NA18956.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+1471C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821726 | |||||||
| chrX:16821792 | C | T | 190 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(187): Show |
199 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.498+1537C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821792 | |||||||
| chrX:16821807 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.498+1552G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821807 | |||||||
| chrX:16821817 | T | C | 5 | a0001c0001t0001g0228 a0001c0001t0003g0086 a0001c0002t0002g0049 others(2): Show |
5 | HG02886.hp1 NA18952.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+1562T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821817 | |||||||
| chrX:16821867 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0117 others(6): Show |
9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.498+1612G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821867 | |||||||
| chrX:16821886 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.498+1631C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821886 | |||||||
| chrX:16821926 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+1671A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16821926 | |||||||
| chrX:16822319 | C | T | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.498+2064C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822319 | |||||||
| chrX:16822478 | C | G | 1 | a0001c0002t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.498+2223C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822478 | |||||||
| chrX:16822840 | C | T | 2 | a0001c0002t0002g0056 a0001c0002t0002g0247 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.498+2585C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822840 | |||||||
| chrX:16822846 | G | A | 12 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0065 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.498+2591G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822846 | |||||||
| chrX:16822864 | G | A | 40 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0009 others(37): Show |
46 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.498+2609G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16822864 | |||||||
| chrX:16823301 | A | T | 2 | a0001c0001t0018g0087 a0001c0001t0019g0088 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.498+3046A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823301 | |||||||
| chrX:16823458 | C | CA | 5 | a0001c0001t0005g0021 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01070.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.498+3229dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | ||||||
| chrX:16823458 | CA | C | 214 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(211): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.498+3229delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | ||||||
| chrX:16823458 | CAA | C | 6 | a0001c0001t0001g0122 a0001c0001t0003g0149 a0001c0002t0002g0006 others(3): Show |
7 | HG00733.hp1 NA18522.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.498+3228_498+3229d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823458 | ||||||
| chrX:16823600 | C | T | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.498+3345C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823600 | |||||||
| chrX:16823816 | C | A | 2 | a0001c0001t0001g0098 a0001c0001t0004g0097 |
2 | NA18955.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.498+3561C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16823816 | |||||||
| chrX:16823936 | ACT | A | 39 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0004 others(36): Show |
45 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.498+3686_498+3687d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16823936 | ||||||
| chrX:16824186 | G | A | 1 | a0001c0001t0003g0136 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.499-3908G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824186 | |||||||
| chrX:16824200 | A | G | 2 | a0001c0001t0003g0108 a0001c0001t0003g0144 |
2 | NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.499-3894A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824200 | |||||||
| chrX:16824762 | TA | T | 189 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(186): Show |
198 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.499-3319delA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 16824762 | ||||||
| chrX:16824882 | C | T | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.499-3212C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16824882 | |||||||
| chrX:16826102 | C | A | 21 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0104 others(18): Show |
21 | HG00544.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.499-1992C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826102 | |||||||
| chrX:16826274 | A | G | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.499-1820A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826274 | |||||||
| chrX:16826696 | G | T | 1 | a0001c0004t0026g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-1398G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826696 | |||||||
| chrX:16826708 | G | A | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.499-1386G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826708 | |||||||
| chrX:16826946 | C | A | 2 | a0001c0001t0006g0053 a0001c0001t0006g0054 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.499-1148C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16826946 | |||||||
| chrX:16827148 | G | A | 1 | a0001c0001t0003g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.499-946G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827148 | |||||||
| chrX:16827208 | A | T | 1 | a0001c0001t0015g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.499-886A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827208 | |||||||
| chrX:16827285 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.499-809C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827285 | |||||||
| chrX:16827318 | A | G | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.499-776A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827318 | |||||||
| chrX:16827392 | G | A | 1 | a0001c0001t0023g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.499-702G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827392 | |||||||
