Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23555 |
| ensemblid | ENSG00000099282.10 |
| hgncid | 23298 |
| symbol | TSPAN15 |
| name | tetraspanin 15 |
| refseq_nuc | NM_012339.5 |
| refseq_prot | NP_036471.1 |
| ensembl_nuc | ENST00000373290.7 |
| ensembl_prot | ENSP00000362387.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 69451465 |
| end | 69507666 |
| strand | + |
| ver | v1.2 |
| region | chr10:69451465-69507666 |
| region5000 | chr10:69446465-69512666 |
| regionname0 | TSPAN15_chr10_69451465_69507666 |
| regionname5000 | TSPAN15_chr10_69446465_69512666 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 294 | 325 | 81 | 64 | 121 | 15 | 42 | 87 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | MPRGD others(289): Show |
chr10 | 69446465 | 69512666 |
| a0002 | 0/0 | 294 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | MPRGD others(289): Show |
chr10 | 69446465 | 69512666 |
| a0003 | 0/0 | 294 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | MPRGD others(289): Show |
chr10 | 69446465 | 69512666 |
| a0004 | 0/0 | 294 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | MPRGD others(289): Show |
chr10 | 69446465 | 69512666 |
| a0005 | 0/0 | 294 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | MPRGD others(289): Show |
chr10 | 69446465 | 69512666 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 882 | 325 | 81 | 64 | 121 | 15 | 42 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 | ||
| a0002c0002 | 0/0 | 882 | 11 | 11 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 | ||
| a0003c0003 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 | ||
| a0003c0004 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 | ||
| a0004c0006 | 0/0 | 882 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 | ||
| a0005c0005 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | ATGCC others(877): Show |
chr10 | 69446465 | 69512666 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1702 | 94 | 16 | 15 | 40 | 6 | 17 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0002 | 0/0 | 1701 | 59 | 38 | 13 | 1 | 1 | 6 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1696): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0003 | 1/0 | 1703 | 58 | 5 | 11 | 35 | 2 | 4 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0004 | 0/0 | 1703 | 43 | 1 | 12 | 23 | 5 | 2 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0005 | 0/0 | 1703 | 17 | 1 | 7 | 3 | 0 | 6 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0006 | 0/1 | 1704 | 12 | 3 | 1 | 2 | 0 | 5 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0007 | 0/0 | 1704 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0008 | 0/0 | 1702 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0009 | 0/0 | 1703 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0010 | 0/0 | 1703 | 4 | 1 | 2 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0011 | 0/0 | 1704 | 4 | 0 | 0 | 3 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0012 | 0/0 | 1704 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0013 | 0/0 | 1702 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0014 | 0/0 | 1701 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1696): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0015 | 0/0 | 1703 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0016 | 0/0 | 1703 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0017 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0018 | 0/0 | 1702 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0019 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0020 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1696): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0021 | 0/0 | 1703 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0022 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0023 | 0/0 | 1702 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0024 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0001c0001t0025 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0002c0002t0002 | 0/0 | 1701 | 11 | 11 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1696): Show |
chr10 | 69446465 | 69512666 |
| a0003c0003t0007 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0003c0004t0007 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1699): Show |
chr10 | 69446465 | 69512666 |
| a0004c0006t0003 | 0/0 | 1703 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1698): Show |
chr10 | 69446465 | 69512666 |
| a0005c0005t0001 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | GTCAG others(1697): Show |
chr10 | 69446465 | 69512666 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0009g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0010g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0011g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0011g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0011g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0011g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0012g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0012g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0013g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0017g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0020g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0021g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0022g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0024g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0001c0001t0025g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0002c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0003c0003t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0003c0004t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0004c0006t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| a0005c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0260 | EUR | GBR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00140 | hp1 | a0001 | c0001 | t0010 | g0262 | EUR | GBR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | GBR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0245 | EUR | FIN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00323 | hp2 | a0004 | c0006 | t0003 | g0212 | EUR | FIN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00408 | hp2 | a0001 | c0001 | t0011 | g0311 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00423 | hp1 | a0001 | c0001 | t0022 | g0095 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00597 | hp2 | a0001 | c0001 | t0025 | g0314 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0252 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0289 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0318 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0147 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0302 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0125 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01261 | hp1 | a0001 | c0001 | t0021 | g0254 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0144 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0185 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0310 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | CDX | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | CDX | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CDX | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0261 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0256 | AMR | PEL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0079 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0077 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0250 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0257 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0270 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0298 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0152 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0268 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0067 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0237 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02976 | hp1 | a0003 | c0003 | t0007 | g0244 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0139 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0071 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03098 | hp2 | a0003 | c0004 | t0007 | g0272 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0068 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0247 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0280 | AFR | ESN | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0057 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0308 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0023 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0248 | SAS | PJL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03927 | hp1 | a0001 | c0001 | t0012 | g0249 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0264 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | BEB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18747 | hp1 | a0001 | c0001 | t0019 | g0126 | EAS | CHB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18747 | hp2 | a0001 | c0001 | t0017 | g0307 | EAS | CHB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18969 | hp1 | a0005 | c0005 | t0001 | g0036 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0304 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18982 | hp2 | a0001 | c0001 | t0014 | g0131 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18993 | hp1 | a0001 | c0001 | t0013 | g0285 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19002 | hp2 | a0001 | c0001 | t0013 | g0283 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | LWK | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | LWK | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | LWK | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0274 | AFR | LWK | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0309 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19060 | hp1 | a0001 | c0001 | t0007 | g0243 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19087 | hp2 | a0001 | c0001 | t0024 | g0313 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | YRI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ASW | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ASW | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0162 | EUR | TSI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0188 | EUR | TSI | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | GIH | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0263 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA18955 | hp2 | a0001 | c0001 | t0012 | g0154 | EAS | JPT | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | USA | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0191 | REF | REF | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0184 | REF | REF | TSPAN15_chr10_69446465_69512666 | TSPAN15 | chr10 | 69446465 | 69512666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:69483873 | A | T | 1 | a0004 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.279A>T | p.Gln93His | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/8 | 409/1703 | 279/885 | 93/294 | chr10 | 69483873 | |||
| chr10:69506125 | G | A | 1 | a0003 | 2 | HG02976.hp1 HG03098.hp2 |
missense_variant&splice_region_variant | MODERATE | c.620G>A | p.Arg207His | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 7/8 | 750/1703 | 620/885 | 207/294 | chr10 | 69506125 | |||
| chr10:69506199 | A | G | 1 | a0002 | 11 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
missense_variant | MODERATE | c.694A>G | p.Thr232Ala | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 7/8 | 824/1703 | 694/885 | 232/294 | chr10 | 69506199 | |||
| chr10:69506920 | G | A | 1 | a0005 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.827G>A | p.Gly276Asp | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 957/1703 | 827/885 | 276/294 | chr10 | 69506920 | |||
| chr10:69507665 | T | G | 1 | a0001 | 1 | NA19087.hp2 | splice_region_variant | LOW | c.*687T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | chr10 | 69507665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:69451612 | G | A | 1 | a0003c0003 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.18G>A | p.Ser6Ser | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/8 | 148/1703 | 18/885 | 6/294 | chr10 | 69451612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:69451551 | G | A | 1 | a0001c0001t0016 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/8 | 44 | chr10 | 69451551 | ||||||
| chr10:69451559 | C | T | 3 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0025 |
6 | HG00408.hp2 HG00597.hp2 HG02040.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-36C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/8 | 36 | chr10 | 69451559 | ||||||
| chr10:69507013 | G | A | 1 | a0001c0001t0017 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*35G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 35 | chr10 | 69507013 | ||||||
| chr10:69507127 | C | T | 1 | a0001c0001t0008 | 6 | HG01433.hp2 HG02257.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*149C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 149 | chr10 | 69507127 | ||||||
| chr10:69507167 | T | G | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(4): Show |
29 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*189T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 189 | chr10 | 69507167 | ||||||
| chr10:69507174 | CT | C | 2 | a0001c0001t0008 a0001c0001t0018 |
7 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*199delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 199 | INFO_REALIGN_3_PRIME | chr10 | 69507174 | |||||
| chr10:69507177 | T | C | 1 | a0001c0001t0009 | 5 | HG02922.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*199T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 199 | chr10 | 69507177 | ||||||
| chr10:69507182 | G | C | 2 | a0001c0001t0008 a0001c0001t0018 |
7 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 204 | chr10 | 69507182 | ||||||
| chr10:69507209 | T | A | 1 | a0001c0001t0019 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 231 | chr10 | 69507209 | ||||||
| chr10:69507254 | G | A | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(5): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*276G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 276 | chr10 | 69507254 | ||||||
| chr10:69507280 | T | G | 1 | a0001c0001t0020 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 302 | chr10 | 69507280 | ||||||
| chr10:69507435 | C | T | 1 | a0001c0001t0015 | 2 | HG02451.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*457C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 457 | chr10 | 69507435 | ||||||
| chr10:69507483 | T | C | 2 | a0001c0001t0013 a0001c0001t0022 |
3 | HG00423.hp1 NA18993.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*505T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 505 | chr10 | 69507483 | ||||||
| chr10:69507650 | T | C | 1 | a0001c0001t0021 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 672 | chr10 | 69507650 | ||||||
| chr10:69507651 | G | GT | 1 | a0001c0001t0006 | 11 | HG01192.hp1 HG02602.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*667insT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 667 | INFO_REALIGN_3_PRIME | chr10 | 69507651 | |||||
| chr10:69507651 | GT | G | 5 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0019 others(2): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*666delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 666 | INFO_REALIGN_3_PRIME | chr10 | 69507651 | |||||
| chr10:69507651 | GTT | G | 4 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0020 others(1): Show |
73 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*666delTT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 665 | INFO_REALIGN_3_PRIME | chr10 | 69507651 | |||||
| chr10:69507655 | T | TG | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(3): Show |
14 | HG00408.hp2 HG02040.hp2 HG02976.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*677_*678insG | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 678 | chr10 | 69507655 | ||||||
| chr10:69507656 | T | G | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(7): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*678T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 678 | chr10 | 69507656 | ||||||
| chr10:69507658 | T | G | 3 | a0001c0001t0002 a0001c0001t0020 a0002c0002t0002 |
71 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*680T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 680 | chr10 | 69507658 | ||||||
| chr10:69507659 | T | G | 1 | a0001c0001t0025 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 681 | chr10 | 69507659 | ||||||
| chr10:69507660 | T | G | 6 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(3): Show |
14 | HG00408.hp2 HG02040.hp2 HG02976.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*682T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 682 | chr10 | 69507660 | ||||||
| chr10:69507661 | T | G | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0010 others(3): Show |
67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*683T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 683 | chr10 | 69507661 | ||||||
| chr10:69507662 | T | G | 1 | a0001c0001t0023 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*684T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 684 | chr10 | 69507662 | ||||||
| chr10:69507663 | T | G | 3 | a0001c0001t0002 a0001c0001t0020 a0002c0002t0002 |
71 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 8/8 | 685 | chr10 | 69507663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:69451856 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+166G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451856 | |||||||
| chr10:69451888 | G | T | 75 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+198G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451888 | |||||||
| chr10:69451891 | AGCCGGTT others(3): Show |
A | 2 | a0001c0001t0001g0018 a0001c0001t0003g0017 |
2 | NA18947.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.96+203_96+212delCC others(8): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69451891 | ||||||
| chr10:69451908 | C | G | 75 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+218C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451908 | |||||||
| chr10:69451921 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+231G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451921 | |||||||
| chr10:69451928 | C | T | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+238C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451928 | |||||||
| chr10:69451951 | T | C | 29 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0002g0265 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.96+261T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451951 | |||||||
| chr10:69451965 | C | A | 75 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+275C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451965 | |||||||
| chr10:69451978 | G | A | 21 | a0001c0001t0001g0246 a0001c0001t0003g0251 a0001c0001t0004g0015 others(18): Show |
22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+288G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69451978 | |||||||
| chr10:69452085 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.96+395G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452085 | |||||||
| chr10:69452183 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.96+493G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452183 | |||||||
| chr10:69452189 | A | G | 75 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+499A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452189 | |||||||
| chr10:69452232 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG03017.hp2 HG03710.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+542T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452232 | |||||||
| chr10:69452280 | C | T | 6 | a0001c0001t0001g0240 a0001c0001t0003g0239 a0001c0001t0006g0238 others(3): Show |
6 | HG03453.hp2 HG03831.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+590C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452280 | |||||||
| chr10:69452296 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG01243.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+606G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452296 | |||||||
| chr10:69452335 | G | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+645G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452335 | |||||||
| chr10:69452546 | G | C | 1 | a0001c0001t0004g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.96+856G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452546 | |||||||
| chr10:69452554 | G | A | 84 | a0001c0001t0001g0031 a0001c0001t0001g0246 a0001c0001t0001g0267 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.96+864G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452554 | |||||||
| chr10:69452577 | C | G | 21 | a0001c0001t0001g0246 a0001c0001t0003g0251 a0001c0001t0004g0015 others(18): Show |
22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+887C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452577 | |||||||
| chr10:69452596 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.96+906G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452596 | |||||||
| chr10:69452738 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.96+1048T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452738 | |||||||
| chr10:69452741 | G | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(29): Show |
35 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.96+1051G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452741 | |||||||
| chr10:69452768 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.96+1078G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452768 | |||||||
| chr10:69452858 | G | T | 1 | a0001c0001t0006g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.96+1168G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452858 | |||||||
| chr10:69452865 | C | T | 1 | a0002c0002t0002g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+1175C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69452865 | |||||||
| chr10:69453034 | T | C | 4 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(1): Show |
4 | HG01433.hp2 HG02257.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1344T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453034 | |||||||
| chr10:69453145 | T | TG | 34 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0002g0016 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.96+1461dupG | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69453145 | ||||||
| chr10:69453177 | G | T | 6 | a0001c0001t0001g0240 a0001c0001t0003g0239 a0001c0001t0006g0238 others(3): Show |
6 | HG03453.hp2 HG03831.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1487G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453177 | |||||||
| chr10:69453230 | T | C | 2 | a0002c0002t0002g0062 a0002c0002t0002g0237 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96+1540T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453230 | |||||||
| chr10:69453290 | A | G | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+1600A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453290 | |||||||
| chr10:69453304 | A | T | 1 | a0001c0001t0002g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96+1614A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453304 | |||||||
| chr10:69453376 | A | G | 2 | a0002c0002t0002g0062 a0002c0002t0002g0237 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96+1686A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453376 | |||||||
| chr10:69453377 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.96+1687T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453377 | |||||||
| chr10:69453426 | T | G | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+1736T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453426 | |||||||
| chr10:69453553 | G | C | 1 | a0001c0001t0002g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.96+1863G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453553 | |||||||
| chr10:69453571 | G | A | 118 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.96+1881G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453571 | |||||||
