Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81619 |
| ensemblid | ENSG00000108219.16 |
| hgncid | 23303 |
| symbol | TSPAN14 |
| name | tetraspanin 14 |
| refseq_nuc | NM_030927.4 |
| refseq_prot | NP_112189.2 |
| ensembl_nuc | ENST00000429989.8 |
| ensembl_prot | ENSP00000396270.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 80454310 |
| end | 80522631 |
| strand | + |
| ver | v1.2 |
| region | chr10:80454310-80522631 |
| region5000 | chr10:80449310-80527631 |
| regionname0 | TSPAN14_chr10_80454310_80522631 |
| regionname5000 | TSPAN14_chr10_80449310_80527631 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 810 | 233 | 72 | 62 | 46 | 12 | 39 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | ATGCA others(805): Show |
chr10 | 80449310 | 80527631 | ||
| a0001c0002 | 0/0 | 810 | 15 | 13 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | ATGCA others(805): Show |
chr10 | 80449310 | 80527631 | ||
| a0001c0003 | 0/0 | 810 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | ATGCA others(805): Show |
chr10 | 80449310 | 80527631 | ||
| a0001c0004 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | ATGCA others(805): Show |
chr10 | 80449310 | 80527631 | ||
| a0001c0005 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | ATGCA others(805): Show |
chr10 | 80449310 | 80527631 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5551 | 46 | 2 | 16 | 18 | 2 | 8 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0002 | 0/0 | 5551 | 33 | 18 | 6 | 1 | 1 | 7 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0003 | 1/0 | 5547 | 18 | 2 | 10 | 1 | 3 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5542): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0004 | 0/0 | 5553 | 16 | 0 | 1 | 12 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5548): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0006 | 0/0 | 5551 | 9 | 5 | 2 | 0 | 0 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0007 | 0/0 | 5553 | 8 | 3 | 1 | 1 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5548): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0008 | 0/0 | 5552 | 8 | 1 | 4 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0009 | 0/0 | 5552 | 6 | 3 | 1 | 0 | 0 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0010 | 0/0 | 5551 | 6 | 0 | 4 | 0 | 1 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0011 | 0/0 | 5550 | 6 | 0 | 2 | 0 | 2 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0012 | 0/0 | 5552 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0013 | 0/0 | 5551 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0014 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0015 | 0/0 | 5552 | 4 | 0 | 1 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0016 | 0/0 | 5551 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0017 | 0/0 | 5558 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5553): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0018 | 0/0 | 5551 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0019 | 0/0 | 5551 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0020 | 0/0 | 5551 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0022 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0023 | 0/0 | 5552 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0024 | 0/0 | 5551 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0025 | 0/0 | 5550 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0026 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0027 | 0/0 | 5551 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0028 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0029 | 0/0 | 5551 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0030 | 0/0 | 5551 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0031 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0032 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0033 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0034 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0035 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0036 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0037 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0038 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0039 | 0/0 | 5553 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5548): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0040 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5548): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0041 | 0/1 | 5547 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5542): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0042 | 0/0 | 5547 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5542): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0043 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0044 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0045 | 0/0 | 5552 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0046 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0047 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0048 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0049 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0050 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0051 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0052 | 0/0 | 5551 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0053 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5545): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0055 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0056 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0001t0057 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5541): Show |
chr10 | 80449310 | 80527631 |
| a0001c0002t0005 | 0/0 | 5553 | 11 | 9 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5548): Show |
chr10 | 80449310 | 80527631 |
| a0001c0002t0021 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0002t0054 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5549): Show |
chr10 | 80449310 | 80527631 |
| a0001c0003t0014 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0003t0018 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| a0001c0004t0009 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5547): Show |
chr10 | 80449310 | 80527631 |
| a0001c0005t0006 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | GAACT others(5546): Show |
chr10 | 80449310 | 80527631 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0011g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0011g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0015g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0015g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0015g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0016g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0016g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0017g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0017g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0019g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0019g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0020g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0020g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0022g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0022g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0022g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0024g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0024g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0025g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0025g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0026g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0027g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0027g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0028g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0028g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0029g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0029g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0030g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0031g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0032g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0033g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0034g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0035g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0036g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0037g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0038g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0039g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0040g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0041g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0042g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0043g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0044g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0045g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0046g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0047g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0048g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0049g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0050g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0051g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0052g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0053g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0055g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0056g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0001t0057g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0002t0054g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0003t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0003t0018g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0004t0009g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| a0001c0005t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0042 | g0048 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00140 | hp1 | a0001 | c0001 | t0025 | g0149 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0059 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0188 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00438 | hp1 | a0001 | c0001 | t0015 | g0193 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00438 | hp2 | a0001 | c0001 | t0015 | g0047 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00558 | hp1 | a0001 | c0001 | t0028 | g0225 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00558 | hp2 | a0001 | c0001 | t0028 | g0160 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0237 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00639 | hp2 | a0001 | c0001 | t0031 | g0141 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00642 | hp1 | a0001 | c0001 | t0046 | g0035 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00642 | hp2 | a0001 | c0002 | t0005 | g0094 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0190 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0124 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00741 | hp1 | a0001 | c0001 | t0011 | g0133 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG00741 | hp2 | a0001 | c0001 | t0045 | g0036 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01069 | hp1 | a0001 | c0001 | t0043 | g0029 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01070 | hp2 | a0001 | c0001 | t0044 | g0045 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01074 | hp2 | a0001 | c0001 | t0029 | g0167 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01081 | hp1 | a0001 | c0001 | t0020 | g0150 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0017 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0198 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01099 | hp2 | a0001 | c0001 | t0029 | g0176 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01109 | hp2 | a0001 | c0001 | t0020 | g0148 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0191 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01169 | hp2 | a0001 | c0001 | t0053 | g0135 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0143 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01243 | hp1 | a0001 | c0001 | t0033 | g0122 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01243 | hp2 | a0001 | c0001 | t0027 | g0092 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0034 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0007 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0147 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0066 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0115 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0076 | EUR | IBS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01884 | hp1 | a0001 | c0002 | t0021 | g0183 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01928 | hp1 | a0001 | c0001 | t0015 | g0010 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01975 | hp2 | a0001 | c0001 | t0010 | g0145 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01978 | hp1 | a0001 | c0001 | t0010 | g0142 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02015 | hp1 | a0001 | c0001 | t0055 | g0098 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0224 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02080 | hp1 | a0001 | c0001 | t0049 | g0157 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02145 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CDX | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02258 | hp1 | a0001 | c0001 | t0047 | g0212 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02258 | hp2 | a0001 | c0001 | t0050 | g0226 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0053 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0236 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02451 | hp2 | a0001 | c0001 | t0024 | g0241 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0228 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0222 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0054 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02622 | hp1 | a0001 | c0001 | t0048 | g0121 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0242 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02630 | hp1 | a0001 | c0001 | t0023 | g0014 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0119 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0162 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0052 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02723 | hp2 | a0001 | c0005 | t0006 | g0132 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02735 | hp1 | a0001 | c0001 | t0034 | g0022 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02738 | hp1 | a0001 | c0001 | t0030 | g0146 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02738 | hp2 | a0001 | c0001 | t0032 | g0067 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02809 | hp1 | a0001 | c0003 | t0018 | g0123 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0129 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0002 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0002 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0112 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0238 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02965 | hp2 | a0001 | c0001 | t0057 | g0118 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02970 | hp2 | a0001 | c0001 | t0019 | g0214 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0088 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03017 | hp1 | a0001 | c0001 | t0052 | g0012 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03041 | hp2 | a0001 | c0003 | t0014 | g0120 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0116 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0230 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0110 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0089 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0087 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03195 | hp1 | a0001 | c0001 | t0027 | g0093 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0244 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0125 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0018 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03492 | hp1 | a0001 | c0001 | t0020 | g0117 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03516 | hp1 | a0001 | c0001 | t0040 | g0079 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0057 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03540 | hp1 | a0001 | c0002 | t0005 | g0024 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03540 | hp2 | a0001 | c0001 | t0016 | g0223 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0213 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0161 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03688 | hp1 | a0001 | c0001 | t0011 | g0099 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03704 | hp1 | a0001 | c0001 | t0038 | g0074 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03704 | hp2 | a0001 | c0001 | t0039 | g0127 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0140 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03831 | hp2 | a0001 | c0004 | t0009 | g0096 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03927 | hp1 | a0001 | c0001 | t0011 | g0194 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0131 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04115 | hp2 | a0001 | c0001 | t0051 | g0058 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0075 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04184 | hp2 | a0001 | c0001 | t0015 | g0205 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0077 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04199 | hp2 | a0001 | c0001 | t0009 | g0071 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0104 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0068 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0109 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18522 | hp2 | a0001 | c0001 | t0022 | g0243 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0015 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18942 | hp2 | a0001 | c0001 | t0036 | g0114 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18947 | hp1 | a0001 | c0001 | t0026 | g0159 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0179 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18994 | hp1 | a0001 | c0001 | t0035 | g0221 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0055 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19030 | hp2 | a0001 | c0002 | t0054 | g0016 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19043 | hp2 | a0001 | c0002 | t0021 | g0182 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19063 | hp1 | a0001 | c0001 | t0026 | g0240 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19063 | hp2 | a0001 | c0001 | t0037 | g0101 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0239 | AFR | ASW | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ASW | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20752 | hp1 | a0001 | c0001 | t0011 | g0007 | EUR | TSI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20752 | hp2 | a0001 | c0001 | t0025 | g0187 | EUR | TSI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | GIH | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02109 | hp1 | a0001 | c0001 | t0056 | g0137 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02486 | hp1 | a0001 | c0002 | t0021 | g0185 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0081 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | USA | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | USA | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0056 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0041 | g0245 | REF | REF | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0037 | REF | REF | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:80489284 | C | T | 1 | a0001c0003 | 2 | HG02809.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.51C>T | p.Tyr17Tyr | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/9 | 130/5547 | 51/813 | 17/270 | chr10 | 80489284 | |||
| chr10:80509429 | C | T | 1 | a0001c0005 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.408C>T | p.Asp136Asp | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/9 | 487/5547 | 408/813 | 136/270 | chr10 | 80509429 | |||
| chr10:80516287 | T | C | 1 | a0001c0002 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
synonymous_variant | LOW | c.705T>C | p.Ile235Ile | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/9 | 784/5547 | 705/813 | 235/270 | chr10 | 80516287 | |||
| chr10:80516305 | C | T | 1 | a0001c0004 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.723C>T | p.Ile241Ile | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/9 | 802/5547 | 723/813 | 241/270 | chr10 | 80516305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:80518104 | G | A | 1 | a0001c0001t0023 | 2 | HG02630.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 128 | chr10 | 80518104 | ||||||
| chr10:80518293 | C | G | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*317C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 317 | chr10 | 80518293 | ||||||
| chr10:80518386 | G | A | 1 | a0001c0001t0030 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 410 | chr10 | 80518386 | ||||||
| chr10:80518407 | C | T | 1 | a0001c0001t0029 | 2 | HG01074.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*431C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 431 | chr10 | 80518407 | ||||||
| chr10:80518424 | T | C | 3 | a0001c0001t0010 a0001c0001t0031 a0001c0001t0032 |
8 | HG00140.hp2 HG00639.hp2 HG01192.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 448 | chr10 | 80518424 | ||||||
| chr10:80518469 | C | T | 1 | a0001c0001t0022 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*493C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 493 | chr10 | 80518469 | ||||||
| chr10:80518470 | G | A | 4 | a0001c0001t0018 a0001c0001t0024 a0001c0001t0033 others(1): Show |