| chrX:16827867 | G | A | 1 | a0001c0004t0026g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-227G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827867 | |||||||
| chrX:16827869 | T | A | 1 | a0001c0004t0026g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-225T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 3/9 | chrX | 16827869 | |||||||
| chrX:16829029 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.670-547A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829029 | |||||||
| chrX:16829050 | A | G | 1 | a0001c0001t0003g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.670-526A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829050 | |||||||
| chrX:16829083 | A | G | 1 | a0001c0001t0023g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670-493A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829083 | |||||||
| chrX:16829203 | G | A | 3 | a0001c0002t0002g0039 a0001c0002t0002g0045 a0001c0002t0002g0047 |
3 | HG01192.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.670-373G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 4/9 | chrX | 16829203 | |||||||
| chrX:16829855 | G | C | 2 | a0001c0001t0011g0089 a0001c0001t0011g0161 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.864+85G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16829855 | |||||||
| chrX:16829954 | A | ACT | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+185_864+186dup others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16829954 | ||||||
| chrX:16830182 | A | AT | 165 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(162): Show |
174 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.864+424dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830182 | ||||||
| chrX:16830195 | A | T | 1 | a0001c0001t0015g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.864+425A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830195 | |||||||
| chrX:16830204 | C | T | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+434C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830204 | |||||||
| chrX:16830247 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.864+477A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830247 | |||||||
| chrX:16830395 | C | T | 191 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(188): Show |
200 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.864+625C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830395 | |||||||
| chrX:16830475 | G | T | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.864+705G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830475 | |||||||
| chrX:16830593 | C | G | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+823C>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830593 | |||||||
| chrX:16830664 | T | C | 2 | a0001c0001t0003g0127 a0001c0001t0021g0130 |
2 | NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.864+894T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830664 | |||||||
| chrX:16830697 | A | AT | 6 | a0001c0001t0003g0085 a0001c0001t0003g0125 a0001c0001t0003g0126 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+937dupT | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830697 | ||||||
| chrX:16830745 | A | T | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.864+975A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830745 | |||||||
| chrX:16830830 | C | CGT | 5 | a0001c0001t0001g0033 a0001c0001t0003g0149 a0001c0001t0004g0234 others(2): Show |
5 | HG00140.hp1 HG01243.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1115_864+1116d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGT | 6 | a0001c0001t0001g0168 a0001c0001t0003g0107 a0001c0001t0003g0139 others(3): Show |
6 | HG02040.hp1 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+1113_864+1116d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGT | 9 | a0001c0001t0001g0232 a0001c0001t0003g0140 a0001c0001t0003g0154 others(6): Show |
9 | HG00621.hp1 HG02083.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.864+1111_864+1116d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0114 a0001c0001t0003g0002 a0001c0001t0003g0131 others(5): Show |
10 | HG00280.hp1 HG00438.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1109_864+1116d others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0003g0008 a0001c0001t0003g0108 a0001c0001t0003g0177 others(4): Show |
8 | HG01168.hp1 HG01169.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1107_864+1116d others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(5): Show |
7 | a0001c0001t0001g0117 a0001c0001t0001g0240 a0001c0001t0003g0141 others(4): Show |
7 | HG00735.hp2 HG03453.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+1105_864+1116d others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(7): Show |
8 | a0001c0001t0001g0110 a0001c0001t0001g0171 a0001c0001t0001g0214 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1103_864+1116d others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(9): Show |
4 | a0001c0001t0003g0085 a0001c0001t0003g0135 a0001c0001t0003g0151 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1101_864+1116d others(18): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(11): Show |
9 | a0001c0001t0001g0104 a0001c0001t0001g0112 a0001c0001t0001g0121 others(6): Show |
9 | HG00673.hp1 HG02015.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.864+1099_864+1116d others(20): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(13): Show |
10 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0118 others(7): Show |
11 | HG00639.hp2 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+1097_864+1116d others(22): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(15): Show |
7 | a0001c0001t0001g0119 a0001c0001t0001g0189 a0001c0001t0001g0219 others(4): Show |
8 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1095_864+1116d others(24): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(17): Show |
10 | a0001c0001t0001g0120 a0001c0001t0001g0220 a0001c0001t0001g0233 others(7): Show |
10 | HG00733.hp2 HG01175.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1093_864+1116d others(26): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(19): Show |
6 | a0001c0001t0001g0169 a0001c0001t0001g0190 a0001c0001t0004g0164 others(3): Show |
6 | HG01175.hp2 HG01258.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+1091_864+1116d others(28): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(21): Show |
