Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283578 |
| ensemblid | ENSG00000100580.8 |
| hgncid | 18633 |
| symbol | TMED8 |
| name | transmembrane p24 trafficking protein family member 8 |
| refseq_nuc | NM_213601.3 |
| refseq_prot | NP_998766.1 |
| ensembl_nuc | ENST00000216468.8 |
| ensembl_prot | ENSP00000216468.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77335029 |
| end | 77377094 |
| strand | - |
| ver | v1.2 |
| region | chr14:77335029-77377094 |
| region5000 | chr14:77330029-77382094 |
| regionname0 | TMED8_chr14_77335029_77377094 |
| regionname5000 | TMED8_chr14_77330029_77382094 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 325 | 211 | 39 | 35 | 119 | 4 | 12 | 90 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| a0002 | 0/0 | 325 | 64 | 35 | 9 | 5 | 5 | 10 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLK others(320): Show |
chr14 | 77330029 | 77382094 |
| a0003 | 0/0 | 325 | 49 | 11 | 18 | 1 | 7 | 12 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| a0004 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| a0005 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| a0006 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| a0007 | 0/0 | 325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | MSDLQ others(320): Show |
chr14 | 77330029 | 77382094 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 975 | 207 | 36 | 34 | 119 | 4 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0001c0005 | 0/0 | 975 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0001c0008 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0001c0009 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0002c0002 | 0/0 | 975 | 61 | 33 | 8 | 5 | 5 | 10 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0002c0004 | 0/0 | 975 | 3 | 2 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0003c0003 | 0/0 | 975 | 49 | 11 | 18 | 1 | 7 | 12 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0004c0007 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0005c0006 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0006c0010 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 | ||
| a0007c0011 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ATGTC others(970): Show |
chr14 | 77330029 | 77382094 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7769 | 60 | 0 | 11 | 46 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0002 | 0/0 | 7770 | 36 | 4 | 4 | 27 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0003 | 0/0 | 7760 | 5 | 0 | 1 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0004 | 0/0 | 7771 | 23 | 0 | 9 | 12 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0005 | 0/0 | 7769 | 9 | 5 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0006 | 0/0 | 7771 | 12 | 4 | 3 | 1 | 2 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0007 | 0/0 | 7763 | 7 | 0 | 0 | 6 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7758): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0008 | 0/0 | 7768 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0010 | 0/0 | 7769 | 7 | 7 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0011 | 0/0 | 7767 | 5 | 0 | 2 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7762): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0012 | 0/0 | 7769 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0014 | 0/0 | 7770 | 4 | 0 | 0 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0015 | 0/0 | 7760 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0018 | 0/0 | 7769 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0019 | 0/0 | 7769 | 3 | 0 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0020 | 0/0 | 7766 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7761): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0023 | 0/0 | 7769 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0025 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0026 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0027 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0028 | 0/0 | 7768 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0031 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0033 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0036 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0038 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0040 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0043 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0044 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0045 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0046 | 0/0 | 7797 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7792): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0047 | 1/0 | 7761 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7756): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0050 | 0/0 | 7761 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7756): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0051 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0052 | 0/0 | 7770 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0054 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0055 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7758): Show |
chr14 | 77330029 | 77382094 |
| a0001c0001t0056 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0005t0024 | 0/0 | 7769 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0001c0008t0032 | 0/0 | 7768 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0001c0009t0013 | 0/0 | 7770 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0001 | 0/0 | 7769 | 19 | 1 | 3 | 5 | 4 | 6 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0002 | 0/0 | 7770 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0003 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0005 | 0/0 | 7769 | 5 | 5 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0006 | 0/0 | 7771 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0008 | 0/0 | 7768 | 10 | 8 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0009 | 0/0 | 7769 | 10 | 9 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0012 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0017 | 0/0 | 7769 | 3 | 0 | 2 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0022 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0029 | 0/0 | 7768 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7763): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0037 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0039 | 0/0 | 7769 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0041 | 0/0 | 7769 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0042 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0049 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0002c0002t0053 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7757): Show |
chr14 | 77330029 | 77382094 |
| a0002c0004t0013 | 0/0 | 7770 | 3 | 2 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0002 | 0/0 | 7770 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7765): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0003 | 0/0 | 7760 | 26 | 2 | 13 | 1 | 5 | 5 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0004 | 0/0 | 7771 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0005 | 0/0 | 7769 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0006 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0007 | 0/0 | 7763 | 6 | 1 | 3 | 0 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7758): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0016 | 0/0 | 7760 | 3 | 0 | 0 | 0 | 0 | 3 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0021 | 0/0 | 7769 | 2 | 1 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0022 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0030 | 0/0 | 7762 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7757): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0034 | 0/0 | 7760 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0003c0003t0035 | 0/0 | 7760 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7755): Show |
chr14 | 77330029 | 77382094 |
| a0004c0007t0048 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0005c0006t0005 | 0/0 | 7769 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| a0006c0010t0025 | 0/0 | 7771 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7766): Show |
chr14 | 77330029 | 77382094 |
| a0007c0011t0001 | 0/0 | 7769 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | ACTCG others(7764): Show |
chr14 | 77330029 | 77382094 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0003 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0011g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0011g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0011g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0012g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0014g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0014g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0014g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0015g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0018g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0018g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0019g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0019g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0019g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0020g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0023g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0023g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0025g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0026g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0027g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0028g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0031g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0033g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0038g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0040g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0043g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0044g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0045g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0046g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0047g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0050g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0051g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0052g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0054g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0055g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0001t0056g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0005t0024g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0005t0024g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0008t0032g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0001c0009t0013g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0017g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0017g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0017g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0022g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0029g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0037g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0039g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0041g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0042g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0049g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0002t0053g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0004t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0004t0013g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0002c0004t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0001 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0007g0005 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0016g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0016g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0021g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0021g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0022g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0030g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0034g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0003c0003t0035g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0004c0007t0048g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0005c0006t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0006c0010t0025g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| a0007c0011t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0037 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00099 | hp2 | a0003 | c0003 | t0003 | g0097 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00140 | hp1 | a0003 | c0003 | t0007 | g0005 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00140 | hp2 | a0003 | c0003 | t0003 | g0009 | EUR | GBR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0190 | EUR | FIN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0039 | EUR | FIN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00597 | hp1 | a0001 | c0001 | t0014 | g0289 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00639 | hp1 | a0003 | c0003 | t0003 | g0095 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00642 | hp1 | a0003 | c0003 | t0003 | g0096 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00642 | hp2 | a0002 | c0002 | t0017 | g0055 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00733 | hp1 | a0003 | c0003 | t0007 | g0005 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0236 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00735 | hp1 | a0002 | c0002 | t0017 | g0054 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00738 | hp1 | a0003 | c0003 | t0003 | g0009 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00741 | hp1 | a0003 | c0003 | t0003 | g0104 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01069 | hp2 | a0003 | c0003 | t0007 | g0086 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0167 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01081 | hp1 | a0001 | c0001 | t0056 | g0171 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01081 | hp2 | a0002 | c0004 | t0013 | g0028 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01106 | hp1 | a0003 | c0003 | t0003 | g0116 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01106 | hp2 | a0001 | c0001 | t0051 | g0158 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01109 | hp2 | a0001 | c0005 | t0024 | g0288 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01167 | hp1 | a0003 | c0003 | t0021 | g0092 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0094 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01169 | hp1 | a0003 | c0003 | t0003 | g0008 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01175 | hp1 | a0002 | c0002 | t0041 | g0041 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01243 | hp1 | a0003 | c0003 | t0007 | g0087 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01243 | hp2 | a0002 | c0002 | t0009 | g0059 | AMR | PUR | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01255 | hp1 | a0003 | c0003 | t0003 | g0001 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0156 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01258 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01515 | hp2 | a0003 | c0003 | t0003 | g0111 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01516 | hp1 | a0003 | c0003 | t0030 | g0085 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01516 | hp2 | a0003 | c0003 | t0003 | g0010 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0010 | EUR | IBS | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01884 | hp1 | a0001 | c0001 | t0054 | g0256 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01884 | hp2 | a0004 | c0007 | t0048 | g0117 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0211 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0001 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01981 | hp1 | a0003 | c0003 | t0034 | g0108 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01993 | hp1 | a0003 | c0003 | t0003 | g0107 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01993 | hp2 | a0001 | c0001 | t0045 | g0142 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0101 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02145 | hp1 | a0003 | c0003 | t0022 | g0088 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02145 | hp2 | a0002 | c0002 | t0005 | g0025 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02155 | hp1 | a0001 | c0001 | t0014 | g0291 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02165 | hp1 | a0001 | c0001 | t0028 | g0273 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CDX | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0218 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02273 | hp1 | a0001 | c0001 | t0050 | g0143 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02273 | hp2 | a0003 | c0003 | t0003 | g0098 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02280 | hp1 | a0002 | c0002 | t0009 | g0004 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02280 | hp2 | a0003 | c0003 | t0007 | g0084 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0052 | AMR | PEL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02451 | hp1 | a0003 | c0003 | t0004 | g0103 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02602 | hp1 | a0002 | c0002 | t0008 | g0069 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0214 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02615 | hp2 | a0002 | c0002 | t0037 | g0049 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02622 | hp1 | a0002 | c0002 | t0008 | g0065 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02622 | hp2 | a0002 | c0002 | t0049 | g0026 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0286 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02630 | hp2 | a0003 | c0003 | t0021 | g0089 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02647 | hp1 | a0002 | c0004 | t0013 | g0027 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0219 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02698 | hp1 | a0002 | c0002 | t0008 | g0064 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02698 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02723 | hp1 | a0002 | c0002 | t0006 | g0030 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0215 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02735 | hp1 | a0003 | c0003 | t0002 | g0113 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02735 | hp2 | a0003 | c0003 | t0003 | g0093 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02738 | hp1 | a0001 | c0001 | t0023 | g0257 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02809 | hp1 | a0005 | c0006 | t0005 | g0083 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02809 | hp2 | a0002 | c0002 | t0005 | g0046 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0004 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02818 | hp2 | a0002 | c0002 | t0008 | g0074 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02886 | hp1 | a0001 | c0009 | t0013 | g0126 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02886 | hp2 | a0002 | c0002 | t0008 | g0081 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02895 | hp1 | a0002 | c0002 | t0009 | g0060 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02897 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02922 | hp1 | a0001 | c0001 | t0025 | g0123 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02922 | hp2 | a0002 | c0002 | t0009 | g0004 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02965 | hp1 | a0001 | c0008 | t0032 | g0280 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02965 | hp2 | a0006 | c0010 | t0025 | g0124 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02970 | hp1 | a0002 | c0002 | t0009 | g0057 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02970 | hp2 | a0002 | c0002 | t0008 | g0071 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02976 | hp1 | a0002 | c0002 | t0005 | g0070 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02976 | hp2 | a0002 | c0002 | t0005 | g0051 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0100 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0213 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03041 | hp2 | a0001 | c0005 | t0024 | g0287 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03098 | hp1 | a0003 | c0003 | t0005 | g0118 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0192 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03130 | hp1 | a0002 | c0002 | t0009 | g0058 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0216 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03139 | hp1 | a0002 | c0002 | t0006 | g0063 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03195 | hp2 | a0002 | c0004 | t0013 | g0029 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03225 | hp1 | a0001 | c0001 | t0036 | g0210 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0056 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03239 | hp2 | a0001 | c0001 | t0011 | g0180 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03491 | hp1 | a0002 | c0002 | t0029 | g0024 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0012 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03516 | hp1 | a0002 | c0002 | t0008 | g0072 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03516 | hp2 | a0001 | c0001 | t0020 | g0277 | AFR | ESN | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03540 | hp1 | a0001 | c0001 | t0038 | g0182 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0195 | AFR | GWD | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03579 | hp1 | a0002 | c0002 | t0009 | g0061 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03579 | hp2 | a0002 | c0002 | t0008 | g0068 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03669 | hp1 | a0003 | c0003 | t0007 | g0005 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0099 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03710 | hp1 | a0002 | c0002 | t0039 | g0079 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03710 | hp2 | a0003 | c0003 | t0016 | g0106 | SAS | PJL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03831 | hp1 | a0003 | c0003 | t0016 | g0109 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04184 | hp1 | a0003 | c0003 | t0035 | g0110 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0115 | SAS | BEB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04199 | hp2 | a0003 | c0003 | t0016 | g0105 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04204 | hp1 | a0001 | c0001 | t0033 | g0197 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG04204 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | STU | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18522 | hp1 | a0002 | c0002 | t0008 | g0067 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18906 | hp1 | a0002 | c0002 | t0042 | g0050 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18944 | hp1 | a0001 | c0001 | t0014 | g0292 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18947 | hp1 | a0001 | c0001 | t0018 | g0169 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18948 | hp1 | a0001 | c0001 | t0044 | g0205 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0141 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18970 | hp2 | a0007 | c0011 | t0001 | g0165 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18974 | hp2 | a0001 | c0001 | t0026 | g0279 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18983 | hp1 | a0001 | c0001 | t0052 | g0263 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18983 | hp2 | a0001 | c0001 | t0019 | g0254 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18990 | hp1 | a0001 | c0001 | t0055 | g0130 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA18990 | hp2 | a0001 | c0001 | t0014 | g0290 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0248 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19009 | hp1 | a0001 | c0001 | t0019 | g0249 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19011 | hp2 | a0001 | c0001 | t0027 | g0272 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0112 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19043 | hp2 | a0001 | c0001 | t0031 | g0198 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19058 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19060 | hp1 | a0001 | c0001 | t0018 | g0163 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19077 | hp1 | a0001 | c0001 | t0019 | g0250 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19080 | hp2 | a0001 | c0001 | t0040 | g0150 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19087 | hp2 | a0001 | c0001 | t0043 | g0231 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19089 | hp1 | a0001 | c0001 | t0046 | g0267 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19240 | hp1 | a0002 | c0002 | t0008 | g0066 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA19240 | hp2 | a0003 | c0003 | t0005 | g0091 | AFR | YRI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0191 | AFR | ASW | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ASW | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0237 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0131 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20805 | hp1 | a0002 | c0002 | t0017 | g0053 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0019 | EUR | TSI | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20905 | hp1 | a0001 | c0001 | t0011 | g0012 | SAS | GIH | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20905 | hp2 | a0001 | c0001 | t0023 | g0225 | SAS | GIH | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG01123 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | CLM | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02109 | hp1 | a0002 | c0002 | t0009 | g0062 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0201 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02486 | hp2 | a0002 | c0002 | t0022 | g0082 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02559 | hp1 | a0003 | c0003 | t0005 | g0090 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG02559 | hp2 | a0002 | c0002 | t0005 | g0048 | AFR | ACB | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | MSL | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| HG06807 | hp2 | a0003 | c0003 | t0006 | g0114 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0217 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0102 | AFR | USA | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA21309 | hp1 | a0002 | c0002 | t0053 | g0073 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| NA21309 | hp2 | a0002 | c0002 | t0012 | g0047 | AFR | LWK | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0134 | REF | REF | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0047 | g0258 | REF | REF | TMED8_chr14_77330029_77382094 | TMED8 | chr14 | 77330029 | 77382094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77343185 | C | A | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.753G>T | p.Glu251Asp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 794/7761 | 753/978 | 251/325 | chr14 | 77343185 | |||
| chr14:77346386 | T | A | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.290A>T | p.Asp97Val | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/6 | 331/7761 | 290/978 | 97/325 | chr14 | 77346386 | |||
| chr14:77346432 | G | A | 1 | a0007 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.244C>T | p.Arg82Trp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/6 | 285/7761 | 244/978 | 82/325 | chr14 | 77346432 | |||
| chr14:77377010 | G | T | 1 | a0002 | 64 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.44C>A | p.Pro15His | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 85/7761 | 44/978 | 15/325 | chr14 | 77377010 | |||
| chr14:77377020 | A | G | 2 | a0003 a0004 |
50 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(47): Show |
missense_variant | MODERATE | c.34T>C | p.Ser12Pro | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 75/7761 | 34/978 | 12/325 | chr14 | 77377020 | |||
| chr14:77377025 | G | T | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.29C>A | p.Pro10Gln | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 70/7761 | 29/978 | 10/325 | chr14 | 77377025 | |||
| chr14:77377041 | G | T | 1 | a0002 | 64 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.13C>A | p.Gln5Lys | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 54/7761 | 13/978 | 5/325 | chr14 | 77377041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77341909 | G | A | 2 | a0001c0009 a0002c0004 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.840C>T | p.Tyr280Tyr | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 881/7761 | 840/978 | 280/325 | chr14 | 77341909 | |||
| chr14:77343218 | G | A | 1 | a0001c0005 | 2 | HG01109.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.720C>T | p.Asp240Asp | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 761/7761 | 720/978 | 240/325 | chr14 | 77343218 | |||
| chr14:77343464 | A | G | 1 | a0001c0008 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.474T>C | p.Ala158Ala | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/6 | 515/7761 | 474/978 | 158/325 | chr14 | 77343464 | |||
| chr14:77343743 | A | G | 1 | a0002c0004 | 3 | HG01081.hp2 HG02647.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.408T>C | p.Leu136Leu | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/6 | 449/7761 | 408/978 | 136/325 | chr14 | 77343743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77335088 | T | C | 20 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0018 others(17): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*6683A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6683 | chr14 | 77335088 | ||||||
| chr14:77335127 | G | A | 2 | a0001c0009t0013 a0002c0004t0013 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6644C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6644 | chr14 | 77335127 | ||||||
| chr14:77335145 | G | A | 2 | a0001c0009t0013 a0002c0004t0013 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6626C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6626 | chr14 | 77335145 | ||||||
| chr14:77335171 | T | C | 1 | a0002c0002t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6600A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6600 | chr14 | 77335171 | ||||||
| chr14:77335311 | G | C | 19 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0018 others(16): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*6460C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6460 | chr14 | 77335311 | ||||||
| chr14:77335501 | G | A | 1 | a0003c0003t0034 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6270C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6270 | chr14 | 77335501 | ||||||
| chr14:77335713 | C | T | 1 | a0002c0002t0041 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6058G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6058 | chr14 | 77335713 | ||||||
| chr14:77335724 | G | A | 1 | a0002c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6047C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 6047 | chr14 | 77335724 | ||||||
| chr14:77335851 | A | G | 1 | a0001c0001t0040 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5920T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5920 | chr14 | 77335851 | ||||||
| chr14:77336571 | G | A | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5200C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5200 | chr14 | 77336571 | ||||||
| chr14:77336629 | C | A | 3 | a0001c0001t0038 a0002c0002t0022 a0003c0003t0022 |
3 | HG02145.hp1 HG02486.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5142G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 5142 | chr14 | 77336629 | ||||||
| chr14:77336799 | C | T | 1 | a0001c0001t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4972G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4972 | chr14 | 77336799 | ||||||
| chr14:77336947 | C | T | 1 | a0004c0007t0048 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4824G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4824 | chr14 | 77336947 | ||||||
| chr14:77337004 | C | G | 1 | a0001c0001t0028 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4767G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4767 | chr14 | 77337004 | ||||||
| chr14:77337026 | ATAT | A | 1 | a0001c0001t0020 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4742_*4744delATA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4742 | chr14 | 77337026 | ||||||
| chr14:77337183 | C | T | 2 | a0001c0009t0013 a0002c0004t0013 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4588G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4588 | chr14 | 77337183 | ||||||
| chr14:77337209 | T | C | 4 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0033 others(1): Show |
28 | HG00323.hp1 HG00621.hp2 HG00735.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4562A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4562 | chr14 | 77337209 | ||||||
| chr14:77337250 | G | A | 1 | a0001c0001t0043 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4521C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4521 | chr14 | 77337250 | ||||||
| chr14:77337272 | C | G | 12 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0031 others(9): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4499G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4499 | chr14 | 77337272 | ||||||
| chr14:77337424 | T | G | 1 | a0001c0001t0044 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4347A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4347 | chr14 | 77337424 | ||||||
| chr14:77337446 | T | C | 1 | a0001c0001t0020 | 3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4325A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4325 | chr14 | 77337446 | ||||||
| chr14:77337576 | C | T | 1 | a0003c0003t0021 | 2 | HG01167.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4195G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4195 | chr14 | 77337576 | ||||||
| chr14:77337680 | G | A | 1 | a0001c0001t0045 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4091C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4091 | chr14 | 77337680 | ||||||
| chr14:77337771 | C | A | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4000G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 4000 | chr14 | 77337771 | ||||||