6 | HG01243.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*494G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 494 | chr10 | 80518470 | ||||||
| chr10:80518704 | C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 728 | chr10 | 80518704 | ||||||
| chr10:80519063 | C | T | 1 | a0001c0001t0056 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1087C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1087 | chr10 | 80519063 | ||||||
| chr10:80519158 | T | G | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1182T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1182 | chr10 | 80519158 | ||||||
| chr10:80519174 | C | T | 1 | a0001c0001t0055 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1198 | chr10 | 80519174 | ||||||
| chr10:80519238 | A | T | 3 | a0001c0002t0005 a0001c0002t0021 a0001c0002t0054 |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1262A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1262 | chr10 | 80519238 | ||||||
| chr10:80519305 | G | C | 1 | a0001c0001t0035 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1329 | chr10 | 80519305 | ||||||
| chr10:80519314 | T | C | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0036 others(4): Show |
29 | HG00597.hp2 HG01175.hp2 HG02004.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1338T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1338 | chr10 | 80519314 | ||||||
| chr10:80519343 | G | T | 1 | a0001c0001t0053 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1367 | chr10 | 80519343 | ||||||
| chr10:80519362 | G | T | 1 | a0001c0001t0052 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1386 | chr10 | 80519362 | ||||||
| chr10:80519446 | C | G | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1470C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1470 | chr10 | 80519446 | ||||||
| chr10:80519514 | A | ATTT | 6 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0025 others(3): Show |
15 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1551dupTTT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | |||||
| chr10:80519514 | A | ATTTT | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(29): Show |
145 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1548_*1551dupTTTT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | |||||
| chr10:80519514 | A | ATTTTT | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
51 | HG00597.hp2 HG00735.hp1 HG01081.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1547_*1551dupTTTT others(1): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | |||||
| chr10:80519514 | A | ATTTTTT | 4 | a0001c0001t0040 a0001c0002t0005 a0001c0002t0021 others(1): Show |
16 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1546_*1551dupTTTT others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | |||||
| chr10:80519514 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1541_*1551dupTTTT others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | |||||
| chr10:80519571 | G | A | 1 | a0001c0001t0055 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1595 | chr10 | 80519571 | ||||||
| chr10:80519681 | A | G | 1 | a0001c0001t0042 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1705A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1705 | chr10 | 80519681 | ||||||
| chr10:80519787 | C | T | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1811C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1811 | chr10 | 80519787 | ||||||
| chr10:80519797 | A | G | 1 | a0001c0001t0050 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1821 | chr10 | 80519797 | ||||||
| chr10:80519801 | AT | A | 5 | a0001c0001t0026 a0001c0001t0037 a0001c0001t0044 others(2): Show |
6 | HG01070.hp2 HG01169.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1839delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1839 | INFO_REALIGN_3_PRIME | chr10 | 80519801 | |||||
| chr10:80519822 | C | G | 1 | a0001c0001t0049 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1846 | chr10 | 80519822 | ||||||
| chr10:80519844 | G | A | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1868 | chr10 | 80519844 | ||||||
| chr10:80519867 | G | A | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1891G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1891 | chr10 | 80519867 | ||||||
| chr10:80519894 | C | T | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1918C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1918 | chr10 | 80519894 | ||||||
| chr10:80520059 | T | C | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2083T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2083 | chr10 | 80520059 | ||||||
| chr10:80520171 | C | T | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(13): Show |
90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2195C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2195 | chr10 | 80520171 | ||||||
| chr10:80520204 | C | T | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(7): Show |
71 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2228 | chr10 | 80520204 | ||||||
| chr10:80520326 | A | G | 1 | a0001c0001t0024 | 2 | HG02451.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2350A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2350 | chr10 | 80520326 | ||||||
| chr10:80520381 | T | C | 1 | a0001c0001t0053 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2405T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2405 | chr10 | 80520381 | ||||||
| chr10:80520381 | T | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(53): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2405T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2405 | chr10 | 80520381 | ||||||
| chr10:80520384 | C | T | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(13): Show |
90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2408C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2408 | chr10 | 80520384 | ||||||
| chr10:80520432 | A | G | 3 | a0001c0002t0005 a0001c0002t0021 a0001c0002t0054 |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2456A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2456 | chr10 | 80520432 | ||||||
| chr10:80520543 | C | G | 4 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0048 others(1): Show |
9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2567C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2567 | chr10 | 80520543 | ||||||
| chr10:80520608 | A | G | 1 | a0001c0001t0027 | 2 | HG01243.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2632 | chr10 | 80520608 | ||||||
| chr10:80520631 | G | A | 2 | a0001c0001t0045 a0001c0001t0046 |
2 | HG00642.hp1 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2655G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2655 | chr10 | 80520631 | ||||||
| chr10:80520635 | C | T | 1 | a0001c0001t0039 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2659C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2659 | chr10 | 80520635 | ||||||
| chr10:80520795 | T | G | 3 | a0001c0002t0005 a0001c0002t0021 a0001c0002t0054 |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2819T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2819 | chr10 | 80520795 | ||||||
| chr10:80520954 | G | A | 1 | a0001c0001t0020 | 3 | HG01081.hp1 HG01109.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2978G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2978 | chr10 | 80520954 | ||||||
| chr10:80521445 | T | C | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3469T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3469 | chr10 | 80521445 | ||||||
| chr10:80521493 | T | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0036 others(4): Show |
29 | HG00597.hp2 HG01175.hp2 HG02004.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3517T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3517 | chr10 | 80521493 | ||||||
| chr10:80521684 | T | C | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3708T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3708 | chr10 | 80521684 | ||||||
| chr10:80521851 | G | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3875G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3875 | chr10 | 80521851 | ||||||
| chr10:80521852 | A | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3876A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3876 | chr10 | 80521852 | ||||||
| chr10:80521872 | C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3896C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3896 | chr10 | 80521872 | ||||||
| chr10:80521911 | G | GA | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(11): Show |
51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3954dupA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3955 | INFO_REALIGN_3_PRIME | chr10 | 80521911 | |||||
| chr10:80521911 | GA | G | 7 | a0001c0001t0018 a0001c0001t0024 a0001c0001t0028 others(4): Show |
12 | HG00558.hp1 HG00558.hp2 HG01243.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3954delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3954 | INFO_REALIGN_3_PRIME | chr10 | 80521911 | |||||
| chr10:80521914 | A | G | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3938A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3938 | chr10 | 80521914 | ||||||
| chr10:80521958 | C | T | 2 | a0001c0001t0012 a0001c0001t0023 |
8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3982C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3982 | chr10 | 80521958 | ||||||
| chr10:80522133 | C | T | 3 | a0001c0002t0005 a0001c0002t0021 a0001c0002t0054 |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4157C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4157 | chr10 | 80522133 | ||||||
| chr10:80522426 | G | A | 1 | a0001c0001t0019 | 3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4450G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4450 | chr10 | 80522426 | ||||||
| chr10:80522502 | C | A | 4 | a0001c0001t0004 a0001c0001t0036 a0001c0001t0037 others(1): Show |
19 | HG00597.hp2 HG02004.hp2 HG02074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4526C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4526 | chr10 | 80522502 | ||||||
| chr10:80522560 | A | G | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0016 others(2): Show |
13 | HG01433.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4584A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4584 | chr10 | 80522560 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:80454561 | C | A | 3 | a0001c0001t0001g0009 a0001c0001t0004g0008 a0001c0001t0015g0010 |
3 | HG01167.hp2 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-18+190C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454561 | |||||||
| chr10:80454696 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+325C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454696 | |||||||
| chr10:80454712 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0052g0012 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-18+341G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454712 | |||||||
| chr10:80454715 | G | T | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+344G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454715 | |||||||
| chr10:80454745 | G | A | 7 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(4): Show |
7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+374G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454745 | |||||||
| chr10:80454758 | C | G | 1 | a0001c0001t0024g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+387C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454758 | |||||||
| chr10:80454766 | C | T | 1 | a0001c0001t0026g0240 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-18+395C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454766 | |||||||
| chr10:80454788 | G | C | 1 | a0001c0001t0004g0021 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-18+417G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454788 | |||||||
| chr10:80454830 | A | C | 213 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0069 others(210): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18+459A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454830 | |||||||
| chr10:80454879 | C | T | 6 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0002t0005g0236 others(3): Show |
6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+508C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454879 | |||||||
| chr10:80454941 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+570C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454941 | |||||||
| chr10:80455036 | C | T | 168 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(165): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-18+665C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455036 | |||||||
| chr10:80455065 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(26): Show |
30 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+694G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455065 | |||||||
| chr10:80455121 | C | T | 13 | a0001c0001t0004g0021 a0001c0001t0004g0097 a0001c0001t0004g0100 others(10): Show |
13 | HG02015.hp1 HG03654.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+750C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455121 | |||||||
| chr10:80455207 | C | G | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+836C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455207 | |||||||
| chr10:80455290 | T | C | 1 | a0001c0001t0007g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+919T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455290 | |||||||
| chr10:80455532 | T | C | 174 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(171): Show |
178 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-18+1161T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455532 | |||||||
| chr10:80455868 | C | T | 1 | a0001c0001t0024g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+1497C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455868 | |||||||
| chr10:80455890 | C | T | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+1519C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455890 | |||||||
| chr10:80456046 | C | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+1675C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456046 | |||||||
| chr10:80456111 | A | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(25): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+1740A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456111 | |||||||
| chr10:80456137 | A | G | 1 | a0001c0001t0028g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+1766A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456137 | |||||||
| chr10:80456402 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(26): Show |
30 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+2031A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456402 | |||||||
| chr10:80456492 | A | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+2121A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456492 | |||||||
| chr10:80456552 | A | G | 10 | a0001c0001t0002g0073 a0001c0001t0007g0052 a0001c0001t0007g0075 others(7): Show |
10 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+2181A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456552 | |||||||
| chr10:80456926 | G | A | 124 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(121): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-18+2555G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456926 | |||||||
| chr10:80457271 | C | T | 6 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0002t0005g0236 others(3): Show |
6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+2900C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457271 | |||||||
| chr10:80457371 | T | G | 1 | a0001c0001t0024g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3000T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457371 | |||||||
| chr10:80457405 | T | C | 29 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(26): Show |
29 | HG01081.hp2 HG01175.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+3034T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457405 | |||||||
| chr10:80457435 | C | T | 5 | a0001c0001t0002g0072 a0001c0001t0009g0071 a0001c0001t0012g0018 others(2): Show |
5 | HG02698.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+3064C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457435 | |||||||
| chr10:80457656 | C | G | 1 | a0001c0001t0008g0224 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-18+3285C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457656 | |||||||
| chr10:80457673 | G | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+3302G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457673 | |||||||
| chr10:80457792 | C | T | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+3421C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457792 | |||||||
| chr10:80457874 | A | G | 1 | a0001c0001t0024g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3503A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457874 | |||||||
| chr10:80457953 | G | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+3582G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457953 | |||||||
| chr10:80457983 | T | C | 7 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(4): Show |
7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+3612T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457983 | |||||||
| chr10:80458011 | T | C | 6 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0016g0002 others(3): Show |
8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+3640T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458011 | |||||||
| chr10:80458118 | C | T | 10 | a0001c0001t0002g0073 a0001c0001t0007g0052 a0001c0001t0007g0075 others(7): Show |
10 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3747C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458118 | |||||||
| chr10:80458188 | G | A | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3817G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458188 | |||||||
| chr10:80458214 | A | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0035g0221 |
3 | HG01978.hp2 HG02293.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-18+3843A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458214 | |||||||
| chr10:80458238 | GAGGTGAC others(3): Show |
G | 138 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+3873_-18+3882d others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80458238 | ||||||
| chr10:80458343 | A | G | 6 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0002t0005g0236 others(3): Show |
6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3972A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458343 | |||||||
| chr10:80458350 | G | A | 1 | a0001c0001t0004g0097 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-18+3979G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458350 | |||||||
| chr10:80458350 | G | C | 151 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(148): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-18+3979G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458350 | |||||||
| chr10:80458399 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+4028C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458399 | |||||||
| chr10:80458629 | G | T | 19 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0002g0004 others(16): Show |
21 | HG00140.hp2 HG01123.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4258G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458629 | |||||||
| chr10:80458723 | G | C | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-18+4352G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458723 | |||||||
| chr10:80458766 | G | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4395G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458766 | |||||||
| chr10:80458882 | C | T | 1 | a0001c0001t0028g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+4511C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458882 | |||||||
| chr10:80458903 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0014g0053 a0001c0001t0014g0056 others(4): Show |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+4532C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458903 | |||||||
| chr10:80458916 | A | G | 5 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 others(2): Show |
5 | HG00099.hp1 HG00438.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+4545A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458916 | |||||||
| chr10:80458967 | AT | A | 19 | a0001c0001t0002g0073 a0001c0001t0003g0023 a0001c0001t0006g0111 others(16): Show |
19 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+4610delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80458967 | ||||||
| chr10:80459142 | A | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4771A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459142 | |||||||
| chr10:80459208 | T | C | 138 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+4837T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459208 | |||||||
| chr10:80459310 | T | C | 144 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(141): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-18+4939T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459310 | |||||||
| chr10:80459335 | C | T | 5 | a0001c0001t0006g0046 a0001c0001t0022g0242 a0001c0001t0022g0243 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+4964C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459335 | |||||||
| chr10:80459353 | A | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4982A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459353 | |||||||
| chr10:80459466 | G | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+5095G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459466 | |||||||