5 | a0001c0001t0001g0124 a0001c0001t0001g0211 a0001c0001t0003g0010 others(2): Show |
7 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1089_864+1116d others(30): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(23): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0218 a0001c0001t0001g0226 others(4): Show |
8 | HG01123.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1087_864+1116d others(32): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(25): Show |
8 | a0001c0001t0001g0101 a0001c0001t0001g0122 a0001c0001t0001g0228 others(5): Show |
8 | HG00639.hp1 HG03540.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+1085_864+1116d others(34): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(27): Show |
3 | a0001c0001t0001g0185 a0001c0001t0004g0128 a0001c0001t0007g0064 |
3 | HG00323.hp2 HG02922.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.864+1083_864+1116d others(36): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(29): Show |
4 | a0001c0001t0001g0212 a0001c0001t0001g0217 a0001c0001t0019g0088 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1081_864+1116d others(38): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(31): Show |
1 | a0001c0001t0001g0014 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.864+1079_864+1116d others(40): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(35): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0166 a0001c0001t0016g0115 |
3 | HG01106.hp1 HG02976.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.864+1075_864+1116d others(44): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(37): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0237 |
2 | HG00544.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.864+1073_864+1116d others(46): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(39): Show |
7 | a0001c0001t0001g0162 a0001c0001t0001g0193 a0001c0001t0001g0203 others(4): Show |
7 | HG02293.hp1 HG02970.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1071_864+1116d others(48): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(41): Show |
4 | a0001c0001t0001g0111 a0001c0001t0001g0183 a0001c0001t0004g0094 others(1): Show |
4 | HG02922.hp1 NA18940.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1069_864+1116d others(50): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(43): Show |
3 | a0001c0001t0001g0201 a0001c0001t0004g0095 a0001c0001t0004g0204 |
3 | HG02129.hp1 NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.864+1067_864+1116d others(52): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(45): Show |
1 | a0001c0001t0001g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.864+1065_864+1116d others(54): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(47): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0227 a0001c0001t0001g0243 |
3 | HG00438.hp2 NA19067.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.864+1063_864+1116d others(56): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(49): Show |
1 | a0001c0001t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.864+1061_864+1116d others(58): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(51): Show |
5 | a0001c0001t0001g0145 a0001c0001t0001g0181 a0001c0001t0004g0097 others(2): Show |
5 | HG01928.hp1 NA18955.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(60): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(53): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0205 a0001c0001t0006g0245 |
3 | HG00735.hp1 HG03225.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(62): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(55): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0202 others(1): Show |
4 | HG01981.hp1 NA19011.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(64): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(57): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0195 a0001c0001t0001g0235 others(1): Show |
4 | HG01168.hp2 HG02004.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(66): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(59): Show |
4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0231 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(68): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(61): Show |
3 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0242 |
3 | HG00642.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(70): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(63): Show |
4 | a0001c0001t0001g0160 a0001c0001t0001g0198 a0001c0001t0004g0167 others(1): Show |
4 | HG01255.hp1 HG02970.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1116_864+1117i others(72): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(65): Show |
1 | a0001c0001t0001g0165 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(74): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(67): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0225 a0001c0001t0003g0153 |
3 | HG02074.hp1 NA18980.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(76): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(69): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0207 a0001c0001t0001g0238 |
3 | HG02135.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(78): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(71): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0224 |
2 | HG00609.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.864+1116_864+1117i others(80): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(73): Show |
1 | a0001c0001t0001g0216 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(82): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(75): Show |
1 | a0001c0002t0010g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.864+1116_864+1117i others(84): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(79): Show |
1 | a0001c0001t0001g0209 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(88): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | C | CGTGTGTG others(93): Show |
1 | a0001c0001t0004g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.864+1116_864+1117i others(102): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGT | C | 5 | a0001c0001t0003g0125 a0001c0002t0002g0037 a0001c0002t0002g0043 others(2): Show |
5 | HG01123.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+1115_864+1116d others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGT | C | 7 | a0001c0001t0001g0123 a0001c0002t0002g0001 a0001c0002t0002g0038 others(4): Show |