| chr14:77337812 | A | G | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3959T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3959 | chr14 | 77337812 | ||||||
| chr14:77337967 | C | T | 2 | a0001c0009t0013 a0002c0004t0013 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3804G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3804 | chr14 | 77337967 | ||||||
| chr14:77337982 | G | A | 1 | a0003c0003t0035 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3789C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3789 | chr14 | 77337982 | ||||||
| chr14:77338062 | C | T | 12 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0031 others(9): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3709G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3709 | chr14 | 77338062 | ||||||
| chr14:77338065 | A | T | 1 | a0001c0001t0052 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3706T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3706 | chr14 | 77338065 | ||||||
| chr14:77338077 | T | TAATGGGG others(21): Show |
1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3693_*3694insGGGA others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3693 | chr14 | 77338077 | ||||||
| chr14:77338201 | A | G | 1 | a0003c0003t0016 | 3 | HG03710.hp2 HG03831.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3570T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3570 | chr14 | 77338201 | ||||||
| chr14:77338237 | A | G | 12 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0031 others(9): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3534T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3534 | chr14 | 77338237 | ||||||
| chr14:77338419 | A | G | 1 | a0001c0001t0018 | 3 | NA18947.hp1 NA18962.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3352T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3352 | chr14 | 77338419 | ||||||
| chr14:77338499 | C | T | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(62): Show |
285 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*3272G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 3272 | chr14 | 77338499 | ||||||
| chr14:77338772 | ATATATT | A | 4 | a0001c0001t0007 a0001c0001t0055 a0003c0003t0007 others(1): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2993_*2998delAATA others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2993 | chr14 | 77338772 | ||||||
| chr14:77339033 | G | A | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
275 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2738C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2738 | chr14 | 77339033 | ||||||
| chr14:77339482 | G | C | 1 | a0001c0001t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2289 | chr14 | 77339482 | ||||||
| chr14:77339641 | G | C | 1 | a0001c0005t0024 | 2 | HG01109.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2130C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2130 | chr14 | 77339641 | ||||||
| chr14:77339694 | A | C | 1 | a0002c0002t0039 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2077 | chr14 | 77339694 | ||||||
| chr14:77339711 | C | T | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2060 | chr14 | 77339711 | ||||||
| chr14:77339712 | T | C | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2059A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 2059 | chr14 | 77339712 | ||||||
| chr14:77339948 | T | C | 1 | a0002c0002t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1823A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1823 | chr14 | 77339948 | ||||||
| chr14:77339986 | A | ATGAAGGA others(1): Show |
64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(61): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1784_*1785insCTCC others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1784 | chr14 | 77339986 | ||||||
| chr14:77340143 | T | C | 16 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0031 others(13): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1628A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1628 | chr14 | 77340143 | ||||||
| chr14:77340149 | G | A | 1 | a0001c0001t0051 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1622 | chr14 | 77340149 | ||||||
| chr14:77340215 | G | A | 1 | a0002c0002t0009 | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1556C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1556 | chr14 | 77340215 | ||||||
| chr14:77340457 | G | A | 2 | a0001c0001t0010 a0001c0001t0036 |
8 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1314C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1314 | chr14 | 77340457 | ||||||
| chr14:77340515 | C | G | 4 | a0001c0001t0012 a0001c0001t0038 a0002c0002t0012 others(1): Show |
6 | HG01891.hp2 HG02615.hp2 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1256G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 1256 | chr14 | 77340515 | ||||||
| chr14:77340809 | C | T | 1 | a0002c0002t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*962G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 962 | chr14 | 77340809 | ||||||
| chr14:77340930 | C | CA | 7 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0027 others(4): Show |
47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*840dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | ||||||
| chr14:77340930 | C | CAA | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0025 others(6): Show |
44 | HG00323.hp1 HG00621.hp2 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*839_*840dupTT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | ||||||
| chr14:77340930 | CA | C | 16 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0015 others(13): Show |
59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*840delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 840 | chr14 | 77340930 | ||||||
| chr14:77340954 | G | T | 1 | a0001c0001t0027 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 817 | chr14 | 77340954 | ||||||
| chr14:77341041 | A | G | 1 | a0001c0001t0026 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 730 | chr14 | 77341041 | ||||||
| chr14:77341154 | T | A | 1 | a0001c0001t0055 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 617 | chr14 | 77341154 | ||||||
| chr14:77341219 | G | A | 2 | a0001c0001t0025 a0006c0010t0025 |
2 | HG02922.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*552C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 552 | chr14 | 77341219 | ||||||
| chr14:77341467 | T | TA | 2 | a0001c0009t0013 a0002c0004t0013 |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*303dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 303 | chr14 | 77341467 | ||||||
| chr14:77341631 | AAC | A | 2 | a0001c0001t0011 a0001c0001t0056 |
6 | HG01071.hp2 HG01081.hp1 HG01255.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*138_*139delGT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 6/6 | 138 | chr14 | 77341631 | ||||||
| chr14:77377073 | C | A | 1 | a0001c0001t0014 | 4 | HG00597.hp1 HG02155.hp1 NA18944.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/6 | 20 | chr14 | 77377073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77342003 | T | C | 1 | a0002c0002t0009g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.761-15A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342003 | |||||||
| chr14:77342199 | C | G | 27 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(24): Show |
27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.761-211G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342199 | |||||||
| chr14:77342435 | A | ATCTTTAC others(5): Show |
194 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(191): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.761-448_761-447ins others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342435 | |||||||
| chr14:77342448 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.761-460T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342448 | |||||||
| chr14:77342615 | G | A | 1 | a0001c0001t0007g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.760+563C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342615 | |||||||
| chr14:77342712 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.760+466C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342712 | |||||||
| chr14:77342864 | T | A | 1 | a0001c0001t0055g0130 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.760+314A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342864 | |||||||
| chr14:77342877 | A | G | 1 | a0001c0001t0027g0272 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.760+301T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342877 | |||||||
| chr14:77342963 | G | A | 1 | a0002c0002t0008g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.760+215C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342963 | |||||||
| chr14:77342976 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(206): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.760+202T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 5/5 | chr14 | 77342976 | |||||||
| chr14:77343596 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(91): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.454+101G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/5 | chr14 | 77343596 | |||||||
| chr14:77343635 | G | T | 1 | a0001c0001t0002g0245 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.454+62C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 4/5 | chr14 | 77343635 | |||||||
| chr14:77343851 | G | C | 26 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(23): Show |
26 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.328-28C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77343851 | |||||||
| chr14:77344046 | T | C | 1 | a0001c0001t0023g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-223A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344046 | |||||||
| chr14:77344176 | C | T | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-353G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344176 | |||||||
| chr14:77344200 | A | G | 58 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(55): Show |
68 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.328-377T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344200 | |||||||
| chr14:77344370 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(91): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.328-547C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344370 | |||||||
| chr14:77344434 | T | C | 1 | a0002c0002t0008g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.328-611A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344434 | |||||||
| chr14:77344545 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-722C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344545 | |||||||
| chr14:77344652 | G | A | 2 | a0001c0001t0025g0123 a0006c0010t0025g0124 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-829C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344652 | |||||||
| chr14:77344672 | A | T | 62 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(59): Show |
72 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.328-849T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344672 | |||||||
| chr14:77344715 | C | T | 5 | a0003c0003t0007g0005 a0003c0003t0007g0084 a0003c0003t0007g0086 others(2): Show |
7 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-892G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344715 | |||||||
| chr14:77344792 | CATA | C | 4 | a0001c0001t0007g0127 a0001c0001t0007g0132 a0001c0001t0007g0133 others(1): Show |
4 | NA18953.hp2 NA18967.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-972_328-970del others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344792 | |||||||
| chr14:77344991 | C | A | 1 | a0001c0001t0005g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328-1168G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77344991 | |||||||
| chr14:77345137 | G | A | 1 | a0001c0001t0010g0216 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.327+1212C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345137 | |||||||
| chr14:77345276 | C | T | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+1073G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345276 | |||||||
| chr14:77345374 | G | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0235 a0001c0001t0001g0252 others(2): Show |
5 | HG00597.hp2 HG01981.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+975C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345374 | |||||||
| chr14:77345636 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.327+713C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345636 | |||||||
| chr14:77345638 | G | C | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+711C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345638 | |||||||
| chr14:77345659 | C | CA | 18 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0253 others(15): Show |
20 | HG01175.hp2 HG01496.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+689dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345659 | C | CAA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0129 others(39): Show |
49 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.327+688_327+689dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345659 | C | CAAA | 7 | a0001c0001t0001g0120 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG01433.hp2 HG02602.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+687_327+689dup others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345659 | CA | C | 76 | a0001c0001t0001g0022 a0001c0001t0001g0176 a0001c0001t0001g0199 others(73): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.327+689delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345659 | CAA | C | 9 | a0001c0001t0020g0023 a0001c0001t0038g0182 a0001c0005t0024g0287 others(6): Show |
10 | HG01081.hp2 HG01109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+688_327+689del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345659 | CAAAAAAA others(4): Show |
C | 56 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(53): Show |
66 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.327+679_327+689del others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345659 | |||||||
| chr14:77345708 | A | G | 1 | a0001c0001t0028g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.327+641T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345708 | |||||||
| chr14:77345772 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(179): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.327+577A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345772 | |||||||
| chr14:77345870 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.327+479C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345870 | |||||||
| chr14:77345923 | C | T | 60 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(57): Show |
70 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.327+426G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345923 | |||||||
| chr14:77345924 | G | A | 1 | a0001c0001t0004g0017 | 2 | NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.327+425C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345924 | |||||||
| chr14:77345947 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.327+402G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345947 | |||||||
| chr14:77345968 | C | CA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(86): Show |
100 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.327+380dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | |||||||
| chr14:77345968 | C | CAA | 27 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0145 others(24): Show |
28 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+379_327+380dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | |||||||
| chr14:77345968 | CA | C | 6 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0001c0005t0024g0287 others(3): Show |
8 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+380delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77345968 | |||||||
| chr14:77346073 | C | T | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+276G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346073 | |||||||
| chr14:77346199 | A | T | 194 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(191): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.327+150T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346199 | |||||||
| chr14:77346303 | T | G | 2 | a0001c0001t0006g0019 a0001c0001t0006g0236 |
3 | HG00733.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.327+46A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 3/5 | chr14 | 77346303 | |||||||
| chr14:77346624 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0155 others(1): Show |
4 | HG00408.hp2 NA18948.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-146C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346624 | |||||||
| chr14:77346627 | CA | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-150delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346627 | |||||||
| chr14:77346760 | G | GT | 148 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(145): Show |