| chr10:80459501 | G | GT | 6 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0016g0002 others(3): Show |
8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5131dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80459501 | ||||||
| chr10:80459577 | C | G | 18 | a0001c0001t0002g0073 a0001c0001t0006g0111 a0001c0001t0006g0112 others(15): Show |
18 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+5206C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459577 | |||||||
| chr10:80459698 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-18+5327C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459698 | |||||||
| chr10:80459730 | C | T | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+5359C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459730 | |||||||
| chr10:80459783 | G | A | 6 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0016g0002 others(3): Show |
8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5412G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459783 | |||||||
| chr10:80459836 | C | T | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+5465C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459836 | |||||||
| chr10:80459928 | T | C | 1 | a0001c0001t0016g0002 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18+5557T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459928 | |||||||
| chr10:80460055 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-18+5684A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460055 | |||||||
| chr10:80460102 | T | C | 1 | a0001c0001t0051g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-18+5731T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460102 | |||||||
| chr10:80460115 | G | A | 2 | a0001c0002t0005g0024 a0001c0002t0005g0025 |
2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+5744G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460115 | |||||||
| chr10:80460272 | G | T | 1 | a0001c0001t0007g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18+5901G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460272 | |||||||
| chr10:80460503 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0036g0114 |
2 | NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-18+6132G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460503 | |||||||
| chr10:80460534 | C | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18942.hp1 NA18952.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-18+6163C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460534 | |||||||
| chr10:80460644 | C | G | 1 | a0001c0001t0019g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+6273C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460644 | |||||||
| chr10:80460722 | T | C | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+6351T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460722 | |||||||
| chr10:80460758 | C | T | 120 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0151 others(117): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-18+6387C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460758 | |||||||
| chr10:80460761 | G | C | 1 | a0001c0001t0024g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+6390G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460761 | |||||||
| chr10:80460841 | C | T | 213 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0069 others(210): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18+6470C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460841 | |||||||
| chr10:80460947 | G | A | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-18+6576G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460947 | |||||||
| chr10:80460960 | G | A | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+6589G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460960 | |||||||
| chr10:80461099 | T | G | 13 | a0001c0001t0004g0021 a0001c0001t0004g0097 a0001c0001t0004g0100 others(10): Show |
13 | HG02015.hp1 HG03654.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+6728T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461099 | |||||||
| chr10:80461146 | C | G | 11 | a0001c0001t0002g0073 a0001c0001t0007g0052 a0001c0001t0007g0075 others(8): Show |
11 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+6775C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461146 | |||||||
| chr10:80461495 | C | A | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+7124C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461495 | |||||||
| chr10:80461634 | T | C | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+7263T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461634 | |||||||
| chr10:80461760 | G | A | 2 | a0001c0001t0002g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-18+7389G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461760 | |||||||
| chr10:80461880 | G | T | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+7509G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461880 | |||||||
| chr10:80461915 | CT | C | 16 | a0001c0001t0002g0073 a0001c0001t0007g0052 a0001c0001t0007g0075 others(13): Show |
16 | HG01175.hp2 HG01433.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+7556delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80461915 | ||||||
| chr10:80461915 | CTT | C | 13 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(10): Show |
15 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+7555_-18+7556d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80461915 | ||||||
| chr10:80461967 | G | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+7596G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461967 | |||||||
| chr10:80462146 | C | T | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+7775C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462146 | |||||||
| chr10:80462163 | T | C | 3 | a0001c0001t0023g0014 a0001c0001t0023g0015 a0001c0002t0054g0016 |
3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-18+7792T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462163 | |||||||
| chr10:80462198 | G | A | 1 | a0001c0001t0020g0117 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-18+7827G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462198 | |||||||
| chr10:80462341 | C | G | 32 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(29): Show |
34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+7970C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462341 | |||||||
| chr10:80462347 | A | AATGGGGT others(13): Show |
19 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(16): Show |
21 | HG00639.hp1 HG01074.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+7986_-18+7987i others(22): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80462347 | ||||||
| chr10:80462358 | A | ATGGGATG others(13): Show |
3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+7992_-18+8011d others(22): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80462358 | ||||||
| chr10:80462358 | A | G | 33 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(30): Show |
35 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18+7987A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462358 | |||||||
| chr10:80462422 | C | A | 222 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(219): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-18+8051C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462422 | |||||||
| chr10:80462609 | G | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+8238G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462609 | |||||||
| chr10:80462942 | T | C | 215 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(212): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-18+8571T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462942 | |||||||
| chr10:80463179 | T | A | 32 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(29): Show |
34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+8808T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463179 | |||||||
| chr10:80463183 | G | A | 5 | a0001c0001t0013g0115 a0001c0001t0018g0119 a0001c0001t0019g0116 others(2): Show |
5 | HG01433.hp1 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+8812G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463183 | |||||||
| chr10:80463402 | G | T | 84 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(81): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-18+9031G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463402 | |||||||
| chr10:80463436 | G | T | 1 | a0001c0001t0019g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+9065G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463436 | |||||||
| chr10:80463535 | C | T | 108 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(105): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+9164C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463535 | |||||||
| chr10:80463698 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-18+9327G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463698 | |||||||
| chr10:80463731 | G | A | 2 | a0001c0001t0013g0115 a0001c0001t0019g0116 |
2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+9360G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463731 | |||||||
| chr10:80464011 | A | G | 108 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(105): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+9640A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464011 | |||||||
| chr10:80464045 | G | A | 1 | a0001c0001t0010g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18+9674G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464045 | |||||||
| chr10:80464085 | C | A | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-18+9714C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464085 | |||||||
| chr10:80464183 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+9812C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464183 | |||||||
| chr10:80464540 | G | A | 32 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(29): Show |
34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+10169G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464540 | |||||||
| chr10:80464648 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-18+10277C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464648 | |||||||
| chr10:80464883 | A | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+10512A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464883 | |||||||
| chr10:80465129 | G | A | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+10758G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465129 | |||||||
| chr10:80465141 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-18+10770G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465141 | |||||||
| chr10:80465181 | G | A | 4 | a0001c0001t0020g0117 a0001c0001t0020g0148 a0001c0001t0020g0150 others(1): Show |
4 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+10810G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465181 | |||||||
| chr10:80465239 | A | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+10868A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465239 | |||||||
| chr10:80465245 | C | A | 6 | a0001c0001t0007g0052 a0001c0001t0007g0075 a0001c0001t0007g0077 others(3): Show |
6 | HG01175.hp2 HG01515.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+10874C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465245 | |||||||
| chr10:80465403 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18+11032C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465403 | |||||||
| chr10:80465619 | C | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11248C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465619 | |||||||
| chr10:80465620 | C | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11249C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465620 | |||||||
| chr10:80465681 | A | T | 2 | a0001c0001t0006g0046 a0001c0001t0044g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18+11310A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465681 | |||||||
| chr10:80465705 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+11334T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465705 | |||||||
| chr10:80465807 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0052g0012 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-18+11436G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465807 | |||||||
| chr10:80465854 | C | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11483C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465854 | |||||||
| chr10:80465891 | C | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+11520C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465891 | |||||||
| chr10:80466006 | AG | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+11637delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80466006 | ||||||
| chr10:80466037 | T | C | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11666T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466037 | |||||||
| chr10:80466400 | C | T | 1 | a0001c0001t0007g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+12029C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466400 | |||||||
| chr10:80466483 | T | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+12112T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466483 | |||||||
| chr10:80466509 | C | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(28): Show |
32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+12138C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466509 | |||||||
| chr10:80466619 | A | C | 1 | a0001c0001t0003g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+12248A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466619 | |||||||
| chr10:80466698 | T | C | 23 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(20): Show |
25 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+12327T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466698 | |||||||
| chr10:80466795 | C | T | 7 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12424C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466795 | |||||||
| chr10:80467110 | A | T | 16 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0097 others(13): Show |
16 | HG02004.hp2 HG03654.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18+12739A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467110 | |||||||
| chr10:80467156 | A | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(28): Show |
32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+12785A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467156 | |||||||
| chr10:80467224 | A | G | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12853A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467224 | |||||||
| chr10:80467347 | C | T | 29 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(26): Show |
31 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+12976C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467347 | |||||||
| chr10:80467387 | A | G | 29 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(26): Show |
31 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+13016A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467387 | |||||||
| chr10:80467439 | C | T | 1 | a0001c0003t0018g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+13068C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467439 | |||||||
| chr10:80467447 | G | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13076G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467447 | |||||||
| chr10:80467468 | C | T | 1 | a0001c0001t0019g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+13097C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467468 | |||||||
| chr10:80467684 | T | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+13313T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467684 | |||||||
| chr10:80467739 | C | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(28): Show |
32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+13368C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467739 | |||||||
| chr10:80467750 | C | T | 1 | a0001c0001t0017g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18+13379C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467750 | |||||||
| chr10:80467791 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+13420C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467791 | |||||||
| chr10:80467791 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-18+13420C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467791 | |||||||
| chr10:80467832 | C | G | 1 | a0001c0001t0019g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+13461C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467832 | |||||||
| chr10:80467874 | T | A | 118 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(115): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-18+13503T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467874 | |||||||
| chr10:80467880 | TTA | T | 3 | a0001c0001t0017g0003 a0001c0001t0017g0054 a0001c0001t0017g0055 |
4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13511_-18+1351 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80467880 | ||||||
| chr10:80468241 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+13870A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468241 | |||||||
| chr10:80468243 | T | C | 2 | a0001c0001t0003g0032 a0001c0001t0006g0033 |
2 | HG01257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+13872T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468243 | |||||||
| chr10:80468258 | C | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13887C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468258 | |||||||
| chr10:80468373 | G | T | 5 | a0001c0001t0013g0115 a0001c0001t0018g0119 a0001c0001t0019g0116 others(2): Show |
5 | HG01433.hp1 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+14002G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468373 | |||||||
| chr10:80468431 | A | G | 4 | a0001c0001t0002g0227 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+14060A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468431 | |||||||
| chr10:80468536 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+14165C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468536 | |||||||
| chr10:80468548 | G | A | 6 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0016g0002 others(3): Show |
8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+14177G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468548 | |||||||
| chr10:80468624 | C | T | 1 | a0001c0001t0030g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+14253C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468624 | |||||||
| chr10:80468715 | TA | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+14347delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468715 | ||||||
| chr10:80468718 | A | AT | 107 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(104): Show |
108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+14366dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468718 | ||||||
| chr10:80468718 | AT | A | 24 | a0001c0001t0002g0006 a0001c0001t0002g0060 a0001c0001t0002g0072 others(21): Show |
25 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18+14366delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468718 | ||||||
| chr10:80468824 | T | G | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+14453T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468824 | |||||||
| chr10:80468942 | A | G | 1 | a0001c0003t0018g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+14571A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468942 | |||||||
| chr10:80469205 | C | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(28): Show |
32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+14834C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469205 | |||||||
| chr10:80469347 | GATAA | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(28): Show |
32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+14984_-18+1498 others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80469347 | ||||||
| chr10:80469512 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+15141G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469512 | |||||||
| chr10:80469524 | C | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+15153C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469524 | |||||||
| chr10:80469550 | C | T | 7 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+15179C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469550 | |||||||
| chr10:80469673 | T | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0151 a0001c0001t0001g0155 others(13): Show |
16 | HG00558.hp2 HG00597.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18+15302T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469673 | |||||||
| chr10:80469853 | A | C | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15482A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469853 | |||||||
| chr10:80469878 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-18+15507T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469878 | |||||||
| chr10:80470000 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+15629C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470000 | |||||||
| chr10:80470155 | A | T | 31 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(28): Show |
33 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+15784A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470155 | |||||||
| chr10:80470234 | C | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15863C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470234 | |||||||
| chr10:80470390 | C | T | 215 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(212): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-18+16019C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470390 | |||||||
| chr10:80470398 | C | G | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+16027C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470398 | |||||||
