Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9442 |
| ensemblid | ENSG00000160563.14 |
| hgncid | 2377 |
| symbol | MED27 |
| name | mediator complex subunit 27 |
| refseq_nuc | NM_004269.4 |
| refseq_prot | NP_004260.2 |
| ensembl_nuc | ENST00000292035.10 |
| ensembl_prot | ENSP00000292035.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 131860112 |
| end | 132079867 |
| strand | - |
| ver | v1.2 |
| region | chr9:131860112-132079867 |
| region5000 | chr9:131855112-132084867 |
| regionname0 | MED27_chr9_131860112_132079867 |
| regionname5000 | MED27_chr9_131855112_132084867 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 311 | 273 | 94 | 52 | 101 | 4 | 20 | 75 | MED27_chr9_131855112_132084867 | MED27 | MADVI others(306): Show |
chr9 | 131855112 | 132084867 |
| a0002 | 0/0 | 311 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | MVDVI others(306): Show |
chr9 | 131855112 | 132084867 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 933 | 273 | 94 | 52 | 101 | 4 | 20 | MED27_chr9_131855112_132084867 | MED27 | ATGGC others(928): Show |
chr9 | 131855112 | 132084867 | ||
| a0002c0002 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | ATGGT others(928): Show |
chr9 | 131855112 | 132084867 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1385 | 216 | 80 | 43 | 73 | 4 | 14 | MED27_chr9_131855112_132084867 | MED27 | AGAGC others(1380): Show |
chr9 | 131855112 | 132084867 |
| a0001c0001t0002 | 0/0 | 1385 | 57 | 14 | 9 | 28 | 0 | 6 | MED27_chr9_131855112_132084867 | MED27 | AGAGC others(1380): Show |
chr9 | 131855112 | 132084867 |
| a0002c0002t0001 | 0/0 | 1385 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | AGAGC others(1380): Show |
chr9 | 131855112 | 132084867 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | GIH | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | USA | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | USA | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | USA | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0136 | REF | REF | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132079840 | G | A | 1 | a0002 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.5C>T | p.Ala2Val | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 1/8 | 28/1385 | 5/936 | 2/311 | chr9 | 132079840 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131860193 | T | C | 1 | a0001c0001t0002 | 57 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*345A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 8/8 | 345 | chr9 | 131860193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131861336 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.802-664T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861336 | |||||||
| chr9:131861341 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.802-669G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861341 | |||||||
| chr9:131861516 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.802-844A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861516 | |||||||
| chr9:131861591 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.802-919G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861591 | |||||||
| chr9:131861603 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.802-931C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861603 | |||||||
| chr9:131861705 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802-1033G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861705 | |||||||
| chr9:131861767 | CT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(73): Show |
77 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.802-1096delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861767 | |||||||
| chr9:131861767 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802-1105_802-1096d others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861767 | |||||||
| chr9:131861767 | CTTTTTTT others(5): Show |
C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.802-1107_802-1096d others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861767 | |||||||
| chr9:131861779 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.802-1107A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861779 | |||||||
| chr9:131861825 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.802-1153G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861825 | |||||||
| chr9:131861826 | G | A | 1 | a0001c0001t0002g0002 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.802-1154C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861826 | |||||||
| chr9:131861840 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(4): Show |
7 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.802-1168C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861840 | |||||||
| chr9:131861861 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0080 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.802-1189A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131861861 | |||||||
| chr9:131862123 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.801+940A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862123 | |||||||
| chr9:131862254 | C | G | 3 | a0001c0001t0002g0074 a0001c0001t0002g0125 a0001c0001t0002g0143 |
3 | HG00438.hp2 HG01496.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.801+809G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862254 | |||||||
| chr9:131862266 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.801+797G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862266 | |||||||
| chr9:131862289 | A | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0040 others(19): Show |
22 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.801+774T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862289 | |||||||
| chr9:131862321 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.801+742C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862321 | |||||||
| chr9:131862328 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0002g0200 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.801+735A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862328 | |||||||
| chr9:131862364 | G | A | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.801+699C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862364 | |||||||
| chr9:131862398 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.801+665C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862398 | |||||||
| chr9:131862562 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0040 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+501C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862562 | |||||||
| chr9:131862594 | G | C | 5 | a0001c0001t0002g0092 a0001c0001t0002g0123 a0001c0001t0002g0129 others(2): Show |
5 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+469C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862594 | |||||||
| chr9:131862715 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
69 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.801+348G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862715 | |||||||
| chr9:131862839 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0080 others(7): Show |
10 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.801+224G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 7/7 | chr9 | 131862839 | |||||||
| chr9:131863170 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.724-30C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863170 | |||||||
| chr9:131863190 | G | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0080 others(7): Show |
10 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-50C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863190 | |||||||
| chr9:131863388 | C | T | 90 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.724-248G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863388 | |||||||
| chr9:131863399 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.724-259C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863399 | |||||||
| chr9:131863524 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.724-384C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863524 | |||||||
| chr9:131863622 | TAGCCACA others(33): Show |
T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0073 others(8): Show |
11 | HG01081.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.724-522_724-483del others(40): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863622 | |||||||
| chr9:131863726 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | NA18948.hp1 NA18961.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-586C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863726 | |||||||
| chr9:131863744 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.724-604G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863744 | |||||||
| chr9:131863745 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.724-605C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863745 | |||||||
| chr9:131863757 | C | T | 89 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.724-617G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863757 | |||||||
| chr9:131863770 | G | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
42 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.724-630C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863770 | |||||||
| chr9:131863788 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0216 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.724-648A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863788 | |||||||
| chr9:131863811 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.724-671G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131863811 | |||||||
| chr9:131864007 | G | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.724-867C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864007 | |||||||
| chr9:131864208 | C | A | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.724-1068G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864208 | |||||||
| chr9:131864389 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-1249C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864389 | |||||||
| chr9:131864436 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.724-1296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864436 | |||||||
| chr9:131864469 | A | G | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0021 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.724-1329T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864469 | |||||||
| chr9:131864690 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.724-1550A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864690 | |||||||
| chr9:131864763 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(26): Show |
29 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.724-1623G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864763 | |||||||
| chr9:131864771 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | NA18966.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-1631C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131864771 | |||||||
| chr9:131865085 | A | C | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.724-1945T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865085 | |||||||
| chr9:131865123 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.724-1983G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865123 | |||||||
| chr9:131865196 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-2056C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865196 | |||||||
| chr9:131865215 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.724-2075A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865215 | |||||||
| chr9:131865307 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.724-2167C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865307 | |||||||
| chr9:131865851 | C | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0230 a0001c0001t0001g0249 others(4): Show |
7 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-2711G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131865851 | |||||||
| chr9:131866082 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.724-2942T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866082 | |||||||
| chr9:131866093 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.724-2953G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866093 | |||||||
| chr9:131866262 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724-3122C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866262 | |||||||
| chr9:131866466 | TGCCTCAT others(9): Show |
T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
40 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.724-3342_724-3327d others(18): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866466 | |||||||
| chr9:131866507 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.724-3367G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866507 | |||||||
| chr9:131866772 | C | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.724-3632G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131866772 | |||||||
| chr9:131867012 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(12): Show |
15 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.724-3872C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131867012 | |||||||
| chr9:131867096 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02647.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.724-3956C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131867096 | |||||||
| chr9:131867532 | G | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-4392C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131867532 | |||||||
| chr9:131867843 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.724-4703C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131867843 | |||||||
| chr9:131867856 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-4716C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131867856 | |||||||
| chr9:131868044 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01255.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.724-4904T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868044 | |||||||
| chr9:131868146 | T | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-5006A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868146 | |||||||
| chr9:131868267 | T | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-5127A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868267 | |||||||
| chr9:131868342 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0080 others(6): Show |
9 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.724-5202T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868342 | |||||||
| chr9:131868598 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.724-5458G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868598 | |||||||
| chr9:131868786 | C | G | 35 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0078 others(32): Show |
35 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.724-5646G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868786 | |||||||
| chr9:131868827 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.724-5687C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868827 | |||||||
| chr9:131868839 | C | T | 161 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.724-5699G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868839 | |||||||
| chr9:131868891 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.724-5751G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131868891 | |||||||
| chr9:131869168 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.724-6028C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869168 | |||||||
| chr9:131869204 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.724-6064G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869204 | |||||||
| chr9:131869322 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0079 a0001c0001t0001g0081 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.724-6182A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869322 | |||||||
| chr9:131869391 | C | CA | 79 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
79 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.724-6252dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869391 | |||||||
| chr9:131869391 | C | CAA | 42 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(39): Show |
42 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.724-6253_724-6252d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869391 | |||||||
| chr9:131869619 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0212 a0001c0001t0002g0217 |
3 | HG02055.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.724-6479G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869619 | |||||||
| chr9:131869619 | C | G | 1 | a0001c0001t0002g0156 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.724-6479G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869619 | |||||||
| chr9:131869620 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.724-6480T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869620 | |||||||
| chr9:131869771 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.724-6631C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869771 | |||||||
| chr9:131869807 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0222 a0001c0001t0001g0231 |
3 | HG01943.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.724-6667G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869807 | |||||||
| chr9:131869825 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.724-6685G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131869825 | |||||||
| chr9:131870126 | G | A | 6 | a0001c0001t0001g0073 a0001c0001t0001g0184 a0001c0001t0001g0250 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-6986C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131870126 | |||||||
| chr9:131870181 | A | G | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.724-7041T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131870181 | |||||||
| chr9:131870388 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0002g0217 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.724-7248T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131870388 | |||||||
| chr9:131870622 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.724-7482G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131870622 | |||||||
| chr9:131870886 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.724-7746C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131870886 | |||||||
| chr9:131871090 | C | T | 207 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(204): Show |
207 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.724-7950G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871090 | |||||||
| chr9:131871102 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.724-7962C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871102 | |||||||
| chr9:131871163 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.724-8023G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871163 | |||||||
| chr9:131871178 | C | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-8038G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871178 | |||||||
| chr9:131871197 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-8057A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871197 | |||||||
| chr9:131871379 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0270 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.724-8239A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871379 | |||||||
| chr9:131871381 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0270 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.724-8241T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871381 | |||||||
| chr9:131871634 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.724-8494G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871634 | |||||||
| chr9:131871752 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.724-8612C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871752 | |||||||
| chr9:131871774 | T | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-8634A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871774 | |||||||
| chr9:131871929 | A | G | 212 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.724-8789T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871929 | |||||||
| chr9:131871969 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.724-8829C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871969 | |||||||
| chr9:131871988 | C | CGAGTGCC others(81): Show |
1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.724-8936_724-8849d others(90): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131871988 | |||||||
| chr9:131872042 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.724-8902G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872042 | |||||||
| chr9:131872129 | T | TGGACCAG others(5): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-9001_724-8990d others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872129 | |||||||
| chr9:131872231 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.724-9091G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872231 | |||||||
| chr9:131872374 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-9234G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872374 | |||||||
| chr9:131872396 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.724-9256T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872396 | |||||||
| chr9:131872490 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.724-9350T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872490 | |||||||
| chr9:131872570 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.724-9430G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131872570 | |||||||
| chr9:131873153 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.724-10013C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873153 | |||||||
| chr9:131873377 | G | A | 12 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.724-10237C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873377 | |||||||
| chr9:131873446 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.724-10306G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873446 | |||||||
| chr9:131873617 | A | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0196 a0001c0001t0001g0197 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.723+10441T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873617 | |||||||
| chr9:131873705 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0199 |
2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.723+10353C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873705 | |||||||
| chr9:131873753 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.723+10305G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873753 | |||||||
| chr9:131873777 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.723+10281C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873777 | |||||||
| chr9:131873914 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.723+10144C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131873914 | |||||||
| chr9:131874005 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.723+10053C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874005 | |||||||
| chr9:131874071 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.723+9987C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874071 | |||||||
| chr9:131874103 | C | G | 10 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+9955G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874103 | |||||||
| chr9:131874162 | G | A | 42 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
42 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.723+9896C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874162 | |||||||
| chr9:131874266 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.723+9792A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874266 | |||||||
| chr9:131874449 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.723+9609G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874449 | |||||||
| chr9:131874503 | T | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.723+9555A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874503 | |||||||
| chr9:131874553 | G | T | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.723+9505C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874553 | |||||||
| chr9:131874623 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.723+9435A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874623 | |||||||
| chr9:131874664 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+9394C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874664 | |||||||
| chr9:131874793 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0040 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+9265C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874793 | |||||||
| chr9:131874951 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.723+9107G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131874951 | |||||||
| chr9:131875040 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+9018G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875040 | |||||||
| chr9:131875427 | C | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG01099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.723+8631G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875427 | |||||||
| chr9:131875431 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+8627G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875431 | |||||||
| chr9:131875641 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+8417C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875641 | |||||||
| chr9:131875799 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02976.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.723+8259C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875799 | |||||||
| chr9:131875890 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.723+8168T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875890 | |||||||
| chr9:131875905 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0088 others(9): Show |
12 | HG01243.hp2 HG01261.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.723+8153C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131875905 | |||||||
| chr9:131876040 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723+8018C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876040 | |||||||
| chr9:131876073 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723+7985G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876073 | |||||||
| chr9:131876153 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.723+7905C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876153 | |||||||
| chr9:131876172 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+7886T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876172 | |||||||
| chr9:131876200 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.723+7858A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876200 | |||||||
| chr9:131876326 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.723+7732G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876326 | |||||||
| chr9:131876632 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.723+7426G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131876632 | |||||||
| chr9:131877034 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.723+7024T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131877034 | |||||||
| chr9:131877064 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.723+6994C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131877064 | |||||||
| chr9:131877423 | C | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.723+6635G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131877423 | |||||||
| chr9:131877877 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.723+6181A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131877877 | |||||||
| chr9:131877996 | C | T | 7 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0166 others(4): Show |
7 | HG01074.hp1 HG01175.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.723+6062G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131877996 | |||||||
| chr9:131878002 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.723+6056G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878002 | |||||||
| chr9:131878103 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723+5955G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878103 | |||||||
| chr9:131878143 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.723+5915C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878143 | |||||||
| chr9:131878274 | A | AAAAT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
31 | HG00558.hp2 HG01081.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.723+5780_723+5783d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878274 | |||||||
| chr9:131878274 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0073 a0001c0001t0001g0169 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+5776_723+5783d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878274 | |||||||
| chr9:131878274 | A | AAAATAAA others(5): Show |
6 | a0001c0001t0001g0081 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+5772_723+5783d others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878274 | |||||||
| chr9:131878274 | AAAAT | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG00438.hp2 HG01255.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.723+5780_723+5783d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878274 | |||||||
| chr9:131878274 | AAAATAAA others(1): Show |
A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
16 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.723+5776_723+5783d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878274 | |||||||
| chr9:131878366 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.723+5692G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878366 | |||||||
| chr9:131878484 | A | T | 12 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+5574T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878484 | |||||||
| chr9:131878537 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+5521A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878537 | |||||||
| chr9:131878652 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.723+5406C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878652 | |||||||
| chr9:131878836 | G | A | 57 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0254 others(54): Show |
57 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.723+5222C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131878836 | |||||||
| chr9:131879031 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723+5027A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879031 | |||||||
| chr9:131879176 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.723+4882A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879176 | |||||||
| chr9:131879298 | C | A | 60 | a0001c0001t0001g0072 a0001c0001t0001g0170 a0001c0001t0001g0212 others(57): Show |
60 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.723+4760G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879298 | |||||||
| chr9:131879357 | C | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG02257.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.723+4701G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879357 | |||||||
| chr9:131879543 | T | A | 34 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0113 others(31): Show |
34 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.723+4515A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879543 | |||||||
| chr9:131879734 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.723+4324G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879734 | |||||||
| chr9:131879830 | A | G | 88 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.723+4228T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879830 | |||||||
| chr9:131879904 | G | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
25 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.723+4154C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131879904 | |||||||
| chr9:131880006 | G | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | NA18977.hp2 NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.723+4052C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880006 | |||||||
| chr9:131880044 | T | G | 1 | a0001c0001t0002g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+4014A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880044 | |||||||
| chr9:131880114 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0073 a0001c0001t0001g0201 others(1): Show |
4 | HG01943.hp2 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+3944G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880114 | |||||||
| chr9:131880137 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.723+3921C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880137 | |||||||
| chr9:131880522 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.723+3536G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880522 | |||||||
| chr9:131880565 | T | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+3493A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880565 | |||||||
| chr9:131880671 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.723+3387A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880671 | |||||||
| chr9:131880725 | G | GTT | 4 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+3332_723+3333i others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880725 | |||||||
| chr9:131880768 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.723+3290A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880768 | |||||||
| chr9:131880895 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.723+3163T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880895 | |||||||
| chr9:131880908 | TA | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+3149delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880908 | |||||||
| chr9:131880963 | T | C | 3 | a0001c0001t0002g0074 a0001c0001t0002g0125 a0001c0001t0002g0143 |
3 | HG00438.hp2 HG01496.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.723+3095A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880963 | |||||||
| chr9:131880987 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0172 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.723+3071A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131880987 | |||||||
| chr9:131881025 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.723+3033G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881025 | |||||||
| chr9:131881087 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.723+2971C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881087 | |||||||
| chr9:131881196 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+2862T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881196 | |||||||
| chr9:131881604 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723+2454A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881604 | |||||||
| chr9:131881676 | A | G | 5 | a0001c0001t0002g0021 a0001c0001t0002g0119 a0001c0001t0002g0120 others(2): Show |
5 | NA18940.hp1 NA18961.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+2382T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881676 | |||||||
| chr9:131881787 | C | CCTT | 4 | a0001c0001t0001g0184 a0001c0001t0001g0219 a0001c0001t0002g0021 others(1): Show |
4 | HG02976.hp2 NA19004.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+2268_723+2270d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881787 | |||||||
| chr9:131881800 | C | CT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0213 others(4): Show |
7 | HG02976.hp1 HG03139.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+2257dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(19): Show |
22 | HG00558.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.723+2256_723+2257d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTT | 62 | a0001c0001t0001g0007 a0001c0001t0001g0170 a0001c0001t0001g0172 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.723+2255_723+2257d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTTT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0169 others(6): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+2254_723+2257d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTTTTT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0082 others(8): Show |
11 | HG01943.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+2252_723+2257d others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTTTTTT | 38 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+2251_723+2257d others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTTTTTT others(1): Show |
28 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0088 others(25): Show |
28 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.723+2250_723+2257d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0241 |
2 | HG02165.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.723+2247_723+2257d others(13): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | CT | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG01123.hp2 HG02735.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+2257delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723+2247_723+2257d others(13): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881800 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.723+2246_723+2257d others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881800 | |||||||
| chr9:131881825 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.723+2233C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131881825 | |||||||
| chr9:131882012 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0002g0217 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.723+2046G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882012 | |||||||
| chr9:131882101 | T | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+1957A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882101 | |||||||
| chr9:131882201 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.723+1857A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882201 | |||||||
| chr9:131882281 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.723+1777C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882281 | |||||||
| chr9:131882385 | T | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.723+1673A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882385 | |||||||
| chr9:131882673 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.723+1385G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882673 | |||||||
| chr9:131882709 | C | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.723+1349G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882709 | |||||||
| chr9:131882803 | A | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+1255T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131882803 | |||||||
| chr9:131883098 | G | A | 16 | a0001c0001t0001g0068 a0001c0001t0001g0201 a0001c0001t0001g0223 others(13): Show |
16 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.723+960C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883098 | |||||||
| chr9:131883212 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0230 others(57): Show |
60 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.723+846A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883212 | |||||||
| chr9:131883383 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0230 others(57): Show |
60 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.723+675A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883383 | |||||||
| chr9:131883501 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.723+557A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883501 | |||||||
| chr9:131883543 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0237 |
2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.723+515C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883543 | |||||||
| chr9:131883560 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.723+498C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883560 | |||||||
| chr9:131883760 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
115 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.723+298C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883760 | |||||||
| chr9:131883762 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883762 | |||||||
| chr9:131883789 | A | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.723+269T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883789 | |||||||
| chr9:131883807 | C | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+251G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 6/7 | chr9 | 131883807 | |||||||
| chr9:131884119 | G | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0066 others(3): Show |
6 | NA18942.hp1 NA18950.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-20C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884119 | |||||||
| chr9:131884194 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-95A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884194 | |||||||
| chr9:131884195 | GA | G | 10 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.682-97delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884195 | |||||||
| chr9:131884236 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.682-137C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884236 | |||||||
| chr9:131884410 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.682-311T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884410 | |||||||
| chr9:131884518 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.682-419T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884518 | |||||||
| chr9:131884605 | C | CT | 10 | a0001c0001t0001g0057 a0001c0001t0001g0073 a0001c0001t0001g0111 others(7): Show |
10 | HG01081.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.682-507dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884605 | |||||||
| chr9:131884605 | C | CTT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(8): Show |
11 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.682-508_682-507dup others(2): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884605 | |||||||
| chr9:131884605 | CT | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
101 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.682-507delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884605 | |||||||
| chr9:131884790 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-691A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884790 | |||||||
| chr9:131884910 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.682-811A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131884910 | |||||||
| chr9:131885210 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0247 |
2 | HG00609.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.682-1111G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885210 | |||||||
