Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10972 |
| ensemblid | ENSG00000170348.9 |
| hgncid | 16998 |
| symbol | TMED10 |
| name | transmembrane p24 trafficking protein 10 |
| refseq_nuc | NM_006827.6 |
| refseq_prot | NP_006818.3 |
| ensembl_nuc | ENST00000303575.9 |
| ensembl_prot | ENSP00000303145.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 75131469 |
| end | 75176612 |
| strand | - |
| ver | v1.2 |
| region | chr14:75131469-75176612 |
| region5000 | chr14:75126469-75181612 |
| regionname0 | TMED10_chr14_75131469_75176612 |
| regionname5000 | TMED10_chr14_75126469_75181612 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 219 | 261 | 86 | 48 | 85 | 8 | 32 | 63 | TMED10_chr14_75126469_75181612 | TMED10 | MSGLS others(214): Show |
chr14 | 75126469 | 75181612 |
| a0002 | 0/0 | 219 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | MSGLS others(214): Show |
chr14 | 75126469 | 75181612 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 657 | 242 | 72 | 46 | 85 | 8 | 29 | TMED10_chr14_75126469_75181612 | TMED10 | ATGTC others(652): Show |
chr14 | 75126469 | 75181612 | ||
| a0001c0002 | 0/0 | 657 | 19 | 14 | 2 | 0 | 0 | 3 | TMED10_chr14_75126469_75181612 | TMED10 | ATGTC others(652): Show |
chr14 | 75126469 | 75181612 | ||
| a0002c0003 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | ATGTC others(652): Show |
chr14 | 75126469 | 75181612 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4109 | 95 | 41 | 18 | 20 | 4 | 12 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0002 | 0/1 | 4110 | 68 | 2 | 13 | 42 | 2 | 8 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0003 | 0/0 | 4111 | 22 | 2 | 4 | 11 | 0 | 5 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4106): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0004 | 0/0 | 4109 | 13 | 3 | 1 | 8 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0005 | 0/0 | 4109 | 12 | 3 | 6 | 0 | 1 | 2 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0006 | 0/0 | 4110 | 7 | 5 | 1 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0007 | 1/0 | 4109 | 6 | 3 | 2 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0008 | 0/0 | 4110 | 5 | 1 | 0 | 3 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0009 | 0/0 | 4111 | 4 | 4 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4106): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0010 | 0/0 | 4111 | 3 | 3 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4106): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0011 | 0/0 | 4111 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4106): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0012 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0013 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0014 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0015 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0016 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0001t0017 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0001c0002t0002 | 0/0 | 4110 | 15 | 11 | 2 | 0 | 0 | 2 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| a0001c0002t0003 | 0/0 | 4111 | 3 | 3 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4106): Show |
chr14 | 75126469 | 75181612 |
| a0001c0002t0004 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4104): Show |
chr14 | 75126469 | 75181612 |
| a0002c0003t0002 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | GAGGC others(4105): Show |
chr14 | 75126469 | 75181612 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0013g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0014g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0015g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0016g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0001t0017g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0001c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| a0002c0003t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0031 | EUR | FIN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0232 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0092 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0249 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | KHV | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0211 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0241 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0198 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0233 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0231 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0118 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0234 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0239 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0245 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0237 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0228 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03490 | hp1 | a0001 | c0001 | t0016 | g0174 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03490 | hp2 | a0001 | c0002 | t0004 | g0210 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0044 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03942 | hp1 | a0001 | c0001 | t0008 | g0225 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | STU | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18953 | hp1 | a0001 | c0001 | t0008 | g0236 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0235 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0226 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19054 | hp1 | a0002 | c0003 | t0002 | g0010 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ASW | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0055 | EUR | TSI | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0072 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0182 | AFR | MSL | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0243 | AFR | USA | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0229 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0012 | REF | REF | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0220 | REF | REF | TMED10_chr14_75126469_75181612 | TMED10 | chr14 | 75126469 | 75181612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75176429 | C | T | 1 | a0002 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.151G>A | p.Asp51Asn | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/5 | 184/4109 | 151/660 | 51/219 | chr14 | 75176429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75134960 | G | A | 1 | a0001c0002 | 19 | HG00741.hp2 HG01346.hp2 HG01884.hp1 others(16): Show |
synonymous_variant | LOW | c.585C>T | p.Phe195Phe | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 618/4109 | 585/660 | 195/219 | chr14 | 75134960 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75132336 | T | C | 1 | a0001c0001t0017 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2549 | chr14 | 75132336 | ||||||
| chr14:75132384 | T | TC | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(3): Show |
96 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2500dupG | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | ||||||
| chr14:75132384 | T | TCC | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(1): Show |
30 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2499_*2500dupGG | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | ||||||
| chr14:75132384 | T | TTC | 1 | a0001c0001t0010 | 3 | HG02717.hp1 HG02895.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2500_*2501insGA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2500 | chr14 | 75132384 | ||||||
| chr14:75132396 | CA | C | 4 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(1): Show |
74 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2488delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2488 | chr14 | 75132396 | ||||||
| chr14:75132397 | A | C | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(4): Show |
45 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2488T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2488 | chr14 | 75132397 | ||||||
| chr14:75132398 | A | C | 1 | a0001c0001t0005 | 12 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2487T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2487 | chr14 | 75132398 | ||||||
| chr14:75132426 | A | G | 2 | a0001c0001t0008 a0001c0001t0017 |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2459T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2459 | chr14 | 75132426 | ||||||
| chr14:75132452 | G | A | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(5): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2433C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2433 | chr14 | 75132452 | ||||||
| chr14:75132625 | G | C | 2 | a0001c0001t0008 a0001c0001t0017 |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2260C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 2260 | chr14 | 75132625 | ||||||
| chr14:75132944 | A | G | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(4): Show |
122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1941T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1941 | chr14 | 75132944 | ||||||
| chr14:75133007 | T | C | 1 | a0001c0001t0016 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1878A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1878 | chr14 | 75133007 | ||||||
| chr14:75133832 | C | T | 1 | a0001c0001t0014 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1053 | chr14 | 75133832 | ||||||
| chr14:75133849 | G | A | 2 | a0001c0001t0008 a0001c0001t0017 |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1036C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 1036 | chr14 | 75133849 | ||||||
| chr14:75133994 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 891 | chr14 | 75133994 | ||||||
| chr14:75134258 | C | T | 1 | a0001c0001t0012 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*627G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 627 | chr14 | 75134258 | ||||||
| chr14:75134541 | G | T | 1 | a0001c0001t0011 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*344C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 5/5 | 344 | chr14 | 75134541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75135034 | A | G | 114 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(111): Show |
118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.539-28T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135034 | |||||||
| chr14:75135068 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0016 |
3 | HG01243.hp2 HG01884.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.539-62A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135068 | |||||||
| chr14:75135079 | G | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
84 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.539-73C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135079 | |||||||
| chr14:75135120 | C | CTAACA | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.539-119_539-115dup others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135120 | |||||||
| chr14:75135159 | A | G | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(119): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.539-153T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135159 | |||||||
| chr14:75135260 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.539-254G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135260 | |||||||
| chr14:75135325 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.539-319T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 4/4 | chr14 | 75135325 | |||||||
| chr14:75136131 | A | T | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(119): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.412-245T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136131 | |||||||
| chr14:75136325 | A | C | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-439T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136325 | |||||||
| chr14:75136405 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.412-519G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136405 | |||||||
| chr14:75136536 | A | G | 4 | a0001c0001t0010g0231 a0001c0001t0010g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-650T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136536 | |||||||
| chr14:75136703 | T | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-817A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136703 | |||||||