| chr10:80470541 | T | G | 2 | a0001c0001t0007g0052 a0001c0001t0007g0075 |
2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+16170T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470541 | |||||||
| chr10:80470895 | G | A | 7 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+16524G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470895 | |||||||
| chr10:80470918 | G | A | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+16547G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470918 | |||||||
| chr10:80470933 | G | A | 2 | a0001c0001t0018g0119 a0001c0001t0057g0118 |
2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-18+16562G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470933 | |||||||
| chr10:80470973 | C | T | 1 | a0001c0002t0005g0094 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+16602C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470973 | |||||||
| chr10:80471007 | C | T | 1 | a0001c0001t0004g0008 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-18+16636C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471007 | |||||||
| chr10:80471175 | G | T | 7 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+16804G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471175 | |||||||
| chr10:80471329 | GT | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0061 a0001c0001t0002g0062 |
4 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+16961delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80471329 | ||||||
| chr10:80471584 | A | G | 1 | a0001c0001t0033g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18+17213A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471584 | |||||||
| chr10:80471783 | G | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+17412G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471783 | |||||||
| chr10:80471854 | A | G | 1 | a0001c0001t0038g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-17363A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471854 | |||||||
| chr10:80471992 | T | C | 21 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(18): Show |
22 | HG00639.hp2 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-17225T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471992 | |||||||
| chr10:80472044 | A | G | 1 | a0001c0001t0028g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-17-17173A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472044 | |||||||
| chr10:80472062 | C | G | 7 | a0001c0001t0016g0222 a0001c0001t0016g0223 a0001c0001t0018g0129 others(4): Show |
7 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-17155C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472062 | |||||||
| chr10:80472095 | G | A | 113 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-17-17122G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472095 | |||||||
| chr10:80472203 | G | T | 7 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-17014G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472203 | |||||||
| chr10:80472292 | G | T | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-16925G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472292 | |||||||
| chr10:80472340 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-16877C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472340 | |||||||
| chr10:80472404 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-16813G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472404 | |||||||
| chr10:80472410 | A | G | 7 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(4): Show |
7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-16807A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472410 | |||||||
| chr10:80472413 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-17-16804G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472413 | |||||||
| chr10:80472422 | C | T | 1 | a0001c0001t0035g0221 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-17-16795C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472422 | |||||||
| chr10:80472509 | G | A | 6 | a0001c0001t0016g0222 a0001c0001t0016g0223 a0001c0001t0033g0122 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16708G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472509 | |||||||
| chr10:80472681 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-16536T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472681 | |||||||
| chr10:80472823 | C | G | 1 | a0001c0002t0005g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-16394C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472823 | |||||||
| chr10:80472859 | T | G | 16 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0097 others(13): Show |
16 | HG02004.hp2 HG03654.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-16358T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472859 | |||||||
| chr10:80472885 | T | C | 4 | a0001c0001t0033g0122 a0001c0001t0048g0121 a0001c0003t0014g0120 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-16332T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472885 | |||||||
| chr10:80472950 | G | A | 82 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0070 others(79): Show |
86 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-17-16267G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472950 | |||||||
| chr10:80473000 | T | C | 8 | a0001c0001t0002g0227 a0001c0001t0012g0017 a0001c0001t0012g0018 others(5): Show |
8 | HG01081.hp2 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-16217T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473000 | |||||||
| chr10:80473412 | C | G | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-15805C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473412 | |||||||
| chr10:80473433 | G | C | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-15784G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473433 | |||||||
| chr10:80473469 | C | G | 155 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(152): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-17-15748C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473469 | |||||||
| chr10:80473517 | T | C | 20 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0097 others(17): Show |
20 | HG01243.hp1 HG02004.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-15700T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473517 | |||||||
| chr10:80473599 | C | G | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-15618C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473599 | |||||||
| chr10:80473604 | G | A | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-15613G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473604 | |||||||
| chr10:80473609 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(76): Show |
79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-17-15608G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473609 | |||||||
| chr10:80473615 | G | T | 4 | a0001c0001t0010g0059 a0001c0001t0010g0066 a0001c0001t0010g0125 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15602G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473615 | |||||||
| chr10:80473628 | C | T | 7 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(4): Show |
7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-15589C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473628 | |||||||
| chr10:80473659 | G | C | 1 | a0001c0001t0057g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-15558G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473659 | |||||||
| chr10:80473681 | A | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-15536A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473681 | |||||||
| chr10:80473682 | TG | T | 4 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(1): Show |
4 | HG01081.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-15532delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473682 | ||||||
| chr10:80473684 | GGT | G | 3 | a0001c0001t0023g0014 a0001c0001t0023g0015 a0001c0002t0054g0016 |
3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-15532_-17-1553 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473684 | |||||||
| chr10:80473685 | G | GT | 8 | a0001c0001t0001g0151 a0001c0001t0004g0008 a0001c0001t0004g0177 others(5): Show |
8 | HG00558.hp2 HG02004.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-15516dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473685 | ||||||
| chr10:80473701 | TA | T | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(37): Show |
42 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-17-15513delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473701 | ||||||
| chr10:80473702 | A | T | 175 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-17-15515A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473702 | |||||||
| chr10:80473703 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0028g0160 |
2 | HG00558.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-17-15514A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473703 | |||||||
| chr10:80473727 | T | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-15490T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473727 | |||||||
| chr10:80473729 | G | C | 5 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-15488G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473729 | |||||||
| chr10:80473751 | G | A | 9 | a0001c0001t0002g0181 a0001c0001t0009g0184 a0001c0001t0012g0186 others(6): Show |
10 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-15466G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473751 | |||||||
| chr10:80473784 | G | A | 105 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-17-15433G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473784 | |||||||
| chr10:80473786 | C | G | 27 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(24): Show |
29 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-15431C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473786 | |||||||
| chr10:80473798 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-17-15419C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473798 | |||||||
| chr10:80473863 | C | T | 1 | a0001c0001t0008g0179 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-17-15354C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473863 | |||||||
| chr10:80474135 | C | T | 1 | a0001c0001t0013g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-17-15082C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474135 | |||||||
| chr10:80474171 | A | G | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0231 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-15046A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474171 | |||||||
| chr10:80474286 | C | A | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14931C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474286 | |||||||
| chr10:80474724 | C | T | 30 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0229 others(27): Show |
32 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-17-14493C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474724 | |||||||
| chr10:80474813 | C | T | 1 | a0001c0001t0026g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-17-14404C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474813 | |||||||
| chr10:80474831 | T | G | 86 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0083 others(83): Show |
89 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-14386T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474831 | |||||||
| chr10:80474861 | C | A | 26 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(23): Show |
28 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-14356C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474861 | |||||||
| chr10:80474999 | A | T | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14218A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474999 | |||||||
| chr10:80475021 | G | A | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14196G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475021 | |||||||
| chr10:80475170 | C | T | 16 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(13): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-14047C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475170 | |||||||
| chr10:80475251 | G | C | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13966G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475251 | |||||||
| chr10:80475383 | T | C | 2 | a0001c0001t0022g0242 a0001c0001t0022g0243 |
2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-13834T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475383 | |||||||
| chr10:80475531 | T | A | 1 | a0001c0001t0022g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-13686T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475531 | |||||||
| chr10:80475618 | C | T | 18 | a0001c0001t0002g0073 a0001c0001t0002g0227 a0001c0001t0002g0231 others(15): Show |
18 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-13599C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475618 | |||||||
| chr10:80475640 | T | C | 4 | a0001c0001t0016g0222 a0001c0001t0016g0223 a0001c0002t0005g0057 others(1): Show |
4 | HG00642.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-13577T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475640 | |||||||
| chr10:80475683 | G | A | 6 | a0001c0001t0014g0056 a0001c0001t0016g0002 a0001c0001t0017g0003 others(3): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-13534G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475683 | |||||||
| chr10:80475742 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-17-13475A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475742 | |||||||
| chr10:80475855 | G | A | 22 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(19): Show |
23 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-13362G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475855 | |||||||
| chr10:80475871 | C | T | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-13346C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475871 | |||||||
| chr10:80475881 | G | A | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-13336G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475881 | |||||||
| chr10:80476009 | G | A | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-13208G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476009 | |||||||
| chr10:80476100 | G | A | 1 | a0001c0001t0057g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-13117G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476100 | |||||||
| chr10:80476110 | G | A | 1 | a0001c0001t0014g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-13107G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476110 | |||||||
| chr10:80476145 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-17-13072G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476145 | |||||||
| chr10:80476169 | C | T | 3 | a0001c0001t0023g0014 a0001c0001t0023g0015 a0001c0002t0054g0016 |
3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-13048C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476169 | |||||||
| chr10:80476173 | T | C | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-13044T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476173 | |||||||
| chr10:80476327 | G | A | 28 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(25): Show |
28 | HG00642.hp2 HG01081.hp2 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-12890G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476327 | |||||||
| chr10:80476409 | G | GT | 16 | a0001c0001t0002g0139 a0001c0001t0003g0043 a0001c0001t0003g0049 others(13): Show |
17 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-12784dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GT | G | 71 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0069 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-17-12784delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTT | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0163 a0001c0001t0002g0006 others(14): Show |
18 | HG00741.hp2 HG01167.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-12785_-17-1278 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTTT | G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0028 others(37): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-17-12786_-17-1278 others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTTTT | G | 12 | a0001c0001t0002g0061 a0001c0001t0002g0073 a0001c0001t0002g0181 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-12787_-17-1278 others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTTTTT | G | 6 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0004g0100 others(3): Show |
6 | HG01074.hp1 HG02622.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-12788_-17-1278 others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTTTTTT | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-12789_-17-1278 others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476409 | GTTTTTTT | G | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12790_-17-1278 others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | ||||||
| chr10:80476417 | T | G | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-12800T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476417 | |||||||
| chr10:80476418 | T | G | 1 | a0001c0001t0004g0100 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-17-12799T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476418 | |||||||
| chr10:80476419 | T | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-12798T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476419 | |||||||
| chr10:80476420 | T | G | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12797T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476420 | |||||||
| chr10:80476439 | G | A | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-12778G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476439 | |||||||
| chr10:80476525 | C | T | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-12692C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476525 | |||||||
| chr10:80476625 | C | T | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-12592C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476625 | |||||||
| chr10:80476636 | C | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-12581C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476636 | |||||||
| chr10:80476743 | T | G | 34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(31): Show |
36 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-12474T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476743 | |||||||
| chr10:80476860 | G | A | 1 | a0001c0001t0016g0002 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-12357G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476860 | |||||||
| chr10:80477011 | T | C | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-12206T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477011 | |||||||
| chr10:80477086 | G | A | 3 | a0001c0001t0009g0184 a0001c0002t0021g0182 a0001c0002t0021g0183 |
3 | HG01884.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17-12131G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477086 | |||||||
| chr10:80477222 | C | T | 11 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(8): Show |
12 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-11995C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477222 | |||||||
| chr10:80477370 | A | G | 52 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0151 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-11847A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477370 | |||||||
| chr10:80477592 | G | A | 46 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(43): Show |
49 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-17-11625G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477592 | |||||||
| chr10:80477625 | T | C | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-11592T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477625 | |||||||
| chr10:80478009 | A | G | 4 | a0001c0001t0012g0186 a0001c0001t0023g0014 a0001c0001t0023g0015 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11208A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478009 | |||||||
| chr10:80478139 | A | G | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-11078A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478139 | |||||||
| chr10:80478165 | T | C | 1 | a0001c0001t0011g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-11052T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478165 | |||||||
| chr10:80478232 | T | G | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-10985T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478232 | |||||||
| chr10:80478408 | G | A | 1 | a0001c0001t0031g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-10809G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478408 | |||||||
| chr10:80478625 | A | C | 1 | a0001c0001t0012g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-17-10592A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478625 | |||||||
| chr10:80478641 | G | A | 5 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0113 others(2): Show |
5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-10576G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478641 | |||||||
| chr10:80478647 | C | T | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-17-10570C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478647 | |||||||
| chr10:80478650 | A | G | 1 | a0001c0001t0043g0029 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-17-10567A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478650 | |||||||
| chr10:80478767 | A | G | 1 | a0001c0001t0016g0002 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-10450A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478767 | |||||||