170 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.198-283dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | G | GTT | 54 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0145 others(51): Show |
54 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.198-284_198-283dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | G | GTTT | 8 | a0001c0001t0008g0219 a0002c0002t0008g0066 a0002c0002t0008g0067 others(5): Show |
8 | HG02602.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-285_198-283dup others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | GT | G | 15 | a0001c0001t0003g0193 a0001c0001t0012g0015 a0001c0001t0012g0191 others(12): Show |
16 | HG01167.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.198-283delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | GTT | G | 35 | a0001c0001t0003g0181 a0001c0001t0003g0194 a0001c0001t0003g0196 others(32): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.198-284_198-283del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0009g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198-292_198-283del others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | GTTTTTTT others(4): Show |
G | 7 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(4): Show |
9 | HG02109.hp1 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-293_198-283del others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77346760 | GTTTTTTT others(5): Show |
G | 1 | a0002c0002t0001g0007 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.198-294_198-283del others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77346760 | |||||||
| chr14:77347081 | C | G | 1 | a0002c0002t0022g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.198-603G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347081 | |||||||
| chr14:77347346 | G | A | 9 | a0002c0002t0008g0081 a0002c0002t0009g0004 a0002c0002t0009g0056 others(6): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.198-868C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347346 | |||||||
| chr14:77347413 | C | T | 1 | a0002c0002t0005g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.198-935G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347413 | |||||||
| chr14:77347420 | C | A | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.198-942G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347420 | |||||||
| chr14:77347556 | C | T | 1 | a0001c0001t0054g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198-1078G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347556 | |||||||
| chr14:77347557 | G | A | 7 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0286 others(4): Show |
7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-1079C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347557 | |||||||
| chr14:77347658 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.198-1180C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347658 | |||||||
| chr14:77347813 | A | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-1335T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347813 | |||||||
| chr14:77347868 | A | G | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1390T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77347868 | |||||||
| chr14:77348230 | C | CT | 280 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(277): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.198-1753dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348230 | |||||||
| chr14:77348258 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.198-1780G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348258 | |||||||
| chr14:77348445 | G | A | 2 | a0003c0003t0003g0010 a0003c0003t0003g0111 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.198-1967C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348445 | |||||||
| chr14:77348468 | C | G | 1 | a0001c0001t0006g0236 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.198-1990G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348468 | |||||||
| chr14:77348518 | C | A | 1 | a0001c0001t0008g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.198-2040G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348518 | |||||||
| chr14:77348640 | A | G | 6 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0001c0005t0024g0287 others(3): Show |
7 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-2162T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348640 | |||||||
| chr14:77348668 | T | C | 9 | a0001c0001t0005g0212 a0001c0001t0005g0285 a0001c0001t0010g0211 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-2190A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348668 | |||||||
| chr14:77348731 | GTTTCT | G | 38 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(35): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.198-2258_198-2254d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348731 | |||||||
| chr14:77348941 | T | C | 1 | a0001c0001t0006g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.198-2463A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77348941 | |||||||
| chr14:77349032 | G | A | 1 | a0003c0003t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.198-2554C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349032 | |||||||
| chr14:77349106 | C | CT | 35 | a0001c0001t0001g0138 a0001c0001t0001g0148 a0001c0001t0001g0160 others(32): Show |
35 | HG00323.hp2 HG00423.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+2566dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | |||||||
| chr14:77349106 | C | CTT | 87 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(84): Show |
101 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.197+2565_197+2566d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | |||||||
| chr14:77349106 | C | CTTT | 51 | a0001c0001t0002g0239 a0001c0001t0002g0241 a0001c0001t0003g0181 others(48): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.197+2564_197+2566d others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | |||||||
| chr14:77349106 | C | CTTTT | 24 | a0001c0001t0003g0196 a0001c0001t0004g0186 a0001c0001t0005g0192 others(21): Show |
25 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+2563_197+2566d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | |||||||
| chr14:77349106 | CT | C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0207 a0001c0001t0001g0235 others(5): Show |
9 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+2566delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349106 | |||||||
| chr14:77349241 | T | C | 60 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(57): Show |
70 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.197+2432A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349241 | |||||||
| chr14:77349370 | TGCCTCCC others(2136): Show |
T | 1 | a0001c0001t0001g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.197+160_197+2302de others(1): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349370 | |||||||
| chr14:77349398 | G | A | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+2275C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349398 | |||||||
| chr14:77349750 | A | G | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+1923T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349750 | |||||||
| chr14:77349857 | G | A | 2 | a0001c0001t0020g0023 a0001c0001t0020g0277 |
3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.197+1816C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77349857 | |||||||
| chr14:77350098 | C | T | 15 | a0001c0001t0005g0192 a0001c0001t0012g0015 a0001c0001t0012g0191 others(12): Show |
16 | HG01167.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+1575G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350098 | |||||||
| chr14:77350185 | G | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0226 a0001c0001t0004g0261 others(1): Show |
5 | HG00621.hp2 NA18947.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+1488C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350185 | |||||||
| chr14:77350422 | G | A | 1 | a0001c0001t0036g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197+1251C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350422 | |||||||
| chr14:77350617 | T | C | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.197+1056A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350617 | |||||||
| chr14:77350977 | C | G | 1 | a0001c0001t0002g0238 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.197+696G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350977 | |||||||
| chr14:77350982 | G | A | 1 | a0001c0001t0040g0150 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.197+691C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77350982 | |||||||
| chr14:77351076 | T | C | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.197+597A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351076 | |||||||
| chr14:77351214 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.197+459G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351214 | |||||||
| chr14:77351224 | C | G | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+449G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351224 | |||||||
| chr14:77351262 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0006g0208 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197+411C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351262 | |||||||
| chr14:77351392 | TG | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(286): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.197+280delC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351392 | |||||||
| chr14:77351396 | C | T | 36 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(33): Show |
45 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.197+277G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351396 | |||||||
| chr14:77351402 | G | A | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+271C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351402 | |||||||
| chr14:77351403 | C | A | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.197+270G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351403 | |||||||
| chr14:77351411 | A | AT | 75 | a0001c0001t0001g0022 a0001c0001t0001g0129 a0001c0001t0001g0161 others(72): Show |
78 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.197+261dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351411 | A | ATT | 9 | a0001c0001t0004g0188 a0001c0001t0004g0268 a0001c0001t0006g0286 others(6): Show |
10 | HG00735.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+260_197+261dup others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351411 | AT | A | 35 | a0001c0001t0005g0192 a0001c0001t0007g0011 a0001c0001t0007g0128 others(32): Show |
38 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+261delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351411 | ATT | A | 32 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(29): Show |
41 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.197+260_197+261del others(2): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351411 | ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0005g0051 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197+252_197+261del others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351411 | ATTTTTTT others(6): Show |
A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0221 a0001c0001t0002g0240 others(3): Show |
8 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+249_197+261del others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351411 | |||||||
| chr14:77351436 | G | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(286): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.197+237C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351436 | |||||||
| chr14:77351463 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.197+210C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351463 | |||||||
| chr14:77351534 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.197+139A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 2/5 | chr14 | 77351534 | |||||||
| chr14:77351809 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0011g0156 a0001c0001t0011g0167 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-58A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77351809 | |||||||
| chr14:77351898 | C | A | 1 | a0002c0002t0053g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-147G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77351898 | |||||||
| chr14:77352092 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-341C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352092 | |||||||
| chr14:77352126 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG00609.hp1 NA18747.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.119-375G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352126 | |||||||
| chr14:77352517 | T | G | 1 | a0002c0002t0001g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.119-766A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352517 | |||||||
| chr14:77352537 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-786C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352537 | |||||||
| chr14:77352725 | C | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-974G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352725 | |||||||
| chr14:77352904 | G | A | 13 | a0001c0001t0008g0201 a0001c0001t0008g0219 a0002c0002t0008g0064 others(10): Show |
13 | HG02486.hp1 HG02602.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.119-1153C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352904 | |||||||
| chr14:77352922 | TG | T | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-1172delC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352922 | |||||||
| chr14:77352926 | T | C | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-1175A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77352926 | |||||||
| chr14:77353439 | G | GT | 54 | a0001c0001t0001g0140 a0001c0001t0002g0241 a0001c0001t0003g0181 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-1689dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353439 | |||||||
| chr14:77353439 | GT | G | 5 | a0001c0001t0001g0159 a0001c0001t0020g0023 a0001c0001t0020g0277 others(2): Show |
6 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-1689delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353439 | |||||||
| chr14:77353644 | T | C | 53 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(50): Show |
63 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.119-1893A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353644 | |||||||
| chr14:77353669 | A | C | 53 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(50): Show |
63 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.119-1918T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353669 | |||||||
| chr14:77353692 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0004g0266 |
3 | NA18969.hp2 NA19007.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.119-1941G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353692 | |||||||
| chr14:77353699 | G | A | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.119-1948C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353699 | |||||||
| chr14:77353977 | A | G | 1 | a0002c0002t0008g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.119-2226T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353977 | |||||||
| chr14:77353997 | C | T | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-2246G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77353997 | |||||||
| chr14:77354043 | A | G | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-2292T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354043 | |||||||
| chr14:77354325 | C | T | 1 | a0001c0001t0015g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.119-2574G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354325 | |||||||
| chr14:77354339 | C | T | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-2588G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354339 | |||||||
| chr14:77354373 | G | C | 1 | a0002c0002t0005g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.119-2622C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354373 | |||||||
| chr14:77354763 | G | A | 2 | a0002c0002t0029g0024 a0003c0003t0003g0096 |
2 | HG00642.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.119-3012C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354763 | |||||||
| chr14:77354773 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-3022C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354773 | |||||||
| chr14:77354823 | G | A | 1 | a0002c0002t0008g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-3072C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354823 | |||||||
| chr14:77354943 | G | T | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-3192C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354943 | |||||||
| chr14:77354954 | C | CA | 8 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0009t0013g0126 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-3204dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77354954 | |||||||