| chr14:75136861 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.412-975A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136861 | |||||||
| chr14:75136962 | T | G | 1 | a0001c0001t0002g0136 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.412-1076A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75136962 | |||||||
| chr14:75137015 | C | CT | 7 | a0001c0001t0001g0240 a0001c0001t0002g0149 a0001c0001t0007g0250 others(4): Show |
7 | HG02615.hp2 HG03017.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-1130dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137015 | |||||||
| chr14:75137246 | G | A | 114 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(111): Show |
118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.412-1360C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137246 | |||||||
| chr14:75137514 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.412-1628A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137514 | |||||||
| chr14:75137606 | C | T | 2 | a0001c0001t0008g0226 a0001c0001t0008g0236 |
2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.412-1720G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137606 | |||||||
| chr14:75137622 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.412-1736A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137622 | |||||||
| chr14:75137691 | A | AT | 12 | a0001c0001t0001g0100 a0001c0001t0001g0119 a0001c0001t0002g0202 others(9): Show |
12 | HG01099.hp1 HG01109.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.412-1806dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137691 | |||||||
| chr14:75137691 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.412-1805T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137691 | |||||||
| chr14:75137694 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.412-1808G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137694 | |||||||
| chr14:75137696 | G | GTTTC | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
109 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.412-1814_412-1811d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137696 | |||||||
| chr14:75137708 | CT | C | 115 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(112): Show |
119 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.412-1823delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137708 | |||||||
| chr14:75137708 | CTT | C | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0184 others(2): Show |
5 | HG01099.hp1 HG01884.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1824_412-1823d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137708 | |||||||
| chr14:75137874 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.412-1988T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75137874 | |||||||
| chr14:75138035 | T | G | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2149A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138035 | |||||||
| chr14:75138073 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0184 a0001c0001t0002g0185 others(2): Show |
6 | HG00558.hp1 NA18939.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-2187G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138073 | |||||||
| chr14:75138352 | G | A | 46 | a0001c0001t0002g0007 a0001c0001t0002g0142 a0001c0001t0002g0184 others(43): Show |
49 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.412-2466C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138352 | |||||||
| chr14:75138399 | A | C | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.412-2513T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138399 | |||||||
| chr14:75138501 | A | T | 1 | a0001c0001t0016g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.412-2615T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138501 | |||||||
| chr14:75138812 | C | CT | 22 | a0001c0001t0001g0050 a0001c0001t0001g0088 a0001c0001t0001g0099 others(19): Show |
22 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.412-2927dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | |||||||
| chr14:75138812 | C | CTT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.412-2928_412-2927d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | |||||||
| chr14:75138812 | C | CTTT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
13 | HG00642.hp1 HG01255.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.412-2929_412-2927d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138812 | |||||||
| chr14:75138824 | T | TTA | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2939_412-2938i others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138824 | |||||||
| chr14:75138825 | T | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0172 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.412-2939A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138825 | |||||||
| chr14:75138825 | T | TA | 120 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(117): Show |
124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.412-2940_412-2939i others(3): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138825 | |||||||
| chr14:75138833 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.412-2947T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138833 | |||||||
| chr14:75138901 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-3015A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138901 | |||||||
| chr14:75138982 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0011g0239 a0001c0001t0014g0241 |
3 | HG02615.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.412-3096T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75138982 | |||||||
| chr14:75139089 | A | G | 118 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(115): Show |
122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.412-3203T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139089 | |||||||
| chr14:75139360 | TAATC | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.412-3478_412-3475d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139360 | |||||||
| chr14:75139635 | C | CA | 114 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0100 others(111): Show |
118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.412-3750dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139635 | |||||||
| chr14:75139635 | C | CAA | 11 | a0001c0001t0001g0099 a0001c0001t0003g0167 a0001c0001t0003g0215 others(8): Show |
11 | HG00673.hp1 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.412-3751_412-3750d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75139635 | |||||||
| chr14:75140016 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.412-4130A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140016 | |||||||
| chr14:75140185 | A | C | 2 | a0001c0001t0006g0060 a0001c0001t0006g0064 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.412-4299T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140185 | |||||||
| chr14:75140186 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.412-4300G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140186 | |||||||
| chr14:75140321 | G | A | 1 | a0001c0001t0002g0142 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.412-4435C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140321 | |||||||
| chr14:75140342 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
95 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.412-4456C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140342 | |||||||
| chr14:75140743 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412-4857A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140743 | |||||||
| chr14:75140861 | C | G | 4 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 others(1): Show |
4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-4975G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140861 | |||||||
| chr14:75140863 | C | G | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412-4977G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75140863 | |||||||
| chr14:75141050 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-5164T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141050 | |||||||
| chr14:75141064 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.412-5178G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141064 | |||||||
| chr14:75141083 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.412-5197A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141083 | |||||||
| chr14:75141141 | A | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0138 a0001c0001t0002g0161 others(2): Show |
6 | HG01361.hp2 HG02293.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-5255T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141141 | |||||||
| chr14:75141214 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-5328C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141214 | |||||||
| chr14:75141565 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-5679T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141565 | |||||||
| chr14:75141673 | A | G | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412-5787T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141673 | |||||||
| chr14:75141721 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.412-5835A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141721 | |||||||
| chr14:75141919 | G | A | 1 | a0001c0002t0002g0212 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.411+5745C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141919 | |||||||
| chr14:75141980 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
111 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.411+5684G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75141980 | |||||||
| chr14:75142025 | G | A | 114 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(111): Show |
118 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.411+5639C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142025 | |||||||
| chr14:75142079 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.411+5585T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142079 | |||||||
| chr14:75142333 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.411+5331C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142333 | |||||||
| chr14:75142387 | C | T | 4 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 others(1): Show |
4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+5277G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142387 | |||||||
| chr14:75142565 | A | T | 126 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(123): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.411+5099T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142565 | |||||||
| chr14:75142607 | T | G | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+5057A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142607 | |||||||
| chr14:75142864 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.411+4800A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142864 | |||||||
| chr14:75142890 | G | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4774C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75142890 | |||||||
| chr14:75143181 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+4483C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143181 | |||||||
| chr14:75143297 | C | T | 1 | a0001c0001t0004g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.411+4367G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143297 | |||||||
| chr14:75143467 | G | C | 126 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(123): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.411+4197C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143467 | |||||||
| chr14:75143933 | C | CA | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.411+3730dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143933 | |||||||
| chr14:75143933 | C | CAA | 5 | a0001c0001t0001g0057 a0001c0001t0002g0140 a0001c0001t0002g0221 others(2): Show |
5 | HG03516.hp2 HG03831.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+3729_411+3730d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143933 | |||||||
| chr14:75143987 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.411+3677G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143987 | |||||||
| chr14:75143994 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.411+3670T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75143994 | |||||||
| chr14:75144022 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.411+3642T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144022 | |||||||