| chr10:69453630 | T | A | 32 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0002g0016 others(29): Show |
33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.96+1940T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453630 | |||||||
| chr10:69453894 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
82 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.96+2204C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453894 | |||||||
| chr10:69453899 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+2209T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453899 | |||||||
| chr10:69453995 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.96+2305G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69453995 | |||||||
| chr10:69454022 | G | T | 2 | a0001c0001t0007g0242 a0001c0001t0007g0243 |
2 | NA18960.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.96+2332G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454022 | |||||||
| chr10:69454096 | T | A | 8 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0008g0027 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+2406T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454096 | |||||||
| chr10:69454239 | C | T | 34 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0002g0016 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.96+2549C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454239 | |||||||
| chr10:69454289 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.96+2599G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454289 | |||||||
| chr10:69454345 | T | C | 81 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.96+2655T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454345 | |||||||
| chr10:69454515 | TA | T | 65 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(62): Show |
65 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.96+2836delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69454515 | ||||||
| chr10:69454571 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0032 |
2 | HG01106.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.96+2881C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454571 | |||||||
| chr10:69454714 | G | A | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3024G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454714 | |||||||
| chr10:69454807 | G | A | 1 | a0005c0005t0001g0036 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.96+3117G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454807 | |||||||
| chr10:69454886 | A | G | 6 | a0001c0001t0002g0066 a0001c0001t0008g0069 a0001c0001t0009g0067 others(3): Show |
6 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+3196A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454886 | |||||||
| chr10:69454905 | G | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(16): Show |
25 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.96+3215G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454905 | |||||||
| chr10:69454913 | C | T | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+3223C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454913 | |||||||
| chr10:69454944 | C | T | 2 | a0001c0001t0010g0262 a0001c0001t0010g0263 |
2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.96+3254C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454944 | |||||||
| chr10:69454973 | G | A | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3283G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69454973 | |||||||
| chr10:69455018 | C | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0032 |
2 | HG01106.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.96+3328C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455018 | |||||||
| chr10:69455038 | C | A | 1 | a0001c0001t0003g0037 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.96+3348C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455038 | |||||||
| chr10:69455042 | A | G | 20 | a0001c0001t0001g0246 a0001c0001t0003g0251 a0001c0001t0004g0015 others(17): Show |
21 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3352A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455042 | |||||||
| chr10:69455094 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0006g0247 a0001c0001t0006g0248 others(2): Show |
5 | HG02602.hp2 HG02698.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3404G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455094 | |||||||
| chr10:69455148 | C | CA | 96 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0024 others(93): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.96+3478dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455148 | ||||||
| chr10:69455148 | C | CAA | 22 | a0001c0001t0001g0022 a0001c0001t0001g0267 a0001c0001t0002g0072 others(19): Show |
22 | HG00639.hp1 HG01074.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.96+3477_96+3478dup others(2): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455148 | ||||||
| chr10:69455148 | CA | C | 6 | a0001c0001t0001g0143 a0001c0001t0002g0232 a0001c0001t0003g0233 others(3): Show |
7 | HG01070.hp1 HG01496.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+3478delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455148 | ||||||
| chr10:69455178 | A | G | 10 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+3488A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455178 | |||||||
| chr10:69455327 | G | T | 1 | a0001c0001t0004g0286 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.96+3637G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455327 | |||||||
| chr10:69455342 | CA | C | 10 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+3653delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455342 | |||||||
| chr10:69455351 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.96+3661G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455351 | |||||||
| chr10:69455351 | G | T | 4 | a0001c0001t0004g0015 a0001c0001t0004g0245 a0001c0001t0004g0260 others(1): Show |
5 | HG00099.hp1 HG00280.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+3661G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455351 | |||||||
| chr10:69455387 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0032 |
2 | HG01106.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.96+3697G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455387 | |||||||
| chr10:69455469 | T | G | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3779T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455469 | |||||||
| chr10:69455517 | TCC | T | 3 | a0001c0001t0004g0312 a0001c0001t0004g0315 a0001c0001t0017g0307 |
3 | HG02056.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.96+3829_96+3830del others(2): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455517 | ||||||
| chr10:69455519 | C | T | 41 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(38): Show |
41 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.96+3829C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455519 | |||||||
| chr10:69455520 | CTCTCTTT others(3): Show |
C | 2 | a0001c0001t0002g0021 a0001c0001t0002g0032 |
2 | HG01106.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.96+3844_96+3853del others(10): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455520 | ||||||
| chr10:69455526 | T | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3836T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455526 | |||||||
| chr10:69455530 | T | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3840T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455530 | |||||||
| chr10:69455536 | T | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+3846T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455536 | |||||||
| chr10:69455538 | CTTTCTTT others(2): Show |
C | 17 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.96+3850_96+3858del others(9): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455538 | ||||||
| chr10:69455540 | T | C | 29 | a0001c0001t0001g0303 a0001c0001t0001g0316 a0001c0001t0002g0273 others(26): Show |
29 | HG00408.hp2 HG00597.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+3850T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455540 | |||||||
| chr10:69455542 | CTTTCT | C | 6 | a0001c0001t0004g0286 a0001c0001t0004g0305 a0001c0001t0004g0317 others(3): Show |
6 | HG01074.hp1 HG01175.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+3854_96+3858del others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455542 | ||||||
| chr10:69455544 | T | C | 23 | a0001c0001t0001g0303 a0001c0001t0001g0316 a0001c0001t0002g0273 others(20): Show |
23 | HG00408.hp2 HG00597.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.96+3854T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455544 | |||||||
| chr10:69455548 | T | C | 10 | a0001c0001t0001g0303 a0001c0001t0002g0273 a0001c0001t0002g0275 others(7): Show |
10 | HG01192.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+3858T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455548 | |||||||
| chr10:69455549 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0004g0302 |
2 | HG01192.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.96+3859C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455549 | |||||||
| chr10:69455550 | T | C | 1 | a0001c0001t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.96+3860T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455550 | |||||||
| chr10:69455557 | CTCTTTCT others(12): Show |
C | 1 | a0001c0001t0006g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.96+3887_96+3905del others(19): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455557 | ||||||
| chr10:69455557 | CTCTTTCT others(23): Show |
C | 3 | a0001c0001t0004g0286 a0001c0001t0004g0317 a0001c0001t0004g0318 |
3 | HG01074.hp1 HG01175.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.96+3869_96+3898del others(30): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455557 | ||||||
| chr10:69455559 | CTTTCTTT others(17): Show |
C | 3 | a0001c0001t0004g0287 a0001c0001t0004g0289 a0001c0001t0005g0288 |
3 | HG00741.hp2 HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.96+3872_96+3895del others(24): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(21): Show |
C | 14 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3872_96+3899del others(28): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(27): Show |
C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.96+3872_96+3905del others(34): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(28): Show |
C | 3 | a0001c0001t0002g0279 a0001c0001t0002g0281 a0001c0001t0004g0306 |
3 | HG01496.hp2 HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.96+3871_96+3905del others(35): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(32): Show |
C | 16 | a0001c0001t0001g0303 a0001c0001t0002g0273 a0001c0001t0002g0275 others(13): Show |
16 | HG00408.hp2 HG00597.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.96+3871_96+3909del others(39): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(36): Show |
C | 1 | a0001c0001t0004g0315 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.96+3871_96+3913del others(43): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455559 | CTTTCTTT others(40): Show |
C | 2 | a0001c0001t0001g0316 a0001c0001t0003g0278 |
2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.96+3871_96+3917del others(47): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455559 | ||||||
| chr10:69455560 | TTTCTTTC others(23): Show |
T | 1 | a0001c0001t0012g0304 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.96+3872_96+3901del others(30): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455560 | ||||||
| chr10:69455561 | T | C | 1 | a0001c0001t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.96+3871T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455561 | |||||||
| chr10:69455561 | T | G | 1 | a0001c0001t0010g0252 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.96+3871T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455561 | |||||||
| chr10:69455565 | T | C | 1 | a0001c0001t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.96+3875T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455565 | |||||||
| chr10:69455569 | T | C | 1 | a0001c0001t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.96+3879T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455569 | |||||||
| chr10:69455573 | CTTTTCTT others(26): Show |
C | 1 | a0001c0001t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.96+3885_96+3917del others(33): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455573 | ||||||
| chr10:69455575 | TTTCTTTC others(8): Show |
T | 13 | a0001c0001t0001g0240 a0001c0001t0002g0064 a0001c0001t0002g0065 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+3887_96+3901del others(15): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455575 | ||||||
| chr10:69455576 | T | TCTTTCTT others(13): Show |
1 | a0001c0001t0009g0070 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.96+3886_96+3887ins others(20): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455576 | |||||||
| chr10:69455588 | T | C | 3 | a0001c0001t0004g0287 a0001c0001t0004g0289 a0001c0001t0005g0288 |
3 | HG00741.hp2 HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.96+3898T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455588 | |||||||
| chr10:69455590 | C | CTCTT | 5 | a0001c0001t0001g0142 a0001c0001t0002g0034 a0001c0001t0002g0060 others(2): Show |
5 | HG01175.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+3916_96+3919dup others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455590 | C | CTCTTTCT others(13): Show |
1 | a0001c0001t0008g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(20): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455590 | C | CTCTTTCT others(17): Show |
6 | a0001c0001t0004g0258 a0001c0001t0008g0027 a0001c0001t0008g0029 others(3): Show |
6 | HG00140.hp1 HG01123.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(24): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455590 | C | CTCTTTCT others(21): Show |
2 | a0001c0001t0004g0260 a0001c0001t0016g0261 |
2 | HG00099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(28): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455590 | C | CTCTTTCT others(29): Show |
1 | a0001c0001t0006g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(36): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455590 | C | CTTTCTTT others(19): Show |
1 | a0001c0001t0004g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.96+3901_96+3902ins others(26): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455590 | ||||||
| chr10:69455594 | T | C | 21 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+3904T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455594 | |||||||
| chr10:69455598 | T | C | 26 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(23): Show |
26 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.96+3908T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455598 | |||||||
| chr10:69455602 | T | C | 42 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(39): Show |
42 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.96+3912T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455602 | |||||||
| chr10:69455606 | T | C | 57 | a0001c0001t0001g0150 a0001c0001t0001g0240 a0001c0001t0001g0291 others(54): Show |
57 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.96+3916T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455606 | |||||||
| chr10:69455606 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0003g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(14): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455606 | ||||||
| chr10:69455606 | T | TTCTTTCT others(19): Show |
9 | a0001c0001t0001g0246 a0001c0001t0004g0015 a0001c0001t0004g0245 others(6): Show |
10 | HG00280.hp1 HG00738.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(26): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455606 | ||||||
| chr10:69455606 | T | TTCTTTCT others(23): Show |
3 | a0001c0001t0006g0247 a0001c0001t0006g0248 a0001c0001t0012g0249 |
3 | HG03239.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(30): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455606 | ||||||
| chr10:69455608 | C | CTTTCTTT others(11): Show |
3 | a0001c0001t0001g0267 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG01243.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(18): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455608 | ||||||
| chr10:69455608 | C | CTTTCTTT others(15): Show |
1 | a0001c0001t0008g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(22): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455608 | ||||||
| chr10:69455608 | C | CTTTCTTT others(19): Show |
2 | a0001c0001t0002g0269 a0001c0001t0020g0270 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.96+3919_96+3920ins others(26): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455608 | ||||||
| chr10:69455608 | C | CTTTCTTT others(35): Show |
1 | a0001c0001t0002g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(42): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455608 | ||||||
| chr10:69455608 | C | CTTTCTTT others(55): Show |
1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+3919_96+3920ins others(62): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455608 | ||||||
| chr10:69455615 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.96+3925T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455615 | |||||||
| chr10:69455617 | T | C | 8 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+3927T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455617 | |||||||
| chr10:69455618 | CT | C | 15 | a0001c0001t0004g0287 a0001c0001t0004g0289 a0001c0001t0004g0290 others(12): Show |
15 | HG00408.hp2 HG00741.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+3929delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455618 | |||||||
| chr10:69455619 | T | C | 10 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+3929T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455619 | |||||||
| chr10:69455619 | T | TC | 19 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(16): Show |
19 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+3930dupC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455619 | ||||||
| chr10:69455621 | T | C | 11 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(8): Show |
11 | HG01074.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+3931T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455621 | |||||||
| chr10:69455621 | T | G | 34 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+3931T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455621 | |||||||
| chr10:69455622 | CTCT | C | 13 | a0001c0001t0001g0150 a0001c0001t0001g0240 a0001c0001t0002g0064 others(10): Show |
13 | HG00280.hp2 HG00639.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+3933_96+3935del others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455622 | |||||||
| chr10:69455623 | T | C | 45 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(42): Show |
45 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.96+3933T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455623 | |||||||
| chr10:69455625 | T | C | 63 | a0001c0001t0001g0246 a0001c0001t0001g0291 a0001c0001t0001g0292 others(60): Show |
64 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.96+3935T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455625 | |||||||
| chr10:69455625 | T | TC | 33 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0155 others(30): Show |
39 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.96+3944dupC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69455625 | ||||||
| chr10:69455628 | C | CG | 5 | a0001c0001t0002g0016 a0001c0001t0002g0281 a0001c0001t0002g0282 others(2): Show |
5 | HG01074.hp1 HG02055.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+3938_96+3939ins others(1): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455628 | |||||||
| chr10:69455628 | C | G | 39 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(36): Show |
39 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.96+3938C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455628 | |||||||
| chr10:69455630 | C | CGCT | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3940_96+3941ins others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455630 | |||||||
| chr10:69455727 | T | C | 81 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.96+4037T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455727 | |||||||
| chr10:69455822 | A | T | 35 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0002g0016 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.96+4132A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455822 | |||||||
| chr10:69455902 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+4212C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455902 | |||||||
| chr10:69455935 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.96+4245T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69455935 | |||||||
| chr10:69456043 | C | T | 84 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.96+4353C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456043 | |||||||
| chr10:69456091 | CT | C | 82 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(79): Show |
82 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+4415delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69456091 | ||||||
| chr10:69456280 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.96+4590G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456280 | |||||||
| chr10:69456378 | T | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+4688T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456378 | |||||||
| chr10:69456512 | A | G | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+4822A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456512 | |||||||
| chr10:69456540 | T | G | 1 | a0001c0001t0008g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+4850T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456540 | |||||||
| chr10:69456554 | G | A | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+4864G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456554 | |||||||
| chr10:69456588 | A | T | 2 | a0001c0001t0002g0081 a0001c0001t0023g0077 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.96+4898A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456588 | |||||||
| chr10:69456589 | G | A | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+4899G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456589 | |||||||
| chr10:69456643 | G | T | 2 | a0001c0001t0005g0009 a0001c0001t0005g0059 |
3 | NA18968.hp1 NA18982.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.96+4953G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456643 | |||||||
| chr10:69456699 | A | C | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+5009A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456699 | |||||||
| chr10:69456735 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.96+5045A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456735 | |||||||
| chr10:69456795 | C | T | 11 | a0001c0001t0001g0267 a0001c0001t0002g0265 a0001c0001t0002g0266 others(8): Show |
11 | HG01243.hp2 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+5105C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456795 | |||||||
| chr10:69456811 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96+5121A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456811 | |||||||
| chr10:69456813 | G | A | 35 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(32): Show |
35 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.96+5123G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456813 | |||||||
| chr10:69456922 | T | G | 81 | a0001c0001t0001g0246 a0001c0001t0001g0267 a0001c0001t0001g0291 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.96+5232T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456922 | |||||||
| chr10:69456948 | C | G | 1 | a0001c0001t0002g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96+5258C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69456948 | |||||||
| chr10:69457004 | G | A | 46 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(43): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+5314G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457004 | |||||||
| chr10:69457092 | T | C | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+5402T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457092 | |||||||