10 | HG00738.hp1 HG02109.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1113_864+1116d others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGT | C | 17 | a0001c0001t0003g0179 a0001c0001t0005g0023 a0001c0002t0002g0003 others(14): Show |
18 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.864+1111_864+1116d others(8): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGTG others(1): Show |
C | 5 | a0001c0002t0002g0005 a0001c0002t0002g0041 a0001c0002t0002g0058 others(2): Show |
6 | HG00741.hp1 HG01074.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+1109_864+1116d others(10): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0012g0182 a0001c0002t0002g0006 a0001c0002t0002g0057 others(6): Show |
10 | HG01943.hp1 HG02080.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+1107_864+1116d others(12): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGTG others(5): Show |
C | 4 | a0001c0001t0003g0138 a0001c0002t0002g0039 a0001c0002t0002g0045 others(1): Show |
4 | HG01192.hp1 HG01433.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1105_864+1116d others(14): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGTG others(7): Show |
C | 1 | a0001c0002t0002g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.864+1103_864+1116d others(16): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830830 | CGTGTGTG others(9): Show |
C | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.864+1101_864+1116d others(18): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 16830830 | ||||||
| chrX:16830887 | A | G | 17 | a0001c0001t0001g0188 a0001c0001t0003g0178 a0001c0001t0006g0053 others(14): Show |
17 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+1117A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830887 | |||||||
| chrX:16830915 | A | C | 12 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0117 others(9): Show |
12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.864+1145A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830915 | |||||||
| chrX:16830915 | A | T | 12 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0065 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.864+1145A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16830915 | |||||||
| chrX:16831184 | A | C | 1 | a0001c0005t0006g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.864+1414A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16831184 | |||||||
| chrX:16831878 | G | T | 1 | a0001c0001t0003g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.865-745G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16831878 | |||||||
| chrX:16832000 | A | T | 1 | a0004c0007t0008g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.865-623A>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832000 | |||||||
| chrX:16832463 | C | A | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
174 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.865-160C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832463 | |||||||
| chrX:16832467 | G | A | 1 | a0001c0002t0002g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.865-156G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 5/9 | chrX | 16832467 | |||||||
| chrX:16832808 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.984+66T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16832808 | |||||||
| chrX:16832915 | GGT | G | 3 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0179 |
3 | HG03098.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.984+184_984+185del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16832915 | ||||||
| chrX:16833419 | T | G | 1 | a0001c0001t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.984+677T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833419 | |||||||
| chrX:16833433 | C | T | 4 | a0001c0001t0023g0158 a0002c0003t0003g0090 a0002c0003t0003g0175 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.984+691C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833433 | |||||||
| chrX:16833442 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.984+700G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833442 | |||||||
| chrX:16833485 | C | T | 2 | a0001c0002t0002g0055 a0001c0002t0002g0246 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.984+743C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833485 | |||||||
| chrX:16833486 | G | A | 1 | a0001c0005t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.984+744G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833486 | |||||||
| chrX:16833624 | T | TAC | 7 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(4): Show |
7 | HG02451.hp1 HG02970.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-640_985-639dup others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | ||||||
| chrX:16833624 | T | TACAC | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.985-642_985-639dup others(4): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | ||||||
| chrX:16833624 | TAC | T | 16 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(13): Show |
16 | HG00642.hp1 HG00733.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.985-640_985-639del others(2): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 16833624 | ||||||
| chrX:16833946 | A | G | 1 | a0001c0006t0002g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.985-337A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16833946 | |||||||
| chrX:16834168 | T | A | 8 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0021 others(5): Show |
8 | HG01070.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.985-115T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834168 | |||||||
| chrX:16834186 | G | C | 1 | a0001c0005t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.985-97G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834186 | |||||||
| chrX:16834204 | A | C | 112 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(109): Show |
115 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.985-79A>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834204 | |||||||
| chrX:16834218 | C | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0194 |
2 | NA18972.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.985-65C>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 6/9 | chrX | 16834218 | |||||||