| chr14:75144069 | A | G | 1 | a0001c0002t0003g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.411+3595T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144069 | |||||||
| chr14:75144278 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.411+3386G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144278 | |||||||
| chr14:75144458 | G | A | 3 | a0001c0001t0002g0202 a0001c0001t0002g0205 a0001c0001t0003g0206 |
3 | HG01099.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.411+3206C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144458 | |||||||
| chr14:75144478 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+3186T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144478 | |||||||
| chr14:75144489 | C | T | 3 | a0001c0001t0002g0202 a0001c0001t0002g0205 a0001c0001t0003g0206 |
3 | HG01099.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.411+3175G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144489 | |||||||
| chr14:75144581 | C | T | 3 | a0001c0001t0002g0194 a0001c0001t0002g0209 a0001c0001t0004g0208 |
3 | HG02080.hp2 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.411+3083G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144581 | |||||||
| chr14:75144609 | AGTCCACA others(18): Show |
A | 1 | a0001c0001t0005g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+3030_411+3054d others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144609 | |||||||
| chr14:75144617 | G | A | 4 | a0001c0002t0002g0008 a0001c0002t0002g0193 a0001c0002t0002g0213 others(1): Show |
5 | HG00741.hp2 HG01346.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+3047C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144617 | |||||||
| chr14:75144752 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.411+2912G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144752 | |||||||
| chr14:75144782 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+2882G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144782 | |||||||
| chr14:75144819 | G | A | 1 | a0001c0001t0008g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.411+2845C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144819 | |||||||
| chr14:75144856 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.411+2808C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75144856 | |||||||
| chr14:75145322 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.411+2342G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145322 | |||||||
| chr14:75145324 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2340T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145324 | |||||||
| chr14:75145380 | C | A | 126 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(123): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.411+2284G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145380 | |||||||
| chr14:75145519 | C | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+2145G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145519 | |||||||
| chr14:75145769 | C | T | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+1895G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145769 | |||||||
| chr14:75145770 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.411+1894T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75145770 | |||||||
| chr14:75146146 | C | A | 1 | a0001c0001t0002g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.411+1518G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146146 | |||||||
| chr14:75146388 | C | G | 6 | a0001c0001t0002g0126 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG00738.hp2 HG01256.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+1276G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146388 | |||||||
| chr14:75146406 | A | G | 1 | a0001c0001t0004g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.411+1258T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146406 | |||||||
| chr14:75146475 | C | T | 8 | a0001c0001t0005g0033 a0001c0001t0005g0042 a0001c0001t0005g0043 others(5): Show |
8 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+1189G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146475 | |||||||
| chr14:75146908 | C | CAGAT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.411+752_411+755dup others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | |||||||
| chr14:75146908 | C | CAGATAGA others(1): Show |
59 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0034 others(56): Show |
60 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.411+748_411+755dup others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | |||||||
| chr14:75146908 | C | CAGATAGA others(5): Show |
17 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0002g0137 others(14): Show |
18 | HG00741.hp2 HG01256.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.411+744_411+755dup others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | |||||||
| chr14:75146908 | C | CAGATAGA others(9): Show |
2 | a0001c0001t0002g0148 a0001c0001t0002g0195 |
2 | HG03654.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.411+740_411+755dup others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | |||||||
| chr14:75146908 | CAGAT | C | 14 | a0001c0001t0001g0057 a0001c0001t0002g0015 a0001c0001t0002g0131 others(11): Show |
14 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+752_411+755del others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146908 | |||||||
| chr14:75146928 | T | C | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+736A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75146928 | |||||||
| chr14:75147184 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.411+480A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147184 | |||||||
| chr14:75147185 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0014 a0001c0001t0005g0045 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.411+469_411+478dup others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(7): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+478_411+479ins others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG03130.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+478_411+479ins others(15): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0004g0013 a0001c0001t0005g0043 a0001c0001t0005g0044 others(1): Show |
4 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+468_411+478dup others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0016 a0001c0001t0005g0042 a0001c0001t0005g0093 |
3 | HG01261.hp2 HG02630.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.411+467_411+478dup others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0005g0033 a0001c0001t0005g0173 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.411+466_411+478dup others(13): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(7): Show |
7 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0121 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+465_411+478dup others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0081 a0001c0001t0009g0071 a0001c0001t0009g0079 |
3 | HG02145.hp2 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.411+464_411+478dup others(15): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0117 a0001c0001t0009g0072 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.411+463_411+478dup others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.411+461_411+478dup others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | GT | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0069 others(3): Show |
6 | HG00741.hp1 HG01981.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+478delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | GTT | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.411+477_411+478del others(2): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147185 | GTTTTTTT | G | 110 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(107): Show |
114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.411+472_411+478del others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147185 | |||||||
| chr14:75147188 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.411+476A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147188 | |||||||
| chr14:75147191 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0001g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.411+472_411+473ins others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147191 | |||||||
| chr14:75147287 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+377G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147287 | |||||||
| chr14:75147431 | C | T | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+233G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 3/4 | chr14 | 75147431 | |||||||
| chr14:75147801 | A | ACCCG | 111 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(108): Show |
115 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.338-68_338-65dupCG others(2): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147801 | |||||||
| chr14:75147805 | G | C | 1 | a0001c0001t0003g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.338-68C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147805 | |||||||
| chr14:75147852 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-115T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75147852 | |||||||
| chr14:75148139 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0014g0241 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.338-402A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148139 | |||||||
| chr14:75148185 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-448T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148185 | |||||||
| chr14:75148222 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.338-485C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148222 | |||||||
| chr14:75148514 | AATC | A | 3 | a0001c0001t0002g0133 a0001c0001t0004g0152 a0001c0001t0004g0170 |
3 | NA18954.hp1 NA18981.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.338-780_338-778del others(3): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148514 | |||||||
| chr14:75148524 | T | C | 126 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(123): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.338-787A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148524 | |||||||
| chr14:75148543 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
97 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.338-806G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148543 | |||||||
| chr14:75148565 | C | T | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.338-828G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148565 | |||||||
| chr14:75148890 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.338-1153T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148890 | |||||||
| chr14:75148923 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.338-1186T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148923 | |||||||
| chr14:75148976 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.338-1239C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148976 | |||||||
| chr14:75148992 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0004g0014 |
2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.338-1255G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75148992 | |||||||
| chr14:75149279 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.338-1542A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149279 | |||||||
| chr14:75149472 | A | ATAAAT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.338-1736_338-1735i others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149472 | |||||||
| chr14:75149781 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-2044G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149781 | |||||||
| chr14:75149837 | GCT | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2102_338-2101d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149837 | |||||||
| chr14:75149840 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2103G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149840 | |||||||
| chr14:75149842 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2105A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149842 | |||||||
| chr14:75149845 | CTGT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2111_338-2109d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149845 | |||||||