| chr10:69457124 | A | G | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+5434A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457124 | |||||||
| chr10:69457126 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+5436G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457126 | |||||||
| chr10:69457266 | G | T | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+5576G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457266 | |||||||
| chr10:69457269 | T | G | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+5579T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457269 | |||||||
| chr10:69457271 | T | G | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+5581T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457271 | |||||||
| chr10:69457272 | T | G | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+5582T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457272 | |||||||
| chr10:69457274 | C | G | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+5584C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457274 | |||||||
| chr10:69457309 | G | T | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+5619G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457309 | |||||||
| chr10:69457334 | C | T | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+5644C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457334 | |||||||
| chr10:69457375 | G | A | 36 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.96+5685G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457375 | |||||||
| chr10:69457857 | T | C | 87 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(84): Show |
93 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.96+6167T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457857 | |||||||
| chr10:69457968 | C | T | 1 | a0001c0001t0024g0313 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.96+6278C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69457968 | |||||||
| chr10:69458028 | C | T | 42 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0300 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.96+6338C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458028 | |||||||
| chr10:69458078 | C | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96+6388C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458078 | |||||||
| chr10:69458099 | G | A | 1 | a0001c0001t0004g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.96+6409G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458099 | |||||||
| chr10:69458108 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | NA18941.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.96+6418G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458108 | |||||||
| chr10:69458256 | C | CAGG | 80 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(77): Show |
89 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+6569_96+6571dup others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69458256 | ||||||
| chr10:69458272 | T | G | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+6582T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458272 | |||||||
| chr10:69458273 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.96+6583C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458273 | |||||||
| chr10:69458303 | C | A | 79 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(76): Show |
88 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96+6613C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458303 | |||||||
| chr10:69458312 | G | A | 1 | a0001c0001t0017g0307 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.96+6622G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458312 | |||||||
| chr10:69458338 | T | C | 40 | a0001c0001t0001g0293 a0001c0001t0001g0300 a0001c0001t0001g0301 others(37): Show |
42 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.96+6648T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458338 | |||||||
| chr10:69458604 | C | T | 3 | a0001c0001t0005g0002 a0001c0001t0005g0149 a0001c0001t0005g0160 |
6 | HG00639.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+6914C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458604 | |||||||
| chr10:69458632 | C | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.96+6942C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458632 | |||||||
| chr10:69458711 | T | C | 1 | a0001c0001t0018g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.96+7021T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458711 | |||||||
| chr10:69458730 | A | G | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+7040A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458730 | |||||||
| chr10:69458742 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+7052A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458742 | |||||||
| chr10:69458776 | A | T | 1 | a0001c0001t0003g0231 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+7086A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458776 | |||||||
| chr10:69458782 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+7092G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458782 | |||||||
| chr10:69458810 | C | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(44): Show |
54 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.96+7120C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458810 | |||||||
| chr10:69458830 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+7140C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458830 | |||||||
| chr10:69458831 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.96+7141G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458831 | |||||||
| chr10:69458890 | G | C | 15 | a0001c0001t0003g0251 a0001c0001t0004g0015 a0001c0001t0004g0245 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+7200G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458890 | |||||||
| chr10:69458934 | C | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(44): Show |
54 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.96+7244C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458934 | |||||||
| chr10:69458963 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7273G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69458963 | |||||||
| chr10:69459067 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | NA18942.hp1 NA18949.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+7377C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459067 | |||||||
| chr10:69459104 | A | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7414A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459104 | |||||||
| chr10:69459105 | C | CA | 17 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0164 others(14): Show |
17 | HG01891.hp2 HG01978.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+7435dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459105 | ||||||
| chr10:69459105 | CA | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(22): Show |
26 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.96+7435delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459105 | ||||||
| chr10:69459116 | AAAAAAAA others(3): Show |
A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(18): Show |
27 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.96+7429_96+7438del others(10): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459116 | ||||||
| chr10:69459118 | AAAAAAAA others(1): Show |
A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG01081.hp2 HG01167.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+7431_96+7438del others(8): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459118 | ||||||
| chr10:69459120 | AAAAAAC | A | 48 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0303 others(45): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.96+7433_96+7438del others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459120 | ||||||
| chr10:69459121 | AAAAAC | A | 9 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0002g0016 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+7434_96+7438del others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459121 | ||||||
| chr10:69459123 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.96+7433A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459123 | |||||||
| chr10:69459125 | A | C | 2 | a0001c0001t0003g0226 a0004c0006t0003g0212 |
2 | HG00323.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.96+7435A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459125 | |||||||
| chr10:69459125 | AC | A | 10 | a0001c0001t0002g0032 a0001c0001t0002g0266 a0001c0001t0002g0271 others(7): Show |
10 | HG01433.hp2 HG02257.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+7436delC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459125 | |||||||
| chr10:69459126 | C | A | 21 | a0001c0001t0002g0021 a0001c0001t0002g0064 a0001c0001t0002g0065 others(18): Show |
21 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+7436C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459126 | |||||||
| chr10:69459133 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7443A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459133 | |||||||
| chr10:69459170 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7480T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459170 | |||||||
| chr10:69459208 | TCA | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7519_96+7520del others(2): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459208 | |||||||
| chr10:69459223 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.96+7533C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459223 | |||||||
| chr10:69459310 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.96+7620A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459310 | |||||||
| chr10:69459435 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7745G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459435 | |||||||
| chr10:69459548 | CAGAG | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7863_96+7866del others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459548 | ||||||
| chr10:69459585 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.96+7895C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459585 | |||||||
| chr10:69459617 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+7927G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459617 | |||||||
| chr10:69459629 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7939G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459629 | |||||||
| chr10:69459654 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+7964G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459654 | |||||||
| chr10:69459661 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+7971T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459661 | |||||||
| chr10:69459708 | G | A | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+8018G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459708 | |||||||
| chr10:69459729 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+8039A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459729 | |||||||
| chr10:69459780 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.96+8090G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459780 | |||||||
| chr10:69459805 | GCCT | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.96+8120_96+8122del others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459805 | ||||||
| chr10:69459879 | C | T | 1 | a0001c0001t0008g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+8189C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459879 | |||||||
| chr10:69459920 | A | AC | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.96+8240dupC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459920 | ||||||
| chr10:69459922 | C | CT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(4): Show |
8 | HG00280.hp2 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+8232_96+8233ins others(1): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459922 | |||||||
| chr10:69459930 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(4): Show |
8 | HG00280.hp2 HG01071.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+8240C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69459930 | |||||||
| chr10:69459930 | C | CA | 83 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(80): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.96+8241dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69459930 | ||||||
| chr10:69460012 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+8322T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460012 | |||||||
| chr10:69460016 | G | GGAGAT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0135 a0001c0001t0001g0227 others(6): Show |
9 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8376_96+8380dup others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460016 | GGAGAT | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+8376_96+8380del others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460016 | GGAGATGA others(3): Show |
G | 39 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0088 others(36): Show |
46 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+8371_96+8380del others(10): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460016 | GGAGATGA others(8): Show |
G | 76 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.96+8366_96+8380del others(15): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460016 | GGAGATGA others(13): Show |
G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8361_96+8380del others(20): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460016 | GGAGATGA others(18): Show |
G | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8356_96+8380del others(25): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460016 | ||||||
| chr10:69460055 | A | ATGAGATG others(193): Show |
1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+8380_96+8381ins others(200): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69460055 | ||||||
| chr10:69460122 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+8432C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460122 | |||||||
| chr10:69460282 | C | T | 1 | a0001c0001t0014g0131 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.96+8592C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460282 | |||||||
| chr10:69460284 | C | A | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+8594C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460284 | |||||||
| chr10:69460293 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+8603G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460293 | |||||||
| chr10:69460300 | G | A | 1 | a0001c0001t0003g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.96+8610G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460300 | |||||||
| chr10:69460343 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8653G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460343 | |||||||
| chr10:69460430 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+8740A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460430 | |||||||
| chr10:69460541 | C | G | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8851C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460541 | |||||||
| chr10:69460653 | C | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+8963C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460653 | |||||||
| chr10:69460676 | T | C | 105 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(102): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.96+8986T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460676 | |||||||
| chr10:69460681 | G | C | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+8991G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460681 | |||||||
| chr10:69460726 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.96+9036A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460726 | |||||||
| chr10:69460781 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+9091G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460781 | |||||||
| chr10:69460955 | C | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+9265C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69460955 | |||||||
| chr10:69461025 | G | A | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+9335G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461025 | |||||||
| chr10:69461076 | G | T | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.96+9386G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461076 | |||||||
| chr10:69461093 | G | A | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.96+9403G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461093 | |||||||
| chr10:69461109 | G | A | 3 | a0001c0001t0009g0068 a0001c0001t0009g0070 a0001c0001t0009g0071 |
3 | HG03041.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.96+9419G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461109 | |||||||
| chr10:69461290 | T | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+9600T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461290 | |||||||
| chr10:69461291 | A | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+9601A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461291 | |||||||
| chr10:69461361 | G | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0245 a0001c0001t0004g0260 |
4 | HG00099.hp1 HG00280.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+9671G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461361 | |||||||
| chr10:69461372 | A | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+9682A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461372 | |||||||
| chr10:69461457 | C | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.96+9767C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461457 | |||||||
| chr10:69461518 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.96+9828T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461518 | |||||||
| chr10:69461574 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+9884C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461574 | |||||||
| chr10:69461742 | A | C | 1 | a0001c0001t0003g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.96+10052A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461742 | |||||||
| chr10:69461761 | GT | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10073delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69461761 | ||||||
| chr10:69461804 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.96+10114G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461804 | |||||||
| chr10:69461918 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.96+10228C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461918 | |||||||
| chr10:69461928 | C | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(108): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.96+10238C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461928 | |||||||
| chr10:69461932 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.96+10242C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461932 | |||||||
| chr10:69461955 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+10265G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461955 | |||||||
| chr10:69461981 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.96+10291C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461981 | |||||||
| chr10:69461988 | A | G | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+10298A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69461988 | |||||||
| chr10:69462009 | C | T | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+10319C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462009 | |||||||
| chr10:69462028 | C | T | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+10338C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462028 | |||||||
| chr10:69462039 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10349G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462039 | |||||||
| chr10:69462059 | T | C | 138 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.96+10369T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462059 | |||||||
| chr10:69462155 | G | GT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0031 others(85): Show |
89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+10491dupT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | G | GTT | 6 | a0001c0001t0001g0155 a0001c0001t0003g0225 a0001c0001t0004g0130 others(3): Show |
6 | HG00544.hp1 HG01167.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+10490_96+10491d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | G | GTTT | 14 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0156 others(11): Show |
21 | HG00280.hp2 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+10489_96+10491d others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | G | GTTTT | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0004g0153 others(6): Show |
9 | HG00639.hp1 HG01071.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+10488_96+10491d others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.96+10475_96+10491d others(19): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | GT | G | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0034 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+10491delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462155 | GTT | G | 6 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0002g0279 others(3): Show |
6 | HG02922.hp1 HG03130.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+10490_96+10491d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462155 | ||||||
| chr10:69462162 | T | TTTTG | 49 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.96+10475_96+10476i others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462162 | ||||||
| chr10:69462163 | T | TTTG | 9 | a0001c0001t0001g0316 a0001c0001t0002g0076 a0001c0001t0002g0080 others(6): Show |
9 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+10475_96+10476i others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462163 | ||||||
| chr10:69462163 | T | TTTTG | 6 | a0001c0001t0015g0079 a0002c0002t0002g0012 a0002c0002t0002g0013 others(3): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+10476_96+10477i others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69462163 | ||||||
| chr10:69462167 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+10477T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462167 | |||||||
| chr10:69462173 | T | G | 6 | a0001c0001t0015g0079 a0002c0002t0002g0012 a0002c0002t0002g0013 others(3): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+10483T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462173 | |||||||
| chr10:69462212 | C | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10522C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462212 | |||||||
| chr10:69462290 | C | T | 5 | a0001c0001t0001g0240 a0001c0001t0007g0137 a0001c0001t0007g0241 others(2): Show |
5 | NA18948.hp1 NA18960.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+10600C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462290 | |||||||
| chr10:69462397 | T | C | 105 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(102): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.96+10707T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462397 | |||||||
| chr10:69462447 | G | C | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+10757G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462447 | |||||||
| chr10:69462537 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10847A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462537 | |||||||
| chr10:69462581 | C | T | 21 | a0001c0001t0003g0168 a0001c0001t0003g0169 a0001c0001t0003g0170 others(18): Show |
21 | HG00423.hp2 HG00438.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+10891C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462581 | |||||||
| chr10:69462600 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.96+10910G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462600 | |||||||
| chr10:69462640 | T | G | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+10950T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462640 | |||||||
| chr10:69462643 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10953G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462643 | |||||||