| chr14:77355154 | T | TTG | 137 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(134): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.119-3405_119-3404d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355154 | |||||||
| chr14:77355198 | C | CT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(95): Show |
108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.119-3448dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355198 | |||||||
| chr14:77355198 | CT | C | 9 | a0001c0001t0010g0218 a0002c0002t0009g0004 a0002c0002t0009g0056 others(6): Show |
11 | HG01243.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-3448delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355198 | |||||||
| chr14:77355265 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(204): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.119-3514T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355265 | |||||||
| chr14:77355425 | A | T | 2 | a0001c0001t0031g0198 a0004c0007t0048g0117 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.119-3674T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355425 | |||||||
| chr14:77355442 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-3691G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355442 | |||||||
| chr14:77355448 | G | A | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-3697C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355448 | |||||||
| chr14:77355536 | G | A | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-3785C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77355536 | |||||||
| chr14:77356068 | G | A | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-4317C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356068 | |||||||
| chr14:77356077 | T | G | 1 | a0001c0001t0002g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.119-4326A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356077 | |||||||
| chr14:77356269 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.119-4518A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356269 | |||||||
| chr14:77356346 | T | C | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-4595A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356346 | |||||||
| chr14:77356378 | G | A | 1 | a0002c0002t0005g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.119-4627C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356378 | |||||||
| chr14:77356612 | A | C | 45 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(42): Show |
49 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.119-4861T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356612 | |||||||
| chr14:77356910 | A | G | 27 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(24): Show |
27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-5159T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77356910 | |||||||
| chr14:77357004 | C | T | 1 | a0001c0008t0032g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-5253G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357004 | |||||||
| chr14:77357026 | A | C | 1 | a0001c0001t0002g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.119-5275T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357026 | |||||||
| chr14:77357202 | G | C | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-5451C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357202 | |||||||
| chr14:77357570 | T | G | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-5819A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357570 | |||||||
| chr14:77357722 | C | G | 194 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(191): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.119-5971G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357722 | |||||||
| chr14:77357953 | A | G | 231 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0199 others(228): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.119-6202T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77357953 | |||||||
| chr14:77358066 | G | A | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-6315C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358066 | |||||||
| chr14:77358124 | C | CA | 61 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0168 others(58): Show |
71 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.119-6374dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | |||||||
| chr14:77358124 | C | CAA | 6 | a0001c0001t0033g0197 a0002c0002t0002g0080 a0002c0002t0029g0024 others(3): Show |
6 | HG00741.hp1 HG02055.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-6375_119-6374d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | |||||||
| chr14:77358124 | CA | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(78): Show |
92 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.119-6374delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358124 | |||||||
| chr14:77358163 | C | T | 1 | a0001c0001t0004g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.119-6412G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358163 | |||||||
| chr14:77358181 | T | TCA | 4 | a0001c0001t0005g0209 a0001c0005t0024g0287 a0002c0002t0005g0070 others(1): Show |
4 | HG01175.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-6432_119-6431d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | |||||||
| chr14:77358181 | T | TCACACAC others(1): Show |
12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-6438_119-6431d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | |||||||
| chr14:77358181 | TCA | T | 64 | a0001c0001t0001g0139 a0001c0001t0001g0278 a0001c0001t0003g0181 others(61): Show |
74 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.119-6432_119-6431d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | |||||||
| chr14:77358181 | TCACACAC others(1): Show |
T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(80): Show |
94 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.119-6438_119-6431d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358181 | |||||||
| chr14:77358282 | C | G | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-6531G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358282 | |||||||
| chr14:77358308 | C | CT | 7 | a0001c0001t0001g0120 a0001c0001t0001g0138 a0001c0001t0001g0173 others(4): Show |
7 | HG01256.hp2 HG01361.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-6558dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358308 | |||||||
| chr14:77358325 | G | A | 1 | a0001c0001t0006g0018 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.119-6574C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358325 | |||||||
| chr14:77358362 | C | T | 1 | a0002c0002t0053g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.119-6611G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358362 | |||||||
| chr14:77358564 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.119-6813A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358564 | |||||||
| chr14:77358577 | G | A | 1 | a0003c0003t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-6826C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358577 | |||||||
| chr14:77358588 | C | T | 54 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.119-6837G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358588 | |||||||
| chr14:77358900 | G | T | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-7149C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77358900 | |||||||
| chr14:77359046 | C | G | 1 | a0002c0002t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.119-7295G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359046 | |||||||
| chr14:77359232 | C | G | 3 | a0001c0001t0006g0019 a0001c0001t0006g0236 a0001c0001t0006g0237 |
4 | HG00733.hp2 HG01433.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7481G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359232 | |||||||
| chr14:77359399 | TAA | T | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7650_119-7649d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359399 | |||||||
| chr14:77359403 | A | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(200): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.119-7652T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359403 | |||||||
| chr14:77359508 | T | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0247 |
2 | NA18964.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.119-7757A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359508 | |||||||
| chr14:77359547 | T | G | 1 | a0001c0001t0028g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.119-7796A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359547 | |||||||
| chr14:77359563 | A | G | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7812T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359563 | |||||||
| chr14:77359592 | C | T | 2 | a0001c0001t0006g0019 a0001c0001t0006g0236 |
3 | HG00733.hp2 HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.119-7841G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359592 | |||||||
| chr14:77359826 | G | C | 1 | a0002c0002t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.119-8075C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359826 | |||||||
| chr14:77359899 | G | GA | 37 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0194 others(34): Show |
46 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.119-8149dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77359899 | |||||||
| chr14:77360025 | A | C | 1 | a0001c0001t0002g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.119-8274T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360025 | |||||||
| chr14:77360168 | T | C | 1 | a0001c0008t0032g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-8417A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360168 | |||||||
| chr14:77360201 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-8450C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360201 | |||||||
| chr14:77360538 | A | C | 27 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(24): Show |
27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-8787T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360538 | |||||||
| chr14:77360559 | CT | C | 33 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(30): Show |
34 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.119-8809delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360559 | |||||||
| chr14:77360973 | C | CT | 13 | a0001c0001t0001g0160 a0001c0001t0001g0264 a0001c0001t0043g0231 others(10): Show |
15 | HG00099.hp1 HG00673.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-9223dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | |||||||
| chr14:77360973 | CT | C | 156 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(153): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.119-9223delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | |||||||
| chr14:77360973 | CTT | C | 7 | a0001c0001t0002g0230 a0001c0001t0006g0248 a0001c0001t0014g0291 others(4): Show |
7 | HG01081.hp2 HG02155.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-9224_119-9223d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360973 | |||||||
| chr14:77360994 | T | C | 1 | a0002c0002t0017g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.119-9243A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77360994 | |||||||
| chr14:77361054 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.119-9303C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361054 | |||||||
| chr14:77361277 | C | T | 1 | a0001c0001t0010g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-9526G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361277 | |||||||
| chr14:77361410 | T | C | 7 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0286 others(4): Show |
7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-9659A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361410 | |||||||
| chr14:77361681 | T | C | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-9930A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361681 | |||||||
| chr14:77361682 | T | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-9931A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361682 | |||||||
| chr14:77361704 | TAG | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(204): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.119-9955_119-9954d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361704 | |||||||
| chr14:77361758 | T | G | 1 | a0001c0001t0004g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.119-10007A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361758 | |||||||
| chr14:77361860 | G | A | 8 | a0001c0001t0005g0212 a0001c0001t0010g0211 a0001c0001t0010g0213 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-10109C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361860 | |||||||
| chr14:77361914 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(80): Show |
94 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.119-10163G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361914 | |||||||
| chr14:77361918 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.119-10167A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77361918 | |||||||
| chr14:77362087 | C | T | 4 | a0003c0003t0007g0084 a0003c0003t0007g0086 a0003c0003t0007g0087 others(1): Show |
4 | HG01069.hp2 HG01243.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-10336G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362087 | |||||||
| chr14:77362126 | G | T | 33 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(30): Show |
34 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.119-10375C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362126 | |||||||
| chr14:77362236 | T | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-10485A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362236 | |||||||
| chr14:77362449 | T | C | 1 | a0001c0001t0033g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.119-10698A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362449 | |||||||
| chr14:77362518 | T | C | 4 | a0001c0001t0002g0251 a0001c0001t0019g0249 a0001c0001t0019g0250 others(1): Show |
4 | NA18952.hp2 NA18983.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-10767A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362518 | |||||||
| chr14:77362782 | T | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11031A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362782 | |||||||
| chr14:77362824 | G | T | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11073C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362824 | |||||||
| chr14:77362867 | A | G | 76 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0020 others(73): Show |
87 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.119-11116T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362867 | |||||||
| chr14:77362869 | G | A | 2 | a0001c0001t0044g0205 a0002c0002t0001g0007 |
3 | HG01515.hp1 HG01517.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.119-11118C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77362869 | |||||||
| chr14:77363023 | T | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-11272A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363023 | |||||||
| chr14:77363062 | C | G | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-11311G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363062 | |||||||
| chr14:77363130 | A | G | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.119-11379T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363130 | |||||||
| chr14:77363140 | C | G | 1 | a0001c0001t0005g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.119-11389G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363140 | |||||||
| chr14:77363210 | C | T | 2 | a0002c0004t0013g0027 a0002c0004t0013g0028 |
2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.119-11459G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363210 | |||||||
| chr14:77363395 | G | A | 1 | a0002c0002t0029g0024 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.119-11644C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363395 | |||||||
| chr14:77363563 | G | A | 2 | a0001c0001t0007g0132 a0002c0002t0009g0057 |
2 | HG02970.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.119-11812C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363563 | |||||||
| chr14:77363694 | C | G | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-11943G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77363694 | |||||||
| chr14:77364204 | C | T | 27 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(24): Show |
27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.119-12453G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364204 | |||||||
| chr14:77364383 | A | G | 1 | a0001c0001t0018g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.118+12553T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364383 | |||||||
| chr14:77364456 | G | C | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+12480C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364456 | |||||||
| chr14:77364484 | A | G | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+12452T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364484 | |||||||
| chr14:77364495 | C | T | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+12441G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364495 | |||||||