| chr9:131885221 | G | A | 58 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0249 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.682-1122C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885221 | |||||||
| chr9:131885434 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-1335C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885434 | |||||||
| chr9:131885515 | C | T | 212 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.682-1416G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885515 | |||||||
| chr9:131885633 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0231 |
2 | HG02135.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.682-1534C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885633 | |||||||
| chr9:131885690 | T | G | 1 | a0001c0001t0002g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.682-1591A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885690 | |||||||
| chr9:131885711 | G | A | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.682-1612C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885711 | |||||||
| chr9:131885743 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.682-1644C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885743 | |||||||
| chr9:131885826 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-1727C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885826 | |||||||
| chr9:131885923 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.682-1824C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131885923 | |||||||
| chr9:131886303 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-2204A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886303 | |||||||
| chr9:131886481 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.682-2382G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886481 | |||||||
| chr9:131886663 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.682-2564T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886663 | |||||||
| chr9:131886798 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG02257.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682-2699G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886798 | |||||||
| chr9:131886810 | C | T | 1 | a0001c0001t0002g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.682-2711G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886810 | |||||||
| chr9:131886881 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0216 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.682-2782C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886881 | |||||||
| chr9:131886973 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.682-2874A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131886973 | |||||||
| chr9:131887125 | C | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-3026G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887125 | |||||||
| chr9:131887227 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.682-3128A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887227 | |||||||
| chr9:131887305 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-3206T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887305 | |||||||
| chr9:131887327 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-3228T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887327 | |||||||
| chr9:131887329 | G | A | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.682-3230C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887329 | |||||||
| chr9:131887407 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.682-3308A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887407 | |||||||
| chr9:131887500 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.682-3401A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887500 | |||||||
| chr9:131887814 | A | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-3715T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887814 | |||||||
| chr9:131888025 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.682-3926G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888025 | |||||||
| chr9:131888034 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-3935G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888034 | |||||||
| chr9:131888086 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-3987G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888086 | |||||||
| chr9:131888194 | T | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.682-4095A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888194 | |||||||
| chr9:131888203 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.682-4104G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888203 | |||||||
| chr9:131888334 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0212 a0001c0001t0001g0268 others(1): Show |
4 | HG01099.hp2 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-4235C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888334 | |||||||
| chr9:131888477 | GC | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG02040.hp1 NA18966.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-4379delG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888477 | |||||||
| chr9:131888521 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.682-4422G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888521 | |||||||
| chr9:131888660 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(4): Show |
7 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-4561G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888660 | |||||||
| chr9:131888942 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.682-4843G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131888942 | |||||||
| chr9:131889187 | G | C | 1 | a0001c0001t0002g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.681+4698C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889187 | |||||||
| chr9:131889288 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681+4597G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889288 | |||||||
| chr9:131889301 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+4584G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889301 | |||||||
| chr9:131889371 | T | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.681+4514A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889371 | |||||||
| chr9:131889668 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.681+4217G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889668 | |||||||
| chr9:131889912 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.681+3973T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889912 | |||||||
| chr9:131889935 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.681+3950G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131889935 | |||||||
| chr9:131890129 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0001g0194 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+3756C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890129 | |||||||
| chr9:131890178 | G | C | 84 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(81): Show |
84 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.681+3707C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890178 | |||||||
| chr9:131890421 | T | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+3464A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890421 | |||||||
| chr9:131890518 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.681+3367A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890518 | |||||||
| chr9:131890604 | T | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0166 |
3 | HG01074.hp1 HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.681+3281A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890604 | |||||||
| chr9:131890605 | C | T | 3 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0166 |
3 | HG01074.hp1 HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.681+3280G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890605 | |||||||
| chr9:131890813 | A | G | 83 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.681+3072T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890813 | |||||||
| chr9:131890871 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.681+3014C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131890871 | |||||||
| chr9:131891018 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681+2867C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891018 | |||||||
| chr9:131891020 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.681+2865A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891020 | |||||||
| chr9:131891224 | CGTGAAAG others(1): Show |
C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+2653_681+2660d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891224 | |||||||
| chr9:131891238 | G | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+2647C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891238 | |||||||
| chr9:131891601 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681+2284C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891601 | |||||||
| chr9:131891693 | A | C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.681+2192T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891693 | |||||||
| chr9:131891832 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.681+2053C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891832 | |||||||
| chr9:131891837 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+2048C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891837 | |||||||
| chr9:131891929 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.681+1956G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131891929 | |||||||
| chr9:131892027 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+1858C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892027 | |||||||
| chr9:131892460 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+1425T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892460 | |||||||
| chr9:131892625 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.681+1260T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892625 | |||||||
| chr9:131892637 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.681+1248G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892637 | |||||||
| chr9:131892638 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+1247G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892638 | |||||||
| chr9:131892693 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 |
3 | HG02630.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.681+1192T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892693 | |||||||
| chr9:131892729 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681+1156A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892729 | |||||||
| chr9:131892951 | T | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.681+934A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131892951 | |||||||
| chr9:131893155 | T | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.681+730A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893155 | |||||||
| chr9:131893284 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+601G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893284 | |||||||
| chr9:131893333 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA18957.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.681+552C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893333 | |||||||
| chr9:131893389 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.681+496G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893389 | |||||||
| chr9:131893402 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.681+483G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893402 | |||||||
| chr9:131893407 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0081 others(70): Show |
73 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.681+478A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893407 | |||||||
| chr9:131893525 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0001g0194 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+360G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893525 | |||||||
| chr9:131893689 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0178 |
2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.681+196T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893689 | |||||||
| chr9:131893793 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.681+92A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893793 | |||||||
| chr9:131893838 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.681+47G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131893838 | |||||||
| chr9:131894026 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.574-34G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894026 | |||||||
| chr9:131894099 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-107A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894099 | |||||||
| chr9:131894104 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG01081.hp1 HG02109.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-112G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894104 | |||||||
| chr9:131894293 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-301G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894293 | |||||||
| chr9:131894378 | G | A | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-386C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894378 | |||||||
| chr9:131894379 | C | CTATG | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-388_574-387ins others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894379 | |||||||
| chr9:131894489 | G | A | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.574-497C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894489 | |||||||
| chr9:131894621 | T | TA | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
36 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.574-630dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894621 | |||||||
| chr9:131894621 | TA | T | 59 | a0001c0001t0001g0144 a0001c0001t0001g0230 a0001c0001t0001g0231 others(56): Show |
59 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.574-630delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894621 | |||||||
| chr9:131894706 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0053 |
3 | HG02135.hp1 HG02165.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.574-714G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894706 | |||||||
| chr9:131894758 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-766A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894758 | |||||||
| chr9:131894832 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-840C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894832 | |||||||
| chr9:131894929 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0183 |
2 | HG02080.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.574-937C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131894929 | |||||||
| chr9:131895010 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0083 others(4): Show |
7 | HG01081.hp1 HG02109.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-1018A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895010 | |||||||
| chr9:131895039 | C | G | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-1047G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895039 | |||||||
| chr9:131895217 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0096 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.574-1225G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895217 | |||||||
| chr9:131895257 | G | A | 3 | a0001c0001t0002g0074 a0001c0001t0002g0125 a0001c0001t0002g0143 |
3 | HG00438.hp2 HG01496.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.574-1265C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895257 | |||||||
| chr9:131895281 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-1289G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895281 | |||||||
| chr9:131895317 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-1325C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895317 | |||||||
| chr9:131895539 | C | A | 7 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0085 others(4): Show |
7 | HG02615.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-1547G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895539 | |||||||
| chr9:131895547 | G | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.574-1555C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895547 | |||||||
| chr9:131895693 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(75): Show |
78 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.574-1701G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895693 | |||||||
| chr9:131895904 | G | GT | 87 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0014 others(84): Show |
87 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.574-1913dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895904 | |||||||
| chr9:131895968 | G | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-1976C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895968 | |||||||
| chr9:131895981 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.574-1989C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895981 | |||||||
| chr9:131896002 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02622.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.574-2010C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896002 | |||||||
| chr9:131896207 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-2215A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896207 | |||||||
| chr9:131896428 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.574-2436C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896428 | |||||||
| chr9:131896712 | A | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(23): Show |
26 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.574-2720T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896712 | |||||||
| chr9:131896817 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.574-2825G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896817 | |||||||
| chr9:131896834 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | NA18977.hp2 NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.574-2842G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896834 | |||||||
| chr9:131896877 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-2885C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896877 | |||||||
| chr9:131896921 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.574-2929C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896921 | |||||||
| chr9:131896951 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-2959A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131896951 | |||||||
| chr9:131897030 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.574-3038T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897030 | |||||||
| chr9:131897093 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-3101A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897093 | |||||||
| chr9:131897343 | C | G | 58 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0249 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.574-3351G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897343 | |||||||
| chr9:131897419 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-3427C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897419 | |||||||
| chr9:131897498 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-3506G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897498 | |||||||
| chr9:131897499 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0208 a0001c0001t0001g0259 others(4): Show |
7 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-3507C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897499 | |||||||
| chr9:131897539 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG02257.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.574-3547A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897539 | |||||||
| chr9:131897579 | C | T | 214 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.574-3587G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897579 | |||||||
| chr9:131897659 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG02257.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.574-3667C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897659 | |||||||
| chr9:131897728 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.574-3736T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897728 | |||||||
| chr9:131897850 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.574-3858A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897850 | |||||||
| chr9:131897905 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.574-3913T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897905 | |||||||
| chr9:131897929 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.574-3937T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131897929 | |||||||
| chr9:131898101 | A | AT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(14): Show |
17 | HG01175.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-4110dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898101 | |||||||
| chr9:131898101 | A | ATTT | 16 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0223 others(13): Show |
16 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-4112_574-4110d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898101 | |||||||
| chr9:131898144 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.574-4152A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898144 | |||||||
| chr9:131898265 | T | C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.574-4273A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898265 | |||||||
| chr9:131898272 | T | C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.574-4280A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898272 | |||||||
| chr9:131898386 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01943.hp2 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-4394A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898386 | |||||||
| chr9:131898495 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-4503G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898495 | |||||||
| chr9:131898569 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-4577A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898569 | |||||||
| chr9:131898594 | A | AT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0079 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-4603dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898594 | |||||||
| chr9:131898625 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0216 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.574-4633A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898625 | |||||||
| chr9:131898729 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-4737G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898729 | |||||||
| chr9:131898775 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0166 |
3 | HG01074.hp1 HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.574-4783C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898775 | |||||||
| chr9:131898864 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-4872G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898864 | |||||||
| chr9:131898877 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-4885C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898877 | |||||||
| chr9:131898880 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-4888G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898880 | |||||||
| chr9:131898881 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.574-4889C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898881 | |||||||
| chr9:131899652 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-5660G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131899652 | |||||||
| chr9:131899977 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.574-5985G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131899977 | |||||||
| chr9:131900147 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-6155G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131900147 | |||||||
| chr9:131900232 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.574-6240G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131900232 | |||||||
| chr9:131900262 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.574-6270G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131900262 | |||||||
| chr9:131900600 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-6608T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131900600 | |||||||
| chr9:131901022 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.574-7030T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901022 | |||||||
| chr9:131901265 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
64 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.574-7273T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901265 | |||||||
| chr9:131901326 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.574-7334C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901326 | |||||||
| chr9:131901359 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.574-7367T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901359 | |||||||
| chr9:131901452 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0001g0167 |
3 | HG03239.hp1 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.574-7460C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901452 | |||||||
| chr9:131901474 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0222 a0001c0001t0002g0217 |
3 | HG00738.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.574-7482G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901474 | |||||||
| chr9:131901731 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-7739G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901731 | |||||||
| chr9:131901899 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.574-7907C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131901899 | |||||||
| chr9:131902282 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.574-8290C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902282 | |||||||
| chr9:131902324 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.574-8332C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902324 | |||||||
| chr9:131902421 | A | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0250 a0001c0001t0001g0252 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-8429T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902421 | |||||||
| chr9:131902535 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.574-8543C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902535 | |||||||
| chr9:131902562 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.574-8570C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902562 | |||||||
| chr9:131902607 | C | G | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.574-8615G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902607 | |||||||
| chr9:131902727 | A | G | 16 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0169 others(13): Show |
16 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.574-8735T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902727 | |||||||
| chr9:131902730 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-8738G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902730 | |||||||
| chr9:131902740 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574-8748C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902740 | |||||||
| chr9:131902868 | A | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.574-8876T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902868 | |||||||
| chr9:131902993 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01255.hp1 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-9001G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131902993 | |||||||
| chr9:131903044 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.574-9052G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903044 | |||||||
| chr9:131903081 | C | CG | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.574-9090dupC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903081 | |||||||
| chr9:131903122 | A | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.574-9130T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903122 | |||||||
| chr9:131903248 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.574-9256C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903248 | |||||||
| chr9:131903258 | G | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG02647.hp2 HG02895.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-9266C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903258 | |||||||
| chr9:131903316 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-9324A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903316 | |||||||
| chr9:131903644 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-9652A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903644 | |||||||
| chr9:131903655 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.574-9663C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903655 | |||||||
| chr9:131903784 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-9792C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903784 | |||||||
| chr9:131903891 | C | CT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0079 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-9900dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903891 | |||||||
| chr9:131903891 | CT | C | 192 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.574-9900delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903891 | |||||||
| chr9:131903907 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-9915A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903907 | |||||||
| chr9:131903908 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-9916G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903908 | |||||||
| chr9:131903909 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-9917A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903909 | |||||||
| chr9:131904178 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0001g0194 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-10186G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904178 | |||||||
| chr9:131904191 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.574-10199C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904191 | |||||||
| chr9:131904389 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.574-10397A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904389 | |||||||
| chr9:131904538 | T | TG | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
66 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.574-10547_574-1054 others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904538 | |||||||
| chr9:131904539 | C | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.574-10547G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904539 | |||||||
| chr9:131904540 | G | GC | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0068 others(22): Show |
25 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.574-10549_574-1054 others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904540 | |||||||
| chr9:131904549 | C | T | 43 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0043 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.574-10557G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904549 | |||||||
| chr9:131904570 | G | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(61): Show |
64 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.574-10578C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904570 | |||||||
| chr9:131904696 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0002g0217 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.574-10704C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904696 | |||||||
| chr9:131904942 | C | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(61): Show |
64 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.574-10950G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131904942 | |||||||
| chr9:131905084 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.574-11092T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905084 | |||||||
| chr9:131905251 | C | T | 10 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.574-11259G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905251 | |||||||
| chr9:131905327 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.574-11335G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905327 | |||||||
| chr9:131905353 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-11361T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905353 | |||||||
| chr9:131905385 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.574-11393G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905385 | |||||||
| chr9:131905541 | G | A | 7 | a0001c0001t0002g0022 a0001c0001t0002g0032 a0001c0001t0002g0126 others(4): Show |
7 | HG00621.hp2 HG02132.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-11549C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905541 | |||||||
| chr9:131905554 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.574-11562G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905554 | |||||||
| chr9:131905701 | C | CA | 12 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0054 others(9): Show |
12 | HG00408.hp2 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-11710dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905701 | |||||||
| chr9:131905701 | C | CAA | 9 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0001g0169 others(6): Show |
9 | HG01358.hp1 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-11711_574-1171 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905701 | |||||||
| chr9:131905701 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02622.hp1 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.574-11719_574-1171 others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905701 | |||||||
| chr9:131905712 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.574-11738_574-1172 others(22): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905712 | |||||||
| chr9:131905715 | AAAAAAAA others(8): Show |
A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0129 a0001c0001t0002g0141 |
3 | HG00738.hp1 HG01099.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.574-11738_574-1172 others(19): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905715 | |||||||
| chr9:131905716 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.574-11738_574-1172 others(18): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905716 | |||||||
| chr9:131905720 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.574-11738_574-1172 others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905720 | |||||||
| chr9:131905722 | AAAAAACA others(1): Show |
A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0088 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.574-11738_574-1173 others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905722 | |||||||
| chr9:131905723 | AAAAACAG | A | 76 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0044 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.574-11738_574-1173 others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905723 | |||||||
| chr9:131905725 | AAACAG | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0159 others(14): Show |
17 | HG02280.hp2 HG02451.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-11738_574-1173 others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905725 | |||||||
| chr9:131905726 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.574-11734T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905726 | |||||||
| chr9:131905726 | AACAG | A | 16 | a0001c0001t0001g0068 a0001c0001t0001g0160 a0001c0001t0001g0161 others(13): Show |
16 | HG00558.hp2 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-11738_574-1173 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905726 | |||||||
| chr9:131905727 | ACAG | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0150 others(3): Show |
6 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-11738_574-1173 others(7): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905727 | |||||||
| chr9:131905728 | CAGAAAA | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG00438.hp1 HG00621.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.574-11742_574-1173 others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905728 | |||||||
| chr9:131905734 | A | C | 165 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(162): Show |
165 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.574-11742T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905734 | |||||||
| chr9:131905754 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-11762T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131905754 | |||||||
| chr9:131906074 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.574-12082A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906074 | |||||||
| chr9:131906159 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0001g0194 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-12167G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906159 | |||||||
| chr9:131906163 | C | T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(27): Show |
30 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.574-12171G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906163 | |||||||
| chr9:131906450 | A | AGGGGGTC | 197 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.574-12459_574-1245 others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906450 | |||||||
| chr9:131906541 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.574-12549T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906541 | |||||||
| chr9:131906562 | T | C | 197 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.574-12570A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906562 | |||||||
| chr9:131906698 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-12706G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906698 | |||||||
| chr9:131906801 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.574-12809G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906801 | |||||||
| chr9:131906984 | T | C | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.574-12992A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906984 | |||||||
| chr9:131906991 | G | T | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.574-12999C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906991 | |||||||
| chr9:131906997 | A | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.574-13005T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131906997 | |||||||
| chr9:131907197 | CTCTCCCT others(22): Show |
C | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-13234_574-1320 others(33): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907197 | |||||||
| chr9:131907246 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0134 |
3 | NA18983.hp1 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.574-13254G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907246 | |||||||
| chr9:131907321 | T | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.574-13329A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907321 | |||||||
| chr9:131907361 | G | C | 197 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.574-13369C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907361 | |||||||
| chr9:131907374 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-13382G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907374 | |||||||
| chr9:131907401 | G | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-13409C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907401 | |||||||
| chr9:131907419 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0254 |
3 | HG01884.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.574-13427G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907419 | |||||||
| chr9:131907451 | C | T | 14 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0169 others(11): Show |
14 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-13459G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907451 | |||||||
| chr9:131907487 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.574-13495G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907487 | |||||||
| chr9:131907504 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG01256.hp1 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.574-13512G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907504 | |||||||
| chr9:131907558 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-13566G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907558 | |||||||
| chr9:131907586 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-13594G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907586 | |||||||
| chr9:131907587 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.574-13595C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907587 | |||||||
| chr9:131907599 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.574-13607G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907599 | |||||||
| chr9:131907634 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.574-13642G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907634 | |||||||
| chr9:131907638 | A | AC | 7 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0001g0210 others(4): Show |
7 | HG01099.hp1 HG01099.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-13647dupG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907638 | |||||||
| chr9:131907681 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.574-13689G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907681 | |||||||
| chr9:131907768 | T | TTGAGGAG others(33): Show |
33 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.574-13777_574-1377 others(44): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907768 | |||||||
| chr9:131907777 | G | A | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.574-13785C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907777 | |||||||
| chr9:131907826 | C | T | 4 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | HG00408.hp1 HG00438.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-13834G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907826 | |||||||
| chr9:131907867 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.574-13875C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907867 | |||||||
| chr9:131907875 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.574-13883C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907875 | |||||||
| chr9:131907933 | G | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0043 others(40): Show |
43 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.574-13941C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907933 | |||||||