| chr10:69462672 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+10982C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462672 | |||||||
| chr10:69462737 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0146 |
2 | HG01070.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.96+11047G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462737 | |||||||
| chr10:69462737 | G | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+11047G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462737 | |||||||
| chr10:69462753 | G | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+11063G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462753 | |||||||
| chr10:69462850 | T | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+11160T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462850 | |||||||
| chr10:69462924 | C | A | 5 | a0001c0001t0001g0240 a0001c0001t0007g0137 a0001c0001t0007g0241 others(2): Show |
5 | NA18948.hp1 NA18960.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+11234C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462924 | |||||||
| chr10:69462957 | G | T | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.96+11267G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462957 | |||||||
| chr10:69462978 | A | T | 1 | a0001c0001t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.96+11288A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69462978 | |||||||
| chr10:69463022 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.96+11332A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463022 | |||||||
| chr10:69463173 | C | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+11483C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463173 | |||||||
| chr10:69463243 | C | T | 1 | a0001c0001t0004g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.96+11553C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463243 | |||||||
| chr10:69463496 | G | A | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+11806G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463496 | |||||||
| chr10:69463509 | A | C | 2 | a0002c0002t0002g0062 a0002c0002t0002g0237 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96+11819A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463509 | |||||||
| chr10:69463599 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.96+11909C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463599 | |||||||
| chr10:69463674 | G | A | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+11984G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463674 | |||||||
| chr10:69463808 | C | CA | 20 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(17): Show |
20 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.96+12134dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69463808 | ||||||
| chr10:69463808 | C | CAA | 15 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
15 | HG01081.hp2 HG01167.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+12133_96+12134d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69463808 | ||||||
| chr10:69463808 | C | CAAA | 56 | a0001c0001t0001g0014 a0001c0001t0001g0155 a0001c0001t0001g0156 others(53): Show |
63 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+12132_96+12134d others(5): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69463808 | ||||||
| chr10:69463808 | C | CAAAA | 33 | a0001c0001t0001g0150 a0001c0001t0001g0240 a0001c0001t0001g0246 others(30): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.96+12131_96+12134d others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69463808 | ||||||
| chr10:69463931 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12241C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463931 | |||||||
| chr10:69463952 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+12262A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69463952 | |||||||
| chr10:69464005 | C | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0020g0270 |
3 | HG02647.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+12315C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464005 | |||||||
| chr10:69464024 | C | T | 6 | a0001c0001t0015g0079 a0002c0002t0002g0012 a0002c0002t0002g0013 others(3): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12334C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464024 | |||||||
| chr10:69464153 | G | C | 1 | a0001c0001t0002g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.96+12463G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464153 | |||||||
| chr10:69464317 | CAGGG | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+12632_96+12635d others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69464317 | ||||||
| chr10:69464335 | C | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+12645C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464335 | |||||||
| chr10:69464386 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+12696G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464386 | |||||||
| chr10:69464399 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+12709T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464399 | |||||||
| chr10:69464469 | T | A | 138 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.96+12779T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464469 | |||||||
| chr10:69464473 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.96+12783G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464473 | |||||||
| chr10:69464488 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+12798C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464488 | |||||||
| chr10:69464501 | A | G | 1 | a0001c0001t0004g0296 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.96+12811A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464501 | |||||||
| chr10:69464543 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.96+12853G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464543 | |||||||
| chr10:69464565 | T | C | 105 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(102): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.96+12875T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464565 | |||||||
| chr10:69464732 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+13042G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464732 | |||||||
| chr10:69464814 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+13124G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464814 | |||||||
| chr10:69464952 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.96+13262G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69464952 | |||||||
| chr10:69465030 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.96+13340G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465030 | |||||||
| chr10:69465141 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+13451G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465141 | |||||||
| chr10:69465196 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0115 others(7): Show |
12 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+13506C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465196 | |||||||
| chr10:69465197 | G | A | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+13507G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465197 | |||||||
| chr10:69465216 | TTCCCCTG others(4): Show |
T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+13528_96+13538d others(13): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69465216 | ||||||
| chr10:69465230 | G | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+13540G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465230 | |||||||
| chr10:69465271 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+13581C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465271 | |||||||
| chr10:69465324 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+13634C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465324 | |||||||
| chr10:69465514 | G | A | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.96+13824G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465514 | |||||||
| chr10:69465569 | A | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+13879A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465569 | |||||||
| chr10:69465675 | G | GAGCTAGA others(3): Show |
14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+13986_96+13995d others(12): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69465675 | ||||||
| chr10:69465721 | A | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.96+14031A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465721 | |||||||
| chr10:69465778 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14088T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465778 | |||||||
| chr10:69465828 | C | A | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+14138C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465828 | |||||||
| chr10:69465837 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+14147G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465837 | |||||||
| chr10:69465859 | TC | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14173delC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69465859 | ||||||
| chr10:69465873 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+14183C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465873 | |||||||
| chr10:69465905 | A | G | 1 | a0001c0001t0018g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.96+14215A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69465905 | |||||||
| chr10:69466100 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+14410G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466100 | |||||||
| chr10:69466209 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14519T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466209 | |||||||
| chr10:69466232 | T | G | 1 | a0001c0001t0005g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.96+14542T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466232 | |||||||
| chr10:69466267 | G | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.96+14577G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466267 | |||||||
| chr10:69466271 | C | T | 105 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(102): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.96+14581C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466271 | |||||||
| chr10:69466347 | G | A | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+14657G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466347 | |||||||
| chr10:69466380 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14690A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466380 | |||||||
| chr10:69466467 | G | T | 1 | a0001c0001t0004g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.96+14777G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466467 | |||||||
| chr10:69466622 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14932T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466622 | |||||||
| chr10:69466623 | G | T | 2 | a0002c0002t0002g0062 a0002c0002t0002g0237 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96+14933G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466623 | |||||||
| chr10:69466628 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+14938C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466628 | |||||||
| chr10:69466688 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+14998C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466688 | |||||||
| chr10:69466710 | T | C | 138 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.96+15020T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466710 | |||||||
| chr10:69466738 | G | T | 1 | a0001c0001t0007g0243 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.96+15048G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466738 | |||||||
| chr10:69466899 | G | A | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+15209G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466899 | |||||||
| chr10:69466955 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0032 |
2 | HG01106.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.96+15265G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69466955 | |||||||
| chr10:69467034 | C | T | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.96+15344C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467034 | |||||||
| chr10:69467143 | A | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+15453A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467143 | |||||||
| chr10:69467144 | G | A | 6 | a0001c0001t0015g0079 a0002c0002t0002g0012 a0002c0002t0002g0013 others(3): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+15454G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467144 | |||||||
| chr10:69467150 | C | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96+15460C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467150 | |||||||
| chr10:69467152 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+15462T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467152 | |||||||
| chr10:69467191 | G | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.96+15501G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467191 | |||||||
| chr10:69467206 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+15516C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467206 | |||||||
| chr10:69467233 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+15543A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467233 | |||||||
| chr10:69467283 | A | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+15593A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467283 | |||||||
| chr10:69467356 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+15666G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467356 | |||||||
| chr10:69467370 | G | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.96+15680G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467370 | |||||||
| chr10:69467397 | G | A | 105 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(102): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.96+15707G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467397 | |||||||
| chr10:69467454 | A | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+15764A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467454 | |||||||
| chr10:69467502 | T | C | 1 | a0001c0001t0019g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.96+15812T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467502 | |||||||
| chr10:69467570 | C | T | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.96+15880C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467570 | |||||||
| chr10:69467637 | A | AAC | 26 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(23): Show |
27 | HG00099.hp2 HG00621.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.96+15984_96+15985d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467637 | A | AACAC | 14 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0104 others(11): Show |
16 | HG00639.hp2 HG01070.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+15982_96+15985d others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467637 | AAC | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0033 others(64): Show |
74 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.96+15984_96+15985d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467637 | AACACAC | A | 17 | a0001c0001t0001g0246 a0001c0001t0003g0251 a0001c0001t0004g0015 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(15): Show |
intron_variant | MODIFIER | c.96+15980_96+15985d others(8): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467637 | AACACACA others(3): Show |
A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0240 others(5): Show |
8 | NA18942.hp1 NA18948.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+15976_96+15985d others(12): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467637 | AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.96+15972_96+15985d others(16): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467637 | ||||||
| chr10:69467673 | C | A | 97 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.96+15983C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467673 | |||||||
| chr10:69467673 | C | CAA | 4 | a0001c0001t0004g0318 a0001c0001t0009g0073 a0002c0002t0002g0062 others(1): Show |
4 | HG01175.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+15984_96+15985i others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467673 | ||||||
| chr10:69467673 | C | CACAA | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96+15985_96+15986i others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467673 | ||||||
| chr10:69467673 | C | CACACACA others(7): Show |
1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+15985_96+15986i others(16): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467673 | ||||||
| chr10:69467673 | C | CACACACA others(9): Show |
1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+15985_96+15986i others(18): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467673 | ||||||
| chr10:69467759 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.97-15932C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467759 | |||||||
| chr10:69467793 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0291 |
3 | HG00323.hp1 HG01243.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.97-15898A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467793 | |||||||
| chr10:69467831 | T | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15860T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467831 | |||||||
| chr10:69467847 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15844C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467847 | |||||||
| chr10:69467885 | C | G | 124 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(121): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.97-15806C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69467885 | |||||||
| chr10:69467887 | TA | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15798delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69467887 | ||||||
| chr10:69468121 | C | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15570C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468121 | |||||||
| chr10:69468130 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(36): Show |
40 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-15561C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468130 | |||||||
| chr10:69468136 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.97-15555C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468136 | |||||||
| chr10:69468146 | G | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0227 a0001c0001t0006g0167 |
3 | HG02572.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-15545G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468146 | |||||||
| chr10:69468298 | G | T | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-15393G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468298 | |||||||
| chr10:69468303 | G | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-15388G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468303 | |||||||
| chr10:69468364 | A | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-15327A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468364 | |||||||
| chr10:69468366 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15325T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468366 | |||||||
| chr10:69468411 | G | A | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-15280G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468411 | |||||||
| chr10:69468415 | C | T | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15276C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468415 | |||||||
| chr10:69468424 | T | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.97-15267T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468424 | |||||||
| chr10:69468518 | CT | C | 19 | a0001c0001t0001g0240 a0001c0001t0002g0016 a0001c0001t0002g0034 others(16): Show |
19 | HG01256.hp2 HG02647.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-15159delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69468518 | ||||||
| chr10:69468684 | G | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-15007G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468684 | |||||||
| chr10:69468768 | T | TA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(18): Show |
28 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.97-14911dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69468768 | ||||||
| chr10:69468856 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0012g0249 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.97-14835G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468856 | |||||||
| chr10:69468999 | G | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(52): Show |
64 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.97-14692G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69468999 | |||||||
| chr10:69469045 | A | AGGGTTGG others(19): Show |
11 | a0001c0001t0001g0240 a0001c0001t0002g0016 a0001c0001t0002g0034 others(8): Show |
11 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-14643_97-14642i others(28): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69469045 | ||||||
| chr10:69469045 | A | AGGGTTGG others(19): Show |
96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-14643_97-14642i others(28): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69469045 | ||||||
| chr10:69469070 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97-14621G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469070 | |||||||
| chr10:69469078 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.97-14613G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469078 | |||||||
| chr10:69469085 | G | C | 1 | a0001c0001t0005g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.97-14606G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469085 | |||||||
| chr10:69469093 | G | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-14598G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469093 | |||||||
| chr10:69469102 | C | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-14589C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469102 | |||||||
| chr10:69469112 | CT | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-14566delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69469112 | ||||||
| chr10:69469245 | T | A | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-14446T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469245 | |||||||
| chr10:69469330 | C | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-14361C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469330 | |||||||
| chr10:69469352 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-14339G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469352 | |||||||
| chr10:69469353 | C | T | 1 | a0001c0001t0003g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97-14338C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469353 | |||||||
| chr10:69469426 | T | C | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-14265T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469426 | |||||||
| chr10:69469428 | A | T | 1 | a0001c0001t0003g0123 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.97-14263A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469428 | |||||||
| chr10:69469480 | A | G | 5 | a0001c0001t0001g0240 a0001c0001t0007g0137 a0001c0001t0007g0241 others(2): Show |
5 | NA18948.hp1 NA18960.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-14211A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469480 | |||||||
| chr10:69469611 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0003g0183 a0001c0001t0003g0239 others(1): Show |
4 | HG03831.hp2 HG03927.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-14080G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469611 | |||||||
| chr10:69469716 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-13975C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469716 | |||||||
| chr10:69469783 | A | G | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.97-13908A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469783 | |||||||
| chr10:69469826 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-13865A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469826 | |||||||