| chr14:77364496 | G | A | 27 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(24): Show |
27 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.118+12440C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364496 | |||||||
| chr14:77364624 | C | T | 3 | a0001c0001t0005g0209 a0001c0001t0036g0210 a0002c0002t0005g0070 |
3 | HG02109.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.118+12312G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364624 | |||||||
| chr14:77364638 | C | T | 16 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(13): Show |
19 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.118+12298G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364638 | |||||||
| chr14:77364686 | C | T | 25 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(22): Show |
25 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.118+12250G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364686 | |||||||
| chr14:77364922 | C | T | 1 | a0003c0003t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+12014G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77364922 | |||||||
| chr14:77365006 | C | T | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+11930G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365006 | |||||||
| chr14:77365137 | T | C | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+11799A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365137 | |||||||
| chr14:77365189 | T | C | 1 | a0001c0001t0010g0214 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118+11747A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365189 | |||||||
| chr14:77365212 | A | T | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+11724T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365212 | |||||||
| chr14:77365300 | C | T | 1 | a0003c0003t0003g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118+11636G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365300 | |||||||
| chr14:77365317 | C | G | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+11619G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365317 | |||||||
| chr14:77365356 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+11580T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365356 | |||||||
| chr14:77365470 | C | T | 1 | a0001c0001t0008g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+11466G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365470 | |||||||
| chr14:77365641 | C | T | 2 | a0001c0001t0020g0023 a0001c0001t0020g0277 |
3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+11295G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365641 | |||||||
| chr14:77365701 | A | G | 1 | a0003c0003t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118+11235T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365701 | |||||||
| chr14:77365727 | C | T | 2 | a0001c0001t0015g0016 a0001c0001t0015g0195 |
3 | HG03139.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.118+11209G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77365727 | |||||||
| chr14:77366013 | C | A | 1 | a0001c0001t0006g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.118+10923G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366013 | |||||||
| chr14:77366152 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118+10784C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366152 | |||||||
| chr14:77366209 | G | A | 1 | a0003c0003t0022g0088 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118+10727C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366209 | |||||||
| chr14:77366306 | A | C | 2 | a0001c0001t0020g0023 a0001c0001t0020g0277 |
3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+10630T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366306 | |||||||
| chr14:77366325 | C | T | 24 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+10611G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366325 | |||||||
| chr14:77366326 | G | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+10610C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366326 | |||||||
| chr14:77366352 | C | A | 2 | a0001c0001t0020g0023 a0001c0001t0020g0277 |
3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+10584G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366352 | |||||||
| chr14:77366540 | A | G | 96 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0199 others(93): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.118+10396T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366540 | |||||||
| chr14:77366739 | C | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(281): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.118+10197G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366739 | |||||||
| chr14:77366768 | A | T | 1 | a0001c0001t0006g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.118+10168T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366768 | |||||||
| chr14:77366834 | G | A | 2 | a0001c0001t0010g0215 a0001c0001t0010g0216 |
2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.118+10102C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366834 | |||||||
| chr14:77366846 | A | G | 6 | a0001c0001t0001g0278 a0001c0001t0026g0279 a0002c0002t0001g0075 others(3): Show |
6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+10090T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77366846 | |||||||
| chr14:77367032 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118+9904C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367032 | |||||||
| chr14:77367199 | A | G | 1 | a0001c0008t0032g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+9737T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367199 | |||||||
| chr14:77367233 | C | T | 3 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0239 |
3 | HG01175.hp2 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.118+9703G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367233 | |||||||
| chr14:77367240 | T | TA | 96 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0125 others(93): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.118+9695dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | |||||||
| chr14:77367240 | T | TAA | 9 | a0001c0001t0001g0170 a0001c0001t0008g0201 a0001c0001t0018g0169 others(6): Show |
9 | HG02486.hp1 HG02602.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+9694_118+9695d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | |||||||
| chr14:77367240 | TA | T | 10 | a0001c0001t0020g0023 a0001c0001t0025g0123 a0001c0001t0031g0198 others(7): Show |
13 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+9695delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367240 | |||||||
| chr14:77367250 | A | AAAAC | 11 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(8): Show |
14 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+9685_118+9686i others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367250 | |||||||
| chr14:77367254 | A | C | 11 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(8): Show |
14 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+9682T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367254 | |||||||
| chr14:77367299 | C | T | 1 | a0003c0003t0003g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118+9637G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367299 | |||||||
| chr14:77367471 | C | T | 7 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0286 others(4): Show |
7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+9465G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367471 | |||||||
| chr14:77367488 | C | T | 1 | a0003c0003t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118+9448G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367488 | |||||||
| chr14:77367593 | GGGTCTTG others(9): Show |
G | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.118+9327_118+9342d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367593 | |||||||
| chr14:77367698 | T | TC | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+9237_118+9238i others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367698 | |||||||
| chr14:77367762 | C | G | 24 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+9174G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367762 | |||||||
| chr14:77367781 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.118+9155G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367781 | |||||||
| chr14:77367856 | A | G | 1 | a0003c0003t0003g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.118+9080T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367856 | |||||||
| chr14:77367978 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.118+8958C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367978 | |||||||
| chr14:77367984 | G | A | 24 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+8952C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77367984 | |||||||
| chr14:77368057 | T | C | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8879A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368057 | |||||||
| chr14:77368176 | G | A | 24 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(21): Show |
24 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+8760C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368176 | |||||||
| chr14:77368176 | G | T | 35 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(32): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.118+8760C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368176 | |||||||
| chr14:77368277 | A | AT | 187 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(184): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.118+8658dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368277 | |||||||
| chr14:77368284 | T | A | 1 | a0001c0001t0056g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.118+8652A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368284 | |||||||
| chr14:77368465 | T | C | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8471A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368465 | |||||||
| chr14:77368467 | A | ATTAT | 9 | a0002c0002t0008g0064 a0002c0002t0009g0004 a0002c0002t0009g0056 others(6): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+8465_118+8468d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368467 | |||||||
| chr14:77368467 | ATTAT | A | 12 | a0001c0001t0007g0011 a0001c0001t0007g0127 a0001c0001t0007g0128 others(9): Show |
15 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+8465_118+8468d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368467 | |||||||
| chr14:77368501 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.118+8435C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368501 | |||||||
| chr14:77368589 | G | A | 1 | a0001c0001t0054g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.118+8347C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368589 | |||||||
| chr14:77368624 | C | T | 3 | a0001c0001t0002g0221 a0001c0001t0002g0265 a0001c0001t0052g0263 |
3 | HG00423.hp2 HG00558.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.118+8312G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368624 | |||||||
| chr14:77368678 | T | C | 1 | a0003c0003t0003g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118+8258A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368678 | |||||||
| chr14:77368718 | G | A | 2 | a0002c0002t0005g0046 a0002c0002t0005g0051 |
2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.118+8218C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368718 | |||||||
| chr14:77368866 | C | G | 1 | a0002c0002t0008g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+8070G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368866 | |||||||
| chr14:77368900 | C | G | 1 | a0003c0003t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+8036G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368900 | |||||||
| chr14:77368974 | T | C | 1 | a0001c0001t0008g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+7962A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77368974 | |||||||
| chr14:77369071 | G | A | 1 | a0001c0001t0008g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+7865C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369071 | |||||||
| chr14:77369096 | G | A | 156 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0199 others(153): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.118+7840C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369096 | |||||||
| chr14:77369117 | TTAGAA | T | 52 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(49): Show |
62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+7814_118+7818d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369117 | |||||||
| chr14:77369182 | T | C | 1 | a0001c0001t0019g0254 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.118+7754A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369182 | |||||||
| chr14:77369423 | T | TG | 7 | a0001c0001t0001g0278 a0001c0001t0026g0279 a0001c0001t0028g0273 others(4): Show |
7 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+7512dupC | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369423 | |||||||
| chr14:77369551 | G | T | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+7385C>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369551 | |||||||
| chr14:77369770 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(75): Show |
86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.118+7166C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369770 | |||||||
| chr14:77369818 | A | G | 1 | a0002c0002t0001g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.118+7118T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369818 | |||||||
| chr14:77369830 | C | T | 9 | a0001c0001t0004g0014 a0001c0001t0004g0183 a0001c0001t0004g0184 others(6): Show |
10 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+7106G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369830 | |||||||
| chr14:77369900 | G | A | 7 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0286 others(4): Show |
7 | HG02630.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+7036C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77369900 | |||||||
| chr14:77370159 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.118+6777C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370159 | |||||||
| chr14:77370167 | G | A | 4 | a0001c0009t0013g0126 a0002c0004t0013g0027 a0002c0004t0013g0028 others(1): Show |
4 | HG01081.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+6769C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370167 | |||||||
| chr14:77370171 | CA | C | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
7 | HG01070.hp2 HG01256.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6764delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | |||||||
| chr14:77370171 | CAAAAAAA others(3): Show |
C | 191 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0199 others(188): Show |
215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.118+6755_118+6764d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | |||||||
| chr14:77370171 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0220 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.118+6754_118+6764d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370171 | |||||||
| chr14:77370223 | A | G | 1 | a0001c0001t0007g0128 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.118+6713T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370223 | |||||||
| chr14:77370525 | TTG | T | 13 | a0001c0001t0001g0129 a0001c0001t0007g0011 a0001c0001t0007g0127 others(10): Show |
16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+6409_118+6410d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370525 | |||||||
| chr14:77370742 | A | AGT | 7 | a0001c0001t0001g0175 a0001c0001t0002g0276 a0001c0001t0027g0272 others(4): Show |
7 | HG02970.hp1 HG03130.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6192_118+6193d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | A | AGTGT | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0002c0002t0001g0031 |
3 | HG00741.hp2 HG01361.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.118+6190_118+6193d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | A | AGTGTGT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(65): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.118+6188_118+6193d others(8): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0002c0002t0001g0034 |
3 | HG02132.hp1 HG02132.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.118+6186_118+6193d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | AGT | A | 59 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(56): Show |
67 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.118+6192_118+6193d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | AGTGT | A | 8 | a0001c0001t0002g0119 a0001c0001t0006g0284 a0001c0001t0025g0123 others(5): Show |
8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+6190_118+6193d others(6): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370742 | AGTGTGTG others(1): Show |
A | 2 | a0003c0003t0003g0010 a0003c0003t0003g0111 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.118+6186_118+6193d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370742 | |||||||