| chr10:80478986 | A | G | 10 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-10231A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478986 | |||||||
| chr10:80479080 | T | G | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-10137T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479080 | |||||||
| chr10:80479118 | G | T | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-10099G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479118 | |||||||
| chr10:80479162 | G | GT | 5 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0048g0121 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-10052dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80479162 | ||||||
| chr10:80479274 | T | C | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-9943T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479274 | |||||||
| chr10:80479325 | T | C | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-9892T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479325 | |||||||
| chr10:80479372 | C | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-9845C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479372 | |||||||
| chr10:80479553 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-9664C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479553 | |||||||
| chr10:80479640 | C | G | 2 | a0001c0002t0005g0057 a0001c0002t0005g0094 |
2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-9577C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479640 | |||||||
| chr10:80479646 | G | A | 3 | a0001c0001t0018g0119 a0001c0001t0033g0122 a0001c0001t0057g0118 |
3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-9571G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479646 | |||||||
| chr10:80479763 | C | G | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-9454C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479763 | |||||||
| chr10:80479769 | G | A | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-9448G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479769 | |||||||
| chr10:80479773 | C | T | 1 | a0001c0001t0055g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-17-9444C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479773 | |||||||
| chr10:80479797 | G | A | 101 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(98): Show |
106 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.-17-9420G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479797 | |||||||
| chr10:80479900 | T | C | 4 | a0001c0001t0003g0188 a0001c0001t0025g0187 a0001c0001t0045g0036 others(1): Show |
4 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-9317T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479900 | |||||||
| chr10:80479920 | C | T | 4 | a0001c0002t0005g0236 a0001c0002t0005g0237 a0001c0002t0005g0238 others(1): Show |
4 | HG00639.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9297C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479920 | |||||||
| chr10:80479967 | A | C | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-9250A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479967 | |||||||
| chr10:80480040 | C | A | 236 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(233): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-17-9177C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480040 | |||||||
| chr10:80480058 | G | T | 1 | a0001c0001t0011g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-9159G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480058 | |||||||
| chr10:80480096 | T | C | 1 | a0001c0001t0030g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-17-9121T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480096 | |||||||
| chr10:80480106 | G | C | 4 | a0001c0001t0010g0059 a0001c0001t0010g0066 a0001c0001t0010g0125 others(1): Show |
4 | HG00140.hp2 HG01358.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-9111G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480106 | |||||||
| chr10:80480186 | C | A | 100 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(97): Show |
105 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.-17-9031C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480186 | |||||||
| chr10:80480202 | A | G | 1 | a0001c0001t0004g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-17-9015A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480202 | |||||||
| chr10:80480445 | T | A | 20 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0004g0008 others(17): Show |
20 | HG01074.hp1 HG02004.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-8772T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480445 | |||||||
| chr10:80480480 | C | T | 5 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0048g0121 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-8737C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480480 | |||||||
| chr10:80480520 | G | A | 2 | a0001c0001t0018g0119 a0001c0001t0057g0118 |
2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-8697G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480520 | |||||||
| chr10:80480543 | G | A | 104 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(101): Show |
109 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.-17-8674G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480543 | |||||||
| chr10:80480572 | C | T | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-8645C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480572 | |||||||
| chr10:80480582 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-17-8635A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480582 | |||||||
| chr10:80480653 | C | A | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-8564C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480653 | |||||||
| chr10:80480673 | C | T | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-8544C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480673 | |||||||
| chr10:80480697 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-8520G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480697 | |||||||
| chr10:80480814 | A | T | 1 | a0001c0001t0003g0042 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-17-8403A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480814 | |||||||
| chr10:80480955 | A | C | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-8262A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480955 | |||||||
| chr10:80481004 | C | G | 84 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(81): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-8213C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481004 | |||||||
| chr10:80481186 | G | A | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-8031G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481186 | |||||||
| chr10:80481375 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-17-7842C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481375 | |||||||
| chr10:80481527 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17-7690A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481527 | |||||||
| chr10:80481538 | T | C | 2 | a0001c0002t0005g0057 a0001c0002t0005g0094 |
2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-7679T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481538 | |||||||
| chr10:80481612 | C | T | 5 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0113 others(2): Show |
5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-7605C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481612 | |||||||
| chr10:80481687 | G | A | 1 | a0001c0001t0012g0018 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-7530G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481687 | |||||||
| chr10:80481689 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17-7528G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481689 | |||||||
| chr10:80481728 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-7489C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481728 | |||||||
| chr10:80481766 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-7451C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481766 | |||||||
| chr10:80481782 | C | T | 3 | a0001c0001t0018g0119 a0001c0001t0033g0122 a0001c0001t0057g0118 |
3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-7435C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481782 | |||||||
| chr10:80481783 | G | A | 7 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(4): Show |
7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-7434G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481783 | |||||||
| chr10:80481921 | T | C | 7 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-7296T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481921 | |||||||
| chr10:80481945 | G | A | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-7272G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481945 | |||||||
| chr10:80482054 | A | G | 8 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(5): Show |
8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-7163A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482054 | |||||||
| chr10:80482082 | G | A | 9 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-7135G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482082 | |||||||
| chr10:80482174 | T | C | 105 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(102): Show |
108 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17-7043T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482174 | |||||||
| chr10:80482235 | A | G | 1 | a0001c0001t0006g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-6982A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482235 | |||||||
| chr10:80482347 | C | G | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-6870C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482347 | |||||||
| chr10:80482350 | AATCTCAG others(442): Show |
A | 7 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(4): Show |
7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-6861_-17-6413d others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482350 | ||||||
| chr10:80482400 | C | T | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-6817C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482400 | |||||||
| chr10:80482413 | A | C | 1 | a0001c0001t0004g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-17-6804A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482413 | |||||||
| chr10:80482477 | G | C | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6740G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482477 | |||||||
| chr10:80482511 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-6706C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482511 | |||||||
| chr10:80482537 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0189 a0001c0001t0015g0205 |
3 | HG03017.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-17-6680C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482537 | |||||||
| chr10:80482547 | C | G | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-6670C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482547 | |||||||
| chr10:80482659 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-6558C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482659 | |||||||
| chr10:80482732 | C | CT | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0002t0005g0236 others(2): Show |
5 | HG00639.hp1 HG01515.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-6465dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | ||||||
| chr10:80482732 | CT | C | 64 | a0001c0001t0001g0172 a0001c0001t0001g0217 a0001c0001t0002g0004 others(61): Show |
68 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17-6465delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | ||||||
| chr10:80482732 | CTT | C | 37 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(34): Show |
38 | HG00642.hp2 HG01069.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-6466_-17-6465d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | ||||||
| chr10:80482766 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-17-6451G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482766 | |||||||
| chr10:80483017 | GAGCCACT others(6): Show |
G | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-6194_-17-6182d others(15): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483017 | ||||||
| chr10:80483401 | A | G | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5816A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483401 | |||||||
| chr10:80483741 | C | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5476C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483741 | |||||||
| chr10:80483896 | G | A | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-5321G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483896 | |||||||
| chr10:80483911 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-5279_-17-5266d others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CA | C | 18 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-5266delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAA | C | 15 | a0001c0001t0003g0041 a0001c0001t0003g0152 a0001c0001t0006g0034 others(12): Show |
16 | HG01071.hp2 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-5267_-17-5266d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAA | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0151 a0001c0001t0001g0156 others(15): Show |
19 | HG00639.hp1 HG00735.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-5268_-17-5266d others(5): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAA | C | 32 | a0001c0001t0001g0069 a0001c0001t0001g0153 a0001c0001t0001g0163 others(29): Show |
32 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-17-5269_-17-5266d others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAA | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0070 others(33): Show |
36 | HG00140.hp1 HG00597.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-5270_-17-5266d others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAA | C | 8 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0009g0184 others(5): Show |
8 | HG01192.hp1 HG01515.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5271_-17-5266d others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA | C | 6 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0055 others(3): Show |
8 | HG02145.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5272_-17-5266d others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0002g0181 a0001c0001t0013g0087 a0001c0001t0017g0054 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5273_-17-5266d others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0073 a0001c0001t0009g0230 a0001c0001t0013g0088 others(4): Show |
7 | HG01433.hp1 HG02809.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-5274_-17-5266d others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(3): Show |
C | 19 | a0001c0001t0002g0061 a0001c0001t0002g0064 a0001c0001t0002g0065 others(16): Show |
19 | HG00642.hp1 HG00741.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5275_-17-5266d others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(4): Show |
C | 30 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(27): Show |
33 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-5276_-17-5266d others(13): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(5): Show |
C | 18 | a0001c0001t0002g0060 a0001c0001t0002g0072 a0001c0001t0002g0210 others(15): Show |
18 | HG01074.hp1 HG02004.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-5277_-17-5266d others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0004g0100 a0001c0001t0016g0222 a0001c0001t0016g0223 |
3 | HG02572.hp2 HG03540.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-5278_-17-5266d others(15): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0011g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-5280_-17-5266d others(17): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0012g0017 a0001c0001t0023g0014 a0001c0001t0050g0226 |
3 | HG01081.hp2 HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-17-5282_-17-5266d others(19): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(3): Show |
6 | HG02559.hp1 HG02723.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-5283_-17-5266d others(20): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483911 | CAAAAAAA others(12): Show |
C | 2 | a0001c0002t0005g0057 a0001c0002t0005g0094 |
2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-5284_-17-5266d others(21): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | ||||||
| chr10:80483966 | A | T | 9 | a0001c0001t0007g0044 a0001c0001t0007g0052 a0001c0001t0007g0075 others(6): Show |
9 | HG01175.hp2 HG02486.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-5251A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483966 | |||||||
| chr10:80484073 | C | T | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-5144C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484073 | |||||||
| chr10:80484129 | C | A | 24 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(21): Show |
25 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-5088C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484129 | |||||||
| chr10:80484176 | C | A | 5 | a0001c0001t0014g0053 a0001c0001t0014g0056 a0001c0001t0048g0121 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5041C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484176 | |||||||
| chr10:80484200 | G | A | 113 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-17-5017G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484200 | |||||||
| chr10:80484230 | A | G | 236 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(233): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-17-4987A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484230 | |||||||
| chr10:80484325 | A | T | 42 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-17-4892A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484325 | |||||||
| chr10:80484451 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-4766C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484451 | |||||||
| chr10:80484452 | G | A | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-4765G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484452 | |||||||
| chr10:80485045 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-4172C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485045 | |||||||
| chr10:80485047 | A | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-4170A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485047 | |||||||
| chr10:80485200 | C | CGT | 90 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(87): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-17-4006_-17-4005d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80485200 | ||||||
| chr10:80485306 | G | A | 10 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-3911G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485306 | |||||||
| chr10:80485363 | T | C | 1 | a0001c0003t0018g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-17-3854T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485363 | |||||||
| chr10:80485437 | C | T | 1 | a0001c0001t0009g0230 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-3780C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485437 | |||||||
| chr10:80485520 | C | A | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-3697C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485520 | |||||||
| chr10:80485587 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-3630C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485587 | |||||||
| chr10:80485668 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-17-3549C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485668 | |||||||
| chr10:80485721 | C | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-3496C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485721 | |||||||
| chr10:80485752 | A | G | 7 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(4): Show |
7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3465A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485752 | |||||||
| chr10:80485754 | C | G | 99 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(96): Show |
104 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.-17-3463C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485754 | |||||||
| chr10:80485874 | C | T | 1 | a0001c0001t0028g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-17-3343C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485874 | |||||||
| chr10:80485911 | A | C | 9 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(6): Show |
9 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-3306A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485911 | |||||||
| chr10:80485989 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0015g0193 |
2 | HG00438.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-17-3228A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485989 | |||||||
| chr10:80486343 | C | T | 3 | a0001c0001t0019g0109 a0001c0001t0019g0116 a0001c0001t0019g0214 |
3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-17-2874C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486343 | |||||||
| chr10:80486409 | G | A | 1 | a0001c0001t0047g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-2808G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486409 | |||||||
| chr10:80486595 | A | C | 9 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(6): Show |
9 | HG00642.hp2 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-2622A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486595 | |||||||
| chr10:80486611 | C | G | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-2606C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486611 | |||||||
| chr10:80486772 | A | G | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-2445A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486772 | |||||||