| chr10:69469938 | G | A | 1 | a0005c0005t0001g0036 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.97-13753G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469938 | |||||||
| chr10:69469948 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-13743G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469948 | |||||||
| chr10:69469973 | A | G | 182 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(179): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.97-13718A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69469973 | |||||||
| chr10:69470087 | G | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-13604G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470087 | |||||||
| chr10:69470261 | G | A | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-13430G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470261 | |||||||
| chr10:69470356 | A | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.97-13335A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470356 | |||||||
| chr10:69470366 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97-13325G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470366 | |||||||
| chr10:69470436 | A | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-13255A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470436 | |||||||
| chr10:69470490 | C | T | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-13201C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470490 | |||||||
| chr10:69470578 | C | G | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.97-13113C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470578 | |||||||
| chr10:69470595 | C | T | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.97-13096C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470595 | |||||||
| chr10:69470702 | C | T | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-12989C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470702 | |||||||
| chr10:69470816 | C | T | 5 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0087 others(2): Show |
7 | HG01891.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-12875C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470816 | |||||||
| chr10:69470868 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-12823T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470868 | |||||||
| chr10:69470908 | G | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-12783G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470908 | |||||||
| chr10:69470933 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-12758A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470933 | |||||||
| chr10:69470965 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.97-12726C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69470965 | |||||||
| chr10:69471031 | C | T | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-12660C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471031 | |||||||
| chr10:69471032 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-12659G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471032 | |||||||
| chr10:69471036 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-12655C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471036 | |||||||
| chr10:69471066 | C | T | 1 | a0001c0001t0010g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.97-12625C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471066 | |||||||
| chr10:69471136 | G | C | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-12555G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471136 | |||||||
| chr10:69471196 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-12495G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471196 | |||||||
| chr10:69471274 | T | C | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-12417T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471274 | |||||||
| chr10:69471312 | C | T | 138 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.97-12379C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471312 | |||||||
| chr10:69471429 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97-12262C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471429 | |||||||
| chr10:69471446 | A | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-12245A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471446 | |||||||
| chr10:69471551 | T | TTCTCTCT others(1): Show |
17 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-12139_97-12132d others(10): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69471551 | ||||||
| chr10:69471551 | T | TTCTTTCT others(5): Show |
14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-12137_97-12136i others(14): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69471551 | ||||||
| chr10:69471560 | A | T | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-12131A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471560 | |||||||
| chr10:69471625 | G | T | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-12066G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471625 | |||||||
| chr10:69471738 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-11953C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471738 | |||||||
| chr10:69471761 | C | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.97-11930C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471761 | |||||||
| chr10:69471812 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-11879C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471812 | |||||||
| chr10:69471813 | A | G | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-11878A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471813 | |||||||
| chr10:69471839 | A | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-11852A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471839 | |||||||
| chr10:69471940 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97-11751C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69471940 | |||||||
| chr10:69472034 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-11657A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472034 | |||||||
| chr10:69472091 | A | C | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.97-11600A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472091 | |||||||
| chr10:69472182 | G | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.97-11509G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472182 | |||||||
| chr10:69472184 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-11507C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472184 | |||||||
| chr10:69472196 | C | T | 127 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(124): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.97-11495C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472196 | |||||||
| chr10:69472197 | A | G | 129 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(126): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.97-11494A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472197 | |||||||
| chr10:69472220 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0005g0144 |
3 | HG01496.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.97-11471A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472220 | |||||||
| chr10:69472263 | G | A | 8 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(5): Show |
8 | HG02717.hp2 HG02809.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-11428G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472263 | |||||||
| chr10:69472419 | A | G | 16 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
16 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97-11272A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472419 | |||||||
| chr10:69472428 | A | C | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-11263A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472428 | |||||||
| chr10:69472551 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-11140G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472551 | |||||||
| chr10:69472743 | G | A | 1 | a0001c0001t0007g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-10948G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472743 | |||||||
| chr10:69472957 | A | G | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-10734A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472957 | |||||||
| chr10:69472987 | C | G | 3 | a0001c0001t0006g0247 a0001c0001t0006g0248 a0001c0001t0006g0250 |
3 | HG02602.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.97-10704C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69472987 | |||||||
| chr10:69473145 | C | T | 1 | a0002c0002t0002g0280 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.97-10546C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473145 | |||||||
| chr10:69473167 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-10524G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473167 | |||||||
| chr10:69473349 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-10342A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473349 | |||||||
| chr10:69473379 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.97-10312G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473379 | |||||||
| chr10:69473488 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-10203G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473488 | |||||||
| chr10:69473501 | CAG | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-10187_97-10186d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69473501 | ||||||
| chr10:69473573 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-10118A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473573 | |||||||
| chr10:69473588 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.97-10103C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473588 | |||||||
| chr10:69473752 | T | G | 1 | a0001c0001t0016g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97-9939T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473752 | |||||||
| chr10:69473888 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97-9803T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473888 | |||||||
| chr10:69473948 | T | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0020g0270 |
3 | HG02647.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.97-9743T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69473948 | |||||||
| chr10:69474062 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-9629T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474062 | |||||||
| chr10:69474107 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-9584C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474107 | |||||||
| chr10:69474129 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-9562C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474129 | |||||||
| chr10:69474437 | G | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-9254G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474437 | |||||||
| chr10:69474535 | T | C | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-9156T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474535 | |||||||
| chr10:69474543 | T | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-9148T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474543 | |||||||
| chr10:69474553 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-9138T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474553 | |||||||
| chr10:69474605 | A | G | 3 | a0001c0001t0004g0151 a0001c0001t0004g0153 a0001c0001t0012g0154 |
3 | HG02027.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.97-9086A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474605 | |||||||
| chr10:69474635 | G | A | 1 | a0001c0001t0004g0317 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.97-9056G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474635 | |||||||
| chr10:69474713 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.97-8978C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474713 | |||||||
| chr10:69474937 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-8754C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474937 | |||||||
| chr10:69474949 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.97-8742G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474949 | |||||||
| chr10:69474964 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-8727T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69474964 | |||||||
| chr10:69475018 | C | T | 1 | a0001c0001t0018g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97-8673C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475018 | |||||||
| chr10:69475020 | C | T | 5 | a0001c0001t0002g0020 a0001c0001t0002g0148 a0001c0001t0002g0165 others(2): Show |
5 | HG02145.hp2 HG02165.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-8671C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475020 | |||||||
| chr10:69475034 | T | C | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-8657T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475034 | |||||||
| chr10:69475164 | C | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-8527C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475164 | |||||||
| chr10:69475237 | G | T | 6 | a0001c0001t0015g0079 a0002c0002t0002g0012 a0002c0002t0002g0013 others(3): Show |
8 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-8454G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475237 | |||||||
| chr10:69475267 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0003g0225 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.97-8424A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475267 | |||||||
| chr10:69475293 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-8398G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475293 | |||||||
| chr10:69475572 | T | G | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-8119T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475572 | |||||||
| chr10:69475828 | T | G | 1 | a0001c0001t0008g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-7863T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475828 | |||||||
| chr10:69475832 | T | C | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.97-7859T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475832 | |||||||
| chr10:69475844 | A | G | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-7847A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475844 | |||||||
| chr10:69475854 | A | G | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-7837A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475854 | |||||||
| chr10:69475909 | C | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-7782C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475909 | |||||||
| chr10:69475990 | C | A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-7701C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69475990 | |||||||
| chr10:69476028 | G | A | 1 | a0001c0001t0008g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.97-7663G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476028 | |||||||
| chr10:69476032 | T | C | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-7659T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476032 | |||||||
| chr10:69476388 | C | T | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-7303C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476388 | |||||||
| chr10:69476389 | G | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-7302G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476389 | |||||||
| chr10:69476423 | G | A | 32 | a0001c0001t0001g0118 a0001c0001t0002g0021 a0001c0001t0002g0032 others(29): Show |
32 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.97-7268G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476423 | |||||||
| chr10:69476496 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.97-7195G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476496 | |||||||
| chr10:69476522 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.97-7169A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476522 | |||||||
| chr10:69476556 | C | G | 2 | a0001c0001t0002g0269 a0001c0001t0020g0270 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.97-7135C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476556 | |||||||
| chr10:69476566 | C | CA | 43 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0150 others(40): Show |
50 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.97-7110dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69476566 | ||||||
| chr10:69476566 | C | CAA | 8 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-7111_97-7110dup others(2): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69476566 | ||||||
| chr10:69476566 | CA | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0136 others(8): Show |
13 | HG01255.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.97-7110delA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69476566 | ||||||
| chr10:69476581 | A | AT | 3 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0005g0144 |
3 | HG01496.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.97-7110_97-7109ins others(1): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476581 | |||||||
| chr10:69476598 | G | T | 1 | a0001c0001t0007g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-7093G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476598 | |||||||
| chr10:69476639 | G | C | 1 | a0001c0001t0003g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.97-7052G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476639 | |||||||
| chr10:69476739 | C | T | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.97-6952C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476739 | |||||||
| chr10:69476740 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97-6951G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476740 | |||||||
| chr10:69476752 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.97-6939G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476752 | |||||||
| chr10:69476816 | C | T | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-6875C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476816 | |||||||
| chr10:69476982 | T | G | 2 | a0001c0001t0001g0224 a0001c0001t0003g0225 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.97-6709T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69476982 | |||||||
| chr10:69477174 | C | T | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.97-6517C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477174 | |||||||
| chr10:69477175 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97-6516G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477175 | |||||||
| chr10:69477237 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-6454T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477237 | |||||||
| chr10:69477287 | A | T | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-6404A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477287 | |||||||
| chr10:69477292 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-6399A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477292 | |||||||
| chr10:69477376 | A | G | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-6315A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477376 | |||||||
| chr10:69477488 | A | G | 1 | a0001c0001t0004g0306 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.97-6203A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477488 | |||||||
| chr10:69477489 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-6202T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477489 | |||||||
| chr10:69477626 | C | T | 15 | a0001c0001t0003g0251 a0001c0001t0004g0015 a0001c0001t0004g0245 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-6065C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477626 | |||||||
| chr10:69477627 | G | A | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-6064G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477627 | |||||||
| chr10:69477678 | G | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-6013G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477678 | |||||||
| chr10:69477682 | C | T | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-6009C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477682 | |||||||
| chr10:69477698 | G | C | 1 | a0001c0001t0003g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97-5993G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477698 | |||||||
| chr10:69477705 | G | C | 7 | a0001c0001t0003g0182 a0001c0001t0003g0196 a0001c0001t0003g0197 others(4): Show |
7 | HG01256.hp2 HG01346.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-5986G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477705 | |||||||
| chr10:69477718 | A | C | 1 | a0001c0001t0003g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.97-5973A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477718 | |||||||
| chr10:69477780 | C | A | 51 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.97-5911C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477780 | |||||||
| chr10:69477989 | C | T | 2 | a0001c0001t0002g0016 a0003c0004t0007g0272 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.97-5702C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69477989 | |||||||
| chr10:69478100 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0003g0004 |
5 | NA18939.hp1 NA18947.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5591C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478100 | |||||||
| chr10:69478131 | AGCAGTGT others(12): Show |
A | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-5519_97-5501del others(19): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69478131 | ||||||
| chr10:69478165 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-5526A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478165 | |||||||
| chr10:69478211 | T | C | 33 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(30): Show |
33 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-5480T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478211 | |||||||
| chr10:69478308 | T | G | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5383T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478308 | |||||||
| chr10:69478355 | C | T | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-5336C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478355 | |||||||
| chr10:69478398 | A | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5293A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478398 | |||||||
| chr10:69478413 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-5278C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478413 | |||||||
| chr10:69478493 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-5198C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478493 | |||||||
| chr10:69478602 | G | C | 9 | a0001c0001t0001g0293 a0001c0001t0004g0043 a0001c0001t0004g0290 others(6): Show |
9 | HG02056.hp2 HG02071.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-5089G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478602 | |||||||
| chr10:69478613 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5078G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478613 | |||||||
| chr10:69478653 | C | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-5038C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478653 | |||||||
| chr10:69478816 | G | T | 31 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(28): Show |
31 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-4875G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478816 | |||||||
| chr10:69478862 | G | A | 51 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.97-4829G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478862 | |||||||
| chr10:69478925 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.97-4766C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69478925 | |||||||
| chr10:69479114 | C | T | 5 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0087 others(2): Show |
7 | HG01891.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-4577C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479114 | |||||||
| chr10:69479173 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0003g0225 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.97-4518G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479173 | |||||||