| chr14:75149849 | A | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.338-2112T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149849 | |||||||
| chr14:75149964 | G | A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+2068C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75149964 | |||||||
| chr14:75150110 | A | C | 4 | a0001c0001t0001g0058 a0001c0001t0002g0006 a0001c0001t0002g0138 others(1): Show |
5 | NA18982.hp1 NA18984.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+1922T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150110 | |||||||
| chr14:75150149 | C | T | 2 | a0001c0001t0002g0189 a0001c0001t0003g0199 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.337+1883G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150149 | |||||||
| chr14:75150226 | G | T | 1 | a0001c0001t0003g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.337+1806C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150226 | |||||||
| chr14:75150319 | C | T | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.337+1713G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150319 | |||||||
| chr14:75150737 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
6 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1295C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150737 | |||||||
| chr14:75150770 | G | A | 1 | a0001c0001t0007g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.337+1262C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75150770 | |||||||
| chr14:75151022 | C | T | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1010G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151022 | |||||||
| chr14:75151116 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.337+916C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151116 | |||||||
| chr14:75151215 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0007g0243 |
2 | HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.337+817C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151215 | |||||||
| chr14:75151425 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.337+607C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151425 | |||||||
| chr14:75151426 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.337+606G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151426 | |||||||
| chr14:75151431 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+601G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151431 | |||||||
| chr14:75151457 | G | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.337+575C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151457 | |||||||
| chr14:75151849 | T | C | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+183A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151849 | |||||||
| chr14:75151872 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.337+160G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 2/4 | chr14 | 75151872 | |||||||
| chr14:75152218 | G | A | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-75C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152218 | |||||||
| chr14:75152332 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.226-189G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152332 | |||||||
| chr14:75152391 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.226-248T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152391 | |||||||
| chr14:75152397 | C | T | 6 | a0001c0001t0006g0075 a0001c0001t0006g0076 a0001c0001t0009g0071 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-254G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152397 | |||||||
| chr14:75152415 | T | G | 126 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(123): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.226-272A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152415 | |||||||
| chr14:75152421 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.226-278A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152421 | |||||||
| chr14:75152431 | A | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-288T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152431 | |||||||
| chr14:75152490 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-347G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152490 | |||||||
| chr14:75152586 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226-443C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152586 | |||||||
| chr14:75152604 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.226-461T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152604 | |||||||
| chr14:75152765 | G | C | 12 | a0001c0001t0002g0131 a0001c0001t0002g0134 a0001c0001t0002g0146 others(9): Show |
12 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.226-622C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152765 | |||||||
| chr14:75152847 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0230 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.226-704G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152847 | |||||||
| chr14:75152894 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226-751A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75152894 | |||||||
| chr14:75153075 | T | C | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-932A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153075 | |||||||
| chr14:75153275 | AAAAAAC | A | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-1138_226-1133d others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153275 | |||||||
| chr14:75153315 | T | TA | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.226-1173dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153315 | |||||||
| chr14:75153416 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226-1273A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153416 | |||||||
| chr14:75153550 | G | C | 1 | a0001c0002t0002g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-1407C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153550 | |||||||
| chr14:75153777 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0002g0032 a0001c0001t0002g0138 a0001c0001t0002g0155 others(2): Show |
5 | HG01081.hp2 HG01257.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-1642_226-1635d others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | |||||||
| chr14:75153777 | C | CTTTTTTT others(2): Show |
117 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(114): Show |
121 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.226-1643_226-1635d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | |||||||
| chr14:75153777 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0222 a0001c0001t0010g0231 a0001c0001t0010g0233 others(1): Show |
4 | HG01109.hp2 HG01981.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1644_226-1635d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153777 | |||||||
| chr14:75153855 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-1712G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153855 | |||||||
| chr14:75153862 | C | T | 1 | a0001c0001t0005g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.226-1719G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75153862 | |||||||
| chr14:75154168 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226-2025C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154168 | |||||||
| chr14:75154237 | CA | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.226-2095delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154237 | |||||||
| chr14:75154317 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.226-2174C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154317 | |||||||
| chr14:75154373 | G | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-2230C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154373 | |||||||
| chr14:75154385 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.226-2242G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154385 | |||||||
| chr14:75154401 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
84 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.226-2259dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAA | 29 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(26): Show |
30 | HG00621.hp1 HG01192.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.226-2260_226-2259d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0068 others(5): Show |
8 | HG01243.hp1 HG01981.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-2261_226-2259d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(1): Show |
22 | a0001c0001t0002g0030 a0001c0001t0002g0032 a0001c0001t0002g0130 others(19): Show |
22 | HG00423.hp1 HG01496.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.226-2266_226-2259d others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(2): Show |
48 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0026 others(45): Show |
51 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.226-2267_226-2259d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(3): Show |
26 | a0001c0001t0002g0028 a0001c0001t0002g0128 a0001c0001t0002g0136 others(23): Show |
27 | HG00544.hp2 HG00741.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.226-2268_226-2259d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0002g0203 a0001c0001t0002g0218 a0001c0001t0002g0219 others(6): Show |
9 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2269_226-2259d others(13): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0205 a0001c0001t0003g0204 a0001c0001t0003g0206 |
3 | HG01099.hp1 HG01257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.226-2270_226-2259d others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0002g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.226-2272_226-2259d others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(8): Show |
2 | a0001c0002t0002g0183 a0001c0002t0003g0182 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.226-2273_226-2259d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0002g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.226-2274_226-2259d others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | CA | C | 6 | a0001c0001t0007g0243 a0001c0001t0008g0225 a0001c0001t0008g0226 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-2259delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226-2268_226-2259d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154401 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0002g0189 a0001c0001t0003g0199 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.226-2272_226-2259d others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154401 | |||||||
| chr14:75154542 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.226-2399C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154542 | |||||||
| chr14:75154824 | C | T | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-2681G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154824 | |||||||
| chr14:75154963 | CT | C | 15 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0029 others(12): Show |
15 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2821delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154963 | |||||||
| chr14:75154964 | T | C | 2 | a0001c0001t0004g0152 a0001c0001t0004g0170 |
2 | NA18954.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.226-2821A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154964 | |||||||
| chr14:75154965 | T | C | 1 | a0001c0001t0004g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.226-2822A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75154965 | |||||||
| chr14:75155020 | G | A | 3 | a0001c0001t0002g0160 a0001c0001t0002g0168 a0001c0001t0003g0159 |
3 | HG03704.hp2 HG03942.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.226-2877C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155020 | |||||||
| chr14:75155208 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0081 others(2): Show |
5 | HG02647.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-3065G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155208 | |||||||
| chr14:75155219 | C | T | 1 | a0001c0001t0006g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.226-3076G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155219 | |||||||
| chr14:75155589 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-3446G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155589 | |||||||
| chr14:75155711 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
6 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-3568A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155711 | |||||||