| chr14:77370767 | A | G | 4 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0005g0025 others(1): Show |
5 | HG02145.hp2 HG02622.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+6169T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370767 | |||||||
| chr14:77370817 | T | C | 5 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0286 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+6119A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370817 | |||||||
| chr14:77370864 | G | A | 2 | a0001c0005t0024g0287 a0001c0005t0024g0288 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.118+6072C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370864 | |||||||
| chr14:77370904 | A | G | 1 | a0001c0001t0008g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+6032T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370904 | |||||||
| chr14:77370933 | T | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(95): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.118+6003A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77370933 | |||||||
| chr14:77371028 | T | C | 1 | a0001c0001t0023g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.118+5908A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371028 | |||||||
| chr14:77371289 | A | G | 13 | a0001c0001t0001g0129 a0001c0001t0007g0011 a0001c0001t0007g0127 others(10): Show |
16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+5647T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371289 | |||||||
| chr14:77371311 | G | A | 1 | a0002c0002t0008g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+5625C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77371311 | |||||||
| chr14:77372101 | G | A | 9 | a0001c0001t0005g0212 a0001c0001t0005g0285 a0001c0001t0010g0211 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4835C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372101 | |||||||
| chr14:77372121 | C | T | 156 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0001g0199 others(153): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.118+4815G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372121 | |||||||
| chr14:77372163 | A | G | 52 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(49): Show |
62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+4773T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372163 | |||||||
| chr14:77372338 | C | G | 1 | a0002c0002t0001g0033 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.118+4598G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372338 | |||||||
| chr14:77372413 | C | T | 12 | a0001c0001t0005g0209 a0001c0001t0005g0212 a0001c0001t0005g0285 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+4523G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372413 | |||||||
| chr14:77372416 | A | G | 1 | a0003c0003t0003g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.118+4520T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372416 | |||||||
| chr14:77372420 | T | C | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4516A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372420 | |||||||
| chr14:77372640 | A | C | 7 | a0001c0001t0008g0201 a0002c0002t0008g0064 a0002c0002t0008g0065 others(4): Show |
7 | HG02486.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+4296T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372640 | |||||||
| chr14:77372714 | T | G | 13 | a0001c0001t0001g0129 a0001c0001t0007g0011 a0001c0001t0007g0127 others(10): Show |
16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+4222A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372714 | |||||||
| chr14:77372752 | C | T | 1 | a0001c0001t0052g0263 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118+4184G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372752 | |||||||
| chr14:77372830 | T | G | 1 | a0005c0006t0005g0083 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118+4106A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372830 | |||||||
| chr14:77372905 | A | AT | 2 | a0001c0001t0011g0012 a0001c0001t0028g0273 |
3 | HG02165.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.118+4030dupA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372905 | |||||||
| chr14:77372905 | A | ATTT | 3 | a0001c0001t0001g0177 a0002c0002t0001g0032 a0002c0002t0001g0077 |
3 | HG01978.hp2 HG02056.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.118+4030_118+4031i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372905 | |||||||
| chr14:77372906 | T | TTA | 5 | a0001c0001t0001g0125 a0001c0001t0001g0264 a0001c0001t0052g0263 others(2): Show |
5 | HG00673.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+4028_118+4029d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118+4020_118+4029d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0119 a0001c0001t0004g0185 |
2 | HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.118+4014_118+4029d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | T | TTTTTTAT others(5): Show |
1 | a0001c0001t0002g0259 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.118+4029_118+4030i others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTA | T | 5 | a0001c0001t0001g0207 a0001c0001t0002g0206 a0001c0001t0006g0208 others(2): Show |
5 | HG02055.hp1 HG03516.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+4028_118+4029d others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(1): Show |
T | 2 | a0001c0001t0007g0011 a0001c0001t0007g0127 |
3 | NA18946.hp1 NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.118+4022_118+4029d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(3): Show |
T | 5 | a0001c0001t0006g0204 a0001c0001t0006g0283 a0001c0001t0012g0191 others(2): Show |
5 | HG00735.hp1 HG01123.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+4020_118+4029d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(5): Show |
T | 2 | a0001c0001t0006g0284 a0002c0002t0012g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118+4018_118+4029d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(7): Show |
T | 16 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(13): Show |
17 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+4016_118+4029d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(9): Show |
T | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.118+4014_118+4029d others(18): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372906 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0014g0289 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.118+4012_118+4029d others(20): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372906 | |||||||
| chr14:77372907 | TA | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0173 others(6): Show |
9 | HG00609.hp2 HG01109.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4028delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATA | T | 15 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(12): Show |
15 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+4026_118+4028d others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATA | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0138 others(12): Show |
15 | HG00621.hp1 HG01256.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.118+4024_118+4028d others(7): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0140 others(13): Show |
18 | HG00408.hp2 HG00558.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.118+4022_118+4028d others(9): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA others(2): Show |
T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0137 a0001c0001t0001g0145 others(7): Show |
10 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4020_118+4028d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA others(4): Show |
T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0161 others(5): Show |
10 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4018_118+4028d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA others(16): Show |
T | 1 | a0002c0002t0001g0007 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.118+4006_118+4028d others(25): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA others(18): Show |
T | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+4004_118+4028d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372907 | TATATATA others(20): Show |
T | 1 | a0002c0002t0022g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+4002_118+4028d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372907 | |||||||
| chr14:77372908 | A | T | 19 | a0001c0001t0001g0129 a0001c0001t0002g0241 a0001c0001t0002g0245 others(16): Show |
22 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+4028T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372908 | |||||||
| chr14:77372910 | A | T | 10 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0173 others(7): Show |
10 | HG00609.hp2 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+4026T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372910 | |||||||
| chr14:77372912 | A | T | 14 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0166 others(11): Show |
14 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+4024T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372912 | |||||||
| chr14:77372914 | A | T | 13 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0152 others(10): Show |
13 | HG00621.hp1 HG01256.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+4022T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372914 | |||||||
| chr14:77372916 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0140 others(12): Show |
17 | HG00408.hp2 HG00558.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+4020T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372916 | |||||||
| chr14:77372918 | A | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0137 a0001c0001t0001g0145 others(6): Show |
9 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4018T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372918 | |||||||
| chr14:77372920 | A | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0038g0182 others(4): Show |
9 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+4016T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372920 | |||||||
| chr14:77372924 | ATATATAT others(22): Show |
A | 1 | a0003c0003t0021g0092 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.118+3983_118+4011d others(31): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372924 | |||||||
| chr14:77372926 | ATATATAT others(20): Show |
A | 3 | a0002c0002t0053g0073 a0003c0003t0005g0118 a0003c0003t0021g0089 |
3 | HG02630.hp2 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.118+3983_118+4009d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372926 | |||||||
| chr14:77372928 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0036g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+3983_118+4007d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372928 | |||||||
| chr14:77372930 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0010g0214 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118+3982_118+4005d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | |||||||
| chr14:77372930 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0005g0209 a0002c0002t0005g0070 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.118+3981_118+4005d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | |||||||
| chr14:77372930 | ATATATAT others(21): Show |
A | 1 | a0002c0002t0008g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.118+3978_118+4005d others(30): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372930 | |||||||
| chr14:77372931 | TATATATA others(14): Show |
T | 1 | a0001c0001t0004g0244 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.118+3984_118+4004d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372931 | |||||||
| chr14:77372932 | A | T | 1 | a0002c0002t0001g0007 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.118+4004T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0006 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.118+3983_118+4003d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(15): Show |
A | 2 | a0003c0003t0003g0010 a0003c0003t0003g0111 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.118+3982_118+4003d others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(17): Show |
A | 4 | a0001c0001t0005g0212 a0001c0001t0005g0285 a0001c0001t0010g0217 others(1): Show |
4 | HG02257.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+3980_118+4003d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0010g0213 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.118+3979_118+4003d others(27): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(23): Show |
A | 1 | a0002c0002t0008g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.118+3974_118+4003d others(32): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(24): Show |
A | 1 | a0002c0002t0008g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+3973_118+4003d others(33): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(25): Show |
A | 3 | a0001c0001t0008g0201 a0002c0002t0008g0065 a0002c0002t0008g0067 |
3 | HG02486.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.118+3972_118+4003d others(34): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372932 | ATATATAT others(26): Show |
A | 1 | a0002c0002t0008g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.118+3971_118+4003d others(35): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372932 | |||||||
| chr14:77372934 | A | T | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+4002T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0014g0292 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.118+3983_118+4001d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0014g0290 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.118+3982_118+4001d others(22): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(14): Show |
A | 5 | a0002c0002t0009g0058 a0002c0002t0009g0059 a0002c0002t0009g0060 others(2): Show |
5 | HG01243.hp2 HG02109.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+3981_118+4001d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(15): Show |
A | 1 | a0002c0002t0009g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118+3980_118+4001d others(24): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0010g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.118+3979_118+4001d others(25): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0010g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.118+3978_118+4001d others(26): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(20): Show |
A | 1 | a0005c0006t0005g0083 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118+3975_118+4001d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372934 | ATATATAT others(23): Show |
A | 1 | a0002c0002t0008g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.118+3972_118+4001d others(32): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372934 | |||||||
| chr14:77372935 | TATATATA others(8): Show |
T | 3 | a0001c0001t0002g0239 a0002c0002t0005g0048 a0006c0010t0025g0124 |
3 | HG01175.hp2 HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.118+3986_118+4000d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372935 | |||||||
| chr14:77372936 | A | T | 1 | a0002c0002t0022g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+4000T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | |||||||
| chr14:77372936 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0025g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.118+3983_118+3999d others(19): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | |||||||
| chr14:77372936 | ATATATAT others(12): Show |
A | 1 | a0003c0003t0005g0091 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+3981_118+3999d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | |||||||
| chr14:77372936 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0010g0216 a0002c0002t0009g0056 a0002c0002t0009g0057 |
3 | HG02970.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3999d others(23): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372936 | |||||||
| chr14:77372937 | TATATATA others(8): Show |
T | 1 | a0003c0003t0004g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118+3984_118+3998d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372937 | |||||||
| chr14:77372938 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0015g0016 a0002c0002t0005g0051 a0002c0002t0029g0024 others(1): Show |
4 | HG02698.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3983_118+3997d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | |||||||
| chr14:77372938 | ATATATAT others(12): Show |
A | 1 | a0002c0002t0009g0004 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3997d others(21): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | |||||||
| chr14:77372938 | ATATATAT others(20): Show |
A | 1 | a0002c0002t0008g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.118+3971_118+3997d others(29): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372938 | |||||||
| chr14:77372939 | TATATATA others(6): Show |
T | 1 | a0002c0002t0037g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.118+3984_118+3996d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372939 | |||||||