| chrX:16834819 | A | G | 3 | a0001c0004t0025g0018 a0001c0004t0026g0016 a0001c0004t0027g0017 |
3 | HG01884.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+462A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16834819 | |||||||
| chrX:16834984 | C | T | 3 | a0001c0002t0002g0041 a0001c0002t0002g0061 a0001c0002t0002g0062 |
3 | HG01074.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1059+627C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16834984 | |||||||
| chrX:16835006 | G | C | 1 | a0001c0002t0002g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1059+649G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835006 | |||||||
| chrX:16835153 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1059+796A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835153 | |||||||
| chrX:16835667 | G | A | 2 | a0001c0002t0002g0056 a0001c0002t0002g0247 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1059+1310G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835667 | |||||||
| chrX:16835732 | CTT | C | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0063 |
3 | NA18952.hp1 NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1059+1376_1059+137 others(6): Show |
TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835732 | |||||||
| chrX:16835902 | T | C | 1 | a0001c0001t0004g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1059+1545T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835902 | |||||||
| chrX:16835995 | C | T | 166 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0093 others(163): Show |
175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1060-1598C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16835995 | |||||||
| chrX:16836248 | T | A | 1 | a0001c0001t0004g0234 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-1345T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16836248 | |||||||
| chrX:16836494 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1060-1099C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16836494 | |||||||
| chrX:16837207 | G | T | 1 | a0001c0002t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1060-386G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837207 | |||||||
| chrX:16837295 | G | C | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1060-298G>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837295 | |||||||
| chrX:16837315 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0217 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1060-278C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837315 | |||||||
| chrX:16837534 | T | C | 2 | a0001c0002t0002g0036 a0001c0002t0002g0068 |
2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1060-59T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 7/9 | chrX | 16837534 | |||||||
| chrX:16837842 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0196 |
3 | HG03139.hp1 NA18522.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1152+157A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16837842 | |||||||
| chrX:16837941 | G | T | 1 | a0001c0001t0003g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1152+256G>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16837941 | |||||||
| chrX:16838026 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1152+341G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16838026 | |||||||
| chrX:16838719 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1152+1034G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16838719 | |||||||
| chrX:16839479 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1153-342C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 8/9 | chrX | 16839479 | |||||||
| chrX:16840552 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1248+636T>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840552 | |||||||
| chrX:16840642 | C | T | 1 | a0001c0001t0022g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1248+726C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840642 | |||||||
| chrX:16840653 | T | C | 168 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(165): Show |
177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1248+737T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840653 | |||||||
| chrX:16840703 | C | T | 1 | a0001c0001t0015g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1249-725C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840703 | |||||||
| chrX:16840842 | A | G | 1 | a0001c0002t0002g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1249-586A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840842 | |||||||
| chrX:16840950 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1249-478G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840950 | |||||||
| chrX:16840963 | A | G | 1 | a0001c0001t0012g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1249-465A>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16840963 | |||||||
| chrX:16841012 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1249-416T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841012 | |||||||
| chrX:16841021 | T | C | 3 | a0001c0001t0001g0162 a0001c0001t0004g0128 a0001c0001t0004g0204 |
3 | NA18968.hp1 NA18974.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1249-407T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841021 | |||||||
| chrX:16841022 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1249-406C>T | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841022 | |||||||
| chrX:16841054 | G | A | 2 | a0001c0001t0003g0172 a0001c0001t0003g0177 |
2 | HG02738.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1249-374G>A | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841054 | |||||||
| chrX:16841092 | T | G | 1 | a0001c0001t0003g0107 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1249-336T>G | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841092 | |||||||
| chrX:16841156 | T | C | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0033 others(164): Show |
176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1249-272T>C | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | chrX | 16841156 | |||||||
| chrX:16841193 | C | CA | 40 | a0001c0001t0001g0096 a0001c0001t0001g0109 a0001c0001t0001g0145 others(37): Show |
40 | HG00438.hp2 HG00642.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1249-222dupA | TXLNG | ENSG00000086712.13 | transcript | ENST00000380122.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 16841193 |