| chr14:75155783 | C | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-3640G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75155783 | |||||||
| chr14:75156145 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0172 |
2 | HG01256.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.226-4002G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156145 | |||||||
| chr14:75156341 | T | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-4198A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156341 | |||||||
| chr14:75156550 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0004g0123 |
2 | HG02074.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.226-4407G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156550 | |||||||
| chr14:75156784 | T | C | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(119): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.226-4641A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156784 | |||||||
| chr14:75156916 | A | AAAAAG | 106 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0063 others(103): Show |
108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.226-4778_226-4774d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(3): Show |
56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(53): Show |
60 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.226-4783_226-4774d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(8): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(25): Show |
31 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.226-4788_226-4774d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(13): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
12 | HG01243.hp1 HG01358.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-4793_226-4774d others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(18): Show |
1 | a0001c0001t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-4798_226-4774d others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(23): Show |
1 | a0001c0001t0005g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.226-4803_226-4774d others(32): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | AAAAAGAA others(28): Show |
6 | a0001c0001t0005g0033 a0001c0001t0005g0042 a0001c0001t0005g0043 others(3): Show |
6 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-4808_226-4774d others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | A | G | 1 | a0001c0001t0003g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.226-4773T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | AAAAAG | A | 9 | a0001c0001t0002g0160 a0001c0001t0007g0250 a0001c0001t0007g0251 others(6): Show |
9 | HG03130.hp1 HG03195.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-4778_226-4774d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.226-4783_226-4774d others(12): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75156916 | AAAAAGAA others(8): Show |
A | 1 | a0001c0001t0009g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-4788_226-4774d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75156916 | |||||||
| chr14:75157063 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-4920A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157063 | |||||||
| chr14:75157075 | T | G | 4 | a0001c0001t0010g0231 a0001c0001t0010g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-4932A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157075 | |||||||
| chr14:75157285 | T | C | 118 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(115): Show |
122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-5142A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157285 | |||||||
| chr14:75157292 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.226-5149A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157292 | |||||||
| chr14:75157431 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-5288G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157431 | |||||||
| chr14:75157603 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-5460A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157603 | |||||||
| chr14:75157642 | CAT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-5501_226-5500d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157642 | |||||||
| chr14:75157647 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.226-5504G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157647 | |||||||
| chr14:75157760 | C | T | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(119): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.226-5617G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75157760 | |||||||
| chr14:75158444 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0101 |
2 | NA18979.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.226-6301G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158444 | |||||||
| chr14:75158648 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226-6505C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158648 | |||||||
| chr14:75158849 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.226-6706C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158849 | |||||||
| chr14:75158855 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.226-6712A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158855 | |||||||
| chr14:75158883 | C | CA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0108 others(3): Show |
7 | NA18747.hp2 NA18955.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-6741dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158883 | |||||||
| chr14:75158919 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.226-6776G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158919 | |||||||
| chr14:75158925 | A | AAAAT | 3 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 |
3 | NA18953.hp1 NA18954.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.226-6786_226-6783d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158925 | |||||||
| chr14:75158953 | T | A | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-6810A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158953 | |||||||
| chr14:75158973 | A | G | 1 | a0001c0001t0005g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.226-6830T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158973 | |||||||
| chr14:75158979 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-6836C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75158979 | |||||||
| chr14:75159339 | A | C | 122 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0015 others(119): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.226-7196T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159339 | |||||||
| chr14:75159428 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-7285A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159428 | |||||||
| chr14:75159457 | A | C | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-7314T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159457 | |||||||
| chr14:75159554 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-7411A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75159554 | |||||||
| chr14:75160012 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.226-7869C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160012 | |||||||
| chr14:75160233 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.226-8090C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160233 | |||||||
| chr14:75160303 | T | C | 1 | a0001c0001t0012g0118 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.226-8160A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160303 | |||||||
| chr14:75160394 | AT | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-8252delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160394 | |||||||
| chr14:75160616 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-8473A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160616 | |||||||
| chr14:75160918 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-8775G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160918 | |||||||
| chr14:75160998 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-8855A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75160998 | |||||||
| chr14:75161470 | C | G | 1 | a0001c0002t0003g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.226-9327G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161470 | |||||||
| chr14:75161496 | AG | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.226-9354delC | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161496 | |||||||
| chr14:75161696 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226-9553A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161696 | |||||||
| chr14:75161790 | C | A | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226-9647G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161790 | |||||||
| chr14:75161809 | A | G | 5 | a0001c0001t0007g0244 a0001c0001t0007g0249 a0001c0001t0007g0250 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-9666T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161809 | |||||||
| chr14:75161968 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.226-9825T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161968 | |||||||
| chr14:75161998 | G | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-9855C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75161998 | |||||||
| chr14:75162021 | C | CCGGGG | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-9883_226-9879d others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162021 | |||||||
| chr14:75162022 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.226-9879G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162022 | |||||||
| chr14:75162153 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0120 |
2 | HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.226-10010A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162153 | |||||||
| chr14:75162182 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.226-10039A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162182 | |||||||
| chr14:75162252 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
138 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.226-10109T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162252 | |||||||
| chr14:75162352 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(8): Show |
15 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-10209T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162352 | |||||||
| chr14:75162697 | CCTGACAA others(26): Show |
C | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.226-10587_226-1055 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162697 | |||||||
| chr14:75162702 | C | T | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-10559G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162702 | |||||||
| chr14:75162741 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.226-10598G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162741 | |||||||
| chr14:75162884 | T | C | 2 | a0001c0001t0002g0209 a0001c0001t0004g0208 |
2 | HG02080.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.226-10741A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75162884 | |||||||
| chr14:75163039 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0138 a0001c0001t0002g0161 others(2): Show |
6 | HG01361.hp2 HG02293.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-10896T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163039 | |||||||
| chr14:75163042 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.226-10899G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163042 | |||||||
| chr14:75163079 | T | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-10936A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163079 | |||||||
| chr14:75163081 | A | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
86 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.226-10938T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163081 | |||||||
| chr14:75163145 | GGGA | G | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-11005_226-1100 others(7): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163145 | |||||||
| chr14:75163214 | C | G | 5 | a0001c0001t0007g0244 a0001c0001t0007g0249 a0001c0001t0007g0250 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-11071G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163214 | |||||||