| chr10:69479198 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-4493G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479198 | |||||||
| chr10:69479241 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.97-4450G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479241 | |||||||
| chr10:69479425 | T | C | 32 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(29): Show |
32 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.97-4266T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479425 | |||||||
| chr10:69479474 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.97-4217C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479474 | |||||||
| chr10:69479495 | T | C | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-4196T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479495 | |||||||
| chr10:69479514 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.97-4177G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479514 | |||||||
| chr10:69479777 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.97-3914G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479777 | |||||||
| chr10:69479808 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.97-3883C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69479808 | |||||||
| chr10:69480143 | A | C | 2 | a0001c0001t0001g0018 a0001c0001t0003g0017 |
2 | NA18947.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.97-3548A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480143 | |||||||
| chr10:69480175 | T | C | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-3516T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480175 | |||||||
| chr10:69480228 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.97-3463C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480228 | |||||||
| chr10:69480284 | A | G | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3407A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480284 | |||||||
| chr10:69480337 | A | AT | 64 | a0001c0001t0001g0049 a0001c0001t0001g0240 a0001c0001t0001g0246 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.97-3344dupT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69480337 | ||||||
| chr10:69480385 | C | G | 1 | a0001c0001t0003g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.97-3306C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480385 | |||||||
| chr10:69480422 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 |
3 | HG02615.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.97-3269G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480422 | |||||||
| chr10:69480601 | C | T | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-3090C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480601 | |||||||
| chr10:69480789 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97-2902C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480789 | |||||||
| chr10:69480818 | T | C | 127 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(124): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.97-2873T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480818 | |||||||
| chr10:69480993 | C | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(40): Show |
52 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.97-2698C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69480993 | |||||||
| chr10:69481079 | C | T | 1 | a0001c0001t0003g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.97-2612C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481079 | |||||||
| chr10:69481116 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.97-2575A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481116 | |||||||
| chr10:69481156 | A | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-2535A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481156 | |||||||
| chr10:69481278 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97-2413C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481278 | |||||||
| chr10:69481399 | A | G | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-2292A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481399 | |||||||
| chr10:69481487 | G | A | 1 | a0001c0001t0008g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-2204G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481487 | |||||||
| chr10:69481587 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-2104A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481587 | |||||||
| chr10:69481653 | C | T | 32 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(29): Show |
32 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.97-2038C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481653 | |||||||
| chr10:69481654 | G | C | 1 | a0001c0001t0003g0189 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.97-2037G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481654 | |||||||
| chr10:69481756 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.97-1935C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69481756 | |||||||
| chr10:69482068 | C | CA | 47 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0064 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.97-1609dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69482068 | ||||||
| chr10:69482083 | C | A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-1608C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482083 | |||||||
| chr10:69482211 | C | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-1480C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482211 | |||||||
| chr10:69482262 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(59): Show |
69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.97-1429C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482262 | |||||||
| chr10:69482513 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.97-1178G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482513 | |||||||
| chr10:69482528 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-1163G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482528 | |||||||
| chr10:69482552 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97-1139C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482552 | |||||||
| chr10:69482553 | G | A | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.97-1138G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482553 | |||||||
| chr10:69482604 | T | G | 1 | a0001c0001t0007g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-1087T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482604 | |||||||
| chr10:69482640 | G | A | 7 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0062 others(4): Show |
9 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-1051G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482640 | |||||||
| chr10:69482673 | A | T | 118 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(115): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.97-1018A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482673 | |||||||
| chr10:69482692 | AAC | A | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-995_97-994delCA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69482692 | ||||||
| chr10:69482705 | A | G | 97 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0022 others(94): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.97-986A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482705 | |||||||
| chr10:69482726 | GC | G | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-962delC | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69482726 | ||||||
| chr10:69482729 | C | T | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-962C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482729 | |||||||
| chr10:69482785 | C | G | 1 | a0001c0001t0003g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.97-906C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482785 | |||||||
| chr10:69482899 | A | G | 51 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.97-792A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482899 | |||||||
| chr10:69482911 | T | G | 2 | a0001c0001t0001g0164 a0001c0001t0006g0167 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-780T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482911 | |||||||
| chr10:69482965 | ATTT | A | 118 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(115): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.97-716_97-714delTT others(1): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69482965 | ||||||
| chr10:69482972 | T | G | 11 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0048 others(8): Show |
11 | HG00323.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-719T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482972 | |||||||
| chr10:69482975 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.97-716T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482975 | |||||||
| chr10:69482978 | G | T | 10 | a0001c0001t0002g0201 a0001c0001t0003g0182 a0001c0001t0003g0196 others(7): Show |
10 | HG01099.hp1 HG01256.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-713G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69482978 | |||||||
| chr10:69483012 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.97-679C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483012 | |||||||
| chr10:69483019 | C | T | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-672C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483019 | |||||||
| chr10:69483027 | T | C | 128 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(125): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.97-664T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483027 | |||||||
| chr10:69483189 | A | C | 118 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(115): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.97-502A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483189 | |||||||
| chr10:69483223 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-468C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483223 | |||||||
| chr10:69483234 | C | G | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.97-457C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483234 | |||||||
| chr10:69483276 | C | T | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-415C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483276 | |||||||
| chr10:69483278 | G | A | 128 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(125): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.97-413G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483278 | |||||||
| chr10:69483293 | G | C | 1 | a0001c0001t0003g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-398G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483293 | |||||||
| chr10:69483351 | TCA | T | 10 | a0001c0001t0001g0240 a0001c0001t0001g0291 a0001c0001t0002g0034 others(7): Show |
10 | HG00323.hp1 HG02717.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-335_97-334delCA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69483351 | ||||||
| chr10:69483402 | AAGGACAC others(1): Show |
A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-286_97-279delGA others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 69483402 | ||||||
| chr10:69483567 | C | G | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.97-124C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483567 | |||||||
| chr10:69483637 | G | T | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.97-54G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 1/7 | chr10 | 69483637 | |||||||
| chr10:69483904 | G | A | 1 | a0005c0005t0001g0036 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.282+28G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69483904 | |||||||
| chr10:69484082 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0005g0144 |
3 | HG01496.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.282+206G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484082 | |||||||
| chr10:69484289 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.282+413T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484289 | |||||||
| chr10:69484314 | G | A | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.282+438G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484314 | |||||||
| chr10:69484467 | G | T | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.282+591G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484467 | |||||||
| chr10:69484472 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.282+596G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484472 | |||||||
| chr10:69484595 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
71 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.283-546G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484595 | |||||||
| chr10:69484639 | G | A | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.283-502G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484639 | |||||||
| chr10:69484705 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283-436C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484705 | |||||||
| chr10:69484717 | G | C | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.283-424G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484717 | |||||||
| chr10:69484767 | A | G | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283-374A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484767 | |||||||
| chr10:69484823 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.283-318G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484823 | |||||||
| chr10:69484858 | C | T | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.283-283C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484858 | |||||||
| chr10:69484982 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283-159C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69484982 | |||||||
| chr10:69485031 | C | T | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.283-110C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69485031 | |||||||
| chr10:69485076 | C | A | 136 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(133): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.283-65C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69485076 | |||||||
| chr10:69485106 | C | T | 4 | a0001c0001t0002g0187 a0001c0001t0002g0201 a0001c0001t0002g0203 others(1): Show |
4 | HG02622.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-35C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 2/7 | chr10 | 69485106 | |||||||
| chr10:69485494 | G | A | 1 | a0001c0001t0004g0107 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.357+279G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485494 | |||||||
| chr10:69485520 | T | C | 17 | a0001c0001t0001g0246 a0001c0001t0003g0251 a0001c0001t0004g0015 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+305T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485520 | |||||||
| chr10:69485542 | A | G | 136 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(133): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.357+327A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485542 | |||||||
| chr10:69485682 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.357+467G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485682 | |||||||
| chr10:69485694 | T | C | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.357+479T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485694 | |||||||
| chr10:69485759 | G | T | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.357+544G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485759 | |||||||
| chr10:69485775 | GT | G | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+561delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485775 | |||||||
| chr10:69485776 | TG | T | 165 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(162): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.357+567delG | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69485776 | ||||||
| chr10:69485777 | G | C | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+562G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485777 | |||||||
| chr10:69485779 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+564G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485779 | |||||||
| chr10:69485861 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.357+646A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485861 | |||||||
| chr10:69485898 | C | A | 1 | a0001c0001t0003g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.357+683C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485898 | |||||||
| chr10:69485943 | A | C | 1 | a0001c0001t0003g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.357+728A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69485943 | |||||||
| chr10:69486146 | C | T | 137 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(134): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.357+931C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486146 | |||||||
| chr10:69486162 | T | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+947T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486162 | |||||||
| chr10:69486176 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.357+961C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486176 | |||||||
| chr10:69486186 | G | T | 6 | a0001c0001t0004g0253 a0001c0001t0004g0255 a0001c0001t0004g0256 others(3): Show |
6 | HG01261.hp1 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+971G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486186 | |||||||
| chr10:69486297 | G | A | 1 | a0001c0001t0012g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.357+1082G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486297 | |||||||
| chr10:69486424 | CT | C | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+1218delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69486424 | ||||||
| chr10:69486433 | T | A | 1 | a0001c0001t0016g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.357+1218T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486433 | |||||||
| chr10:69486501 | CAGTCAT | C | 40 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(37): Show |
40 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+1289_357+1294d others(8): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69486501 | ||||||
| chr10:69486548 | C | T | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+1333C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486548 | |||||||
| chr10:69486618 | T | TTCAGCAG others(299): Show |
1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+1418_357+1419i others(308): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69486618 | ||||||
| chr10:69486630 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.357+1415T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486630 | |||||||
| chr10:69486664 | T | C | 1 | a0001c0001t0015g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.357+1449T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486664 | |||||||
| chr10:69486676 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1461C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486676 | |||||||
| chr10:69486685 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1470C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486685 | |||||||
| chr10:69486713 | A | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1498A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486713 | |||||||
| chr10:69486824 | A | G | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+1609A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486824 | |||||||
| chr10:69486873 | C | G | 1 | a0001c0001t0003g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.357+1658C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486873 | |||||||
| chr10:69486879 | G | A | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+1664G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486879 | |||||||
| chr10:69486884 | C | T | 2 | a0002c0002t0002g0013 a0002c0002t0002g0140 |
3 | HG01891.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.357+1669C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486884 | |||||||
| chr10:69486891 | C | T | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.357+1676C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69486891 | |||||||
| chr10:69487089 | C | T | 14 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1874C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487089 | |||||||
| chr10:69487113 | G | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+1898G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487113 | |||||||
| chr10:69487168 | C | G | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1953C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487168 | |||||||
| chr10:69487185 | C | T | 40 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(37): Show |
40 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+1970C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487185 | |||||||
| chr10:69487293 | A | G | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+2078A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487293 | |||||||
| chr10:69487307 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+2092C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487307 | |||||||
| chr10:69487528 | G | A | 2 | a0001c0001t0001g0267 a0003c0004t0007g0272 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.357+2313G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487528 | |||||||
| chr10:69487653 | T | C | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+2438T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487653 | |||||||
| chr10:69487803 | T | A | 40 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(37): Show |
40 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+2588T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487803 | |||||||
| chr10:69487835 | T | C | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+2620T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487835 | |||||||
| chr10:69487869 | G | A | 23 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(20): Show |
23 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.357+2654G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487869 | |||||||
| chr10:69487911 | T | C | 40 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(37): Show |
40 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+2696T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487911 | |||||||
| chr10:69487911 | T | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.357+2696T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487911 | |||||||
| chr10:69487955 | C | T | 8 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+2740C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487955 | |||||||
| chr10:69487958 | C | T | 52 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.357+2743C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69487958 | |||||||
| chr10:69488052 | A | T | 1 | a0001c0001t0003g0200 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.357+2837A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488052 | |||||||
| chr10:69488164 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+2949G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488164 | |||||||
| chr10:69488292 | G | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
41 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.357+3077G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488292 | |||||||
| chr10:69488472 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+3257G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488472 | |||||||
| chr10:69488488 | A | C | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+3273A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488488 | |||||||
| chr10:69488491 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+3276G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488491 | |||||||
| chr10:69488493 | C | G | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+3278C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488493 | |||||||
| chr10:69488539 | C | A | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+3324C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488539 | |||||||
| chr10:69488625 | C | T | 12 | a0001c0001t0002g0034 a0001c0001t0002g0064 a0001c0001t0002g0065 others(9): Show |