| chr9:131907963 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.574-13971C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907963 | |||||||
| chr9:131907965 | G | T | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.574-13973C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131907965 | |||||||
| chr9:131908019 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-14027G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908019 | |||||||
| chr9:131908143 | C | CG | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.574-14152dupC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908143 | |||||||
| chr9:131908147 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG03139.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.574-14155G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908147 | |||||||
| chr9:131908161 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.574-14169C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908161 | |||||||
| chr9:131908225 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.574-14233C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908225 | |||||||
| chr9:131908237 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.574-14245G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908237 | |||||||
| chr9:131908238 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 |
3 | HG02630.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.574-14246C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908238 | |||||||
| chr9:131908241 | C | T | 211 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.574-14249G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908241 | |||||||
| chr9:131908273 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0072 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.574-14281G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908273 | |||||||
| chr9:131908477 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-14485G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908477 | |||||||
| chr9:131908874 | TA | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0015 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.574-14883delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908874 | |||||||
| chr9:131908916 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.574-14924G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908916 | |||||||
| chr9:131908917 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.574-14925C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908917 | |||||||
| chr9:131909015 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-15023A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909015 | |||||||
| chr9:131909081 | A | T | 1 | a0001c0001t0001g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.574-15089T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909081 | |||||||
| chr9:131909120 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-15128G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909120 | |||||||
| chr9:131909252 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0170 others(65): Show |
68 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.574-15260A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909252 | |||||||
| chr9:131909440 | G | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0129 a0001c0001t0002g0141 |
3 | HG00738.hp1 HG01099.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.574-15448C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909440 | |||||||
| chr9:131909483 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-15491C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909483 | |||||||
| chr9:131909563 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.574-15571G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909563 | |||||||
| chr9:131909654 | G | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0201 others(14): Show |
17 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.574-15662C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909654 | |||||||
| chr9:131909684 | T | A | 79 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(76): Show |
79 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.574-15692A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909684 | |||||||
| chr9:131909732 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.574-15740A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909732 | |||||||
| chr9:131909823 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.574-15831T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909823 | |||||||
| chr9:131909998 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0212 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.574-16006C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131909998 | |||||||
| chr9:131910163 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.574-16171G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910163 | |||||||
| chr9:131910260 | A | C | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.574-16268T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910260 | |||||||
| chr9:131910370 | C | A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0169 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-16378G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910370 | |||||||
| chr9:131910498 | A | T | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.574-16506T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910498 | |||||||
| chr9:131910639 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00544.hp1 HG00621.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-16647C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910639 | |||||||
| chr9:131910674 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-16682G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910674 | |||||||
| chr9:131910683 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.574-16691T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910683 | |||||||
| chr9:131910820 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0219 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.574-16828A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910820 | |||||||
| chr9:131910831 | T | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.574-16839A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910831 | |||||||
| chr9:131910850 | G | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.574-16858C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910850 | |||||||
| chr9:131910919 | C | A | 1 | a0001c0001t0001g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.574-16927G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910919 | |||||||
| chr9:131910931 | T | C | 66 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0031 others(63): Show |
66 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.574-16939A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131910931 | |||||||
| chr9:131911038 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG02886.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.574-17046T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911038 | |||||||
| chr9:131911039 | TAAAC | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
19 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.574-17051_574-1704 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911039 | |||||||
| chr9:131911161 | A | C | 32 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0113 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.574-17169T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911161 | |||||||
| chr9:131911433 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-17441G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911433 | |||||||
| chr9:131911581 | A | C | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-17589T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911581 | |||||||
| chr9:131911764 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-17772G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911764 | |||||||
| chr9:131911995 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.574-18003T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131911995 | |||||||
| chr9:131912071 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.574-18079G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912071 | |||||||
| chr9:131912160 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.574-18168C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912160 | |||||||
| chr9:131912190 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.574-18198C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912190 | |||||||
| chr9:131912249 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-18257A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912249 | |||||||
| chr9:131912328 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.574-18336G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912328 | |||||||
| chr9:131912425 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-18433T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912425 | |||||||
| chr9:131912514 | G | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-18522C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912514 | |||||||
| chr9:131912661 | C | T | 74 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0075 others(71): Show |
74 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.574-18669G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131912661 | |||||||
| chr9:131913064 | C | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-19072G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913064 | |||||||
| chr9:131913366 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0247 |
2 | HG00609.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.574-19374G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913366 | |||||||
| chr9:131913606 | C | T | 64 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0060 others(61): Show |
64 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.574-19614G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913606 | |||||||
| chr9:131913709 | C | A | 116 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(113): Show |
116 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.574-19717G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913709 | |||||||
| chr9:131913873 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.574-19881C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913873 | |||||||
| chr9:131913944 | C | CTTCA | 108 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(105): Show |
108 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.574-19956_574-1995 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913944 | |||||||
| chr9:131913994 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.574-20002C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131913994 | |||||||
| chr9:131914011 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.574-20019C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914011 | |||||||
| chr9:131914181 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.574-20189T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914181 | |||||||
| chr9:131914328 | C | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-20336G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914328 | |||||||
| chr9:131914415 | C | T | 66 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0124 others(63): Show |
66 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.574-20423G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914415 | |||||||
| chr9:131914458 | A | G | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-20466T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914458 | |||||||
| chr9:131914684 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.574-20692C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914684 | |||||||
| chr9:131914815 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-20823A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914815 | |||||||
| chr9:131914894 | T | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-20902A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131914894 | |||||||
| chr9:131915030 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0208 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-21038A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131915030 | |||||||
| chr9:131915141 | G | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0083 others(12): Show |
15 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.574-21149C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131915141 | |||||||
| chr9:131915267 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-21275C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131915267 | |||||||
| chr9:131915352 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.574-21360A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131915352 | |||||||
| chr9:131916042 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.574-22050T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916042 | |||||||
| chr9:131916288 | C | T | 210 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.574-22296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916288 | |||||||
| chr9:131916290 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-22298G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916290 | |||||||
| chr9:131916392 | C | T | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.574-22400G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916392 | |||||||
| chr9:131916411 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-22419G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916411 | |||||||
| chr9:131916533 | G | C | 106 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(103): Show |
106 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.574-22541C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131916533 | |||||||
| chr9:131917198 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573+22183C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917198 | |||||||
| chr9:131917277 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.573+22104T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917277 | |||||||
| chr9:131917378 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.573+22003C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917378 | |||||||
| chr9:131917378 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.573+22003C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917378 | |||||||
| chr9:131917471 | G | C | 75 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0075 others(72): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+21910C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917471 | |||||||
| chr9:131917503 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.573+21878T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917503 | |||||||
| chr9:131917512 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+21869G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917512 | |||||||
| chr9:131917558 | G | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+21823C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917558 | |||||||
| chr9:131917569 | A | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0068 others(28): Show |
31 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.573+21812T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917569 | |||||||
| chr9:131917632 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(4): Show |
7 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+21749G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917632 | |||||||
| chr9:131917731 | G | A | 113 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(110): Show |
113 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.573+21650C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917731 | |||||||
| chr9:131917734 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG00621.hp1 HG02132.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.573+21647T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917734 | |||||||
| chr9:131917743 | G | A | 113 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(110): Show |
113 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.573+21638C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131917743 | |||||||
| chr9:131918222 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+21159A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918222 | |||||||
| chr9:131918374 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573+21007G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918374 | |||||||
| chr9:131918472 | G | GCAAA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0054 others(5): Show |
8 | HG00408.hp2 HG03688.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+20905_573+2090 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918472 | |||||||
| chr9:131918504 | C | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573+20877G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918504 | |||||||
| chr9:131918700 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+20681G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918700 | |||||||
| chr9:131918900 | G | A | 75 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0061 others(72): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+20481C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131918900 | |||||||
| chr9:131919068 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.573+20313G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919068 | |||||||
| chr9:131919114 | A | G | 204 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.573+20267T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919114 | |||||||
| chr9:131919169 | G | A | 74 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0075 others(71): Show |
74 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.573+20212C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919169 | |||||||
| chr9:131919325 | G | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+20056C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919325 | |||||||
| chr9:131919363 | G | A | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(82): Show |
85 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.573+20018C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919363 | |||||||
| chr9:131919460 | A | AT | 39 | a0001c0001t0001g0061 a0001c0001t0001g0124 a0001c0001t0002g0002 others(36): Show |
39 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.573+19920dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919460 | |||||||
| chr9:131919541 | A | G | 44 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0068 others(41): Show |
44 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.573+19840T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919541 | |||||||
| chr9:131919792 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.573+19589A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919792 | |||||||
| chr9:131919811 | C | CT | 93 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(90): Show |
93 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.573+19569dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919811 | |||||||
| chr9:131919811 | C | CTT | 33 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0083 others(30): Show |
33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.573+19568_573+1956 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919811 | |||||||
| chr9:131919894 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.573+19487G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919894 | |||||||
| chr9:131920623 | G | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+18758C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920623 | |||||||
| chr9:131920690 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.573+18691C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920690 | |||||||
| chr9:131920718 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+18663T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920718 | |||||||
| chr9:131920719 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+18662C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920719 | |||||||
| chr9:131920722 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+18659C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920722 | |||||||
| chr9:131920732 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+18649G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920732 | |||||||
| chr9:131920804 | G | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+18577C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920804 | |||||||
| chr9:131920814 | T | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573+18567A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131920814 | |||||||
| chr9:131921243 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573+18138C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921243 | |||||||
| chr9:131921358 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.573+18023C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921358 | |||||||
| chr9:131921477 | ACCATC | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0083 others(12): Show |
15 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+17899_573+1790 others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921477 | |||||||
| chr9:131921485 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0016 |
2 | HG01943.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.573+17896C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921485 | |||||||
| chr9:131921561 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+17820A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921561 | |||||||
| chr9:131921858 | T | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+17523A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921858 | |||||||
| chr9:131921944 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.573+17437C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131921944 | |||||||
| chr9:131922023 | T | C | 219 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(216): Show |
219 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.573+17358A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922023 | |||||||
| chr9:131922028 | A | AG | 25 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0031 others(22): Show |
25 | HG00544.hp1 HG01099.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.573+17352dupC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922028 | |||||||
| chr9:131922066 | A | C | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.573+17315T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922066 | |||||||
| chr9:131922081 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01255.hp1 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+17300A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922081 | |||||||
| chr9:131922122 | C | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.573+17259G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922122 | |||||||
| chr9:131922254 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+17127T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922254 | |||||||
| chr9:131922432 | G | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+16949C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922432 | |||||||
| chr9:131922442 | CT | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.573+16938delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922442 | |||||||
| chr9:131922491 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+16890T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922491 | |||||||
| chr9:131922592 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.573+16789G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922592 | |||||||
| chr9:131922635 | C | CTTTTT | 91 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(88): Show |
91 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.573+16745_573+1674 others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922635 | |||||||
| chr9:131922640 | C | A | 91 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(88): Show |
91 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.573+16741G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131922640 | |||||||
| chr9:131923099 | G | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG02257.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.573+16282C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923099 | |||||||
| chr9:131923226 | T | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0248 |
3 | HG02895.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.573+16155A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923226 | |||||||
| chr9:131923227 | C | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0248 |
3 | HG02895.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.573+16154G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923227 | |||||||
| chr9:131923412 | G | T | 62 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0124 others(59): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.573+15969C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923412 | |||||||
| chr9:131923635 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.573+15746G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923635 | |||||||
| chr9:131923677 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.573+15704C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923677 | |||||||
| chr9:131923969 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.573+15412T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923969 | |||||||
| chr9:131923979 | T | C | 75 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(72): Show |
75 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.573+15402A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131923979 | |||||||
| chr9:131924000 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0086 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.573+15381A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924000 | |||||||
| chr9:131924211 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.573+15170C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924211 | |||||||
| chr9:131924440 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.573+14941T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924440 | |||||||
| chr9:131924544 | T | C | 8 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+14837A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924544 | |||||||
| chr9:131924751 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.573+14630G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924751 | |||||||
| chr9:131924804 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.573+14577A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924804 | |||||||
| chr9:131924868 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.573+14513A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924868 | |||||||
| chr9:131924934 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.573+14447T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131924934 | |||||||
| chr9:131925011 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.573+14370C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925011 | |||||||
| chr9:131925069 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.573+14312G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925069 | |||||||
| chr9:131925496 | A | AAATAAAT others(36): Show |
1 | a0001c0001t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.573+13842_573+1388 others(47): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925496 | |||||||
| chr9:131925550 | T | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0089 others(3): Show |
6 | HG01081.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+13831A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925550 | |||||||
| chr9:131925732 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+13649T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925732 | |||||||
| chr9:131925784 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.573+13597C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925784 | |||||||
| chr9:131925787 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+13594C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925787 | |||||||
| chr9:131925971 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.573+13410T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131925971 | |||||||
| chr9:131926017 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.573+13364C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926017 | |||||||
| chr9:131926080 | T | G | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+13301A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926080 | |||||||
| chr9:131926286 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.573+13095C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926286 | |||||||
| chr9:131926292 | GT | G | 5 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+13088delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926292 | |||||||
| chr9:131926439 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+12942G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926439 | |||||||
| chr9:131926465 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.573+12916G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926465 | |||||||
| chr9:131926562 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.573+12819G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926562 | |||||||
| chr9:131926780 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+12601T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926780 | |||||||
| chr9:131926783 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.573+12598A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131926783 | |||||||
| chr9:131927718 | T | G | 1 | a0001c0001t0002g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.573+11663A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131927718 | |||||||
| chr9:131927753 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+11628C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131927753 | |||||||
| chr9:131927770 | A | G | 9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0181 others(6): Show |
9 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+11611T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131927770 | |||||||
| chr9:131927827 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.573+11554A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131927827 | |||||||
| chr9:131927900 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0070 |
2 | NA18950.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.573+11481C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131927900 | |||||||
| chr9:131928015 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+11366T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131928015 | |||||||
| chr9:131928468 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.573+10913T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131928468 | |||||||
| chr9:131928706 | G | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.573+10675C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131928706 | |||||||
| chr9:131928964 | T | A | 6 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(3): Show |
6 | HG02809.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+10417A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131928964 | |||||||
| chr9:131929105 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.573+10276G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929105 | |||||||
| chr9:131929164 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0248 |
3 | HG02895.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.573+10217C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929164 | |||||||
| chr9:131929219 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.573+10162G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929219 | |||||||
| chr9:131929303 | G | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0174 others(6): Show |
9 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.573+10078C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929303 | |||||||
| chr9:131929463 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+9918C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929463 | |||||||
| chr9:131929465 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.573+9916G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929465 | |||||||
| chr9:131929589 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.573+9792G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929589 | |||||||
| chr9:131929654 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.573+9727G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929654 | |||||||
| chr9:131929697 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+9684T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929697 | |||||||
| chr9:131929857 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.573+9524G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929857 | |||||||
| chr9:131929957 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.573+9424T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131929957 | |||||||
| chr9:131930032 | C | CAG | 7 | a0001c0001t0001g0007 a0001c0001t0001g0086 a0001c0001t0001g0111 others(4): Show |
7 | HG02451.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+9347_573+9348d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930032 | C | CAGAGAGA others(1): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0037 others(5): Show |
8 | HG01891.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+9341_573+9348d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930032 | C | CAGAGAGA others(3): Show |
1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.573+9339_573+9348d others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930032 | C | CAGAGAGA others(11): Show |
1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.573+9348_573+9349i others(20): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930032 | C | CAGAGAGA others(17): Show |
1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.573+9348_573+9349i others(26): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930032 | CAG | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0114 a0001c0001t0001g0239 others(5): Show |
8 | HG00544.hp1 HG00621.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+9347_573+9348d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930032 | |||||||
| chr9:131930080 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
15 | HG01496.hp2 HG01943.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+9301C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930080 | |||||||
| chr9:131930144 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0208 others(8): Show |
11 | HG01074.hp1 HG01175.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+9237A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930144 | |||||||
| chr9:131930147 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.573+9234C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930147 | |||||||
| chr9:131930204 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.573+9177T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930204 | |||||||
| chr9:131930210 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.573+9171A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930210 | |||||||
| chr9:131930564 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+8817G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930564 | |||||||
| chr9:131930578 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.573+8803A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930578 | |||||||
| chr9:131930611 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0071 |
2 | HG02040.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.573+8770G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930611 | |||||||
| chr9:131930811 | G | C | 1 | a0001c0001t0001g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.573+8570C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930811 | |||||||
| chr9:131930906 | T | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0058 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+8475A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930906 | |||||||
| chr9:131930974 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+8407C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131930974 | |||||||
| chr9:131931003 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0258 |
2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.573+8378A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931003 | |||||||
| chr9:131931003 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.573+8378A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931003 | |||||||
| chr9:131931105 | T | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+8276A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931105 | |||||||
| chr9:131931116 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+8265C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931116 | |||||||
| chr9:131931628 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.573+7753G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931628 | |||||||
| chr9:131931642 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+7739C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931642 | |||||||
| chr9:131931800 | GAATATCA others(46): Show |
G | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.573+7528_573+7580d others(55): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131931800 | |||||||
| chr9:131932014 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.573+7367T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932014 | |||||||
| chr9:131932035 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+7346T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932035 | |||||||
| chr9:131932093 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.573+7288G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932093 | |||||||
| chr9:131932241 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.573+7140G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932241 | |||||||
| chr9:131932245 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.573+7136G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932245 | |||||||
| chr9:131932308 | GA | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.573+7072delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932308 | |||||||
| chr9:131932382 | G | GA | 211 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
211 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.573+6998dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932382 | |||||||
| chr9:131932396 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+6985C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932396 | |||||||
| chr9:131932401 | G | T | 59 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(56): Show |
59 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.573+6980C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932401 | |||||||
| chr9:131932476 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.573+6905A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932476 | |||||||
| chr9:131932522 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+6859G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932522 | |||||||
| chr9:131932710 | C | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+6671G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932710 | |||||||
| chr9:131933009 | C | CAAAAACC others(361): Show |
1 | a0001c0001t0001g0207 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573+6371_573+6372i others(370): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933009 | |||||||
| chr9:131933094 | T | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(84): Show |
87 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.573+6287A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933094 | |||||||
| chr9:131933175 | A | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+6206T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933175 | |||||||
| chr9:131933265 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+6116G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933265 | |||||||
| chr9:131933325 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0207 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.573+6056A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933325 | |||||||
| chr9:131933599 | T | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01255.hp1 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+5782A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933599 | |||||||
| chr9:131933661 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.573+5720G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933661 | |||||||
| chr9:131933752 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.573+5629A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933752 | |||||||
| chr9:131933908 | G | A | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0262 others(2): Show |
5 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+5473C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131933908 | |||||||
| chr9:131934394 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+4987C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131934394 | |||||||
| chr9:131934550 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.573+4831G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131934550 | |||||||
| chr9:131935166 | C | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.573+4215G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935166 | |||||||
| chr9:131935200 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
5 | NA18948.hp1 NA18961.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+4181G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935200 | |||||||
| chr9:131935509 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+3872C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935509 | |||||||
| chr9:131935519 | C | T | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+3862G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935519 | |||||||
| chr9:131935702 | C | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+3679G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935702 | |||||||
| chr9:131935708 | G | A | 60 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(57): Show |
60 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.573+3673C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935708 | |||||||
| chr9:131935725 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.573+3656C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935725 | |||||||
| chr9:131935808 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.573+3573T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131935808 | |||||||
| chr9:131936034 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0096 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.573+3347C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936034 | |||||||