| chr14:75163250 | C | T | 2 | a0001c0001t0007g0250 a0001c0001t0007g0251 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.226-11107G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163250 | |||||||
| chr14:75163254 | C | T | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226-11111G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163254 | |||||||
| chr14:75163269 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
89 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.226-11126G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163269 | |||||||
| chr14:75163294 | T | C | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-11151A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163294 | |||||||
| chr14:75163294 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.226-11151A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163294 | |||||||
| chr14:75163310 | T | C | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-11167A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163310 | |||||||
| chr14:75163358 | T | C | 4 | a0001c0001t0010g0231 a0001c0001t0010g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-11215A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163358 | |||||||
| chr14:75163507 | C | T | 1 | a0001c0001t0007g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.226-11364G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163507 | |||||||
| chr14:75163552 | C | CA | 24 | a0001c0001t0001g0039 a0001c0001t0002g0029 a0001c0001t0002g0130 others(21): Show |
25 | HG00621.hp2 HG00741.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.226-11410dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | |||||||
| chr14:75163552 | CA | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
110 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.226-11410delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | |||||||
| chr14:75163552 | CAAAAAA | C | 5 | a0001c0001t0007g0244 a0001c0001t0007g0249 a0001c0001t0007g0250 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-11415_226-1141 others(10): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163552 | |||||||
| chr14:75163587 | C | T | 2 | a0001c0001t0005g0054 a0001c0001t0005g0055 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.226-11444G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163587 | |||||||
| chr14:75163675 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-11532C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75163675 | |||||||
| chr14:75164072 | C | T | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-11929G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164072 | |||||||
| chr14:75164211 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.226-12068C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164211 | |||||||
| chr14:75164229 | C | CT | 54 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0020 others(51): Show |
54 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.226-12087dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164229 | |||||||
| chr14:75164238 | T | TC | 4 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 others(1): Show |
4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-12096_226-1209 others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164238 | |||||||
| chr14:75164309 | G | GCACAAAA others(26): Show |
1 | a0001c0001t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225+12045_225+1204 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164309 | |||||||
| chr14:75164312 | A | C | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225+12043T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164312 | |||||||
| chr14:75164324 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.225+12031C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164324 | |||||||
| chr14:75164380 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.225+11975G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164380 | |||||||
| chr14:75164426 | T | A | 1 | a0001c0001t0003g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.225+11929A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164426 | |||||||
| chr14:75164492 | A | G | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+11863T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164492 | |||||||
| chr14:75164532 | AAT | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0131 a0001c0001t0002g0186 others(2): Show |
6 | NA18939.hp1 NA18953.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+11821_225+1182 others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164532 | AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0081 a0001c0001t0006g0080 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.225+11811_225+1182 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164532 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.225+11809_225+1182 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164532 | AATATATA others(9): Show |
A | 1 | a0001c0001t0004g0247 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.225+11807_225+1182 others(20): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164532 | AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.225+11801_225+1182 others(26): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164532 | AATATATA others(19): Show |
A | 56 | a0001c0001t0002g0006 a0001c0001t0002g0026 a0001c0001t0002g0028 others(53): Show |
57 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.225+11797_225+1182 others(30): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164532 | |||||||
| chr14:75164545 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0002g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.225+11777_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164545 | |||||||
| chr14:75164546 | TATATATA others(18): Show |
T | 3 | a0001c0001t0003g0124 a0001c0001t0003g0129 a0001c0001t0004g0170 |
3 | HG03831.hp1 NA19012.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.225+11784_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164546 | |||||||
| chr14:75164546 | TATATATA others(20): Show |
T | 1 | a0001c0001t0002g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.225+11782_225+1180 others(31): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164546 | |||||||
| chr14:75164547 | ATATATAT others(26): Show |
A | 3 | a0001c0001t0008g0226 a0001c0001t0008g0236 a0001c0001t0017g0237 |
3 | HG03195.hp2 NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.225+11775_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164547 | |||||||
| chr14:75164547 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0008g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225+11774_225+1180 others(38): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164547 | |||||||
| chr14:75164548 | TATATATA others(18): Show |
T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0130 |
2 | NA18990.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.225+11782_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164548 | |||||||
| chr14:75164549 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0008g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.225+11773_225+1180 others(37): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164549 | |||||||
| chr14:75164551 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+11773_225+1180 others(35): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164551 | |||||||
| chr14:75164553 | ATATATAT others(18): Show |
A | 5 | a0001c0001t0002g0127 a0001c0001t0005g0044 a0001c0001t0007g0243 others(2): Show |
5 | HG01361.hp1 HG01496.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11777_225+1180 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164553 | |||||||
| chr14:75164553 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225+11775_225+1180 others(31): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164553 | |||||||
| chr14:75164555 | ATATATAT others(16): Show |
A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(6): Show |
9 | HG01243.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+11777_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | |||||||
| chr14:75164555 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0036 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.225+11776_225+1179 others(28): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | |||||||
| chr14:75164555 | ATATATAT others(18): Show |
A | 9 | a0001c0001t0005g0033 a0001c0001t0005g0042 a0001c0001t0005g0043 others(6): Show |
9 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164555 | |||||||
| chr14:75164556 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.225+11780_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164556 | |||||||
| chr14:75164557 | ATATATAT others(14): Show |
A | 12 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00280.hp2 HG00741.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+11777_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | |||||||
| chr14:75164557 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.225+11776_225+1179 others(26): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | |||||||
| chr14:75164557 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0005g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.225+11774_225+1179 others(28): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | |||||||
| chr14:75164557 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0005g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+11773_225+1179 others(29): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164557 | |||||||
| chr14:75164558 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225+11778_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164558 | |||||||
| chr14:75164559 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0016g0174 |
3 | HG01891.hp2 HG02809.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.225+11777_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | |||||||
| chr14:75164559 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0111 others(1): Show |
4 | HG02818.hp1 HG04228.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+11776_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | |||||||
| chr14:75164559 | ATATATAT others(14): Show |
A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0052 others(20): Show |
24 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | |||||||
| chr14:75164559 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+11773_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164559 | |||||||
| chr14:75164561 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+11777_225+1179 others(21): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164561 | ATATATAT others(11): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0022 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11776_225+1179 others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164561 | ATATATAT others(12): Show |
A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(14): Show |
17 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164561 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00639.hp2 HG03831.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11774_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164561 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0248 a0001c0001t0005g0056 |
3 | HG02895.hp2 HG03471.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.225+11773_225+1179 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164561 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0014g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+11771_225+1179 others(27): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164561 | |||||||
| chr14:75164563 | ATATATAT others(10): Show |
A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0057 others(1): Show |
4 | HG00140.hp1 HG02976.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11775_225+1179 others(21): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | |||||||
| chr14:75164563 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+11773_225+1179 others(23): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | |||||||
| chr14:75164563 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225+11772_225+1179 others(24): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164563 | |||||||
| chr14:75164565 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225+11776_225+1178 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164565 | |||||||
| chr14:75164565 | ATATATAT others(8): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0059 others(1): Show |