| chr10:80486989 | T | C | 2 | a0001c0001t0002g0134 a0001c0001t0053g0135 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-17-2228T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486989 | |||||||
| chr10:80486992 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-17-2225C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486992 | |||||||
| chr10:80486993 | A | G | 232 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(229): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-17-2224A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486993 | |||||||
| chr10:80487029 | C | T | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-17-2188C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487029 | |||||||
| chr10:80487133 | C | G | 2 | a0001c0002t0005g0057 a0001c0002t0005g0094 |
2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-2084C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487133 | |||||||
| chr10:80487283 | C | G | 1 | a0001c0001t0004g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-17-1934C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487283 | |||||||
| chr10:80487288 | C | T | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1929C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487288 | |||||||
| chr10:80487335 | G | A | 3 | a0001c0001t0018g0119 a0001c0001t0033g0122 a0001c0001t0057g0118 |
3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-1882G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487335 | |||||||
| chr10:80487368 | G | A | 1 | a0001c0001t0022g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-1849G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487368 | |||||||
| chr10:80487383 | A | G | 140 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-17-1834A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487383 | |||||||
| chr10:80487466 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-17-1751T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487466 | |||||||
| chr10:80487517 | G | A | 2 | a0001c0001t0012g0018 a0001c0001t0012g0019 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-17-1700G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487517 | |||||||
| chr10:80487531 | G | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-1686G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487531 | |||||||
| chr10:80487620 | A | G | 3 | a0001c0002t0005g0236 a0001c0002t0005g0237 a0001c0002t0005g0238 |
3 | HG00639.hp1 HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-1597A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487620 | |||||||
| chr10:80487703 | A | G | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1514A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487703 | |||||||
| chr10:80487745 | G | C | 1 | a0001c0001t0008g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-1472G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487745 | |||||||
| chr10:80488025 | G | A | 5 | a0001c0001t0018g0119 a0001c0001t0020g0148 a0001c0001t0020g0150 others(2): Show |
5 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-1192G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488025 | |||||||
| chr10:80488043 | C | A | 5 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0054 others(2): Show |
7 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-1174C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488043 | |||||||
| chr10:80488052 | G | A | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-1165G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488052 | |||||||
| chr10:80488078 | G | A | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1139G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488078 | |||||||
| chr10:80488159 | G | A | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1058G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488159 | |||||||
| chr10:80488172 | C | T | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1045C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488172 | |||||||
| chr10:80488276 | C | T | 20 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-941C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488276 | |||||||
| chr10:80488414 | T | C | 4 | a0001c0001t0003g0050 a0001c0001t0022g0242 a0001c0001t0022g0243 others(1): Show |
4 | HG01175.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-803T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488414 | |||||||
| chr10:80488715 | A | G | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-502A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488715 | |||||||
| chr10:80488723 | A | G | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-494A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488723 | |||||||
| chr10:80489051 | G | A | 1 | a0001c0001t0009g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-17-166G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489051 | |||||||
| chr10:80489070 | T | A | 1 | a0001c0001t0029g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-17-147T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489070 | |||||||
| chr10:80489073 | C | T | 1 | a0001c0001t0006g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-144C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489073 | |||||||
| chr10:80489352 | C | T | 42 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.81+38C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489352 | |||||||
| chr10:80489404 | A | G | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+90A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489404 | |||||||
| chr10:80489426 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.81+112G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489426 | |||||||
| chr10:80489996 | G | A | 202 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(199): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.81+682G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489996 | |||||||
| chr10:80490018 | G | A | 2 | a0001c0001t0003g0040 a0001c0001t0003g0042 |
2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.81+704G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490018 | |||||||
| chr10:80490093 | A | C | 1 | a0001c0001t0012g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.81+779A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490093 | |||||||
| chr10:80490203 | T | C | 2 | a0001c0001t0006g0046 a0001c0001t0044g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.81+889T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490203 | |||||||
| chr10:80490279 | C | T | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+965C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490279 | |||||||
| chr10:80490486 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+1172G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490486 | |||||||
| chr10:80490499 | A | C | 131 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(128): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.81+1185A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490499 | |||||||
| chr10:80490769 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0015g0205 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.81+1455T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490769 | |||||||
| chr10:80490816 | A | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(47): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1502A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490816 | |||||||
| chr10:80491075 | T | C | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+1761T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491075 | |||||||
| chr10:80491085 | G | T | 1 | a0001c0001t0008g0224 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.81+1771G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491085 | |||||||
| chr10:80491128 | A | G | 1 | a0001c0001t0019g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+1814A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491128 | |||||||
| chr10:80491182 | C | T | 3 | a0001c0002t0021g0182 a0001c0002t0021g0183 a0001c0002t0021g0185 |
3 | HG01884.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81+1868C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491182 | |||||||
| chr10:80491293 | A | T | 50 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(47): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1979A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491293 | |||||||
| chr10:80491374 | C | T | 2 | a0001c0001t0003g0051 a0001c0001t0042g0048 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.81+2060C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491374 | |||||||
| chr10:80491623 | T | C | 2 | a0001c0001t0018g0119 a0001c0001t0057g0118 |
2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.81+2309T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491623 | |||||||
| chr10:80491758 | T | C | 39 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(36): Show |
41 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.81+2444T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491758 | |||||||
| chr10:80491788 | C | A | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+2474C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491788 | |||||||
| chr10:80492013 | G | A | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+2699G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492013 | |||||||
| chr10:80492200 | T | A | 2 | a0001c0001t0007g0081 a0001c0001t0050g0226 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.81+2886T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492200 | |||||||
| chr10:80492440 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.81+3126G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492440 | |||||||
| chr10:80492582 | C | G | 20 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3268C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492582 | |||||||
| chr10:80492845 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+3531G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492845 | |||||||
| chr10:80492941 | C | T | 4 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0054 others(1): Show |
6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+3627C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492941 | |||||||
| chr10:80492980 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.81+3666A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492980 | |||||||
| chr10:80493030 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+3716A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493030 | |||||||
| chr10:80493199 | A | G | 1 | a0001c0001t0012g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+3885A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493199 | |||||||
| chr10:80493275 | G | C | 3 | a0001c0001t0002g0060 a0001c0001t0002g0072 a0001c0001t0009g0071 |
3 | HG02698.hp1 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.81+3961G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493275 | |||||||
| chr10:80493378 | G | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+4064G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493378 | |||||||
| chr10:80493758 | G | A | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+4444G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493758 | |||||||
| chr10:80493879 | C | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+4565C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493879 | |||||||
| chr10:80493945 | C | A | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+4631C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493945 | |||||||
| chr10:80494086 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+4772T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494086 | |||||||
| chr10:80494131 | T | A | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+4817T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494131 | |||||||
| chr10:80494154 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.81+4840A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494154 | |||||||
| chr10:80494228 | C | T | 229 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(226): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.81+4914C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494228 | |||||||
| chr10:80494291 | A | G | 230 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(227): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.81+4977A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494291 | |||||||
| chr10:80494402 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.81+5088C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494402 | |||||||
| chr10:80494632 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+5318G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494632 | |||||||
| chr10:80494684 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81+5370G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494684 | |||||||
| chr10:80494734 | C | T | 113 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.81+5420C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494734 | |||||||
| chr10:80494804 | A | G | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+5490A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494804 | |||||||
| chr10:80494841 | AT | A | 4 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0054 others(1): Show |
6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+5530delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80494841 | ||||||
| chr10:80494843 | T | A | 4 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0054 others(1): Show |
6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+5529T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494843 | |||||||
| chr10:80495183 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.81+5869A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495183 | |||||||
| chr10:80495293 | A | G | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+5979A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495293 | |||||||
| chr10:80495295 | C | T | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+5981C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495295 | |||||||
| chr10:80495335 | C | CTG | 4 | a0001c0001t0003g0039 a0001c0001t0004g0104 a0001c0001t0034g0022 others(1): Show |
4 | HG01361.hp1 HG02735.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+6063_81+6064dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495335 | ||||||
| chr10:80495355 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0010g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81+6045_81+6068del others(24): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495355 | ||||||
| chr10:80495361 | GTGTGTGT others(11): Show |
G | 4 | a0001c0001t0006g0046 a0001c0001t0014g0056 a0001c0001t0044g0045 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+6051_81+6068del others(18): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495361 | ||||||
| chr10:80495363 | GTGTGTGT others(9): Show |
G | 104 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(101): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.81+6053_81+6068del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495363 | ||||||
| chr10:80495365 | GTGTGTGT others(7): Show |
G | 6 | a0001c0001t0001g0220 a0001c0001t0002g0139 a0001c0001t0020g0117 others(3): Show |
6 | HG00558.hp1 HG01978.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+6055_81+6068del others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495365 | ||||||
| chr10:80495367 | GTGTGTGT others(5): Show |
G | 4 | a0001c0001t0001g0195 a0001c0001t0009g0184 a0001c0001t0022g0242 others(1): Show |
4 | HG02622.hp2 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+6057_81+6068del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495367 | ||||||
| chr10:80495369 | GTGTGTGT others(3): Show |
G | 14 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(11): Show |
14 | HG00642.hp2 HG01074.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+6059_81+6068del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495369 | ||||||
| chr10:80495371 | GTGTGTGT others(1): Show |
G | 7 | a0001c0001t0002g0232 a0001c0001t0016g0002 a0001c0001t0017g0003 others(4): Show |
9 | HG02145.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+6061_81+6068del others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495371 | ||||||
| chr10:80495373 | GTGTGTA | G | 49 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(46): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+6063_81+6068del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495373 | ||||||
| chr10:80495375 | GTGTA | G | 8 | a0001c0001t0004g0107 a0001c0001t0007g0044 a0001c0001t0007g0080 others(5): Show |
8 | HG00639.hp1 HG00642.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+6066_81+6069del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495375 | ||||||
| chr10:80495377 | GTA | G | 25 | a0001c0001t0003g0030 a0001c0001t0003g0040 a0001c0001t0003g0042 others(22): Show |
25 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.81+6065_81+6066del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495377 | ||||||
| chr10:80495379 | A | G | 21 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0003g0023 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+6065A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495379 | |||||||
| chr10:80495595 | G | T | 1 | a0001c0002t0005g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81+6281G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495595 | |||||||
| chr10:80495641 | A | G | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+6327A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495641 | |||||||
| chr10:80495684 | A | G | 12 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(9): Show |
12 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+6370A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495684 | |||||||
| chr10:80496018 | G | A | 120 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(117): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.81+6704G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496018 | |||||||
| chr10:80496082 | T | C | 1 | a0001c0001t0028g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.81+6768T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496082 | |||||||
| chr10:80496097 | A | G | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81+6783A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496097 | |||||||
| chr10:80496129 | A | G | 2 | a0001c0001t0002g0072 a0001c0001t0009g0071 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81+6815A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496129 | |||||||
| chr10:80496161 | A | G | 15 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(12): Show |
15 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+6847A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496161 | |||||||
| chr10:80496394 | C | G | 1 | a0001c0001t0007g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+7080C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496394 | |||||||
| chr10:80496406 | A | G | 1 | a0001c0001t0018g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+7092A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496406 | |||||||
| chr10:80496427 | C | T | 20 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+7113C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496427 | |||||||
| chr10:80496464 | G | A | 1 | a0001c0001t0004g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+7150G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496464 | |||||||
| chr10:80496502 | T | C | 122 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(119): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.81+7188T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496502 | |||||||
| chr10:80496718 | CT | C | 10 | a0001c0001t0001g0009 a0001c0001t0002g0134 a0001c0001t0002g0136 others(7): Show |
10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+7408delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80496718 | ||||||
| chr10:80496758 | A | T | 16 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+7444A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496758 | |||||||
| chr10:80496766 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.81+7452C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496766 | |||||||
| chr10:80496782 | G | C | 8 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(5): Show |
8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+7468G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496782 | |||||||
| chr10:80496786 | T | TATTCTAA others(7): Show |
8 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(5): Show |
8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+7472_81+7473ins others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496786 | |||||||
| chr10:80496842 | A | G | 1 | a0001c0001t0009g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81+7528A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496842 | |||||||
| chr10:80497047 | C | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0175 |
2 | NA18950.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.82-7681C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497047 | |||||||
| chr10:80497047 | C | T | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.82-7681C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497047 | |||||||
| chr10:80497364 | C | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(127): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.82-7364C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497364 | |||||||
| chr10:80497419 | G | A | 20 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-7309G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497419 | |||||||
| chr10:80497436 | A | G | 1 | a0001c0002t0005g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82-7292A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497436 | |||||||