| chr9:131936062 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+3319C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936062 | |||||||
| chr9:131936091 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+3290G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936091 | |||||||
| chr9:131936132 | C | CA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0065 others(4): Show |
7 | HG01175.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+3248dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936132 | |||||||
| chr9:131936132 | CA | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0072 others(14): Show |
17 | HG01109.hp1 HG01891.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.573+3248delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936132 | |||||||
| chr9:131936143 | A | T | 57 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0098 others(54): Show |
57 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.573+3238T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936143 | |||||||
| chr9:131936147 | A | AAAAG | 8 | a0001c0001t0001g0033 a0001c0001t0001g0062 a0001c0001t0001g0093 others(5): Show |
8 | HG01943.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+3230_573+3233d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936147 | |||||||
| chr9:131936147 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0002g0022 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.573+3234T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936147 | |||||||
| chr9:131936631 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.573+2750A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936631 | |||||||
| chr9:131936760 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.573+2621G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936760 | |||||||
| chr9:131936822 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.573+2559G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936822 | |||||||
| chr9:131936903 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.573+2478C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131936903 | |||||||
| chr9:131937079 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.573+2302C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937079 | |||||||
| chr9:131937134 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+2247G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937134 | |||||||
| chr9:131937222 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+2159T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937222 | |||||||
| chr9:131937574 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.573+1807C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937574 | |||||||
| chr9:131937604 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.573+1777G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937604 | |||||||
| chr9:131937829 | CT | C | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
103 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.573+1551delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937829 | |||||||
| chr9:131937887 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+1494C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131937887 | |||||||
| chr9:131938041 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
192 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.573+1340T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938041 | |||||||
| chr9:131938065 | C | A | 1 | a0001c0001t0002g0153 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.573+1316G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938065 | |||||||
| chr9:131938074 | G | T | 80 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0072 others(77): Show |
80 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.573+1307C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938074 | |||||||
| chr9:131938148 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+1233C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938148 | |||||||
| chr9:131938331 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.573+1050G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938331 | |||||||
| chr9:131938452 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+929G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938452 | |||||||
| chr9:131938484 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.573+897T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938484 | |||||||
| chr9:131938597 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.573+784G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938597 | |||||||
| chr9:131938674 | A | G | 60 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(57): Show |
60 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.573+707T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938674 | |||||||
| chr9:131938734 | A | C | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
192 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.573+647T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938734 | |||||||
| chr9:131938955 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573+426G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938955 | |||||||
| chr9:131938989 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+392T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938989 | |||||||
| chr9:131938992 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573+389G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131938992 | |||||||
| chr9:131939082 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | NA18948.hp1 NA18961.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+299A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131939082 | |||||||
| chr9:131939497 | T | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-23A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939497 | |||||||
| chr9:131939770 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939770 | |||||||
| chr9:131939826 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.480-352C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939826 | |||||||
| chr9:131939881 | C | G | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480-407G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939881 | |||||||
| chr9:131939900 | C | CT | 6 | a0001c0001t0001g0071 a0001c0001t0001g0078 a0001c0001t0001g0086 others(3): Show |
6 | HG02055.hp1 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-427dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939900 | |||||||
| chr9:131939900 | CT | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0118 others(8): Show |
11 | HG01074.hp1 HG01175.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.480-427delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939900 | |||||||
| chr9:131939900 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.480-437_480-427del others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939900 | |||||||
| chr9:131939997 | C | G | 1 | a0001c0001t0002g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.480-523G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131939997 | |||||||
| chr9:131940073 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): Show |
198 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.480-599G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131940073 | |||||||
| chr9:131940152 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0097 others(4): Show |
7 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.480-678C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131940152 | |||||||
| chr9:131940191 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.480-717G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131940191 | |||||||
| chr9:131940362 | C | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-888G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131940362 | |||||||
| chr9:131941274 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480-1800C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941274 | |||||||
| chr9:131941309 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0209 a0001c0001t0002g0217 |
3 | HG01943.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.480-1835C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941309 | |||||||
| chr9:131941560 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-2086G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941560 | |||||||
| chr9:131941769 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
13 | HG01081.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.480-2295G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941769 | |||||||
| chr9:131941817 | A | AT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(53): Show |
57 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.480-2344dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATT | 13 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(10): Show |
13 | HG00544.hp2 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.480-2345_480-2344d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0097 a0001c0001t0001g0209 others(3): Show |
6 | HG01943.hp2 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-2346_480-2344d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0184 others(2): Show |
5 | HG02630.hp2 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-2347_480-2344d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT | 8 | a0001c0001t0001g0075 a0001c0001t0001g0249 a0001c0001t0001g0254 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.480-2350_480-2344d others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(1): Show |
29 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0161 others(26): Show |
29 | HG00438.hp2 HG00558.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.480-2351_480-2344d others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0124 a0001c0001t0001g0159 a0001c0001t0001g0160 others(11): Show |
14 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-2352_480-2344d others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(3): Show |
11 | a0001c0001t0001g0096 a0001c0001t0001g0163 a0001c0001t0001g0182 others(8): Show |
11 | HG00621.hp2 HG01928.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.480-2353_480-2344d others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0169 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.480-2354_480-2344d others(13): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0181 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-2355_480-2344d others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.480-2356_480-2344d others(15): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.480-2366_480-2344d others(25): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | AT | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0070 others(24): Show |
27 | HG00544.hp1 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.480-2344delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941817 | ATT | A | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.480-2345_480-2344d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941817 | |||||||
| chr9:131941881 | A | G | 69 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0093 others(66): Show |
69 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.480-2407T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941881 | |||||||
| chr9:131941886 | C | T | 62 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.480-2412G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941886 | |||||||
| chr9:131942115 | G | A | 6 | a0001c0001t0001g0124 a0001c0001t0002g0092 a0001c0001t0002g0123 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-2641C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131942115 | |||||||
| chr9:131942534 | C | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-3060G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131942534 | |||||||
| chr9:131942600 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.480-3126T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131942600 | |||||||
| chr9:131943031 | A | G | 63 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0001g0124 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.480-3557T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943031 | |||||||
| chr9:131943066 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.480-3592T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943066 | |||||||
| chr9:131943122 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
213 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.480-3648A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943122 | |||||||
| chr9:131943812 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.480-4338G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943812 | |||||||
| chr9:131943849 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.480-4375A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943849 | |||||||
| chr9:131943874 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0254 |
3 | HG01884.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.480-4400G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943874 | |||||||
| chr9:131943995 | G | A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0001c0001t0001g0254 |
3 | HG01884.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.480-4521C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131943995 | |||||||
| chr9:131944196 | C | G | 24 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0157 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.480-4722G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944196 | |||||||
| chr9:131944318 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.480-4844G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944318 | |||||||
| chr9:131944361 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.480-4887G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944361 | |||||||
| chr9:131944481 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.480-5007A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944481 | |||||||
| chr9:131944530 | C | CT | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0096 others(22): Show |
25 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.480-5057dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944530 | |||||||
| chr9:131944530 | CT | C | 57 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(54): Show |
57 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.480-5057delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944530 | |||||||
| chr9:131944610 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.480-5136G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944610 | |||||||
| chr9:131944828 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480-5354C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944828 | |||||||
| chr9:131944829 | G | T | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480-5355C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131944829 | |||||||
| chr9:131945447 | C | T | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-5973G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945447 | |||||||
| chr9:131945546 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-6072A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945546 | |||||||
| chr9:131945795 | TA | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): Show |
53 | HG00558.hp2 HG00621.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.480-6322delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945795 | |||||||
| chr9:131945881 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.480-6407A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945881 | |||||||
| chr9:131945968 | T | TA | 10 | a0001c0001t0001g0043 a0001c0001t0001g0073 a0001c0001t0001g0093 others(7): Show |
10 | HG01361.hp2 HG01928.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480-6495dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945968 | |||||||
| chr9:131945978 | A | AC | 58 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0001g0124 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.480-6505_480-6504i others(3): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131945978 | |||||||
| chr9:131946098 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-6624C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946098 | |||||||
| chr9:131946244 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-6770G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946244 | |||||||
| chr9:131946248 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.480-6774G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946248 | |||||||
| chr9:131946290 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.480-6816C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946290 | |||||||
| chr9:131946402 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.480-6928G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946402 | |||||||
| chr9:131946574 | A | G | 63 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0001g0124 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.480-7100T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131946574 | |||||||
| chr9:131947140 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.480-7666C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947140 | |||||||
| chr9:131947481 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0250 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.480-8007G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947481 | |||||||
| chr9:131947667 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.480-8193G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947667 | |||||||
| chr9:131947738 | T | C | 8 | a0001c0001t0001g0096 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.480-8264A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947738 | |||||||
| chr9:131947743 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-8269A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947743 | |||||||
| chr9:131947933 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.480-8459A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947933 | |||||||
| chr9:131947977 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-8503C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131947977 | |||||||
| chr9:131948036 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-8562A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948036 | |||||||
| chr9:131948119 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.480-8645A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948119 | |||||||
| chr9:131948224 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.480-8750G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948224 | |||||||
| chr9:131948249 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-8775G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948249 | |||||||
| chr9:131948360 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.480-8886C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948360 | |||||||
| chr9:131948468 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-8994A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948468 | |||||||
| chr9:131948502 | CA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(176): Show |
180 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.480-9029delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948502 | |||||||
| chr9:131948505 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-9031T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948505 | |||||||
| chr9:131948508 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0233 |
2 | HG02622.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.480-9034T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948508 | |||||||
| chr9:131948509 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0271 a0001c0001t0002g0108 others(1): Show |
4 | HG00558.hp1 HG01943.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-9035T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948509 | |||||||
| chr9:131948514 | A | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.480-9040T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948514 | |||||||
| chr9:131948571 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-9097T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948571 | |||||||
| chr9:131948585 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-9111G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948585 | |||||||
| chr9:131948990 | A | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-9516T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131948990 | |||||||
| chr9:131949178 | T | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480-9704A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949178 | |||||||
| chr9:131949212 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-9738A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949212 | |||||||
| chr9:131949377 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
38 | HG00408.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.480-9903C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949377 | |||||||
| chr9:131949479 | A | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.480-10005T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949479 | |||||||
| chr9:131949636 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0208 a0001c0001t0001g0211 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-10162T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949636 | |||||||
| chr9:131949655 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.480-10181C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949655 | |||||||
| chr9:131949836 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.480-10362A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949836 | |||||||
| chr9:131949840 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.480-10366G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949840 | |||||||
| chr9:131949841 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.480-10367C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949841 | |||||||
| chr9:131949889 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.480-10415A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949889 | |||||||
| chr9:131949939 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.480-10465A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131949939 | |||||||
| chr9:131950005 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.480-10531A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950005 | |||||||
| chr9:131950163 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0209 a0001c0001t0002g0217 |
3 | HG01943.hp2 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.480-10689G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950163 | |||||||
| chr9:131950189 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.480-10715T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950189 | |||||||
| chr9:131950204 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(14): Show |
17 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.480-10730G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950204 | |||||||
| chr9:131950356 | G | C | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.480-10882C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950356 | |||||||
| chr9:131950435 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480-10961C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950435 | |||||||
| chr9:131950454 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-10980G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950454 | |||||||
| chr9:131950536 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.480-11062C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950536 | |||||||
| chr9:131950575 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.480-11101G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950575 | |||||||
| chr9:131950734 | A | C | 93 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0072 others(90): Show |
93 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.480-11260T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131950734 | |||||||
| chr9:131951067 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(14): Show |
17 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.480-11593C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951067 | |||||||
| chr9:131951177 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.480-11703C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951177 | |||||||
| chr9:131951207 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-11733C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951207 | |||||||
| chr9:131951246 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480-11772A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951246 | |||||||
| chr9:131951442 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-11968T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951442 | |||||||
| chr9:131951541 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.480-12067G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951541 | |||||||
| chr9:131951677 | C | T | 59 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(56): Show |
59 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.480-12203G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951677 | |||||||
| chr9:131951982 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-12508T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131951982 | |||||||
| chr9:131952140 | C | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
103 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.480-12666G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952140 | |||||||
| chr9:131952173 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(14): Show |
17 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.480-12699G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952173 | |||||||
| chr9:131952299 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.480-12825C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952299 | |||||||
| chr9:131952492 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-13018A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952492 | |||||||
| chr9:131952493 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-13019A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952493 | |||||||
| chr9:131952599 | G | GC | 4 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-13126dupG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952599 | |||||||
| chr9:131952733 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG00621.hp1 HG02132.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.480-13259G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952733 | |||||||
| chr9:131952809 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-13335G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131952809 | |||||||
| chr9:131953093 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-13619G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953093 | |||||||
| chr9:131953530 | C | T | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
5 | HG01255.hp2 HG01258.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-14056G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953530 | |||||||
| chr9:131953564 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.480-14090T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953564 | |||||||
| chr9:131953762 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
16 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.480-14288A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953762 | |||||||
| chr9:131953777 | G | T | 1 | a0001c0001t0002g0003 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.480-14303C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953777 | |||||||
| chr9:131953793 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.480-14319A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953793 | |||||||
| chr9:131953802 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.480-14328T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953802 | |||||||
| chr9:131953818 | CT | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(139): Show |
143 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.480-14345delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953818 | |||||||
| chr9:131953818 | CTT | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0051 others(20): Show |
23 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.480-14346_480-1434 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953818 | |||||||
| chr9:131953978 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-14504G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131953978 | |||||||
| chr9:131954281 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480-14807C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131954281 | |||||||
| chr9:131954296 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.480-14822C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131954296 | |||||||
| chr9:131954500 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.480-15026A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131954500 | |||||||
| chr9:131954581 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480-15107A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131954581 | |||||||
| chr9:131954778 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.480-15304A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131954778 | |||||||
| chr9:131955033 | TG | T | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-15560delC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955033 | |||||||
| chr9:131955183 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.480-15709G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955183 | |||||||
| chr9:131955229 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.480-15755A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955229 | |||||||
| chr9:131955252 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-15778G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955252 | |||||||
| chr9:131955356 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0129 a0001c0001t0002g0141 |
3 | HG00738.hp1 HG01099.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.480-15882A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955356 | |||||||
| chr9:131955547 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-16073A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955547 | |||||||
| chr9:131955617 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.480-16143G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955617 | |||||||
| chr9:131955682 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480-16208T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955682 | |||||||
| chr9:131955694 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.480-16220G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955694 | |||||||
| chr9:131955927 | AAAAG | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-16457_480-1645 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955927 | |||||||
| chr9:131955931 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.480-16457C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131955931 | |||||||
| chr9:131956240 | A | T | 63 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.480-16766T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956240 | |||||||
| chr9:131956293 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-16819C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956293 | |||||||
| chr9:131956437 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.480-16963C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956437 | |||||||
| chr9:131956572 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.480-17098G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956572 | |||||||
| chr9:131956613 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.480-17139A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956613 | |||||||
| chr9:131956614 | C | CA | 13 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0065 others(10): Show |
13 | HG00609.hp1 HG00609.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.480-17141dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956614 | |||||||
| chr9:131956712 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.480-17238A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956712 | |||||||
| chr9:131956731 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.480-17257A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956731 | |||||||
| chr9:131956818 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.480-17344A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956818 | |||||||
| chr9:131956825 | TA | T | 15 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0159 others(12): Show |
15 | HG01169.hp1 HG01255.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.480-17352delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131956825 | |||||||
| chr9:131957082 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-17608A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957082 | |||||||
| chr9:131957158 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-17684T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957158 | |||||||
| chr9:131957216 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-17742A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957216 | |||||||
| chr9:131957262 | A | C | 4 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-17788T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957262 | |||||||
| chr9:131957265 | C | CT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00140.hp1 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.480-17792dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957265 | |||||||
| chr9:131957664 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480-18190G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957664 | |||||||
| chr9:131957666 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.480-18192T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957666 | |||||||
| chr9:131957801 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-18327C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957801 | |||||||
| chr9:131957857 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-18383A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957857 | |||||||
| chr9:131957897 | TA | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0093 others(6): Show |
9 | HG02040.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-18424delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957897 | |||||||
| chr9:131957909 | A | G | 8 | a0001c0001t0001g0096 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.480-18435T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957909 | |||||||
| chr9:131957910 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.480-18436T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957910 | |||||||
| chr9:131957924 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.480-18450T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957924 | |||||||
| chr9:131957953 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.480-18479C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957953 | |||||||
| chr9:131957981 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.480-18507G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131957981 | |||||||
| chr9:131958062 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.480-18588T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958062 | |||||||
| chr9:131958181 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
197 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.480-18707G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958181 | |||||||
| chr9:131958248 | G | GT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0096 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-18775dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958248 | |||||||
| chr9:131958306 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0209 a0001c0001t0001g0213 others(3): Show |
6 | HG01943.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-18832C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958306 | |||||||
| chr9:131958333 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480-18859G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958333 | |||||||
| chr9:131958391 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0096 others(15): Show |
18 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.480-18917C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958391 | |||||||
| chr9:131958392 | T | C | 89 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0072 others(86): Show |
89 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.480-18918A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958392 | |||||||
| chr9:131958541 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.480-19067G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958541 | |||||||
| chr9:131958598 | T | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0124 others(61): Show |
64 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.480-19124A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958598 | |||||||
| chr9:131958756 | G | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
16 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.480-19282C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958756 | |||||||
| chr9:131958971 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.480-19497A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131958971 | |||||||
| chr9:131959084 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0097 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.480-19610C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959084 | |||||||
| chr9:131959118 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-19644G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959118 | |||||||
| chr9:131959321 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-19847G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959321 | |||||||
| chr9:131959393 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0097 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.480-19919C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959393 | |||||||
| chr9:131959453 | A | C | 1 | a0001c0001t0002g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.480-19979T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959453 | |||||||
| chr9:131959597 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.480-20123C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959597 | |||||||
| chr9:131959821 | G | T | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.480-20347C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959821 | |||||||
| chr9:131959910 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.480-20436C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959910 | |||||||
| chr9:131960047 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.480-20573T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960047 | |||||||
| chr9:131960326 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.480-20852C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960326 | |||||||
| chr9:131960465 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.480-20991C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960465 | |||||||
| chr9:131960498 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.480-21024G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960498 | |||||||
| chr9:131960571 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-21097C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960571 | |||||||
| chr9:131960629 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.480-21155A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960629 | |||||||
| chr9:131960654 | C | T | 4 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-21180G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960654 | |||||||
| chr9:131960669 | T | C | 63 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.480-21195A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960669 | |||||||
| chr9:131960810 | T | C | 98 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.480-21336A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960810 | |||||||
| chr9:131960929 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-21455C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131960929 | |||||||
| chr9:131961280 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0183 |
3 | HG02080.hp2 NA18986.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.480-21806G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961280 | |||||||
| chr9:131961355 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG00639.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.480-21881C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961355 | |||||||
| chr9:131961402 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.480-21928A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961402 | |||||||
| chr9:131961619 | CTG | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0210 a0001c0001t0002g0076 others(1): Show |
4 | HG00408.hp2 HG03688.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-22147_480-2214 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961619 | |||||||
| chr9:131961650 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.480-22176C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961650 | |||||||
| chr9:131961679 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.480-22205G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961679 | |||||||
| chr9:131961804 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.480-22330G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131961804 | |||||||
| chr9:131962145 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-22671A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962145 | |||||||
| chr9:131962297 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.480-22823G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962297 | |||||||
| chr9:131962532 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0072 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.480-23058G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962532 | |||||||
| chr9:131962543 | AT | A | 79 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0075 others(76): Show |
79 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.480-23070delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962543 | |||||||
| chr9:131962543 | ATT | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
117 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.480-23071_480-2307 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962543 | |||||||
| chr9:131962958 | C | T | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-23484G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131962958 | |||||||
| chr9:131963013 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.480-23539T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963013 | |||||||
| chr9:131963048 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0128 |