12 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+3410C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488625 | |||||||
| chr10:69488638 | G | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0108 others(11): Show |
14 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.357+3423G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488638 | |||||||
| chr10:69488877 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 |
3 | HG01891.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.357+3662G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69488877 | |||||||
| chr10:69489065 | T | G | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+3850T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489065 | |||||||
| chr10:69489068 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
61 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.357+3853A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489068 | |||||||
| chr10:69489137 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+3922G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489137 | |||||||
| chr10:69489159 | A | G | 2 | a0001c0001t0003g0037 a0001c0001t0003g0045 |
2 | NA19004.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.357+3944A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489159 | |||||||
| chr10:69489198 | C | T | 9 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(6): Show |
9 | HG02717.hp2 HG02809.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+3983C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489198 | |||||||
| chr10:69489249 | C | G | 95 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(92): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.357+4034C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489249 | |||||||
| chr10:69489297 | G | A | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+4082G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489297 | |||||||
| chr10:69489388 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0006g0023 |
2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.357+4173C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489388 | |||||||
| chr10:69489389 | G | A | 41 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(38): Show |
41 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.357+4174G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489389 | |||||||
| chr10:69489398 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.357+4183G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489398 | |||||||
| chr10:69489569 | G | C | 43 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(40): Show |
52 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.357+4354G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489569 | |||||||
| chr10:69489656 | A | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0003g0001 |
5 | HG01975.hp1 HG01978.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+4441A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489656 | |||||||
| chr10:69489690 | C | G | 7 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0062 others(4): Show |
9 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+4475C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489690 | |||||||
| chr10:69489741 | G | A | 9 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+4526G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489741 | |||||||
| chr10:69489761 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.357+4546C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489761 | |||||||
| chr10:69489796 | T | C | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4581T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489796 | |||||||
| chr10:69489797 | G | T | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0078 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4582G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489797 | |||||||
| chr10:69489831 | C | T | 9 | a0001c0001t0002g0187 a0001c0001t0002g0273 a0001c0001t0002g0275 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+4616C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489831 | |||||||
| chr10:69489911 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.357+4696C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69489911 | |||||||
| chr10:69490052 | C | T | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.357+4837C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490052 | |||||||
| chr10:69490194 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+4979C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490194 | |||||||
| chr10:69490230 | A | G | 1 | a0001c0001t0004g0286 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.357+5015A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490230 | |||||||
| chr10:69490274 | G | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0106 others(3): Show |
6 | NA18941.hp1 NA18944.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+5059G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490274 | |||||||
| chr10:69490282 | C | T | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+5067C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490282 | |||||||
| chr10:69490401 | T | G | 39 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(36): Show |
39 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.357+5186T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490401 | |||||||
| chr10:69490402 | G | A | 39 | a0001c0001t0001g0240 a0001c0001t0002g0021 a0001c0001t0002g0032 others(36): Show |
39 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.357+5187G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490402 | |||||||
| chr10:69490433 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.358-5161A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490433 | |||||||
| chr10:69490523 | A | C | 136 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(133): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.358-5071A>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490523 | |||||||
| chr10:69490563 | A | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.358-5031A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490563 | |||||||
| chr10:69490581 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.358-5013C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490581 | |||||||
| chr10:69490587 | A | G | 177 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(174): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.358-5007A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490587 | |||||||
| chr10:69490922 | C | T | 3 | a0001c0001t0005g0005 a0001c0001t0005g0057 a0001c0001t0005g0152 |
5 | HG02683.hp1 HG02738.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-4672C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490922 | |||||||
| chr10:69490942 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.358-4652T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490942 | |||||||
| chr10:69490985 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-4609C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69490985 | |||||||
| chr10:69491044 | G | A | 1 | a0001c0001t0007g0242 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.358-4550G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491044 | |||||||
| chr10:69491051 | G | A | 8 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-4543G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491051 | |||||||
| chr10:69491170 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.358-4424C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491170 | |||||||
| chr10:69491233 | T | A | 3 | a0001c0001t0005g0002 a0001c0001t0005g0149 a0001c0001t0005g0160 |
6 | HG00639.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-4361T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491233 | |||||||
| chr10:69491237 | G | C | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-4357G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491237 | |||||||
| chr10:69491252 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.358-4342C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491252 | |||||||
| chr10:69491473 | C | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02717.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.358-4121C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491473 | |||||||
| chr10:69491505 | G | A | 8 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-4089G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491505 | |||||||
| chr10:69491530 | T | TTGTGTGT others(5): Show |
316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(313): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.358-4058_358-4047d others(14): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69491530 | ||||||
| chr10:69491628 | A | G | 51 | a0001c0001t0001g0246 a0001c0001t0001g0293 a0001c0001t0001g0300 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.358-3966A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491628 | |||||||
| chr10:69491716 | C | T | 17 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(14): Show |
17 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.358-3878C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491716 | |||||||
| chr10:69491744 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.358-3850G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491744 | |||||||
| chr10:69491814 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.358-3780G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491814 | |||||||
| chr10:69491849 | G | A | 2 | a0001c0001t0003g0229 a0001c0001t0003g0230 |
2 | NA18949.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.358-3745G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491849 | |||||||
| chr10:69491851 | C | T | 8 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0082 others(5): Show |
8 | HG02717.hp2 HG02809.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-3743C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491851 | |||||||
| chr10:69491945 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.358-3649C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69491945 | |||||||
| chr10:69492136 | G | T | 1 | a0001c0001t0022g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.358-3458G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492136 | |||||||
| chr10:69492137 | G | T | 1 | a0001c0001t0022g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.358-3457G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492137 | |||||||
| chr10:69492242 | A | G | 1 | a0001c0001t0004g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.358-3352A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492242 | |||||||
| chr10:69492287 | C | T | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.358-3307C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492287 | |||||||
| chr10:69492365 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.358-3229C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492365 | |||||||
| chr10:69492372 | C | T | 5 | a0001c0001t0002g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(2): Show |
5 | HG00639.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-3222C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492372 | |||||||
| chr10:69492450 | C | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.358-3144C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492450 | |||||||
| chr10:69492552 | T | C | 1 | a0001c0001t0023g0077 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.358-3042T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492552 | |||||||
| chr10:69492637 | A | AGGAGGCG others(11): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0003g0169 |
3 | HG00609.hp2 NA18961.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.358-2932_358-2915d others(20): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69492637 | ||||||
| chr10:69492637 | AGGAGGCG others(11): Show |
A | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-2932_358-2915d others(20): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69492637 | ||||||
| chr10:69492662 | G | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG00544.hp2 HG02083.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-2932G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492662 | |||||||
| chr10:69492755 | T | G | 3 | a0001c0001t0004g0151 a0001c0001t0004g0153 a0001c0001t0012g0154 |
3 | HG02027.hp2 NA18955.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.358-2839T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492755 | |||||||
| chr10:69492777 | A | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358-2817A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492777 | |||||||
| chr10:69492893 | G | A | 16 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(13): Show |
16 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.358-2701G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492893 | |||||||
| chr10:69492950 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.358-2644C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492950 | |||||||
| chr10:69492984 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.358-2610C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492984 | |||||||
| chr10:69492998 | G | A | 137 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(134): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.358-2596G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69492998 | |||||||
| chr10:69493115 | C | T | 1 | a0001c0001t0007g0137 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.358-2479C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493115 | |||||||
| chr10:69493136 | C | T | 8 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-2458C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493136 | |||||||
| chr10:69493189 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0155 others(19): Show |
29 | HG00280.hp2 HG00639.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.358-2405C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493189 | |||||||
| chr10:69493295 | G | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(93): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.358-2299G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493295 | |||||||
| chr10:69493295 | G | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-2299G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493295 | |||||||
| chr10:69493296 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.358-2298C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493296 | |||||||
| chr10:69493297 | G | A | 8 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-2297G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493297 | |||||||
| chr10:69493391 | C | G | 22 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(19): Show |
22 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.358-2203C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493391 | |||||||
| chr10:69493403 | C | T | 16 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(13): Show |
16 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.358-2191C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493403 | |||||||
| chr10:69493442 | C | T | 22 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(19): Show |
22 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.358-2152C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493442 | |||||||
| chr10:69493470 | C | CT | 71 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0150 others(68): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.358-2104dupT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69493470 | ||||||
| chr10:69493470 | C | CTT | 48 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp2 HG01106.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.358-2105_358-2104d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69493470 | ||||||
| chr10:69493470 | CT | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0221 a0001c0001t0002g0046 others(8): Show |
11 | HG00639.hp2 HG01168.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.358-2104delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69493470 | ||||||
| chr10:69493470 | CTT | C | 11 | a0001c0001t0001g0240 a0001c0001t0002g0034 a0001c0001t0002g0064 others(8): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-2105_358-2104d others(4): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69493470 | ||||||
| chr10:69493521 | A | G | 137 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(134): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.358-2073A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493521 | |||||||
| chr10:69493597 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-1997C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493597 | |||||||
| chr10:69493715 | G | T | 1 | a0001c0001t0004g0112 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.358-1879G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493715 | |||||||
| chr10:69493890 | C | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0032 a0001c0001t0002g0265 others(11): Show |
14 | HG01106.hp1 HG01243.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-1704C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493890 | |||||||
| chr10:69493906 | C | T | 1 | a0001c0001t0003g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.358-1688C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493906 | |||||||
| chr10:69493979 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.358-1615T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69493979 | |||||||
| chr10:69494368 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0003g0004 |
5 | NA18939.hp1 NA18947.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-1226T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494368 | |||||||
| chr10:69494606 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0003g0157 |
2 | HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.358-988C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494606 | |||||||
| chr10:69494651 | T | TA | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0081 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358-941dupA | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 69494651 | ||||||
| chr10:69494662 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0012g0249 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.358-932G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494662 | |||||||
| chr10:69494663 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.358-931G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494663 | |||||||
| chr10:69494765 | C | T | 41 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0164 others(38): Show |
43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.358-829C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494765 | |||||||
| chr10:69494985 | A | G | 1 | a0001c0001t0024g0313 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.358-609A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69494985 | |||||||
| chr10:69495009 | G | A | 31 | a0001c0001t0004g0043 a0001c0001t0004g0051 a0001c0001t0004g0052 others(28): Show |
31 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.358-585G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495009 | |||||||
| chr10:69495077 | A | G | 8 | a0001c0001t0002g0021 a0001c0001t0002g0080 a0001c0001t0002g0145 others(5): Show |
8 | HG00140.hp1 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-517A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495077 | |||||||
| chr10:69495212 | C | T | 6 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(3): Show |
6 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-382C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495212 | |||||||
| chr10:69495334 | C | T | 135 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0032 others(132): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.358-260C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495334 | |||||||
| chr10:69495448 | G | A | 1 | a0001c0001t0006g0238 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.358-146G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495448 | |||||||
| chr10:69495457 | G | A | 3 | a0001c0001t0006g0167 a0001c0001t0006g0217 a0001c0001t0006g0238 |
3 | HG02886.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.358-137G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495457 | |||||||
| chr10:69495483 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.358-111C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495483 | |||||||
| chr10:69495528 | G | A | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-66G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495528 | |||||||
| chr10:69495549 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0003g0133 a0001c0001t0014g0131 |
3 | HG00438.hp2 NA18982.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.358-45G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 3/7 | chr10 | 69495549 | |||||||
| chr10:69495907 | A | G | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+218A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69495907 | |||||||
| chr10:69495991 | T | C | 53 | a0001c0001t0004g0015 a0001c0001t0004g0026 a0001c0001t0004g0112 others(50): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.453+302T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69495991 | |||||||
| chr10:69496155 | T | G | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+466T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496155 | |||||||
| chr10:69496247 | T | A | 31 | a0001c0001t0004g0043 a0001c0001t0004g0051 a0001c0001t0004g0052 others(28): Show |
31 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+558T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496247 | |||||||
| chr10:69496263 | T | A | 1 | a0001c0001t0003g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.453+574T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496263 | |||||||
| chr10:69496320 | C | CAAT | 43 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0002g0032 others(40): Show |
45 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+680_453+682dup others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | C | CAATAAT | 29 | a0001c0001t0002g0021 a0001c0001t0002g0081 a0001c0001t0002g0097 others(26): Show |
33 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.453+677_453+682dup others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | C | CAATAATA others(2): Show |
5 | a0001c0001t0001g0224 a0001c0001t0002g0215 a0001c0001t0004g0043 others(2): Show |
5 | HG00597.hp2 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+674_453+682dup others(9): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | C | CAATAATA others(5): Show |
1 | a0001c0001t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.453+671_453+682dup others(12): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | C | CAATAATA others(8): Show |
1 | a0001c0001t0002g0279 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.453+668_453+682dup others(15): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | CAAT | C | 51 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.453+680_453+682del others(3): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | CAATAAT | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0031 others(20): Show |
25 | HG00280.hp2 HG00621.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.453+677_453+682del others(6): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | CAATAATA others(2): Show |
C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
124 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.453+674_453+682del others(9): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | CAATAATA others(5): Show |
C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0115 others(9): Show |
14 | HG00597.hp1 HG00609.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+671_453+682del others(12): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496320 | CAATAATA others(8): Show |
C | 6 | a0001c0001t0003g0172 a0001c0001t0008g0027 a0001c0001t0008g0028 others(3): Show |
6 | HG02257.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+668_453+682del others(15): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 69496320 | ||||||
| chr10:69496442 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.453+753C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496442 | |||||||