4 | HG00738.hp1 HG02647.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+11775_225+1178 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164565 | |||||||
| chr14:75164567 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.225+11776_225+1178 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164567 | |||||||
| chr14:75164569 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.225+11771_225+1178 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164569 | |||||||
| chr14:75164570 | TATATATA | T | 4 | a0001c0001t0006g0075 a0001c0001t0009g0071 a0001c0001t0009g0077 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+11778_225+1178 others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164570 | |||||||
| chr14:75164571 | A | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0155 a0001c0001t0002g0158 others(2): Show |
5 | HG01884.hp2 NA18939.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+11784T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164571 | |||||||
| chr14:75164573 | A | ATT | 3 | a0001c0001t0002g0203 a0001c0001t0002g0205 a0001c0001t0002g0209 |
3 | HG01257.hp2 NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.225+11781_225+1178 others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164573 | |||||||
| chr14:75164573 | A | T | 51 | a0001c0001t0002g0006 a0001c0001t0002g0133 a0001c0001t0002g0134 others(48): Show |
53 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.225+11782T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164573 | |||||||
| chr14:75164575 | A | T | 77 | a0001c0001t0002g0006 a0001c0001t0002g0026 a0001c0001t0002g0028 others(74): Show |
79 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.225+11780T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164575 | |||||||
| chr14:75164577 | A | ATATATAT others(11): Show |
1 | a0001c0002t0002g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(22): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(14): Show |
1 | a0001c0002t0002g0008 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(25): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(20): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0246 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(14): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(5): Show |
1 | a0001c0002t0002g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(7): Show |
6 | a0001c0001t0002g0195 a0001c0002t0002g0196 a0001c0002t0002g0212 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+11777_225+1177 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(8): Show |
1 | a0001c0002t0002g0008 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.225+11777_225+1177 others(19): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATATAT others(7): Show |
1 | a0001c0002t0003g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(18): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | ATATTTTT others(5): Show |
1 | a0001c0002t0003g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.225+11777_225+1177 others(16): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164577 | A | T | 84 | a0001c0001t0001g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(81): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.225+11778T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164577 | |||||||
| chr14:75164580 | T | A | 1 | a0001c0001t0002g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.225+11775A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164580 | |||||||
| chr14:75164581 | T | A | 2 | a0001c0001t0010g0233 a0001c0001t0010g0234 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.225+11774A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164581 | |||||||
| chr14:75164842 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.225+11513T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164842 | |||||||
| chr14:75164974 | G | A | 1 | a0001c0001t0003g0166 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.225+11381C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75164974 | |||||||
| chr14:75165389 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.225+10966C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165389 | |||||||
| chr14:75165435 | C | A | 1 | a0001c0001t0014g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+10920G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165435 | |||||||
| chr14:75165597 | A | G | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+10758T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165597 | |||||||
| chr14:75165658 | T | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0173 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.225+10697A>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165658 | |||||||
| chr14:75165813 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.225+10542C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165813 | |||||||
| chr14:75165896 | A | G | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0078 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+10459T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165896 | |||||||
| chr14:75165974 | C | CT | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG02622.hp1 HG02723.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+10380dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75165974 | |||||||
| chr14:75166127 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.225+10228G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166127 | |||||||
| chr14:75166144 | G | A | 1 | a0001c0002t0002g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225+10211C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166144 | |||||||
| chr14:75166305 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.225+10050T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166305 | |||||||
| chr14:75166385 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.225+9970C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166385 | |||||||
| chr14:75166547 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+9808C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166547 | |||||||
| chr14:75166563 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.225+9792C>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166563 | |||||||
| chr14:75166772 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.225+9583T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166772 | |||||||
| chr14:75166797 | T | G | 2 | a0001c0001t0008g0226 a0001c0001t0008g0236 |
2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.225+9558A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166797 | |||||||
| chr14:75166939 | CT | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
116 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.225+9415delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75166939 | |||||||
| chr14:75167038 | T | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0108 others(3): Show |
7 | NA18747.hp2 NA18955.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+9317A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167038 | |||||||
| chr14:75167095 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(21): Show |
28 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.225+9260G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167095 | |||||||
| chr14:75167099 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225+9256C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167099 | |||||||
| chr14:75167117 | T | C | 1 | a0001c0001t0005g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+9238A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167117 | |||||||
| chr14:75167250 | ATTCT | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9101_225+9104d others(6): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167250 | |||||||
| chr14:75167446 | G | A | 4 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 others(1): Show |
4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+8909C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75167446 | |||||||
| chr14:75168031 | T | G | 1 | a0001c0001t0003g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.225+8324A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168031 | |||||||
| chr14:75168198 | C | T | 1 | a0001c0001t0005g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+8157G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168198 | |||||||
| chr14:75168354 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225+8001A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168354 | |||||||
| chr14:75168495 | GA | G | 4 | a0001c0001t0008g0226 a0001c0001t0008g0235 a0001c0001t0008g0236 others(1): Show |
4 | HG03195.hp2 NA18953.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+7859delT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168495 | |||||||
| chr14:75168670 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225+7685C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168670 | |||||||
| chr14:75168841 | T | G | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+7514A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168841 | |||||||
| chr14:75168902 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225+7453G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168902 | |||||||
| chr14:75168950 | T | C | 1 | a0001c0001t0012g0118 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+7405A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75168950 | |||||||
| chr14:75169008 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+7347G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169008 | |||||||
| chr14:75169013 | A | G | 1 | a0001c0001t0003g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.225+7342T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169013 | |||||||
| chr14:75169058 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.225+7297C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169058 | |||||||
| chr14:75169273 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+7082A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169273 | |||||||
| chr14:75169486 | C | T | 3 | a0001c0001t0005g0054 a0001c0001t0005g0055 a0001c0001t0005g0056 |
3 | HG00741.hp1 HG02895.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.225+6869G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169486 | |||||||
| chr14:75169646 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01243.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+6709C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75169646 | |||||||
| chr14:75170047 | GAAATACA others(2): Show |
G | 6 | a0001c0001t0007g0243 a0001c0001t0007g0244 a0001c0001t0007g0249 others(3): Show |
6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+6299_225+6307d others(11): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170047 | |||||||
| chr14:75170084 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+6271C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170084 | |||||||
| chr14:75170087 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225+6268G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170087 | |||||||
| chr14:75170104 | G | C | 1 | a0001c0001t0005g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.225+6251C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170104 | |||||||
| chr14:75170152 | C | T | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG00544.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.225+6203G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170152 | |||||||
| chr14:75170258 | G | A | 4 | a0001c0001t0010g0231 a0001c0001t0010g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+6097C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170258 | |||||||
| chr14:75170264 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
134 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.225+6091G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170264 | |||||||
| chr14:75170284 | G | A | 1 | a0001c0001t0017g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.225+6071C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170284 | |||||||
| chr14:75170648 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.225+5707T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170648 | |||||||
| chr14:75170656 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
142 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+5699T>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170656 | |||||||