2 | HG00558.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.480-23574C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963048 | |||||||
| chr9:131963281 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-23807C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963281 | |||||||
| chr9:131963415 | T | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(14): Show |
17 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.480-23941A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963415 | |||||||
| chr9:131963471 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-23997T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963471 | |||||||
| chr9:131963615 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.480-24141C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963615 | |||||||
| chr9:131963777 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-24303A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963777 | |||||||
| chr9:131963833 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.480-24359A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963833 | |||||||
| chr9:131963925 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.480-24451G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131963925 | |||||||
| chr9:131964249 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.480-24775T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964249 | |||||||
| chr9:131964326 | G | GAGGTGAT others(709): Show |
1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(720): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(640): Show |
5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(651): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(832): Show |
4 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG02647.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(843): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(724): Show |
1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(735): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(724): Show |
1 | a0001c0001t0001g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(735): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(832): Show |
1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(843): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(832): Show |
3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.480-24853_480-2485 others(843): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(829): Show |
7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(4): Show |
7 | NA18948.hp1 NA18950.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(840): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(727): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.480-24853_480-2485 others(738): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(724): Show |
45 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0098 others(42): Show |
45 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(735): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(724): Show |
1 | a0001c0001t0001g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.480-24853_480-2485 others(735): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(727): Show |
5 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG00408.hp1 HG00438.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(738): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(727): Show |
14 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(11): Show |
14 | HG00621.hp1 HG02132.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(738): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(748): Show |
1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(759): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(730): Show |
1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.480-24853_480-2485 others(741): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(718): Show |
1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(729): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(730): Show |
63 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0075 others(60): Show |
63 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(741): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GAGGTGAT others(850): Show |
1 | a0001c0001t0002g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.480-24853_480-2485 others(861): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GTGGTGCT others(667): Show |
1 | a0001c0001t0001g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.480-24853_480-2485 others(678): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964326 | G | GTGGTGCT others(712): Show |
5 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0184 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-24853_480-2485 others(723): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964326 | |||||||
| chr9:131964377 | A | ATGGTGAT others(5): Show |
1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-24915_480-2490 others(16): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964377 | |||||||
| chr9:131964394 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.480-24920C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964394 | |||||||
| chr9:131964593 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-25119A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964593 | |||||||
| chr9:131964854 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-25380G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131964854 | |||||||
| chr9:131965225 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-25751G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965225 | |||||||
| chr9:131965305 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-25831C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965305 | |||||||
| chr9:131965307 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.480-25833C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965307 | |||||||
| chr9:131965714 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.480-26240C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965714 | |||||||
| chr9:131965756 | A | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG02647.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-26282T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965756 | |||||||
| chr9:131965940 | T | C | 4 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-26466A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131965940 | |||||||
| chr9:131966016 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.480-26542G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966016 | |||||||
| chr9:131966094 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480-26620C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966094 | |||||||
| chr9:131966103 | C | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG01099.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.480-26629G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966103 | |||||||
| chr9:131966199 | T | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01258.hp1 HG01261.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-26725A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966199 | |||||||
| chr9:131966199 | T | TA | 17 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0001g0170 others(14): Show |
17 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.480-26726dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966199 | |||||||
| chr9:131966199 | T | TAA | 54 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0104 others(51): Show |
54 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.480-26727_480-2672 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966199 | |||||||
| chr9:131966216 | C | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.480-26742G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966216 | |||||||
| chr9:131966221 | C | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.480-26747G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966221 | |||||||
| chr9:131966221 | C | CAAAACCA | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.480-26754_480-2674 others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966221 | |||||||
| chr9:131966326 | G | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0002g0091 |
3 | HG02622.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.480-26852C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966326 | |||||||
| chr9:131966383 | C | CA | 10 | a0001c0001t0001g0101 a0001c0001t0001g0114 a0001c0001t0001g0115 others(7): Show |
10 | HG00609.hp1 NA18951.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-26910dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00140.hp1 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.480-26915_480-2691 others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(3): Show |
6 | HG01258.hp1 HG01261.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-26916_480-2691 others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0176 a0001c0001t0001g0178 others(2): Show |
5 | HG00639.hp1 HG01261.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-26919_480-2691 others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0175 a0001c0001t0001g0177 others(3): Show |
6 | HG00735.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-26920_480-2691 others(15): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0148 others(1): Show |
4 | HG01109.hp1 HG03209.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-26921_480-2691 others(16): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(6): Show |
30 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0139 others(27): Show |
30 | HG00558.hp1 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.480-26922_480-2691 others(17): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(7): Show |
42 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0082 others(39): Show |
42 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.480-26923_480-2691 others(18): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0086 others(6): Show |
9 | HG00738.hp1 HG01255.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-26924_480-2691 others(19): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0261 |
2 | HG02622.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.480-26925_480-2691 others(20): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.480-26926_480-2691 others(21): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(12): Show |
9 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
9 | HG00735.hp1 HG00738.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(23): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(13): Show |
8 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0067 others(5): Show |
8 | HG00544.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(24): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(14): Show |
9 | a0001c0001t0001g0066 a0001c0001t0001g0137 a0001c0001t0001g0191 others(6): Show |
9 | HG00621.hp1 HG02132.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(25): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0222 others(1): Show |
4 | HG01346.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(26): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(16): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0157 others(3): Show |
6 | HG01175.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(27): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(17): Show |
15 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG01081.hp1 HG01361.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(28): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(18): Show |
7 | a0001c0001t0001g0037 a0001c0001t0001g0142 a0001c0001t0001g0170 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(29): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(19): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(8): Show |
12 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(30): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(20): Show |
5 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0103 others(2): Show |
5 | HG01346.hp1 HG01981.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(31): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(21): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0210 others(2): Show |
5 | HG00438.hp1 HG02165.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(32): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(22): Show |
4 | a0001c0001t0001g0201 a0001c0001t0001g0209 a0001c0001t0001g0234 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(33): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(23): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0247 a0001c0001t0001g0269 |
3 | HG00609.hp2 HG01099.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.480-26910_480-2690 others(34): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(24): Show |
10 | a0001c0001t0001g0055 a0001c0001t0001g0182 a0001c0001t0001g0216 others(7): Show |
10 | HG01255.hp1 HG02559.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(35): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(25): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG00741.hp1 HG01496.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-26910_480-2690 others(36): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(28): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0049 |
2 | HG02135.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.480-26910_480-2690 others(39): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0054 |
2 | HG00408.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.480-26910_480-2690 others(40): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(41): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.480-26910_480-2690 others(43): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0019 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(45): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0215 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(47): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(37): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0214 |
2 | HG03453.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.480-26910_480-2690 others(48): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(39): Show |
1 | a0001c0001t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(50): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(42): Show |
1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(53): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CAAAAAAA others(43): Show |
1 | a0001c0001t0001g0213 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.480-26910_480-2690 others(54): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CACAAAAA others(23): Show |
1 | a0001c0001t0001g0065 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(34): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966383 | C | CACAAAAA others(24): Show |
1 | a0002c0002t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.480-26910_480-2690 others(35): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966383 | |||||||
| chr9:131966430 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.480-26956C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966430 | |||||||
| chr9:131966734 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-27260C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966734 | |||||||
| chr9:131966884 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480-27410C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966884 | |||||||
| chr9:131966954 | T | A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-27480A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131966954 | |||||||
| chr9:131967030 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-27556C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967030 | |||||||
| chr9:131967124 | T | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.480-27650A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967124 | |||||||
| chr9:131967259 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.480-27785G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967259 | |||||||
| chr9:131967485 | C | CT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0169 others(15): Show |
18 | HG00621.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.480-28012dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967485 | |||||||
| chr9:131967485 | CT | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0233 others(3): Show |
6 | HG02523.hp2 HG02735.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-28012delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967485 | |||||||
| chr9:131967486 | T | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG02647.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-28012A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967486 | |||||||
| chr9:131967487 | T | A | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480-28013A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967487 | |||||||
| chr9:131967818 | A | AT | 66 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0075 others(63): Show |
66 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.480-28345dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967818 | |||||||
| chr9:131967818 | AT | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0170 others(3): Show |
6 | HG00609.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-28345delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967818 | |||||||
| chr9:131967839 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480-28365C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967839 | |||||||
| chr9:131967974 | T | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0101 a0001c0001t0001g0109 others(6): Show |
9 | HG02080.hp2 HG02129.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-28500A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131967974 | |||||||
| chr9:131968220 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.480-28746G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968220 | |||||||
| chr9:131968226 | A | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01891.hp1 HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.480-28752T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968226 | |||||||
| chr9:131968265 | G | A | 5 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG02647.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-28791C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968265 | |||||||
| chr9:131968447 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-28973G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968447 | |||||||
| chr9:131968463 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.480-28989G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968463 | |||||||
| chr9:131968471 | CA | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(64): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.480-28998delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968471 | |||||||
| chr9:131968471 | CAA | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(103): Show |
107 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.480-28999_480-2899 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968471 | |||||||
| chr9:131968471 | CAAA | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
65 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.480-29000_480-2899 others(7): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968471 | |||||||
| chr9:131968471 | CAAAA | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0093 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.480-29001_480-2899 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968471 | |||||||
| chr9:131968496 | C | T | 10 | a0001c0001t0001g0070 a0001c0001t0001g0257 a0001c0001t0001g0259 others(7): Show |
10 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-29022G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968496 | |||||||
| chr9:131968802 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-29328C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968802 | |||||||
| chr9:131968884 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.480-29410G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968884 | |||||||
| chr9:131968885 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.480-29411C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968885 | |||||||
| chr9:131968959 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.480-29485A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131968959 | |||||||
| chr9:131969127 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-29653C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969127 | |||||||
| chr9:131969137 | C | T | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-29663G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969137 | |||||||
| chr9:131969138 | G | A | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0155 others(1): Show |
4 | HG02148.hp1 HG02273.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-29664C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969138 | |||||||
| chr9:131969207 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.480-29733C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969207 | |||||||
| chr9:131969218 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480-29744C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969218 | |||||||
| chr9:131969452 | G | A | 51 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0001g0139 others(48): Show |
51 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.480-29978C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969452 | |||||||
| chr9:131969482 | CT | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0079 a0001c0001t0001g0080 others(21): Show |
24 | HG01081.hp1 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.480-30009delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969482 | |||||||
| chr9:131969501 | G | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0209 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.480-30027C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969501 | |||||||
| chr9:131969606 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.480-30132C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969606 | |||||||
| chr9:131969731 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG02647.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480-30257G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969731 | |||||||
| chr9:131969969 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(67): Show |
71 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.480-30495C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131969969 | |||||||
| chr9:131970282 | C | A | 25 | a0001c0001t0001g0088 a0001c0001t0001g0219 a0001c0001t0001g0228 others(22): Show |
25 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.480-30808G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970282 | |||||||
| chr9:131970359 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.480-30885C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970359 | |||||||
| chr9:131970441 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480-30967G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970441 | |||||||
| chr9:131970543 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.480-31069G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970543 | |||||||
| chr9:131970608 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.480-31134C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970608 | |||||||
| chr9:131970641 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480-31167C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970641 | |||||||
| chr9:131970665 | C | T | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-31191G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970665 | |||||||
| chr9:131970984 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.480-31510T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131970984 | |||||||
| chr9:131971140 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.480-31666A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971140 | |||||||
| chr9:131971340 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.480-31866C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971340 | |||||||
| chr9:131971363 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.480-31889C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971363 | |||||||
| chr9:131971498 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-32024T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971498 | |||||||
| chr9:131971503 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.480-32029C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971503 | |||||||
| chr9:131971581 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-32107C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971581 | |||||||
| chr9:131971658 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480-32184C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971658 | |||||||
| chr9:131971709 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.480-32235T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971709 | |||||||
| chr9:131971903 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.480-32429C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131971903 | |||||||
| chr9:131972232 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-32758G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131972232 | |||||||
| chr9:131972244 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.480-32770A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131972244 | |||||||
| chr9:131972548 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480-33074G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131972548 | |||||||
| chr9:131972739 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-33265C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131972739 | |||||||
| chr9:131973428 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-33954G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973428 | |||||||
| chr9:131973457 | C | CT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(132): Show |
136 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.480-33984dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973457 | |||||||
| chr9:131973457 | C | CTT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0072 others(5): Show |
8 | HG01255.hp1 HG02622.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.480-33985_480-3398 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973457 | |||||||
| chr9:131973460 | T | TTC | 16 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.480-33987_480-3398 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973460 | |||||||
| chr9:131973482 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-34008T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973482 | |||||||
| chr9:131973519 | G | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
66 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.480-34045C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973519 | |||||||
| chr9:131973521 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.480-34047C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973521 | |||||||
| chr9:131973578 | T | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.480-34104A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973578 | |||||||
| chr9:131973612 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.480-34138G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973612 | |||||||
| chr9:131973626 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.480-34152G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973626 | |||||||
| chr9:131973650 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.480-34176C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973650 | |||||||
| chr9:131973867 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
156 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.480-34393C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973867 | |||||||
| chr9:131973873 | G | C | 29 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0219 others(26): Show |
29 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.480-34399C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973873 | |||||||
| chr9:131973883 | A | AT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.480-34410dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973883 | |||||||
| chr9:131973883 | AT | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0222 others(7): Show |
10 | HG02486.hp2 HG02976.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-34410delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973883 | |||||||
| chr9:131973919 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0182 others(4): Show |
7 | HG01943.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-34445A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131973919 | |||||||
| chr9:131974004 | T | C | 10 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(7): Show |
10 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.480-34530A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974004 | |||||||
| chr9:131974005 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-34531C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974005 | |||||||
| chr9:131974233 | T | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.480-34759A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974233 | |||||||
| chr9:131974359 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.480-34885A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974359 | |||||||
| chr9:131974453 | T | C | 6 | a0001c0001t0001g0124 a0001c0001t0002g0092 a0001c0001t0002g0123 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-34979A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974453 | |||||||
| chr9:131974465 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.480-34991T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974465 | |||||||
| chr9:131974473 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.480-34999A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974473 | |||||||
| chr9:131974506 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-35032A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974506 | |||||||
| chr9:131974615 | C | A | 40 | a0001c0001t0001g0075 a0001c0001t0001g0124 a0001c0001t0001g0148 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.480-35141G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974615 | |||||||
| chr9:131974866 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480-35392G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974866 | |||||||
| chr9:131974924 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.480-35450A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131974924 | |||||||
| chr9:131975212 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.480-35738G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975212 | |||||||
| chr9:131975255 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.480-35781T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975255 | |||||||
| chr9:131975259 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.480-35785A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975259 | |||||||
| chr9:131975264 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.480-35790T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975264 | |||||||
| chr9:131975385 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480-35911G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975385 | |||||||
| chr9:131975787 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | NA18956.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.480-36313T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975787 | |||||||
| chr9:131975972 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.480-36498C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131975972 | |||||||
| chr9:131976077 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01943.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.480-36603C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131976077 | |||||||
| chr9:131976176 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.480-36702C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131976176 | |||||||
| chr9:131976237 | G | A | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
5 | NA18948.hp1 NA18961.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.480-36763C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131976237 | |||||||
| chr9:131976257 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG01099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.480-36783G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131976257 | |||||||
| chr9:131976941 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.479+37396G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131976941 | |||||||
| chr9:131977143 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.479+37194C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977143 | |||||||
| chr9:131977160 | C | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+37177G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977160 | |||||||
| chr9:131977223 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+37114G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977223 | |||||||
| chr9:131977512 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.479+36825G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977512 | |||||||
| chr9:131977552 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.479+36785C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977552 | |||||||
| chr9:131977599 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+36738G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977599 | |||||||
| chr9:131977705 | C | T | 13 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
13 | HG01081.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+36632G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977705 | |||||||
| chr9:131977865 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.479+36472G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131977865 | |||||||
| chr9:131978028 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.479+36309G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978028 | |||||||
| chr9:131978150 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+36187A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978150 | |||||||
| chr9:131978297 | T | C | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+36040A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978297 | |||||||
| chr9:131978317 | A | T | 4 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+36020T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978317 | |||||||
| chr9:131978419 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.479+35918T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978419 | |||||||
| chr9:131978532 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.479+35805A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978532 | |||||||
| chr9:131978689 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.479+35648T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978689 | |||||||
| chr9:131978743 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+35594A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978743 | |||||||
| chr9:131978893 | T | C | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+35444A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131978893 | |||||||
| chr9:131979019 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+35318A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979019 | |||||||
| chr9:131979030 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479+35307T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979030 | |||||||
| chr9:131979047 | T | C | 20 | a0001c0001t0001g0070 a0001c0001t0001g0223 a0001c0001t0001g0224 others(17): Show |
20 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.479+35290A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979047 | |||||||
| chr9:131979112 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG02040.hp1 NA18966.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+35225A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979112 | |||||||
| chr9:131979130 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479+35207G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979130 | |||||||
| chr9:131979156 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.479+35181G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979156 | |||||||
| chr9:131979483 | CA | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.479+34853delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979483 | |||||||
| chr9:131979483 | CAA | C | 104 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(101): Show |
104 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.479+34852_479+3485 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979483 | |||||||
| chr9:131979483 | CAAA | C | 86 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(83): Show |
86 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.479+34851_479+3485 others(7): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979483 | |||||||
| chr9:131979483 | CAAAA | C | 7 | a0001c0001t0001g0104 a0001c0001t0001g0147 a0001c0001t0001g0185 others(4): Show |
7 | HG01358.hp1 HG01361.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+34850_479+3485 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979483 | |||||||
| chr9:131979798 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.479+34539G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979798 | |||||||
| chr9:131979831 | A | ATGGC | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
165 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.479+34502_479+3450 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979831 | |||||||
| chr9:131979831 | A | ATGGCTGG others(5): Show |
65 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(62): Show |
65 | HG00140.hp2 HG00609.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.479+34494_479+3450 others(16): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979831 | |||||||
| chr9:131979831 | A | ATGGCTGG others(9): Show |
6 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+34490_479+3450 others(20): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979831 | |||||||
| chr9:131979831 | A | ATGGCTGG others(13): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(5): Show |
8 | HG00621.hp1 HG02132.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+34486_479+3450 others(24): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979831 | |||||||
| chr9:131979831 | A | ATGGCTGG others(17): Show |
1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.479+34482_479+3450 others(28): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979831 | |||||||
| chr9:131979887 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.479+34450A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131979887 | |||||||
| chr9:131980207 | T | G | 93 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0075 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.479+34130A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980207 | |||||||
| chr9:131980361 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+33976A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980361 | |||||||
| chr9:131980502 | T | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(12): Show |
15 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.479+33835A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980502 | |||||||
| chr9:131980532 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.479+33805G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980532 | |||||||
| chr9:131980624 | A | C | 6 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG02647.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+33713T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980624 | |||||||
| chr9:131980838 | C | T | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+33499G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980838 | |||||||
| chr9:131980859 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+33478A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980859 | |||||||
| chr9:131980908 | T | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.479+33429A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980908 | |||||||
| chr9:131980920 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.479+33417T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131980920 | |||||||
| chr9:131981013 | A | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0169 others(16): Show |
19 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.479+33324T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981013 | |||||||
| chr9:131981106 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.479+33231G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981106 | |||||||
| chr9:131981189 | A | C | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+33148T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981189 | |||||||
| chr9:131981374 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.479+32963G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981374 | |||||||
| chr9:131981409 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+32928C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981409 | |||||||
| chr9:131981584 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.479+32753C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981584 | |||||||
| chr9:131981594 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.479+32743C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981594 | |||||||
| chr9:131981669 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479+32668C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981669 | |||||||
| chr9:131981730 | C | G | 4 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+32607G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981730 | |||||||
| chr9:131981777 | G | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.479+32560C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131981777 | |||||||
| chr9:131982084 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.479+32253G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131982084 | |||||||
| chr9:131982319 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.479+32018G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131982319 | |||||||
| chr9:131982710 | A | G | 105 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+31627T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131982710 | |||||||
| chr9:131982797 | A | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.479+31540T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131982797 | |||||||
| chr9:131982982 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.479+31355G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131982982 | |||||||
| chr9:131983095 | C | T | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.479+31242G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983095 | |||||||