| chr10:80497814 | T | C | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.82-6914T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497814 | |||||||
| chr10:80497845 | CTGGGAGG others(5): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-6880_82-6869del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80497845 | ||||||
| chr10:80497954 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.82-6774C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497954 | |||||||
| chr10:80497964 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-6764C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497964 | |||||||
| chr10:80497980 | G | A | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-6748G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497980 | |||||||
| chr10:80498159 | A | T | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-6569A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498159 | |||||||
| chr10:80498265 | C | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(6): Show |
10 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-6463C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498265 | |||||||
| chr10:80498390 | T | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82-6338T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498390 | |||||||
| chr10:80498478 | A | T | 1 | a0001c0001t0003g0050 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.82-6250A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498478 | |||||||
| chr10:80498484 | C | T | 1 | a0001c0001t0011g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82-6244C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498484 | |||||||
| chr10:80498518 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.82-6210G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498518 | |||||||
| chr10:80498795 | C | G | 1 | a0001c0001t0007g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82-5933C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498795 | |||||||
| chr10:80498862 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82-5866A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498862 | |||||||
| chr10:80498959 | G | A | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-5769G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498959 | |||||||
| chr10:80499049 | G | A | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-5679G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499049 | |||||||
| chr10:80499060 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-5668C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499060 | |||||||
| chr10:80499461 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.82-5267G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499461 | |||||||
| chr10:80499472 | G | A | 1 | a0001c0001t0030g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.82-5256G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499472 | |||||||
| chr10:80499741 | G | T | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82-4987G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499741 | |||||||
| chr10:80499763 | C | T | 1 | a0001c0002t0005g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82-4965C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499763 | |||||||
| chr10:80499764 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82-4964G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499764 | |||||||
| chr10:80499916 | AAAG | A | 119 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(116): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.82-4808_82-4806del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80499916 | ||||||
| chr10:80499973 | GGCAGCCA others(9): Show |
G | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-4742_82-4727del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80499973 | ||||||
| chr10:80500088 | C | T | 4 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0001c0001t0006g0046 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-4640C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500088 | |||||||
| chr10:80500314 | C | CT | 6 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG00280.hp2 HG01074.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-4382dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTT | C | 16 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(13): Show |
17 | HG00642.hp1 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-4383_82-4382del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTT | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(28): Show |
33 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-4384_82-4382del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTTT | C | 16 | a0001c0001t0002g0064 a0001c0001t0002g0181 a0001c0001t0002g0210 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-4385_82-4382del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTTTT | C | 51 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0070 others(48): Show |
52 | HG00621.hp2 HG00642.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.82-4386_82-4382del others(5): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTTTTT | C | 98 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0151 others(95): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.82-4387_82-4382del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTTTTTT | C | 6 | a0001c0001t0001g0202 a0001c0001t0004g0113 a0001c0001t0011g0076 others(3): Show |
6 | HG01070.hp2 HG01515.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4388_82-4382del others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500314 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4391_82-4382del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | ||||||
| chr10:80500351 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0025g0187 |
2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.82-4377C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500351 | |||||||
| chr10:80500543 | G | A | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.82-4185G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500543 | |||||||
| chr10:80500557 | G | T | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-4171G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500557 | |||||||
| chr10:80500571 | CGCCTCCC others(25): Show |
C | 1 | a0001c0002t0005g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.82-4142_82-4111del others(32): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500571 | ||||||
| chr10:80500586 | T | C | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4142T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500586 | |||||||
| chr10:80500702 | A | T | 2 | a0001c0001t0001g0189 a0001c0001t0015g0205 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.82-4026A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500702 | |||||||
| chr10:80501105 | G | GT | 18 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(15): Show |
18 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-3609dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501105 | ||||||
| chr10:80501105 | GT | G | 194 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(191): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.82-3609delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501105 | ||||||
| chr10:80501119 | T | C | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-3609T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501119 | |||||||
| chr10:80501120 | C | T | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-3608C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501120 | |||||||
| chr10:80501121 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-3607T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501121 | |||||||
| chr10:80501150 | G | C | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-3578G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501150 | |||||||
| chr10:80501209 | C | T | 1 | a0001c0001t0040g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82-3519C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501209 | |||||||
| chr10:80501214 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-3514C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501214 | |||||||
| chr10:80501270 | A | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-3458A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501270 | |||||||
| chr10:80501285 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-3443C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501285 | |||||||
| chr10:80501286 | CT | C | 96 | a0001c0001t0001g0175 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
99 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.82-3422delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501286 | ||||||
| chr10:80501286 | CTT | C | 122 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(119): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.82-3423_82-3422del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501286 | ||||||
| chr10:80501326 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.82-3402A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501326 | |||||||
| chr10:80501687 | A | G | 20 | a0001c0001t0001g0163 a0001c0001t0004g0008 a0001c0001t0004g0021 others(17): Show |
20 | HG00597.hp2 HG02004.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.82-3041A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501687 | |||||||
| chr10:80501900 | CGTT | C | 20 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-2823_82-2821del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501900 | ||||||
| chr10:80501978 | G | C | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-2750G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501978 | |||||||
| chr10:80502204 | G | A | 1 | a0001c0001t0009g0230 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.82-2524G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502204 | |||||||
| chr10:80502309 | C | T | 1 | a0001c0001t0047g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82-2419C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502309 | |||||||
| chr10:80502328 | C | G | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-2400C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502328 | |||||||
| chr10:80502552 | A | C | 3 | a0001c0001t0019g0109 a0001c0001t0019g0116 a0001c0001t0019g0214 |
3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.82-2176A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502552 | |||||||
| chr10:80502651 | G | T | 25 | a0001c0001t0001g0207 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
27 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-2077G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502651 | |||||||
| chr10:80502658 | G | A | 1 | a0001c0001t0033g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-2070G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502658 | |||||||
| chr10:80502683 | C | T | 1 | a0001c0001t0028g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.82-2045C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502683 | |||||||
| chr10:80502692 | G | A | 24 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0139 others(21): Show |
25 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.82-2036G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502692 | |||||||
| chr10:80502735 | G | A | 4 | a0001c0001t0016g0002 a0001c0001t0017g0003 a0001c0001t0017g0054 others(1): Show |
6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1993G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502735 | |||||||
| chr10:80502758 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.82-1970G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502758 | |||||||
| chr10:80502768 | A | G | 11 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-1960A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502768 | |||||||
| chr10:80503070 | C | T | 50 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(47): Show |
53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.82-1658C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503070 | |||||||
| chr10:80503120 | TG | T | 119 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(116): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.82-1604delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80503120 | ||||||
| chr10:80503214 | C | T | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82-1514C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503214 | |||||||
| chr10:80503757 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.82-971A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503757 | |||||||
| chr10:80503826 | G | A | 1 | a0001c0001t0004g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82-902G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503826 | |||||||
| chr10:80503927 | G | C | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.82-801G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503927 | |||||||
| chr10:80504082 | C | G | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82-646C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504082 | |||||||
| chr10:80504126 | A | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-602A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504126 | |||||||
| chr10:80504168 | C | G | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-560C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504168 | |||||||
| chr10:80504198 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0070 others(18): Show |
21 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.82-530A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504198 | |||||||
| chr10:80504390 | C | T | 1 | a0001c0001t0033g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-338C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504390 | |||||||
| chr10:80504524 | A | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-204A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504524 | |||||||
| chr10:80504667 | G | A | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-61G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504667 | |||||||
| chr10:80504933 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.132+155C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80504933 | |||||||
| chr10:80504973 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.132+195G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80504973 | |||||||
| chr10:80505013 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.132+235A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505013 | |||||||
| chr10:80505057 | A | G | 139 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(136): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.132+279A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505057 | |||||||
| chr10:80505079 | G | A | 1 | a0001c0001t0047g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.132+301G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505079 | |||||||
| chr10:80505096 | C | T | 10 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(7): Show |
10 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+318C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505096 | |||||||
| chr10:80505515 | A | G | 229 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(226): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.132+737A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505515 | |||||||
| chr10:80506086 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.133-1142C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506086 | |||||||
| chr10:80506158 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0061 a0001c0001t0002g0062 |
4 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-1070A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506158 | |||||||
| chr10:80506676 | T | C | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-552T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506676 | |||||||
| chr10:80506690 | C | T | 1 | a0001c0001t0009g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133-538C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506690 | |||||||
| chr10:80506707 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-521C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506707 | |||||||
| chr10:80506920 | C | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-308C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506920 | |||||||
| chr10:80507049 | C | T | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.133-179C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80507049 | |||||||
| chr10:80507096 | G | A | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-132G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80507096 | |||||||
| chr10:80507480 | C | G | 21 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(18): Show |
22 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+106C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507480 | |||||||
| chr10:80507824 | A | C | 1 | a0001c0001t0002g0136 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.279+450A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507824 | |||||||
| chr10:80507855 | A | G | 40 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(37): Show |
41 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.279+481A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507855 | |||||||
| chr10:80507855 | A | T | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.279+481A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507855 | |||||||
| chr10:80507881 | C | G | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+507C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507881 | |||||||
| chr10:80508032 | A | G | 10 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(7): Show |
10 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+658A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508032 | |||||||
| chr10:80508068 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+694C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508068 | |||||||
| chr10:80508094 | G | A | 30 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(27): Show |
32 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.279+720G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508094 | |||||||
| chr10:80508119 | C | CTT | 6 | a0001c0001t0018g0119 a0001c0001t0019g0109 a0001c0001t0019g0116 others(3): Show |
6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+758_279+759dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 80508119 | ||||||
| chr10:80508133 | T | TTG | 8 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(5): Show |
8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+759_279+760ins others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508133 | |||||||
| chr10:80508133 | T | TTTG | 30 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(27): Show |
31 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+759_279+760ins others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508133 | |||||||
| chr10:80508140 | G | A | 1 | a0001c0004t0009g0096 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.279+766G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508140 | |||||||
| chr10:80508169 | G | T | 1 | a0001c0001t0030g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.279+795G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508169 | |||||||
| chr10:80508189 | A | C | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+815A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508189 | |||||||
| chr10:80508260 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.279+886C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508260 | |||||||
| chr10:80508364 | C | T | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 |
3 | HG02723.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.280-937C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508364 | |||||||
| chr10:80508365 | G | A | 2 | a0001c0001t0047g0212 a0001c0001t0050g0226 |
2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.280-936G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508365 | |||||||
| chr10:80508398 | G | T | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.280-903G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508398 | |||||||
| chr10:80508410 | G | T | 1 | a0001c0001t0012g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-891G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508410 | |||||||
| chr10:80508413 | C | T | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-888C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508413 | |||||||
| chr10:80508684 | G | T | 1 | a0001c0001t0006g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-617G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508684 | |||||||
| chr10:80508687 | C | T | 3 | a0001c0001t0018g0119 a0001c0001t0033g0122 a0001c0001t0057g0118 |
3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.280-614C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508687 | |||||||
| chr10:80508834 | T | A | 1 | a0001c0001t0050g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.280-467T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508834 | |||||||
| chr10:80509021 | A | G | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-280A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509021 | |||||||
| chr10:80509120 | G | A | 1 | a0001c0001t0018g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280-181G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509120 | |||||||
| chr10:80509175 | G | A | 19 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(16): Show |
19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-126G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509175 | |||||||
| chr10:80509482 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(121): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.450+11C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509482 | |||||||