| chr14:75170761 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.225+5594T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75170761 | |||||||
| chr14:75171196 | GGAA | G | 6 | a0001c0001t0005g0033 a0001c0001t0005g0042 a0001c0001t0005g0043 others(3): Show |
6 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+5156_225+5158d others(5): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171196 | |||||||
| chr14:75171234 | A | G | 3 | a0001c0001t0007g0249 a0001c0001t0007g0250 a0001c0001t0007g0251 |
3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.225+5121T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171234 | |||||||
| chr14:75171237 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225+5118C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171237 | |||||||
| chr14:75171264 | C | G | 1 | a0001c0001t0008g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+5091G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171264 | |||||||
| chr14:75171281 | A | AT | 15 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.225+5073dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171281 | |||||||
| chr14:75171281 | AT | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0008g0226 others(2): Show |
5 | HG02486.hp1 HG03041.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+5073delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171281 | |||||||
| chr14:75171336 | G | A | 4 | a0001c0001t0010g0231 a0001c0001t0010g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+5019C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171336 | |||||||
| chr14:75171342 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+5013G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171342 | |||||||
| chr14:75171512 | T | G | 1 | a0001c0001t0004g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225+4843A>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171512 | |||||||
| chr14:75171592 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225+4763A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171592 | |||||||
| chr14:75171690 | A | AGAAACAT others(32): Show |
107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
114 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.225+4626_225+4664d others(41): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171690 | |||||||
| chr14:75171929 | C | CT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
9 | HG02622.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.225+4425dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171929 | |||||||
| chr14:75171958 | T | C | 1 | a0001c0001t0004g0031 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.225+4397A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75171958 | |||||||
| chr14:75172075 | G | GGAAGAAC others(8): Show |
1 | a0001c0001t0004g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.225+4265_225+4279d others(17): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172075 | |||||||
| chr14:75172311 | C | CT | 6 | a0001c0001t0007g0243 a0001c0001t0007g0244 a0001c0001t0007g0249 others(3): Show |
6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+4043dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172311 | |||||||
| chr14:75172311 | CT | C | 6 | a0001c0001t0002g0032 a0001c0001t0002g0171 a0001c0001t0008g0226 others(3): Show |
6 | HG02735.hp2 HG03195.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+4043delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172311 | |||||||
| chr14:75172393 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225+3962G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172393 | |||||||
| chr14:75172482 | A | T | 1 | a0001c0001t0008g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225+3873T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172482 | |||||||
| chr14:75172519 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.225+3836T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172519 | |||||||
| chr14:75172543 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+3812G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172543 | |||||||
| chr14:75172642 | G | A | 1 | a0001c0001t0003g0222 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225+3713C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172642 | |||||||
| chr14:75172658 | T | C | 1 | a0001c0001t0005g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+3697A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172658 | |||||||
| chr14:75172868 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
137 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.225+3487C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172868 | |||||||
| chr14:75172893 | A | AT | 5 | a0001c0001t0007g0244 a0001c0001t0007g0249 a0001c0001t0007g0250 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+3461dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172893 | |||||||
| chr14:75172893 | AT | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0176 a0001c0001t0002g0032 others(2): Show |
5 | HG01943.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+3461delA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172893 | |||||||
| chr14:75172991 | G | C | 5 | a0001c0001t0001g0230 a0001c0001t0010g0231 a0001c0001t0010g0233 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+3364C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75172991 | |||||||
| chr14:75173087 | T | C | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+3268A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173087 | |||||||
| chr14:75173151 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+3204G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173151 | |||||||
| chr14:75173243 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0173 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.225+3112G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173243 | |||||||
| chr14:75173342 | T | C | 5 | a0001c0001t0001g0230 a0001c0001t0010g0231 a0001c0001t0010g0233 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+3013A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173342 | |||||||
| chr14:75173380 | A | G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0184 a0001c0001t0002g0185 others(3): Show |
7 | HG00558.hp1 NA18939.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+2975T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173380 | |||||||
| chr14:75173408 | G | C | 1 | a0001c0001t0004g0223 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.225+2947C>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173408 | |||||||
| chr14:75173487 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+2868C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173487 | |||||||
| chr14:75173545 | C | CT | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+2809dupA | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173545 | |||||||
| chr14:75173556 | A | T | 4 | a0001c0002t0002g0181 a0001c0002t0002g0183 a0001c0002t0002g0227 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+2799T>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173556 | |||||||
| chr14:75173651 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+2704G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173651 | |||||||
| chr14:75173673 | C | T | 5 | a0001c0001t0007g0244 a0001c0001t0007g0249 a0001c0001t0007g0250 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+2682G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173673 | |||||||
| chr14:75173700 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
138 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.225+2655C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173700 | |||||||
| chr14:75173754 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+2601G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173754 | |||||||
| chr14:75173848 | A | G | 1 | a0001c0001t0007g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.225+2507T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75173848 | |||||||
| chr14:75174209 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.225+2146A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174209 | |||||||
| chr14:75174374 | T | C | 1 | a0001c0001t0002g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.225+1981A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174374 | |||||||
| chr14:75174544 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.225+1811A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174544 | |||||||
| chr14:75174695 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.225+1660C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174695 | |||||||
| chr14:75174827 | G | A | 6 | a0001c0001t0008g0225 a0001c0001t0008g0226 a0001c0001t0008g0229 others(3): Show |
6 | HG03195.hp2 HG03942.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+1528C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174827 | |||||||
| chr14:75174838 | C | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
121 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.225+1517G>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75174838 | |||||||
| chr14:75175039 | C | CA | 14 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(11): Show |
15 | HG01081.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+1315dupT | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | |||||||
| chr14:75175039 | C | CAA | 9 | a0001c0001t0001g0230 a0001c0001t0008g0235 a0001c0001t0008g0236 others(6): Show |
9 | HG01109.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+1314_225+1315d others(4): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | |||||||
| chr14:75175039 | CAAAAAA | C | 7 | a0001c0001t0001g0176 a0001c0001t0002g0177 a0001c0001t0003g0178 others(4): Show |
7 | HG00423.hp1 HG00735.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1310_225+1315d others(8): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | |||||||
| chr14:75175039 | CAAAAAAA | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.225+1309_225+1315d others(9): Show |
TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175039 | |||||||
| chr14:75175190 | T | C | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1165A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175190 | |||||||
| chr14:75175291 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1064A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175291 | |||||||
| chr14:75175559 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0011g0239 a0001c0001t0014g0241 |
3 | HG02615.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.225+796C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175559 | |||||||
| chr14:75175588 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.225+767A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175588 | |||||||
| chr14:75175632 | C | A | 6 | a0001c0001t0007g0243 a0001c0001t0007g0244 a0001c0001t0007g0249 others(3): Show |
6 | HG01081.hp1 HG01496.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+723G>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175632 | |||||||
| chr14:75175647 | G | A | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG02056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.225+708C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175647 | |||||||
| chr14:75175831 | A | G | 7 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG00140.hp2 HG00280.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+524T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175831 | |||||||
| chr14:75175843 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225+512C>T | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175843 | |||||||
| chr14:75175860 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(8): Show |
15 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+495T>C | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175860 | |||||||
| chr14:75175974 | C | T | 4 | a0001c0001t0002g0015 a0001c0001t0004g0013 a0001c0001t0004g0014 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+381G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75175974 | |||||||
| chr14:75176085 | T | C | 3 | a0001c0001t0007g0249 a0001c0001t0007g0250 a0001c0001t0007g0251 |
3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.225+270A>G | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75176085 | |||||||
| chr14:75176142 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.225+213G>A | TMED10 | ENSG00000170348.9 | transcript | ENST00000303575.9 | protein_coding | 1/4 | chr14 | 75176142 |