| chr9:131983127 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.479+31210C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983127 | |||||||
| chr9:131983468 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+30869A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983468 | |||||||
| chr9:131983596 | C | A | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+30741G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983596 | |||||||
| chr9:131983780 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.479+30557C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983780 | |||||||
| chr9:131984019 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+30318G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984019 | |||||||
| chr9:131984057 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0071 others(1): Show |
4 | HG02040.hp2 NA18956.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+30280G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984057 | |||||||
| chr9:131984122 | C | G | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+30215G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984122 | |||||||
| chr9:131984578 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.479+29759C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984578 | |||||||
| chr9:131984791 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG03139.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.479+29546T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984791 | |||||||
| chr9:131984890 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+29447T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131984890 | |||||||
| chr9:131985050 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.479+29287A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131985050 | |||||||
| chr9:131985696 | TG | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(12): Show |
15 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.479+28640delC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131985696 | |||||||
| chr9:131985714 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+28623A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131985714 | |||||||
| chr9:131985792 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+28545C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131985792 | |||||||
| chr9:131986388 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.479+27949C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986388 | |||||||
| chr9:131986433 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+27904A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986433 | |||||||
| chr9:131986500 | C | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(262): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.479+27837G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986500 | |||||||
| chr9:131986669 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.479+27668G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986669 | |||||||
| chr9:131986974 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.479+27363G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986974 | |||||||
| chr9:131986999 | A | AT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
112 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.479+27337dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | A | ATT | 27 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0031 others(24): Show |
27 | HG00558.hp1 HG00741.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.479+27336_479+2733 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | A | ATTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0058 others(3): Show |
6 | HG01433.hp1 HG02132.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+27335_479+2733 others(7): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | AT | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0085 others(13): Show |
16 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+27337delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | ATT | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0017 others(19): Show |
22 | HG00621.hp1 HG00639.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.479+27336_479+2733 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.479+27327_479+2733 others(15): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131986999 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.479+27322_479+2733 others(20): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | |||||||
| chr9:131987007 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+27330A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987007 | |||||||
| chr9:131987116 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.479+27221G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987116 | |||||||
| chr9:131987123 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.479+27214C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987123 | |||||||
| chr9:131987339 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+26998A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987339 | |||||||
| chr9:131987352 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.479+26985C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987352 | |||||||
| chr9:131987429 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.479+26908C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987429 | |||||||
| chr9:131987593 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.479+26744A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987593 | |||||||
| chr9:131987801 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+26536T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987801 | |||||||
| chr9:131987895 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+26442C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987895 | |||||||
| chr9:131987997 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.479+26340T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131987997 | |||||||
| chr9:131988066 | T | C | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.479+26271A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988066 | |||||||
| chr9:131988153 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.479+26184A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988153 | |||||||
| chr9:131988364 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.479+25973T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988364 | |||||||
| chr9:131988732 | C | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.479+25605G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988732 | |||||||
| chr9:131988796 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.479+25541A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988796 | |||||||
| chr9:131988886 | GC | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(225): Show |
229 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.479+25450delG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988886 | |||||||
| chr9:131988995 | T | C | 103 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(100): Show |
103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+25342A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988995 | |||||||
| chr9:131989215 | T | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+25122A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989215 | |||||||
| chr9:131989394 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.479+24943G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989394 | |||||||
| chr9:131989575 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.479+24762A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989575 | |||||||
| chr9:131989628 | G | A | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+24709C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989628 | |||||||
| chr9:131989645 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+24692A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989645 | |||||||
| chr9:131989646 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+24691A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989646 | |||||||
| chr9:131989664 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.479+24673C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989664 | |||||||
| chr9:131989986 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.479+24351C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131989986 | |||||||
| chr9:131990194 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0003 |
2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.479+24143C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990194 | |||||||
| chr9:131990196 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.479+24141C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990196 | |||||||
| chr9:131990416 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.479+23921G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990416 | |||||||
| chr9:131990427 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.479+23910G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990427 | |||||||
| chr9:131990428 | A | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.479+23909T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990428 | |||||||
| chr9:131990504 | G | A | 100 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(97): Show |
100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.479+23833C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990504 | |||||||
| chr9:131990569 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00609.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.479+23768C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990569 | |||||||
| chr9:131990605 | G | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.479+23732C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990605 | |||||||
| chr9:131990784 | C | T | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+23553G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990784 | |||||||
| chr9:131990802 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479+23535G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990802 | |||||||
| chr9:131990884 | C | T | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(146): Show |
149 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.479+23453G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990884 | |||||||
| chr9:131990960 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.479+23377T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990960 | |||||||
| chr9:131990961 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.479+23376C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990961 | |||||||
| chr9:131990967 | G | A | 128 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(125): Show |
128 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.479+23370C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990967 | |||||||
| chr9:131991196 | C | CA | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+23140dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991196 | |||||||
| chr9:131991261 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.479+23076G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991261 | |||||||
| chr9:131991407 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.479+22930T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991407 | |||||||
| chr9:131991545 | C | A | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+22792G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991545 | |||||||
| chr9:131991658 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02451.hp1 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.479+22679C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991658 | |||||||
| chr9:131991802 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.479+22535T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991802 | |||||||
| chr9:131991825 | G | A | 25 | a0001c0001t0001g0088 a0001c0001t0001g0219 a0001c0001t0001g0228 others(22): Show |
25 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.479+22512C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991825 | |||||||
| chr9:131991834 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+22503C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991834 | |||||||
| chr9:131991956 | C | T | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+22381G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131991956 | |||||||
| chr9:131992111 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.479+22226G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992111 | |||||||
| chr9:131992112 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.479+22225T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992112 | |||||||
| chr9:131992243 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.479+22094T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992243 | |||||||
| chr9:131992266 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+22071C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992266 | |||||||
| chr9:131992353 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.479+21984G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992353 | |||||||
| chr9:131992577 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479+21760A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992577 | |||||||
| chr9:131992698 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.479+21639C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131992698 | |||||||
| chr9:131993001 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.479+21336T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993001 | |||||||
| chr9:131993030 | G | T | 117 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(114): Show |
117 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.479+21307C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993030 | |||||||
| chr9:131993047 | C | T | 3 | a0001c0001t0002g0074 a0001c0001t0002g0125 a0001c0001t0002g0143 |
3 | HG00438.hp2 HG01496.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.479+21290G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993047 | |||||||
| chr9:131993189 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.479+21148A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993189 | |||||||
| chr9:131993230 | GT | G | 109 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0072 others(106): Show |
109 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.479+21106delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993230 | |||||||
| chr9:131993242 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+21095A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993242 | |||||||
| chr9:131993243 | T | A | 131 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(128): Show |
131 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.479+21094A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993243 | |||||||
| chr9:131993243 | T | TA | 5 | a0001c0001t0001g0048 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.479+21093dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993243 | |||||||
| chr9:131993244 | A | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(11): Show |
14 | HG00738.hp2 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.479+21093T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993244 | |||||||
| chr9:131993478 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.479+20859A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993478 | |||||||
| chr9:131993619 | G | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(8): Show |
11 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+20718C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993619 | |||||||
| chr9:131993631 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.479+20706T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993631 | |||||||
| chr9:131993825 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.479+20512G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993825 | |||||||
| chr9:131993827 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.479+20510A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993827 | |||||||
| chr9:131993919 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.479+20418C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993919 | |||||||
| chr9:131993939 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+20398C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131993939 | |||||||
| chr9:131994191 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479+20146G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994191 | |||||||
| chr9:131994219 | C | A | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.479+20118G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994219 | |||||||
| chr9:131994219 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.479+20118G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994219 | |||||||
| chr9:131994239 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.479+20098G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994239 | |||||||
| chr9:131994363 | T | TCTGCACT others(19): Show |
1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+19948_479+1997 others(30): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994363 | |||||||
| chr9:131994773 | C | A | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.479+19564G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994773 | |||||||
| chr9:131994860 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.479+19477G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994860 | |||||||
| chr9:131994924 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.479+19413C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131994924 | |||||||
| chr9:131995368 | T | G | 93 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.479+18969A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131995368 | |||||||
| chr9:131995922 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.479+18415T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131995922 | |||||||
| chr9:131996160 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+18177A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996160 | |||||||
| chr9:131996192 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.479+18145C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996192 | |||||||
| chr9:131996332 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.479+18005G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996332 | |||||||
| chr9:131996365 | A | G | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.479+17972T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996365 | |||||||
| chr9:131996382 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.479+17955G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996382 | |||||||
| chr9:131996383 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.479+17954C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996383 | |||||||
| chr9:131996566 | G | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+17771C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131996566 | |||||||
| chr9:131997016 | A | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+17321T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997016 | |||||||
| chr9:131997075 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.479+17262A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997075 | |||||||
| chr9:131997088 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0190 a0001c0001t0002g0186 others(3): Show |
6 | HG02735.hp2 HG03704.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+17249A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997088 | |||||||
| chr9:131997347 | G | A | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(8): Show |
11 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+16990C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997347 | |||||||
| chr9:131997472 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+16865T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997472 | |||||||
| chr9:131997521 | C | T | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+16816G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997521 | |||||||
| chr9:131997529 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
80 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.479+16808C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997529 | |||||||
| chr9:131997658 | C | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0169 others(13): Show |
16 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+16679G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997658 | |||||||
| chr9:131997685 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479+16652A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997685 | |||||||
| chr9:131997803 | C | T | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.479+16534G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997803 | |||||||
| chr9:131997874 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.479+16463G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131997874 | |||||||
| chr9:131998093 | G | A | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+16244C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998093 | |||||||
| chr9:131998142 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+16195C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998142 | |||||||
| chr9:131998252 | T | TA | 11 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(8): Show |
11 | HG00558.hp2 HG02080.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.479+16084dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998252 | |||||||
| chr9:131998282 | CT | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0169 others(13): Show |
16 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+16054delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998282 | |||||||
| chr9:131998441 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.479+15896G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998441 | |||||||
| chr9:131998454 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+15883G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998454 | |||||||
| chr9:131998496 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+15841A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998496 | |||||||
| chr9:131998531 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+15806G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998531 | |||||||
| chr9:131998532 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479+15805C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998532 | |||||||
| chr9:131998540 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0169 others(17): Show |
20 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.479+15797A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998540 | |||||||
| chr9:131998615 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0157 a0001c0001t0001g0185 others(1): Show |
4 | HG01361.hp2 HG01981.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+15722G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998615 | |||||||
| chr9:131998770 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479+15567A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998770 | |||||||
| chr9:131998995 | T | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG03139.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.479+15342A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131998995 | |||||||
| chr9:131999256 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.479+15081T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131999256 | |||||||
| chr9:131999278 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+15059A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131999278 | |||||||
| chr9:131999418 | C | T | 101 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(98): Show |
101 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.479+14919G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131999418 | |||||||
| chr9:131999666 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.479+14671G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131999666 | |||||||
| chr9:132000036 | G | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0188 |
2 | HG00621.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.479+14301C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000036 | |||||||
| chr9:132000063 | C | CTCAAAAG others(15): Show |
2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.479+14252_479+1427 others(26): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000063 | |||||||
| chr9:132000063 | CTCAAAAG others(15): Show |
C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.479+14252_479+1427 others(26): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000063 | |||||||
| chr9:132000063 | CTCAAAAG others(37): Show |
C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0078 a0002c0002t0001g0273 |
3 | HG03453.hp2 NA19067.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.479+14230_479+1427 others(48): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000063 | |||||||
| chr9:132000275 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.479+14062G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000275 | |||||||
| chr9:132000381 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.479+13956C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000381 | |||||||
| chr9:132000423 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.479+13914G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000423 | |||||||
| chr9:132000702 | T | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+13635A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000702 | |||||||
| chr9:132000743 | T | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0002g0099 others(1): Show |
4 | HG00140.hp1 HG01123.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+13594A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000743 | |||||||
| chr9:132000752 | A | AT | 7 | a0001c0001t0001g0063 a0001c0001t0001g0181 a0001c0001t0001g0201 others(4): Show |
7 | HG00609.hp2 HG02559.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.479+13584dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000752 | |||||||
| chr9:132000752 | AT | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0199 others(2): Show |
5 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.479+13584delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000752 | |||||||
| chr9:132000753 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+13584A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132000753 | |||||||
| chr9:132001553 | A | G | 103 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(100): Show |
103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+12784T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132001553 | |||||||
| chr9:132001612 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+12725A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132001612 | |||||||
| chr9:132001891 | T | C | 115 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(112): Show |
115 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.479+12446A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132001891 | |||||||
| chr9:132001917 | CT | C | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG02040.hp1 NA18966.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+12419delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132001917 | |||||||
| chr9:132002145 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.479+12192G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002145 | |||||||
| chr9:132002156 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+12181C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002156 | |||||||
| chr9:132002161 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.479+12176A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002161 | |||||||
| chr9:132002200 | C | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+12137G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002200 | |||||||
| chr9:132002225 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00438.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.479+12112A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002225 | |||||||
| chr9:132002265 | T | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+12072A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002265 | |||||||
| chr9:132002422 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.479+11915C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002422 | |||||||
| chr9:132002485 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+11852A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002485 | |||||||
| chr9:132002669 | T | G | 9 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0260 others(6): Show |
9 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.479+11668A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002669 | |||||||
| chr9:132002687 | G | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0043 others(8): Show |
12 | HG00639.hp2 HG00741.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.479+11650C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002687 | |||||||
| chr9:132002736 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02572.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.479+11601T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002736 | |||||||
| chr9:132002786 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.479+11551T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002786 | |||||||
| chr9:132002829 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.479+11508G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002829 | |||||||
| chr9:132002909 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479+11428T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002909 | |||||||
| chr9:132002918 | C | CAAAAAA | 84 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(81): Show |
84 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.479+11413_479+1141 others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002918 | |||||||
| chr9:132002918 | C | CAAAAAAA | 13 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0103 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.479+11412_479+1141 others(11): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002918 | |||||||
| chr9:132002929 | G | A | 122 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
122 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.479+11408C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002929 | |||||||
| chr9:132003050 | G | A | 122 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0072 others(119): Show |
122 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.479+11287C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003050 | |||||||
| chr9:132003092 | TA | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(5): Show |
8 | HG01943.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+11244delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003092 | |||||||
| chr9:132003289 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.479+11048C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003289 | |||||||
| chr9:132003361 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.479+10976A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003361 | |||||||
| chr9:132003433 | G | A | 93 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.479+10904C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003433 | |||||||
| chr9:132003618 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+10719A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003618 | |||||||
| chr9:132003969 | T | TAC | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.479+10366_479+1036 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132003969 | |||||||
| chr9:132004090 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0053 |
2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.479+10247C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004090 | |||||||
| chr9:132004103 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.479+10234C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004103 | |||||||
| chr9:132004275 | A | G | 7 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.479+10062T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004275 | |||||||
| chr9:132004409 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.479+9928T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004409 | |||||||
| chr9:132004566 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.479+9771G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004566 | |||||||
| chr9:132004571 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.479+9766C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004571 | |||||||
| chr9:132004803 | G | A | 120 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
120 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.479+9534C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004803 | |||||||
| chr9:132004864 | A | C | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.479+9473T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132004864 | |||||||
| chr9:132005018 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+9319T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005018 | |||||||
| chr9:132005188 | G | C | 95 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.479+9149C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005188 | |||||||
| chr9:132005805 | A | T | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.479+8532T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005805 | |||||||
| chr9:132005903 | G | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.479+8434C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005903 | |||||||
| chr9:132006041 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479+8296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006041 | |||||||
| chr9:132006056 | C | A | 117 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(114): Show |
117 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.479+8281G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006056 | |||||||
| chr9:132006200 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.479+8137C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006200 | |||||||
| chr9:132006284 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.479+8053G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006284 | |||||||
| chr9:132006410 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+7927A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006410 | |||||||
| chr9:132006621 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.479+7716G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006621 | |||||||
| chr9:132006655 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.479+7682T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006655 | |||||||
| chr9:132006672 | A | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(17): Show |
20 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.479+7665T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006672 | |||||||
| chr9:132006728 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.479+7609C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006728 | |||||||
| chr9:132006796 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.479+7541G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006796 | |||||||
| chr9:132006807 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+7530G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006807 | |||||||
| chr9:132006833 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.479+7504G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006833 | |||||||
| chr9:132006898 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(3): Show |
6 | HG01943.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+7439A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132006898 | |||||||
| chr9:132007236 | G | A | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+7101C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132007236 | |||||||
| chr9:132007396 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0003 |
2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.479+6941A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132007396 | |||||||
| chr9:132007429 | T | A | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.479+6908A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132007429 | |||||||
| chr9:132007513 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+6824A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132007513 | |||||||
| chr9:132007971 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01884.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.479+6366A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132007971 | |||||||
| chr9:132008032 | C | A | 120 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(117): Show |
120 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.479+6305G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008032 | |||||||
| chr9:132008098 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.479+6239A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008098 | |||||||
| chr9:132008235 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.479+6102G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008235 | |||||||
| chr9:132008263 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.479+6074A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008263 | |||||||
| chr9:132008282 | T | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+6055A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008282 | |||||||
| chr9:132008329 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.479+6008G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008329 | |||||||
| chr9:132008385 | A | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.479+5952T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008385 | |||||||
| chr9:132008402 | G | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | NA18942.hp1 NA18950.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.479+5935C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008402 | |||||||
| chr9:132008496 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+5841A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008496 | |||||||
| chr9:132008581 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.479+5756C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008581 | |||||||
| chr9:132008667 | C | T | 103 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(100): Show |
103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+5670G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008667 | |||||||
| chr9:132008718 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.479+5619G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008718 | |||||||
| chr9:132008864 | T | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.479+5473A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132008864 | |||||||
| chr9:132009114 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.479+5223G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009114 | |||||||
| chr9:132009274 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0169 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+5063G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009274 | |||||||
| chr9:132009414 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(3): Show |
6 | HG01943.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.479+4923G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009414 | |||||||
| chr9:132009552 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(11): Show |
14 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.479+4785C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009552 | |||||||
| chr9:132009576 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.479+4761C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009576 | |||||||
| chr9:132009679 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.479+4658G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009679 | |||||||
| chr9:132009883 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.479+4454C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132009883 | |||||||
| chr9:132010145 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(5): Show |
8 | HG00735.hp1 HG01175.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.479+4192G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010145 | |||||||
| chr9:132010364 | T | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.479+3973A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010364 | |||||||
| chr9:132010407 | A | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0056 |
3 | HG00544.hp2 NA18964.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.479+3930T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010407 | |||||||
| chr9:132010594 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.479+3743C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010594 | |||||||
| chr9:132010688 | A | G | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(4): Show |
7 | NA18948.hp1 NA18950.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+3649T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010688 | |||||||
| chr9:132010838 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.479+3499G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010838 | |||||||
| chr9:132010896 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479+3441C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132010896 | |||||||
| chr9:132011103 | T | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.479+3234A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011103 | |||||||
| chr9:132011188 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.479+3149A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011188 | |||||||
| chr9:132011281 | GAA | G | 10 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0159 others(7): Show |
10 | HG01169.hp1 HG01255.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.479+3054_479+3055d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011281 | |||||||
| chr9:132011450 | A | G | 129 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(126): Show |
129 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.479+2887T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011450 | |||||||
| chr9:132011487 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+2850C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011487 | |||||||
| chr9:132011513 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479+2824C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011513 | |||||||
| chr9:132011588 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.479+2749C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011588 | |||||||
| chr9:132011829 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.479+2508G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011829 | |||||||
| chr9:132011945 | C | A | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(8): Show |