| chr10:69496452 | T | C | 10 | a0001c0001t0002g0020 a0001c0001t0002g0039 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+763T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496452 | |||||||
| chr10:69496744 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0003g0169 |
2 | NA18961.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.453+1055T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496744 | |||||||
| chr10:69496883 | T | C | 5 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+1194T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496883 | |||||||
| chr10:69496927 | A | G | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+1238A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69496927 | |||||||
| chr10:69497352 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | NA18941.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.454-928G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497352 | |||||||
| chr10:69497362 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02523.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.454-918C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497362 | |||||||
| chr10:69497458 | G | A | 5 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0070 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-822G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497458 | |||||||
| chr10:69497575 | A | G | 32 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(29): Show |
38 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.454-705A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497575 | |||||||
| chr10:69497742 | G | C | 2 | a0001c0001t0004g0124 a0001c0001t0004g0286 |
2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.454-538G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497742 | |||||||
| chr10:69497871 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.454-409G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497871 | |||||||
| chr10:69497969 | C | T | 1 | a0003c0004t0007g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454-311C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69497969 | |||||||
| chr10:69498031 | C | G | 1 | a0001c0001t0003g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.454-249C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 4/7 | chr10 | 69498031 | |||||||
| chr10:69498477 | T | C | 1 | a0003c0003t0007g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570+81T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498477 | |||||||
| chr10:69498489 | G | C | 1 | a0001c0001t0002g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+93G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498489 | |||||||
| chr10:69498531 | G | A | 12 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(9): Show |
12 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+135G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498531 | |||||||
| chr10:69498553 | G | A | 7 | a0001c0001t0002g0016 a0001c0001t0002g0187 a0001c0001t0002g0201 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+157G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498553 | |||||||
| chr10:69498628 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.570+232A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498628 | |||||||
| chr10:69498805 | C | T | 4 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+409C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498805 | |||||||
| chr10:69498930 | G | T | 35 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(32): Show |
41 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.570+534G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69498930 | |||||||
| chr10:69499108 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.570+712C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499108 | |||||||
| chr10:69499166 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.570+770T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499166 | |||||||
| chr10:69499179 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0108 |
3 | HG02809.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.570+783G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499179 | |||||||
| chr10:69499289 | C | T | 1 | a0001c0001t0003g0123 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.570+893C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499289 | |||||||
| chr10:69499302 | C | T | 35 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(32): Show |
41 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.570+906C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499302 | |||||||
| chr10:69499303 | G | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0080 a0001c0001t0002g0187 others(2): Show |
5 | HG02622.hp1 HG02717.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+907G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499303 | |||||||
| chr10:69499515 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.570+1119T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499515 | |||||||
| chr10:69499639 | A | T | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.570+1243A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499639 | |||||||
| chr10:69499687 | G | T | 1 | a0001c0001t0004g0255 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.570+1291G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499687 | |||||||
| chr10:69499765 | G | A | 4 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1369G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499765 | |||||||
| chr10:69499837 | G | A | 4 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1441G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499837 | |||||||
| chr10:69499913 | C | G | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.570+1517C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499913 | |||||||
| chr10:69499964 | A | T | 4 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1568A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499964 | |||||||
| chr10:69499996 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+1600G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69499996 | |||||||
| chr10:69500501 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0121 others(1): Show |
6 | NA18939.hp1 NA18947.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+2105G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69500501 | |||||||
| chr10:69500517 | A | G | 2 | a0001c0001t0015g0079 a0001c0001t0015g0101 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.570+2121A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69500517 | |||||||
| chr10:69500536 | T | C | 35 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(32): Show |
41 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.570+2140T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69500536 | |||||||
| chr10:69500651 | T | G | 14 | a0001c0001t0007g0137 a0001c0001t0007g0241 a0001c0001t0007g0242 others(11): Show |
14 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.570+2255T>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69500651 | |||||||
| chr10:69501039 | G | A | 2 | a0001c0001t0015g0079 a0001c0001t0015g0101 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.570+2643G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501039 | |||||||
| chr10:69501093 | C | T | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.570+2697C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501093 | |||||||
| chr10:69501163 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.570+2767C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501163 | |||||||
| chr10:69501166 | G | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02523.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.570+2770G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501166 | |||||||
| chr10:69501201 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.570+2805G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501201 | |||||||
| chr10:69501202 | G | A | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.570+2806G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501202 | |||||||
| chr10:69501241 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.570+2845G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501241 | |||||||
| chr10:69501251 | A | G | 6 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(3): Show |
6 | HG01433.hp2 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+2855A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501251 | |||||||
| chr10:69501338 | G | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0057 a0001c0001t0005g0152 |
5 | HG02683.hp1 HG02738.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+2942G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501338 | |||||||
| chr10:69501591 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.571-2847C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501591 | |||||||
| chr10:69501674 | A | G | 12 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(9): Show |
12 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-2764A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501674 | |||||||
| chr10:69501738 | C | T | 13 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(10): Show |
19 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.571-2700C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501738 | |||||||
| chr10:69501773 | A | G | 2 | a0001c0001t0003g0218 a0001c0001t0003g0251 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.571-2665A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501773 | |||||||
| chr10:69501902 | A | G | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.571-2536A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501902 | |||||||
| chr10:69501960 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0187 a0001c0001t0002g0201 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-2478C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501960 | |||||||
| chr10:69501985 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-2453G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69501985 | |||||||
| chr10:69502088 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.571-2350G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502088 | |||||||
| chr10:69502098 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.571-2340T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502098 | |||||||
| chr10:69502117 | TCAGCAGA others(6): Show |
T | 1 | a0001c0001t0021g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.571-2304_571-2292d others(15): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 69502117 | ||||||
| chr10:69502202 | T | C | 5 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0070 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-2236T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502202 | |||||||
| chr10:69502292 | G | T | 119 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.571-2146G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502292 | |||||||
| chr10:69502412 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0232 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.571-2026C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502412 | |||||||
| chr10:69502576 | TG | T | 27 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(24): Show |
33 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.571-1858delG | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 69502576 | ||||||
| chr10:69502639 | C | G | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.571-1799C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69502639 | |||||||
| chr10:69503067 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0187 a0001c0001t0002g0201 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1371C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503067 | |||||||
| chr10:69503068 | G | A | 42 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0032 others(39): Show |
43 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-1370G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503068 | |||||||
| chr10:69503100 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-1338T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503100 | |||||||
| chr10:69503243 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.571-1195A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503243 | |||||||
| chr10:69503261 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.571-1177G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503261 | |||||||
| chr10:69503285 | C | T | 4 | a0001c0001t0010g0252 a0001c0001t0010g0257 a0001c0001t0010g0262 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1153C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503285 | |||||||
| chr10:69503305 | T | A | 6 | a0001c0001t0004g0253 a0001c0001t0004g0255 a0001c0001t0004g0256 others(3): Show |
6 | HG01261.hp1 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1133T>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503305 | |||||||
| chr10:69503344 | C | T | 2 | a0001c0001t0015g0079 a0001c0001t0015g0101 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.571-1094C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503344 | |||||||
| chr10:69503345 | G | A | 23 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(20): Show |
29 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-1093G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503345 | |||||||
| chr10:69503384 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.571-1054C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503384 | |||||||
| chr10:69503508 | C | T | 116 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.571-930C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503508 | |||||||
| chr10:69503552 | G | A | 4 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0205 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-886G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503552 | |||||||
| chr10:69503582 | C | T | 2 | a0001c0001t0001g0292 a0005c0005t0001g0036 |
2 | HG02129.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.571-856C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503582 | |||||||
| chr10:69503645 | G | A | 27 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(24): Show |
33 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.571-793G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503645 | |||||||
| chr10:69503647 | G | A | 116 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.571-791G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503647 | |||||||
| chr10:69503654 | G | A | 4 | a0001c0001t0002g0034 a0001c0001t0002g0064 a0001c0001t0002g0065 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-784G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503654 | |||||||
| chr10:69503662 | G | A | 7 | a0001c0001t0002g0016 a0001c0001t0002g0187 a0001c0001t0002g0201 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-776G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503662 | |||||||
| chr10:69503668 | G | A | 23 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(20): Show |
29 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-770G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503668 | |||||||
| chr10:69503696 | G | T | 34 | a0001c0001t0004g0043 a0001c0001t0004g0051 a0001c0001t0004g0052 others(31): Show |
34 | HG00642.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.571-742G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503696 | |||||||
| chr10:69503699 | G | T | 14 | a0001c0001t0004g0015 a0001c0001t0004g0026 a0001c0001t0004g0112 others(11): Show |
15 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.571-739G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503699 | |||||||
| chr10:69503734 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-704C>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503734 | |||||||
| chr10:69503849 | C | T | 42 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0032 others(39): Show |
43 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-589C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503849 | |||||||
| chr10:69503850 | G | A | 21 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(18): Show |
27 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-588G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503850 | |||||||
| chr10:69503906 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-532A>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503906 | |||||||
| chr10:69503944 | C | T | 1 | a0001c0001t0004g0317 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.571-494C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503944 | |||||||
| chr10:69503956 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0020g0270 |
3 | HG02647.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.571-482A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503956 | |||||||
| chr10:69503961 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.571-477T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503961 | |||||||
| chr10:69503980 | G | T | 12 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(9): Show |
12 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-458G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503980 | |||||||
| chr10:69503985 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | HG00639.hp2 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.571-453G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69503985 | |||||||
| chr10:69504189 | AG | A | 116 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.571-245delG | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 69504189 | ||||||
| chr10:69504201 | C | A | 10 | a0001c0001t0007g0137 a0001c0001t0007g0241 a0001c0001t0007g0242 others(7): Show |
10 | HG00408.hp2 HG00597.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-237C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | chr10 | 69504201 | |||||||
| chr10:69504235 | G | GT | 117 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(114): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.571-197dupT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 69504235 | ||||||
| chr10:69504525 | T | C | 12 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(9): Show |
12 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.618+40T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504525 | |||||||
| chr10:69504565 | G | T | 1 | a0001c0001t0018g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.618+80G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504565 | |||||||
| chr10:69504569 | G | A | 116 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0020 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.618+84G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504569 | |||||||
| chr10:69504569 | G | C | 1 | a0001c0001t0003g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618+84G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504569 | |||||||
| chr10:69504576 | G | T | 6 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(3): Show |
6 | HG01433.hp2 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+91G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504576 | |||||||
| chr10:69504628 | G | C | 1 | a0001c0001t0002g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.618+143G>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504628 | |||||||
| chr10:69504680 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | NA18942.hp1 NA18949.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+195G>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504680 | |||||||
| chr10:69504764 | C | T | 5 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0070 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+279C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504764 | |||||||
| chr10:69504765 | G | A | 4 | a0001c0001t0002g0034 a0001c0001t0002g0064 a0001c0001t0002g0065 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+280G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504765 | |||||||
| chr10:69504862 | G | A | 12 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(9): Show |
12 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.618+377G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69504862 | |||||||
| chr10:69505063 | T | C | 7 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0107 others(4): Show |
7 | HG02027.hp1 NA18939.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+578T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505063 | |||||||
| chr10:69505090 | C | T | 6 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0087 others(3): Show |
8 | HG01891.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.618+605C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505090 | |||||||
| chr10:69505275 | T | C | 10 | a0001c0001t0007g0137 a0001c0001t0007g0241 a0001c0001t0007g0242 others(7): Show |
10 | HG00408.hp2 HG00597.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+790T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505275 | |||||||
| chr10:69505303 | G | A | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.618+818G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505303 | |||||||
| chr10:69505314 | A | G | 7 | a0001c0001t0002g0016 a0001c0001t0002g0187 a0001c0001t0002g0201 others(4): Show |
7 | HG02622.hp1 HG02647.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-810A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505314 | |||||||
| chr10:69505463 | C | A | 1 | a0001c0001t0018g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.619-661C>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505463 | |||||||
| chr10:69505472 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.619-652A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505472 | |||||||
| chr10:69505524 | ACTTCTGG others(6): Show |
A | 39 | a0001c0001t0005g0002 a0001c0001t0005g0005 a0001c0001t0005g0009 others(36): Show |
45 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.619-596_619-584del others(13): Show |
TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 69505524 | ||||||
| chr10:69505567 | C | CT | 6 | a0001c0001t0001g0089 a0001c0001t0002g0066 a0001c0001t0002g0215 others(3): Show |
6 | HG00639.hp2 HG02280.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-542dupT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 69505567 | ||||||
| chr10:69505567 | CT | C | 30 | a0001c0001t0001g0138 a0001c0001t0001g0300 a0001c0001t0005g0002 others(27): Show |
36 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.619-542delT | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 69505567 | ||||||
| chr10:69505703 | C | T | 7 | a0001c0001t0008g0019 a0001c0001t0008g0027 a0001c0001t0008g0028 others(4): Show |
7 | HG01433.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-421C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505703 | |||||||
| chr10:69505769 | T | C | 42 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0032 others(39): Show |
43 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.619-355T>C | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505769 | |||||||
| chr10:69505785 | A | G | 2 | a0001c0001t0004g0294 a0001c0001t0004g0298 |
2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.619-339A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505785 | |||||||
| chr10:69505853 | G | A | 5 | a0001c0001t0009g0067 a0001c0001t0009g0068 a0001c0001t0009g0070 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-271G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505853 | |||||||
| chr10:69505949 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0082 a0001c0001t0002g0083 others(6): Show |
9 | HG01070.hp2 HG01243.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-175A>G | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69505949 | |||||||
| chr10:69506070 | G | A | 2 | a0001c0001t0015g0079 a0001c0001t0015g0101 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.619-54G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69506070 | |||||||
| chr10:69506083 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0001g0109 others(3): Show |
6 | HG00544.hp2 NA18954.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-41C>T | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 6/7 | chr10 | 69506083 | |||||||
| chr10:69506666 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.736-163G>A | TSPAN15 | ENSG00000099282.10 | transcript | ENST00000373290.7 | protein_coding | 7/7 | chr10 | 69506666 |