| chr14:77372940 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0015g0016 a0003c0003t0003g0001 |
2 | HG03471.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3995d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | |||||||
| chr14:77372940 | ATATATAT others(7): Show |
A | 2 | a0003c0003t0003g0001 a0003c0003t0003g0104 |
2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.118+3982_118+3995d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | |||||||
| chr14:77372940 | ATATATAT others(8): Show |
A | 1 | a0003c0003t0034g0108 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.118+3981_118+3995d others(17): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372940 | |||||||
| chr14:77372942 | ATATATAT others(4): Show |
A | 2 | a0003c0003t0003g0009 a0003c0003t0003g0101 |
3 | HG00140.hp2 HG00738.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3993d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | |||||||
| chr14:77372942 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0005g0192 a0002c0002t0006g0030 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.118+3982_118+3993d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | |||||||
| chr14:77372942 | ATATATAT others(6): Show |
A | 1 | a0003c0003t0003g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118+3981_118+3993d others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | |||||||
| chr14:77372942 | ATATATAT others(7): Show |
A | 4 | a0003c0003t0003g0099 a0003c0003t0003g0102 a0003c0003t0003g0107 others(1): Show |
4 | HG01106.hp1 HG01993.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3980_118+3993d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372942 | |||||||
| chr14:77372943 | TATATATA others(2): Show |
T | 2 | a0001c0001t0012g0015 a0002c0002t0017g0055 |
3 | HG00642.hp2 HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.118+3984_118+3992d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372943 | |||||||
| chr14:77372944 | ATATATAT others(2): Show |
A | 5 | a0002c0002t0042g0050 a0003c0003t0007g0005 a0003c0003t0007g0084 others(2): Show |
7 | HG00140.hp1 HG00733.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3983_118+3991d others(11): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | |||||||
| chr14:77372944 | ATATATAT others(3): Show |
A | 1 | a0003c0003t0016g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.118+3982_118+3991d others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | |||||||
| chr14:77372944 | ATATATAT others(5): Show |
A | 2 | a0003c0003t0003g0001 a0003c0003t0003g0098 |
2 | HG01258.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.118+3980_118+3991d others(14): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | |||||||
| chr14:77372944 | ATATATAT others(7): Show |
A | 1 | a0003c0003t0003g0001 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.118+3978_118+3991d others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372944 | |||||||
| chr14:77372946 | ATATATAT others(4): Show |
A | 2 | a0003c0003t0016g0105 a0003c0003t0016g0106 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.118+3979_118+3989d others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372946 | |||||||
| chr14:77372947 | TA | T | 6 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0172 others(3): Show |
6 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3988delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372947 | |||||||
| chr14:77372948 | A | T | 6 | a0001c0001t0020g0023 a0001c0001t0020g0277 a0002c0002t0001g0007 others(3): Show |
7 | HG00741.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3988T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372948 | |||||||
| chr14:77372949 | TA | T | 10 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0154 others(7): Show |
10 | HG00099.hp1 HG01070.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+3986delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372949 | |||||||
| chr14:77372950 | A | ATT | 3 | a0001c0001t0001g0253 a0001c0001t0006g0019 a0001c0001t0006g0236 |
3 | HG00733.hp2 HG01433.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.118+3985_118+3986i others(4): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372950 | |||||||
| chr14:77372950 | A | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0137 a0001c0001t0001g0152 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.118+3986T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372950 | |||||||
| chr14:77372951 | TA | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG02132.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+3984delT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372951 | |||||||
| chr14:77372952 | A | ATAT | 7 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0200 others(4): Show |
7 | HG00544.hp1 HG02165.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+3983_118+3984i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0241 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.118+3983_118+3984i others(16): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | A | ATATATAT others(3): Show |
2 | a0001c0001t0019g0249 a0001c0001t0027g0272 |
2 | NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.118+3983_118+3984i others(12): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | A | ATATATAT others(6): Show |
2 | a0001c0001t0002g0242 a0003c0003t0002g0113 |
2 | HG02056.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.118+3983_118+3984i others(15): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | A | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0137 others(71): Show |
80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.118+3984T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | AT | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0139 a0001c0001t0001g0144 others(4): Show |
7 | HG00735.hp2 HG01433.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+3983delA | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372952 | ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0001g0166 a0001c0001t0011g0156 a0001c0001t0011g0167 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3976_118+3983d others(10): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372952 | |||||||
| chr14:77372953 | T | TA | 7 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0002g0240 others(4): Show |
8 | HG00673.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.118+3982_118+3983i others(3): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | |||||||
| chr14:77372953 | T | TATA | 3 | a0001c0001t0001g0282 a0001c0001t0002g0003 a0001c0001t0002g0230 |
3 | NA18963.hp2 NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.118+3982_118+3983i others(5): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | |||||||
| chr14:77372953 | T | TATATATA others(4): Show |
1 | a0001c0001t0006g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.118+3982_118+3983i others(13): Show |
TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372953 | |||||||
| chr14:77372954 | T | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(8): Show |
11 | HG00673.hp1 HG01978.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+3982A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372954 | |||||||
| chr14:77372955 | T | A | 6 | a0001c0001t0002g0265 a0001c0001t0004g0186 a0001c0001t0004g0187 others(3): Show |
6 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3981A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372955 | |||||||
| chr14:77372956 | T | A | 1 | a0002c0004t0013g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118+3980A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372956 | |||||||
| chr14:77372957 | T | A | 6 | a0001c0001t0004g0186 a0001c0001t0004g0187 a0001c0001t0004g0188 others(3): Show |
6 | HG00323.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+3979A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372957 | |||||||
| chr14:77372958 | T | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3978A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372958 | |||||||
| chr14:77372959 | T | A | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG00323.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.118+3977A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372959 | |||||||
| chr14:77372960 | T | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3976A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372960 | |||||||
| chr14:77372962 | T | A | 3 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0004c0007t0048g0117 |
3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3974A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372962 | |||||||
| chr14:77372963 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0004g0268 |
2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.118+3973A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372963 | |||||||
| chr14:77372964 | T | A | 3 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0004c0007t0048g0117 |
3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3972A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372964 | |||||||
| chr14:77372966 | T | A | 3 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0004c0007t0048g0117 |
3 | HG01884.hp2 NA18941.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.118+3970A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372966 | |||||||
| chr14:77372968 | T | A | 1 | a0001c0001t0002g0271 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.118+3968A>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372968 | |||||||
| chr14:77372991 | C | T | 52 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(49): Show |
62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.118+3945G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77372991 | |||||||
| chr14:77373004 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(74): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.118+3932G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373004 | |||||||
| chr14:77373005 | G | A | 13 | a0001c0001t0001g0129 a0001c0001t0007g0011 a0001c0001t0007g0127 others(10): Show |
16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+3931C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373005 | |||||||
| chr14:77373047 | C | G | 1 | a0001c0008t0032g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+3889G>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373047 | |||||||
| chr14:77373096 | G | C | 1 | a0001c0008t0032g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+3840C>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373096 | |||||||
| chr14:77373170 | A | G | 1 | a0003c0003t0021g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.118+3766T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373170 | |||||||
| chr14:77373302 | T | TA | 13 | a0001c0001t0001g0129 a0001c0001t0007g0011 a0001c0001t0007g0127 others(10): Show |
16 | HG00140.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+3633dupT | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373302 | |||||||
| chr14:77373307 | A | C | 1 | a0001c0001t0008g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118+3629T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373307 | |||||||
| chr14:77373313 | C | A | 3 | a0001c0001t0006g0283 a0001c0001t0006g0286 a0002c0002t0006g0030 |
3 | HG02630.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.118+3623G>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373313 | |||||||
| chr14:77373314 | A | G | 8 | a0002c0002t0009g0004 a0002c0002t0009g0056 a0002c0002t0009g0057 others(5): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+3622T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373314 | |||||||
| chr14:77373393 | A | C | 2 | a0001c0008t0032g0280 a0002c0002t0001g0031 |
2 | HG00741.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.118+3543T>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373393 | |||||||
| chr14:77373706 | T | G | 2 | a0001c0001t0002g0276 a0001c0001t0027g0272 |
2 | NA18989.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.118+3230A>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373706 | |||||||
| chr14:77373713 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(95): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.118+3223A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373713 | |||||||
| chr14:77373756 | G | A | 35 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(32): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.118+3180C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77373756 | |||||||
| chr14:77374024 | G | A | 1 | a0001c0001t0031g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.118+2912C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374024 | |||||||
| chr14:77374615 | A | G | 1 | a0001c0001t0006g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.118+2321T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374615 | |||||||
| chr14:77374751 | C | T | 2 | a0002c0002t0005g0025 a0002c0002t0049g0026 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118+2185G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374751 | |||||||
| chr14:77374824 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(78): Show |
89 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.118+2112C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374824 | |||||||
| chr14:77374936 | A | T | 1 | a0001c0001t0002g0200 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.118+2000T>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374936 | |||||||
| chr14:77374956 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.118+1980G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77374956 | |||||||
| chr14:77375015 | C | T | 54 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0196 others(51): Show |
65 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.118+1921G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375015 | |||||||
| chr14:77375194 | T | C | 1 | a0003c0003t0003g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.118+1742A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375194 | |||||||
| chr14:77375245 | C | T | 9 | a0001c0001t0004g0014 a0001c0001t0004g0183 a0001c0001t0004g0184 others(6): Show |
10 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+1691G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375245 | |||||||
| chr14:77375406 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.118+1530C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375406 | |||||||
| chr14:77375451 | G | A | 1 | a0001c0001t0002g0276 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.118+1485C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375451 | |||||||
| chr14:77375705 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0120 others(103): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.118+1231T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375705 | |||||||
| chr14:77375733 | T | C | 2 | a0001c0001t0020g0023 a0001c0001t0020g0277 |
3 | HG02897.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118+1203A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375733 | |||||||
| chr14:77375802 | T | C | 6 | a0001c0001t0001g0278 a0001c0001t0026g0279 a0002c0002t0001g0075 others(3): Show |
6 | HG00609.hp2 HG00621.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+1134A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77375802 | |||||||
| chr14:77376026 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.118+910G>A | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376026 | |||||||
| chr14:77376103 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+833T>C | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376103 | |||||||
| chr14:77376131 | T | C | 1 | a0002c0002t0039g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118+805A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376131 | |||||||
| chr14:77376314 | T | C | 2 | a0001c0008t0032g0280 a0002c0002t0002g0080 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.118+622A>G | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376314 | |||||||
| chr14:77376552 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.118+384C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376552 | |||||||
| chr14:77376557 | G | A | 2 | a0003c0003t0005g0118 a0004c0007t0048g0117 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.118+379C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376557 | |||||||
| chr14:77376561 | G | A | 1 | a0002c0002t0008g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.118+375C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376561 | |||||||
| chr14:77376823 | G | A | 1 | a0002c0002t0022g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+113C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376823 | |||||||
| chr14:77376877 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.118+59C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376877 | |||||||
| chr14:77376879 | G | A | 7 | a0001c0001t0005g0285 a0001c0001t0006g0283 a0001c0001t0006g0284 others(4): Show |
7 | HG01109.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+57C>T | TMED8 | ENSG00000100580.8 | transcript | ENST00000216468.8 | protein_coding | 1/5 | chr14 | 77376879 |