11 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.479+2392G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011945 | |||||||
| chr9:132011949 | CTT | C | 117 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(114): Show |
117 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.479+2386_479+2387d others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132011949 | |||||||
| chr9:132012111 | G | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.479+2226C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132012111 | |||||||
| chr9:132012667 | A | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.479+1670T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132012667 | |||||||
| chr9:132012752 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.479+1585G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132012752 | |||||||
| chr9:132012803 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.479+1534G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132012803 | |||||||
| chr9:132013618 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.479+719A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132013618 | |||||||
| chr9:132013649 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.479+688A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132013649 | |||||||
| chr9:132013818 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.479+519A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132013818 | |||||||
| chr9:132013960 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.479+377G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132013960 | |||||||
| chr9:132014004 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0169 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+333C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132014004 | |||||||
| chr9:132014211 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+126G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132014211 | |||||||
| chr9:132014219 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.479+118T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132014219 | |||||||
| chr9:132014720 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.349-253C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132014720 | |||||||
| chr9:132014722 | CCAA | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(73): Show |
77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.349-258_349-256del others(3): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132014722 | |||||||
| chr9:132014726 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.349-259G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132014726 | |||||||
| chr9:132014884 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349-417A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132014884 | |||||||
| chr9:132015043 | T | C | 98 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(95): Show |
98 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.349-576A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015043 | |||||||
| chr9:132015078 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-611G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015078 | |||||||
| chr9:132015155 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-688A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015155 | |||||||
| chr9:132015281 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-814A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015281 | |||||||
| chr9:132015447 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-980G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015447 | |||||||
| chr9:132015954 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.349-1487T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132015954 | |||||||
| chr9:132016018 | C | G | 1 | a0001c0001t0002g0258 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.349-1551G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016018 | |||||||
| chr9:132016301 | C | T | 102 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.349-1834G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016301 | |||||||
| chr9:132016477 | C | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.349-2010G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016477 | |||||||
| chr9:132016528 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.349-2061C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016528 | |||||||
| chr9:132016738 | C | T | 105 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(102): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.349-2271G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016738 | |||||||
| chr9:132016819 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.349-2352G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016819 | |||||||
| chr9:132016821 | G | C | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2354C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016821 | |||||||
| chr9:132016866 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.349-2399G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016866 | |||||||
| chr9:132017504 | T | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-3037A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017504 | |||||||
| chr9:132017530 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.349-3063C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017530 | |||||||
| chr9:132017564 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18956.hp1 NA19004.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.349-3097A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017564 | |||||||
| chr9:132017672 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0056 |
3 | HG00544.hp2 NA18964.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.349-3205G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017672 | |||||||
| chr9:132017680 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.349-3213C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017680 | |||||||
| chr9:132017883 | C | A | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-3416G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017883 | |||||||
| chr9:132017990 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01109.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.349-3523G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132017990 | |||||||
| chr9:132018014 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-3547C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018014 | |||||||
| chr9:132018154 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.349-3687T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018154 | |||||||
| chr9:132018313 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-3846A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018313 | |||||||
| chr9:132018324 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-3857G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018324 | |||||||
| chr9:132018680 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-4213G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018680 | |||||||
| chr9:132018686 | C | G | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.349-4219G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018686 | |||||||
| chr9:132018862 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.349-4395C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018862 | |||||||
| chr9:132018867 | A | T | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-4400T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018867 | |||||||
| chr9:132018904 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.349-4437A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018904 | |||||||
| chr9:132018911 | AT | A | 92 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(89): Show |
92 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.349-4445delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018911 | |||||||
| chr9:132018921 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-4454A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132018921 | |||||||
| chr9:132019041 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349-4574C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019041 | |||||||
| chr9:132019106 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.349-4639C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019106 | |||||||
| chr9:132019426 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.349-4959C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019426 | |||||||
| chr9:132019433 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.349-4966A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019433 | |||||||
| chr9:132019507 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.349-5040A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019507 | |||||||
| chr9:132019592 | A | T | 100 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(97): Show |
100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-5125T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019592 | |||||||
| chr9:132019737 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.349-5270G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132019737 | |||||||
| chr9:132020306 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.349-5839C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132020306 | |||||||
| chr9:132020653 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.349-6186A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132020653 | |||||||
| chr9:132020796 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.349-6329C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132020796 | |||||||
| chr9:132021070 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00735.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.349-6603G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021070 | |||||||
| chr9:132021419 | GATT | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(225): Show |
229 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.349-6955_349-6953d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021419 | |||||||
| chr9:132021441 | G | C | 8 | a0001c0001t0001g0072 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-6974C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021441 | |||||||
| chr9:132021500 | C | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-7033G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021500 | |||||||
| chr9:132021504 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349-7037C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021504 | |||||||
| chr9:132021806 | TAGGAAG | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(12): Show |
15 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-7345_349-7340d others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132021806 | |||||||
| chr9:132022007 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.349-7540C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132022007 | |||||||
| chr9:132022279 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | NA18950.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.349-7812A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132022279 | |||||||
| chr9:132022318 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.349-7851C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132022318 | |||||||
| chr9:132022430 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.349-7963C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132022430 | |||||||
| chr9:132022799 | A | G | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-8332T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132022799 | |||||||
| chr9:132023075 | T | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-8608A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023075 | |||||||
| chr9:132023203 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.349-8736A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023203 | |||||||
| chr9:132023210 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(12): Show |
15 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-8744dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023210 | |||||||
| chr9:132023266 | G | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-8799C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023266 | |||||||
| chr9:132023342 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.349-8875G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023342 | |||||||
| chr9:132023481 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.349-9014C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023481 | |||||||
| chr9:132023545 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.349-9078T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023545 | |||||||
| chr9:132023574 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-9107A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023574 | |||||||
| chr9:132023742 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-9275T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023742 | |||||||
| chr9:132023784 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-9317A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132023784 | |||||||
| chr9:132024110 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.349-9643A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024110 | |||||||
| chr9:132024268 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0163 |
2 | HG02523.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.349-9801G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024268 | |||||||
| chr9:132024356 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.349-9889C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024356 | |||||||
| chr9:132024557 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(247): Show |
251 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.349-10090G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024557 | |||||||
| chr9:132024660 | A | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.349-10193T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024660 | |||||||
| chr9:132024748 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349-10281C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024748 | |||||||
| chr9:132024775 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349-10308G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024775 | |||||||
| chr9:132025033 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01943.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349-10566A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025033 | |||||||
| chr9:132025048 | C | G | 1 | a0001c0001t0002g0140 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.349-10581G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025048 | |||||||
| chr9:132025182 | AT | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
221 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.349-10716delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025182 | |||||||
| chr9:132025307 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.349-10840G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025307 | |||||||
| chr9:132025401 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-10934G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025401 | |||||||
| chr9:132025472 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0250 others(1): Show |
4 | HG02257.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-11005C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025472 | |||||||
| chr9:132025489 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-11022T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025489 | |||||||
| chr9:132025551 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-11084T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025551 | |||||||
| chr9:132025603 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.349-11136A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025603 | |||||||
| chr9:132025756 | T | A | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.349-11289A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025756 | |||||||
| chr9:132025786 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349-11319G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025786 | |||||||
| chr9:132025794 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.349-11327A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025794 | |||||||
| chr9:132025837 | G | A | 95 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.349-11370C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025837 | |||||||
| chr9:132025994 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.349-11527T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025994 | |||||||
| chr9:132026142 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.349-11675G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026142 | |||||||
| chr9:132026514 | T | C | 96 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(93): Show |
96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.349-12047A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026514 | |||||||
| chr9:132026768 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-12301G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026768 | |||||||
| chr9:132026785 | A | T | 109 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(106): Show |
109 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.349-12318T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026785 | |||||||
| chr9:132026788 | T | A | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.349-12321A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026788 | |||||||
| chr9:132026885 | CTAT | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.349-12421_349-1241 others(7): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026885 | |||||||
| chr9:132026955 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.349-12488C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132026955 | |||||||
| chr9:132027148 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-12681C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027148 | |||||||
| chr9:132027184 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-12717A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027184 | |||||||
| chr9:132027234 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-12767G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027234 | |||||||
| chr9:132027286 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.349-12819A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027286 | |||||||
| chr9:132027326 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-12859C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027326 | |||||||
| chr9:132027393 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-12926C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027393 | |||||||
| chr9:132027414 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-12947G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027414 | |||||||
| chr9:132027477 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.349-13010G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027477 | |||||||
| chr9:132027488 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.349-13021C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027488 | |||||||
| chr9:132027646 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-13179G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027646 | |||||||
| chr9:132027688 | TGA | T | 6 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0213 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-13223_349-1322 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027688 | |||||||
| chr9:132027693 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.349-13226G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027693 | |||||||
| chr9:132027694 | T | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.349-13227A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027694 | |||||||
| chr9:132027695 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.349-13228T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027695 | |||||||
| chr9:132027734 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.349-13267A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027734 | |||||||
| chr9:132027902 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.349-13435C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132027902 | |||||||
| chr9:132028229 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349-13762G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028229 | |||||||
| chr9:132028338 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.349-13871C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028338 | |||||||
| chr9:132028509 | T | TA | 21 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0073 others(18): Show |
21 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.349-14043dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028509 | |||||||
| chr9:132028509 | TA | T | 8 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0109 others(5): Show |
8 | HG00140.hp2 HG01169.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-14043delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028509 | |||||||
| chr9:132028510 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349-14043T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028510 | |||||||
| chr9:132028594 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-14127C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028594 | |||||||
| chr9:132028657 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-14190A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028657 | |||||||
| chr9:132028870 | C | T | 21 | a0001c0001t0001g0150 a0001c0001t0001g0201 a0001c0001t0001g0223 others(18): Show |
21 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-14403G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028870 | |||||||
| chr9:132028949 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(3): Show |
6 | HG01943.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-14482G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132028949 | |||||||
| chr9:132029423 | CCACAG | C | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-14961_349-1495 others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132029423 | |||||||
| chr9:132029457 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.349-14990T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132029457 | |||||||
| chr9:132029518 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-15051C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132029518 | |||||||
| chr9:132029655 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-15188C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132029655 | |||||||
| chr9:132030003 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.349-15536G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030003 | |||||||
| chr9:132030137 | G | A | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-15670C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030137 | |||||||
| chr9:132030306 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.349-15839T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030306 | |||||||
| chr9:132030414 | AAG | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-15949_349-1594 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030414 | |||||||
| chr9:132030634 | T | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-16167A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030634 | |||||||
| chr9:132030688 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.349-16221A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030688 | |||||||
| chr9:132030886 | C | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG03139.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.349-16419G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132030886 | |||||||
| chr9:132031190 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.349-16723C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031190 | |||||||
| chr9:132031351 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349-16884A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031351 | |||||||
| chr9:132031369 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349-16902T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031369 | |||||||
| chr9:132031738 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(8): Show |
11 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-17271A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031738 | |||||||
| chr9:132031769 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.349-17302C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031769 | |||||||
| chr9:132031793 | G | GA | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-17327dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031793 | |||||||
| chr9:132031876 | T | G | 116 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(113): Show |
116 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.349-17409A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031876 | |||||||
| chr9:132031888 | T | G | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-17421A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132031888 | |||||||
| chr9:132032038 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.349-17571A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032038 | |||||||
| chr9:132032060 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01109.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.349-17593C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032060 | |||||||
| chr9:132032087 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.349-17620A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032087 | |||||||
| chr9:132032260 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.349-17793A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032260 | |||||||
| chr9:132032415 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0073 |
3 | HG00738.hp2 HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.349-17948A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032415 | |||||||
| chr9:132032432 | A | C | 102 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.349-17965T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032432 | |||||||
| chr9:132032604 | T | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-18137A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032604 | |||||||
| chr9:132032837 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.349-18370C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032837 | |||||||
| chr9:132032853 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.349-18386G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032853 | |||||||
| chr9:132032907 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-18440T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132032907 | |||||||
| chr9:132033254 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.349-18787A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033254 | |||||||
| chr9:132033268 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0207 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.349-18801A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033268 | |||||||
| chr9:132033295 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-18828A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033295 | |||||||
| chr9:132033396 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.349-18929G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033396 | |||||||
| chr9:132033449 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-18982A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033449 | |||||||
| chr9:132033749 | C | G | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-19282G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033749 | |||||||
| chr9:132033805 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-19338A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033805 | |||||||
| chr9:132033851 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.349-19384C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033851 | |||||||
| chr9:132033972 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349-19505A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132033972 | |||||||
| chr9:132034312 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.349-19845C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132034312 | |||||||
| chr9:132034355 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-19888T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132034355 | |||||||
| chr9:132034778 | A | C | 122 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(119): Show |
122 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.349-20311T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132034778 | |||||||
| chr9:132034828 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-20361T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132034828 | |||||||
| chr9:132035034 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.349-20567G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035034 | |||||||
| chr9:132035067 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.349-20600C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035067 | |||||||
| chr9:132035146 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-20679C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035146 | |||||||
| chr9:132035194 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-20727A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035194 | |||||||
| chr9:132035609 | C | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(15): Show |
18 | HG01081.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-21142G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035609 | |||||||
| chr9:132035623 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-21156C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035623 | |||||||
| chr9:132035630 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-21163T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035630 | |||||||
| chr9:132035738 | G | A | 25 | a0001c0001t0001g0088 a0001c0001t0001g0219 a0001c0001t0001g0228 others(22): Show |
25 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.349-21271C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035738 | |||||||
| chr9:132035947 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.349-21480A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132035947 | |||||||
| chr9:132036311 | C | T | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-21844G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036311 | |||||||
| chr9:132036315 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-21848G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036315 | |||||||
| chr9:132036587 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349-22120T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036587 | |||||||
| chr9:132036727 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | NA18942.hp1 NA18950.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-22260T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036727 | |||||||
| chr9:132036880 | T | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(225): Show |
229 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.349-22413A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036880 | |||||||
| chr9:132036963 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-22496A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036963 | |||||||
| chr9:132036989 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG00621.hp1 HG02132.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.349-22522C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132036989 | |||||||
| chr9:132037099 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.349-22632G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037099 | |||||||
| chr9:132037227 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
81 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.349-22760G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037227 | |||||||
| chr9:132037291 | C | T | 95 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0075 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.349-22824G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037291 | |||||||
| chr9:132037344 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-22877T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037344 | |||||||
| chr9:132037349 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.349-22882A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037349 | |||||||
| chr9:132037718 | C | CA | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-23252dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037718 | |||||||
| chr9:132037845 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.349-23378G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037845 | |||||||
| chr9:132037851 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-23384G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037851 | |||||||
| chr9:132037962 | G | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | NA18948.hp2 NA18957.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.349-23495C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037962 | |||||||
| chr9:132037984 | T | C | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-23517A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037984 | |||||||
| chr9:132037991 | A | G | 29 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0001c0001t0002g0002 others(26): Show |
29 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-23524T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132037991 | |||||||
| chr9:132038188 | C | CT | 37 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00621.hp1 HG00741.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.349-23722dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038188 | |||||||
| chr9:132038285 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-23818C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038285 | |||||||
| chr9:132038382 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-23915G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038382 | |||||||
| chr9:132038386 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.349-23919C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038386 | |||||||
| chr9:132038439 | G | T | 1 | a0001c0001t0002g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349-23972C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038439 | |||||||
| chr9:132038443 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0002g0032 |
2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.349-23976G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038443 | |||||||
| chr9:132038488 | G | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(13): Show |
16 | HG00609.hp2 HG00621.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-24021C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038488 | |||||||
| chr9:132038701 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-24234C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038701 | |||||||
| chr9:132038836 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
80 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.349-24369C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038836 | |||||||
| chr9:132038959 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.349-24492C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038959 | |||||||
| chr9:132038990 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.349-24523C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038990 | |||||||
| chr9:132038998 | C | T | 90 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0098 others(87): Show |
90 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.349-24531G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132038998 | |||||||
| chr9:132039247 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.349-24780G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039247 | |||||||
| chr9:132039248 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-24781C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039248 | |||||||
| chr9:132039317 | GT | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG02040.hp1 NA18966.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-24851delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039317 | |||||||
| chr9:132039386 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.349-24919G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039386 | |||||||
| chr9:132039566 | T | C | 102 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(99): Show |
102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.349-25099A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039566 | |||||||
| chr9:132039613 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-25146T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039613 | |||||||
| chr9:132039644 | GAACCCTA others(695): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.349-25879_349-2517 others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039644 | |||||||
| chr9:132039661 | AGAGT | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-25198_349-2519 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132039661 | |||||||
| chr9:132040001 | GGACATTT others(5696): Show |
G | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.349-31237_349-2553 others(4): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040001 | |||||||
| chr9:132040429 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.349-25962C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040429 | |||||||
| chr9:132040456 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0207 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.349-25989A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040456 | |||||||
| chr9:132040456 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349-25989A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040456 | |||||||
| chr9:132040620 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-26153T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040620 | |||||||
| chr9:132040705 | G | A | 2 | a0001c0001t0001g0065 a0002c0002t0001g0273 |
2 | NA19067.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.349-26238C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040705 | |||||||
| chr9:132040744 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.349-26277C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040744 | |||||||
| chr9:132040749 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0259 a0001c0001t0002g0099 others(1): Show |
4 | HG00558.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-26282G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040749 | |||||||
| chr9:132040783 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0002g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.349-26316T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040783 | |||||||
| chr9:132040786 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-26319G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132040786 | |||||||
| chr9:132041254 | T | C | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
5 | HG01255.hp2 HG01258.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-26787A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132041254 | |||||||
| chr9:132041317 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG02559.hp1 HG02572.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-26850G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132041317 | |||||||
| chr9:132041493 | A | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.349-27026T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132041493 | |||||||
| chr9:132041801 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.349-27334C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132041801 | |||||||
| chr9:132041801 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.349-27334C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132041801 | |||||||
| chr9:132042194 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.349-27727C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042194 | |||||||
| chr9:132042236 | G | A | 95 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.349-27769C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042236 | |||||||
| chr9:132042294 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-27827T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042294 | |||||||
| chr9:132042438 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.349-27971C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042438 | |||||||
| chr9:132042449 | AGGTAT | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02451.hp1 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.349-27987_349-2798 others(9): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042449 | |||||||
| chr9:132042771 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.349-28304C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132042771 | |||||||
| chr9:132043149 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-28682G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132043149 | |||||||
| chr9:132043301 | A | AT | 5 | a0001c0001t0001g0190 a0001c0001t0002g0186 a0001c0001t0002g0187 others(2): Show |
5 | HG02735.hp2 HG03704.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-28835dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132043301 | |||||||
| chr9:132043301 | AT | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(11): Show |
14 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-28835delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132043301 | |||||||
| chr9:132043618 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(56): Show |
60 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.349-29151G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132043618 | |||||||
| chr9:132043811 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01943.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349-29344G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132043811 | |||||||
| chr9:132044122 | G | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-29655C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044122 | |||||||
| chr9:132044371 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.349-29904A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044371 | |||||||
| chr9:132044433 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349-29966G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044433 | |||||||
| chr9:132044722 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-30255A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044722 | |||||||
| chr9:132044768 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.349-30301T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044768 | |||||||
| chr9:132044881 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.349-30414A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132044881 | |||||||