| chr10:80509705 | T | C | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.450+234T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509705 | |||||||
| chr10:80509816 | C | T | 1 | a0001c0001t0019g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+345C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509816 | |||||||
| chr10:80509837 | C | G | 1 | a0001c0001t0016g0002 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+366C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509837 | |||||||
| chr10:80509855 | A | G | 221 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(218): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.450+384A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509855 | |||||||
| chr10:80509885 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+414C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509885 | |||||||
| chr10:80509971 | A | G | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.450+500A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509971 | |||||||
| chr10:80510023 | C | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0039 others(1): Show |
4 | HG00280.hp2 HG01123.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+552C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510023 | |||||||
| chr10:80510092 | C | G | 227 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.450+621C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510092 | |||||||
| chr10:80510276 | G | A | 112 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(109): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+805G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510276 | |||||||
| chr10:80510412 | A | G | 1 | a0001c0001t0019g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.450+941A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510412 | |||||||
| chr10:80510462 | C | T | 41 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.450+991C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510462 | |||||||
| chr10:80510519 | C | T | 8 | a0001c0001t0002g0073 a0001c0001t0002g0181 a0001c0001t0002g0227 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+1048C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510519 | |||||||
| chr10:80510612 | C | T | 7 | a0001c0001t0014g0056 a0001c0001t0018g0119 a0001c0001t0019g0109 others(4): Show |
7 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+1141C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510612 | |||||||
| chr10:80510648 | G | A | 21 | a0001c0001t0012g0017 a0001c0001t0012g0018 a0001c0001t0012g0019 others(18): Show |
22 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.450+1177G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510648 | |||||||
| chr10:80510715 | AT | A | 9 | a0001c0001t0007g0044 a0001c0001t0007g0052 a0001c0001t0007g0075 others(6): Show |
9 | HG01175.hp2 HG02486.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+1245delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510715 | |||||||
| chr10:80510747 | A | G | 1 | a0001c0001t0011g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.450+1276A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510747 | |||||||
| chr10:80510805 | C | T | 4 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(1): Show |
4 | HG02723.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1334C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510805 | |||||||
| chr10:80510812 | G | A | 3 | a0001c0001t0017g0003 a0001c0001t0017g0054 a0001c0001t0017g0055 |
4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1332G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510812 | |||||||
| chr10:80510924 | A | G | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.451-1220A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510924 | |||||||
| chr10:80510997 | G | A | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.451-1147G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510997 | |||||||
| chr10:80511085 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0015g0205 |
2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.451-1059T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511085 | |||||||
| chr10:80511207 | A | T | 11 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(8): Show |
12 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-937A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511207 | |||||||
| chr10:80511220 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.451-924C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511220 | |||||||
| chr10:80511222 | A | T | 17 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(14): Show |
18 | HG01433.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-922A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511222 | |||||||
| chr10:80511418 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0043g0029 |
2 | HG01069.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.451-726C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511418 | |||||||
| chr10:80511458 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0015g0193 |
2 | HG00438.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.451-686C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511458 | |||||||
| chr10:80511585 | G | A | 230 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(227): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.451-559G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511585 | |||||||
| chr10:80511711 | C | CCT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0166 a0001c0001t0001g0202 others(8): Show |
12 | HG00558.hp1 HG01074.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-373_451-372dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | C | CCTCT | 4 | a0001c0001t0001g0163 a0001c0001t0003g0051 a0001c0001t0004g0102 others(1): Show |
4 | HG01361.hp2 HG02080.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-375_451-372dup others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | C | CCTCTCT | 5 | a0001c0001t0001g0178 a0001c0001t0003g0040 a0001c0001t0004g0103 others(2): Show |
5 | HG00621.hp2 HG02258.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-377_451-372dup others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | C | CCTCTCTC others(3): Show |
4 | a0001c0001t0001g0151 a0001c0001t0004g0113 a0001c0001t0020g0148 others(1): Show |
4 | HG01081.hp1 HG01109.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-381_451-372dup others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | C | CCTCTCTC others(5): Show |
1 | a0001c0001t0001g0199 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-383_451-372dup others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCT | C | 16 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0170 others(13): Show |
16 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-373_451-372del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCT | C | 16 | a0001c0001t0001g0070 a0001c0001t0001g0156 a0001c0001t0001g0192 others(13): Show |
16 | HG00642.hp2 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-375_451-372del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCT | C | 31 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0175 others(28): Show |
32 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.451-377_451-372del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(1): Show |
C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0211 a0001c0001t0002g0072 others(8): Show |
11 | HG01167.hp2 HG01884.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-379_451-372del others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(3): Show |
C | 24 | a0001c0001t0001g0027 a0001c0001t0001g0195 a0001c0001t0001g0209 others(21): Show |
26 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.451-381_451-372del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(5): Show |
C | 29 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0208 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-383_451-372del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(7): Show |
C | 11 | a0001c0001t0001g0154 a0001c0001t0002g0064 a0001c0001t0002g0090 others(8): Show |
11 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-385_451-372del others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(9): Show |
C | 11 | a0001c0001t0002g0006 a0001c0001t0002g0083 a0001c0001t0002g0084 others(8): Show |
12 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-387_451-372del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(11): Show |
C | 5 | a0001c0001t0012g0017 a0001c0001t0018g0119 a0001c0001t0022g0242 others(2): Show |
5 | HG01081.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-389_451-372del others(18): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(13): Show |
C | 4 | a0001c0001t0003g0032 a0001c0001t0012g0213 a0001c0001t0024g0110 others(1): Show |
4 | HG01257.hp1 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-391_451-372del others(20): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(17): Show |
C | 6 | a0001c0001t0011g0007 a0001c0001t0011g0133 a0001c0001t0019g0109 others(3): Show |
7 | HG00741.hp1 HG01255.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-395_451-372del others(24): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511711 | CCTCTCTC others(21): Show |
C | 4 | a0001c0001t0011g0194 a0001c0002t0005g0001 a0001c0002t0005g0228 others(1): Show |
5 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-399_451-372del others(28): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | ||||||
| chr10:80511726 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.451-418C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511726 | |||||||
| chr10:80511761 | TCTCTCTC others(4): Show |
T | 2 | a0001c0001t0010g0066 a0001c0001t0010g0125 |
2 | HG01358.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.451-381_451-371del others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511761 | ||||||
| chr10:80511763 | TCTCTCTC others(2): Show |
T | 3 | a0001c0001t0007g0075 a0001c0001t0030g0146 a0001c0001t0046g0035 |
3 | HG00642.hp1 HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.451-379_451-371del others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511763 | ||||||
| chr10:80511765 | TCTCTCTC | T | 4 | a0001c0001t0001g0189 a0001c0001t0048g0121 a0001c0001t0051g0058 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-377_451-371del others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511765 | ||||||
| chr10:80511769 | TCTC | T | 4 | a0001c0001t0001g0218 a0001c0001t0003g0041 a0001c0001t0006g0112 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-373_451-371del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511769 | ||||||
| chr10:80511771 | T | C | 19 | a0001c0001t0002g0004 a0001c0001t0002g0061 a0001c0001t0002g0062 others(16): Show |
21 | HG01109.hp1 HG01167.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.451-373T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511771 | |||||||
| chr10:80511771 | TC | T | 5 | a0001c0001t0001g0069 a0001c0001t0008g0198 a0001c0001t0039g0127 others(2): Show |
5 | HG01099.hp1 HG01258.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-369delC | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511771 | ||||||
| chr10:80511780 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-353_451-338dup others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511780 | ||||||
| chr10:80511837 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.451-307G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511837 | |||||||
| chr10:80511910 | C | G | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.451-234C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511910 | |||||||
| chr10:80512302 | C | T | 1 | a0001c0001t0040g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.576+33C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512302 | |||||||
| chr10:80512433 | T | C | 17 | a0001c0001t0006g0034 a0001c0001t0006g0046 a0001c0001t0006g0068 others(14): Show |
18 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.576+164T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512433 | |||||||
| chr10:80512455 | T | G | 14 | a0001c0002t0005g0001 a0001c0002t0005g0024 a0001c0002t0005g0025 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.576+186T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512455 | |||||||
| chr10:80512469 | A | G | 3 | a0001c0001t0014g0053 a0001c0001t0048g0121 a0001c0003t0014g0120 |
3 | HG02280.hp1 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.576+200A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512469 | |||||||
| chr10:80512590 | T | C | 3 | a0001c0001t0017g0003 a0001c0001t0017g0054 a0001c0001t0017g0055 |
4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+321T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512590 | |||||||
| chr10:80512631 | C | T | 3 | a0001c0001t0008g0190 a0001c0001t0008g0196 a0001c0001t0008g0198 |
3 | HG00735.hp1 HG01099.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.576+362C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512631 | |||||||
| chr10:80512677 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.576+408A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512677 | |||||||
| chr10:80512750 | G | A | 3 | a0001c0001t0019g0109 a0001c0001t0019g0116 a0001c0001t0019g0214 |
3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.576+481G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512750 | |||||||
| chr10:80512871 | TTTG | T | 41 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0004g0008 others(38): Show |
42 | HG00597.hp2 HG01074.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.576+629_576+631del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | ||||||
| chr10:80512871 | TTTGTTG | T | 14 | a0001c0002t0005g0001 a0001c0002t0005g0024 a0001c0002t0005g0025 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.576+626_576+631del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | ||||||
| chr10:80512871 | TTTGTTGT others(2): Show |
T | 5 | a0001c0001t0016g0222 a0001c0001t0016g0223 a0001c0001t0022g0242 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+623_576+631del others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | ||||||
| chr10:80512871 | TTTGTTGT others(5): Show |
T | 167 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(164): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.576+620_576+631del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | ||||||
| chr10:80513039 | C | T | 2 | a0001c0001t0006g0046 a0001c0001t0044g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.576+770C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513039 | |||||||
| chr10:80513185 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577-834C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513185 | |||||||
| chr10:80513323 | T | C | 188 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(185): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.577-696T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513323 | |||||||
| chr10:80513509 | G | A | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.577-510G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513509 | |||||||
| chr10:80513680 | G | A | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.577-339G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513680 | |||||||
| chr10:80513784 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.577-235G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513784 | |||||||
| chr10:80513884 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-135G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513884 | |||||||
| chr10:80513885 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-134C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513885 | |||||||
| chr10:80514012 | C | A | 1 | a0001c0001t0016g0002 | 2 | HG02896.hp1 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.577-7C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80514012 | |||||||
| chr10:80514486 | G | T | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.621+423G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514486 | |||||||
| chr10:80514666 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.621+603G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514666 | |||||||
| chr10:80514818 | G | A | 4 | a0001c0001t0011g0007 a0001c0001t0011g0076 a0001c0001t0011g0133 others(1): Show |
5 | HG00741.hp1 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+755G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514818 | |||||||
| chr10:80515231 | C | T | 3 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 |
3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.622-973C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515231 | |||||||
| chr10:80515335 | C | T | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.622-869C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515335 | |||||||
| chr10:80515346 | C | T | 2 | a0001c0001t0024g0110 a0001c0001t0024g0241 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.622-858C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515346 | |||||||
| chr10:80515798 | C | A | 5 | a0001c0001t0004g0102 a0001c0001t0004g0103 a0001c0001t0004g0113 others(2): Show |
5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-406C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515798 | |||||||
| chr10:80515833 | G | A | 9 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(6): Show |
9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-371G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515833 | |||||||
| chr10:80515931 | A | G | 14 | a0001c0002t0005g0001 a0001c0002t0005g0024 a0001c0002t0005g0025 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-273A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515931 | |||||||
| chr10:80515938 | G | A | 4 | a0001c0001t0022g0242 a0001c0001t0022g0243 a0001c0001t0022g0244 others(1): Show |
4 | HG02258.hp2 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-266G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515938 | |||||||
| chr10:80516009 | C | T | 14 | a0001c0002t0005g0001 a0001c0002t0005g0024 a0001c0002t0005g0025 others(11): Show |
15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-195C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516009 | |||||||
| chr10:80516025 | A | G | 9 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(6): Show |
9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-179A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516025 | |||||||
| chr10:80516039 | G | T | 55 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(52): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.622-165G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516039 | |||||||
| chr10:80516067 | G | A | 3 | a0001c0002t0021g0182 a0001c0002t0021g0183 a0001c0002t0021g0185 |
3 | HG01884.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.622-137G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516067 | |||||||
| chr10:80516129 | C | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0207 |
3 | HG01192.hp1 HG01358.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.622-75C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516129 | |||||||
| chr10:80516363 | T | C | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 |
3 | HG02723.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.741+40T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516363 | |||||||
| chr10:80516439 | A | T | 12 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(9): Show |
13 | HG01433.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.741+116A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516439 | |||||||
| chr10:80516525 | C | T | 1 | a0001c0001t0013g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.741+202C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516525 | |||||||
| chr10:80516975 | C | T | 2 | a0001c0001t0007g0078 a0001c0001t0038g0074 |
2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.741+652C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516975 | |||||||
| chr10:80517036 | C | T | 1 | a0001c0001t0057g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.741+713C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517036 | |||||||
| chr10:80517039 | G | T | 1 | a0001c0001t0027g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.741+716G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517039 | |||||||
| chr10:80517359 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.742-546A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517359 | |||||||
| chr10:80517541 | G | C | 235 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(232): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.742-364G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517541 | |||||||
| chr10:80517554 | C | T | 9 | a0001c0001t0013g0087 a0001c0001t0013g0088 a0001c0001t0013g0089 others(6): Show |
9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.742-351C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517554 | |||||||
| chr10:80517585 | G | A | 36 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(33): Show |
38 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.742-320G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517585 | |||||||
| chr10:80517651 | G | C | 20 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0063 others(17): Show |
20 | HG00597.hp2 HG02004.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.742-254G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517651 | |||||||
| chr10:80517682 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.742-223T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517682 | |||||||
| chr10:80517811 | C | T | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.742-94C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517811 | |||||||
| chr10:80517854 | C | T | 1 | a0001c0001t0008g0131 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.742-51C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517854 |