| chr9:132045127 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-30660C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045127 | |||||||
| chr9:132045244 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-30777A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045244 | |||||||
| chr9:132045362 | T | C | 6 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0213 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-30895A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045362 | |||||||
| chr9:132045413 | T | TACAC | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-30950_349-3094 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045413 | TAC | T | 48 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(45): Show |
48 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.349-30948_349-3094 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045413 | TACAC | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.349-30950_349-3094 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045413 | TACACAC | T | 89 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0023 others(86): Show |
89 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.349-30952_349-3094 others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045413 | TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0001g0184 others(11): Show |
14 | HG01099.hp2 HG02257.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-30954_349-3094 others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045413 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-30956_349-3094 others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045413 | |||||||
| chr9:132045432 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.349-30965T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045432 | |||||||
| chr9:132045455 | G | C | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.349-30988C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045455 | |||||||
| chr9:132045831 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349-31364A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045831 | |||||||
| chr9:132045842 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.349-31375C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132045842 | |||||||
| chr9:132046003 | A | G | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+31439T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046003 | |||||||
| chr9:132046046 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+31396A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046046 | |||||||
| chr9:132046098 | A | G | 96 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(93): Show |
96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.348+31344T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046098 | |||||||
| chr9:132046146 | C | T | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
5 | HG01255.hp2 HG01258.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+31296G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046146 | |||||||
| chr9:132046282 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+31160C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046282 | |||||||
| chr9:132046551 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.348+30891G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046551 | |||||||
| chr9:132046643 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+30799G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046643 | |||||||
| chr9:132046724 | C | T | 28 | a0001c0001t0001g0088 a0001c0001t0001g0219 a0001c0001t0001g0228 others(25): Show |
28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.348+30718G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132046724 | |||||||
| chr9:132047047 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.348+30395C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047047 | |||||||
| chr9:132047225 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.348+30217C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047225 | |||||||
| chr9:132047307 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+30135G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047307 | |||||||
| chr9:132047441 | G | GAC | 23 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0109 others(20): Show |
23 | HG01884.hp1 HG02040.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.348+29999_348+3000 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACAC | 150 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(147): Show |
151 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.348+29997_348+3000 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACACAC | 38 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0064 others(35): Show |
38 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.348+29995_348+3000 others(10): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACACACA others(1): Show |
11 | a0001c0001t0001g0017 a0001c0001t0001g0072 a0001c0001t0001g0075 others(8): Show |
11 | HG01928.hp1 HG02622.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+29993_348+3000 others(12): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACACACA others(3): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0199 others(1): Show |
4 | HG01261.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+29991_348+3000 others(14): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACACACA others(5): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG01256.hp1 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.348+29989_348+3000 others(16): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | G | GACACACA others(7): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0016 |
2 | HG01943.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.348+29987_348+3000 others(18): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | GAC | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0144 others(10): Show |
13 | HG00609.hp1 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+29999_348+3000 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047441 | GACAC | G | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(8): Show |
11 | HG00558.hp2 HG02080.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+29997_348+3000 others(8): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047441 | |||||||
| chr9:132047469 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+29973G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047469 | |||||||
| chr9:132047491 | G | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02451.hp1 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.348+29951C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047491 | |||||||
| chr9:132047524 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0002g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.348+29918C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132047524 | |||||||
| chr9:132048206 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.348+29236G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132048206 | |||||||
| chr9:132048345 | G | A | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+29097C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132048345 | |||||||
| chr9:132048361 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(9): Show |
12 | HG00558.hp2 HG02080.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+29081G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132048361 | |||||||
| chr9:132048627 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.348+28815G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132048627 | |||||||
| chr9:132048730 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.348+28712C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132048730 | |||||||
| chr9:132049084 | A | G | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00621.hp1 HG02132.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+28358T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049084 | |||||||
| chr9:132049091 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.348+28351C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049091 | |||||||
| chr9:132049099 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.348+28343C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049099 | |||||||
| chr9:132049150 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.348+28292G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049150 | |||||||
| chr9:132049346 | A | C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02809.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.348+28096T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049346 | |||||||
| chr9:132049565 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+27877A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049565 | |||||||
| chr9:132049823 | A | C | 1 | a0002c0002t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.348+27619T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049823 | |||||||
| chr9:132049859 | A | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.348+27583T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049859 | |||||||
| chr9:132049937 | T | G | 2 | a0001c0001t0001g0216 a0001c0001t0002g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.348+27505A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132049937 | |||||||
| chr9:132050006 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.348+27436A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050006 | |||||||
| chr9:132050498 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+26944G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050498 | |||||||
| chr9:132050504 | A | G | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0157 others(2): Show |
5 | HG01358.hp1 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+26938T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050504 | |||||||
| chr9:132050651 | G | C | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+26791C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050651 | |||||||
| chr9:132050681 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.348+26761G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050681 | |||||||
| chr9:132050768 | C | A | 132 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(129): Show |
132 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.348+26674G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050768 | |||||||
| chr9:132050888 | T | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+26554A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132050888 | |||||||
| chr9:132051253 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348+26189A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051253 | |||||||
| chr9:132051262 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.348+26180T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051262 | |||||||
| chr9:132051467 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.348+25975C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051467 | |||||||
| chr9:132051509 | C | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+25933G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051509 | |||||||
| chr9:132051571 | T | A | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.348+25871A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051571 | |||||||
| chr9:132051828 | T | G | 1 | a0001c0001t0002g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.348+25614A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051828 | |||||||
| chr9:132051863 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00609.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.348+25579A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132051863 | |||||||
| chr9:132052059 | C | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+25383G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052059 | |||||||
| chr9:132052066 | G | C | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.348+25376C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052066 | |||||||
| chr9:132052206 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.348+25236T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052206 | |||||||
| chr9:132052227 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+25215A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052227 | |||||||
| chr9:132052396 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.348+25046G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052396 | |||||||
| chr9:132052578 | TA | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(250): Show |
254 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.348+24863delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052578 | |||||||
| chr9:132052580 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+24862T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052580 | |||||||
| chr9:132052685 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01255.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.348+24757G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052685 | |||||||
| chr9:132052709 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0250 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.348+24733A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132052709 | |||||||
| chr9:132053161 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+24281C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053161 | |||||||
| chr9:132053218 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.348+24224C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053218 | |||||||
| chr9:132053249 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0169 others(10): Show |
13 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+24193C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053249 | |||||||
| chr9:132053253 | CA | C | 21 | a0001c0001t0001g0150 a0001c0001t0001g0201 a0001c0001t0001g0223 others(18): Show |
21 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.348+24188delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053253 | |||||||
| chr9:132053264 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.348+24178T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053264 | |||||||
| chr9:132053264 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+24178T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053264 | |||||||
| chr9:132053265 | A | T | 3 | a0001c0001t0001g0164 a0001c0001t0002g0099 a0001c0001t0002g0151 |
3 | HG01433.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+24177T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053265 | |||||||
| chr9:132053266 | A | T | 6 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
6 | HG00140.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+24176T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053266 | |||||||
| chr9:132053267 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.348+24175T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053267 | |||||||
| chr9:132053270 | G | T | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.348+24172C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053270 | |||||||
| chr9:132053350 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0169 a0001c0001t0001g0170 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+24092G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053350 | |||||||
| chr9:132053365 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+24077A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053365 | |||||||
| chr9:132053414 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.348+24028C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053414 | |||||||
| chr9:132053609 | A | G | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0081 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+23833T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053609 | |||||||
| chr9:132053624 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.348+23818G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053624 | |||||||
| chr9:132053644 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.348+23798T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053644 | |||||||
| chr9:132053735 | T | C | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.348+23707A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053735 | |||||||
| chr9:132053992 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.348+23450A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132053992 | |||||||
| chr9:132054056 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+23386C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054056 | |||||||
| chr9:132054113 | T | C | 41 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0088 others(38): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.348+23329A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054113 | |||||||
| chr9:132054219 | C | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+23223G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054219 | |||||||
| chr9:132054253 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+23189C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054253 | |||||||
| chr9:132054273 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.348+23169T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054273 | |||||||
| chr9:132054481 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.348+22961G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054481 | |||||||
| chr9:132054612 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+22830C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054612 | |||||||
| chr9:132054675 | G | A | 14 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG01081.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.348+22767C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054675 | |||||||
| chr9:132054821 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.348+22621A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054821 | |||||||
| chr9:132054826 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(119): Show |
123 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.348+22616A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132054826 | |||||||
| chr9:132055092 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348+22350C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055092 | |||||||
| chr9:132055391 | G | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+22051C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055391 | |||||||
| chr9:132055421 | T | A | 99 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(96): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.348+22021A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055421 | |||||||
| chr9:132055472 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.348+21970G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055472 | |||||||
| chr9:132055535 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+21907C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055535 | |||||||
| chr9:132055560 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.348+21882A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055560 | |||||||
| chr9:132055608 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.348+21834G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055608 | |||||||
| chr9:132055630 | C | G | 100 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0075 others(97): Show |
100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.348+21812G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055630 | |||||||
| chr9:132055714 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+21728G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055714 | |||||||
| chr9:132055883 | C | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.348+21559G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132055883 | |||||||
| chr9:132056005 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348+21437A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132056005 | |||||||
| chr9:132056166 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.348+21276G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132056166 | |||||||
| chr9:132056296 | G | A | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+21146C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132056296 | |||||||
| chr9:132056656 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.348+20786A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132056656 | |||||||
| chr9:132057216 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
256 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.348+20226T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057216 | |||||||
| chr9:132057298 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+20144A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057298 | |||||||
| chr9:132057433 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0218 |
3 | HG02280.hp2 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.348+20009C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057433 | |||||||
| chr9:132057433 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+20009C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057433 | |||||||
| chr9:132057542 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+19900C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057542 | |||||||
| chr9:132057599 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+19843A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057599 | |||||||
| chr9:132057784 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348+19658G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057784 | |||||||
| chr9:132057956 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+19486C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132057956 | |||||||
| chr9:132058343 | C | T | 95 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0096 others(92): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.348+19099G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058343 | |||||||
| chr9:132058351 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+19091C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058351 | |||||||
| chr9:132058674 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.348+18768C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058674 | |||||||
| chr9:132058701 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0218 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.348+18741G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058701 | |||||||
| chr9:132058713 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.348+18729G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058713 | |||||||
| chr9:132058757 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.348+18685T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058757 | |||||||
| chr9:132058969 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.348+18473C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132058969 | |||||||
| chr9:132059167 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+18275G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059167 | |||||||
| chr9:132059187 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+18255G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059187 | |||||||
| chr9:132059288 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348+18154C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059288 | |||||||
| chr9:132059435 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.348+18007A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059435 | |||||||
| chr9:132059482 | T | C | 5 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
5 | HG01169.hp1 HG01433.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+17960A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059482 | |||||||
| chr9:132059533 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+17909G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059533 | |||||||
| chr9:132059554 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.348+17888A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059554 | |||||||
| chr9:132059599 | G | T | 39 | a0001c0001t0001g0088 a0001c0001t0001g0174 a0001c0001t0001g0175 others(36): Show |
39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.348+17843C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059599 | |||||||
| chr9:132059601 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+17841A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059601 | |||||||
| chr9:132059711 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0272 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.348+17731G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059711 | |||||||
| chr9:132059822 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.348+17620C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132059822 | |||||||
| chr9:132060285 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.348+17157A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060285 | |||||||
| chr9:132060464 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+16978T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060464 | |||||||
| chr9:132060502 | T | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+16940A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060502 | |||||||
| chr9:132060516 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+16926A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060516 | |||||||
| chr9:132060560 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+16882G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060560 | |||||||
| chr9:132060587 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+16855G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060587 | |||||||
| chr9:132060898 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.348+16544C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132060898 | |||||||
| chr9:132061021 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348+16421T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061021 | |||||||
| chr9:132061241 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+16201G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061241 | |||||||
| chr9:132061272 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.348+16170G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061272 | |||||||
| chr9:132061301 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+16141T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061301 | |||||||
| chr9:132061321 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.348+16121G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061321 | |||||||
| chr9:132061452 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0002g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.348+15990C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061452 | |||||||
| chr9:132061584 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01943.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.348+15858A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061584 | |||||||
| chr9:132061638 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+15804C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061638 | |||||||
| chr9:132061734 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.348+15708T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061734 | |||||||
| chr9:132061736 | C | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01081.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+15706G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132061736 | |||||||
| chr9:132062108 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.348+15334G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062108 | |||||||
| chr9:132062273 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0003 |
2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.348+15169G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062273 | |||||||
| chr9:132062293 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+15149G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062293 | |||||||
| chr9:132062555 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+14887G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062555 | |||||||
| chr9:132062616 | AT | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
128 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.348+14825delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062616 | |||||||
| chr9:132062616 | ATT | A | 6 | a0001c0001t0001g0154 a0001c0001t0002g0095 a0001c0001t0002g0152 others(3): Show |
6 | HG02129.hp1 HG02129.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+14824_348+1482 others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062616 | |||||||
| chr9:132062668 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348+14774T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062668 | |||||||
| chr9:132062992 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.348+14450C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062992 | |||||||
| chr9:132063603 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.348+13839C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132063603 | |||||||
| chr9:132063970 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.348+13472G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132063970 | |||||||
| chr9:132064221 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.348+13221C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132064221 | |||||||
| chr9:132064239 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.348+13203G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132064239 | |||||||
| chr9:132064309 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+13133C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132064309 | |||||||
| chr9:132064846 | G | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+12596C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132064846 | |||||||
| chr9:132064867 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01943.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.348+12575T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132064867 | |||||||
| chr9:132065051 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+12391T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065051 | |||||||
| chr9:132065086 | A | G | 1 | a0001c0001t0002g0022 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.348+12356T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065086 | |||||||
| chr9:132065195 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348+12247G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065195 | |||||||
| chr9:132065261 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02109.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+12181G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065261 | |||||||
| chr9:132065360 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.348+12082C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065360 | |||||||
| chr9:132065382 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+12060G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065382 | |||||||
| chr9:132065424 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.348+12018G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065424 | |||||||
| chr9:132065606 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0073 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.348+11836G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065606 | |||||||
| chr9:132065645 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.348+11797G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065645 | |||||||
| chr9:132065805 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(54): Show |
58 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.348+11637G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065805 | |||||||
| chr9:132065919 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.348+11523G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132065919 | |||||||
| chr9:132066181 | T | C | 2 | a0001c0001t0001g0065 a0002c0002t0001g0273 |
2 | NA19067.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.348+11261A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132066181 | |||||||
| chr9:132066447 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.348+10995G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132066447 | |||||||
| chr9:132066503 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+10939G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132066503 | |||||||
| chr9:132066601 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+10841C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132066601 | |||||||
| chr9:132066986 | G | C | 28 | a0001c0001t0001g0078 a0001c0001t0001g0219 a0001c0001t0001g0228 others(25): Show |
28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.348+10456C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132066986 | |||||||
| chr9:132067120 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.348+10322G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067120 | |||||||
| chr9:132067168 | G | A | 13 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
13 | HG01081.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+10274C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067168 | |||||||
| chr9:132067233 | CCATGCCC others(14): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.348+10188_348+1020 others(25): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067233 | |||||||
| chr9:132067287 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+10155C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067287 | |||||||
| chr9:132067710 | T | TTTG | 10 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(7): Show |
10 | HG00621.hp1 HG01891.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+9729_348+9731d others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067710 | |||||||
| chr9:132067734 | C | T | 10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(7): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+9708G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067734 | |||||||
| chr9:132067804 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0208 a0001c0001t0001g0211 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+9638G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067804 | |||||||
| chr9:132067816 | ATTCTCCT others(22): Show |
A | 1 | a0001c0001t0001g0019 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.348+9597_348+9625d others(31): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132067816 | |||||||
| chr9:132068138 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+9304C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068138 | |||||||
| chr9:132068191 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.348+9251C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068191 | |||||||
| chr9:132068199 | C | G | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348+9243G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068199 | |||||||
| chr9:132068204 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.348+9238C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068204 | |||||||
| chr9:132068295 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.348+9147G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068295 | |||||||
| chr9:132068390 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+9052G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068390 | |||||||
| chr9:132068392 | C | T | 15 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(12): Show |
15 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+9050G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068392 | |||||||
| chr9:132068411 | G | A | 15 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(12): Show |
15 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+9031C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068411 | |||||||
| chr9:132068468 | G | C | 5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+8974C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068468 | |||||||
| chr9:132068545 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(259): Show |
263 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.348+8897A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068545 | |||||||
| chr9:132068582 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | NA18942.hp1 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+8860A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068582 | |||||||
| chr9:132068602 | A | T | 98 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0093 others(95): Show |
98 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.348+8840T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068602 | |||||||
| chr9:132068639 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+8803C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068639 | |||||||
| chr9:132068922 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+8520G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132068922 | |||||||
| chr9:132069034 | G | T | 10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(7): Show |
10 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+8408C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132069034 | |||||||
| chr9:132069041 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(116): Show |
120 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.348+8401C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132069041 | |||||||
| chr9:132069208 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348+8234T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132069208 | |||||||
| chr9:132069615 | A | T | 1 | a0001c0001t0001g0257 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.348+7827T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132069615 | |||||||
| chr9:132070110 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+7332G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070110 | |||||||
| chr9:132070275 | G | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+7167C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070275 | |||||||
| chr9:132070325 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.348+7117C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070325 | |||||||
| chr9:132070359 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.348+7083G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070359 | |||||||
| chr9:132070411 | G | T | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.348+7031C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070411 | |||||||
| chr9:132070601 | A | ACCAGGGG others(23): Show |
1 | a0001c0001t0001g0019 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.348+6840_348+6841i others(32): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070601 | |||||||
| chr9:132070682 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.348+6760G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070682 | |||||||
| chr9:132070686 | AATATCTG others(8): Show |
A | 108 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0075 others(105): Show |
108 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.348+6741_348+6755d others(17): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070686 | |||||||
| chr9:132070703 | G | A | 108 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0075 others(105): Show |
108 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.348+6739C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070703 | |||||||
| chr9:132070709 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.348+6733C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070709 | |||||||
| chr9:132070857 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0002g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.348+6585C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132070857 | |||||||
| chr9:132071045 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+6397C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071045 | |||||||
| chr9:132071314 | G | A | 13 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(10): Show |
13 | HG01169.hp1 HG01255.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+6128C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071314 | |||||||
| chr9:132071349 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348+6093A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071349 | |||||||
| chr9:132071407 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+6035G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071407 | |||||||
| chr9:132071417 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+6025G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071417 | |||||||
| chr9:132071418 | A | G | 106 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0075 others(103): Show |
106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.348+6024T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071418 | |||||||
| chr9:132071429 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.348+6013T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071429 | |||||||
| chr9:132071501 | ACACT | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02559.hp1 HG03516.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+5937_348+5940d others(6): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071501 | |||||||
| chr9:132071529 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348+5913G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071529 | |||||||
| chr9:132071654 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02559.hp1 HG03516.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+5788C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071654 | |||||||
| chr9:132071663 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+5779C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071663 | |||||||
| chr9:132071729 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.348+5713C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071729 | |||||||
| chr9:132071735 | T | C | 133 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(130): Show |
133 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.348+5707A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071735 | |||||||
| chr9:132071857 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+5585G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071857 | |||||||
| chr9:132071880 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+5562G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071880 | |||||||
| chr9:132071992 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+5450G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132071992 | |||||||
| chr9:132072144 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.348+5298G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072144 | |||||||
| chr9:132072163 | T | G | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+5279A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072163 | |||||||
| chr9:132072548 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.348+4894G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072548 | |||||||
| chr9:132072591 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+4851C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072591 | |||||||
| chr9:132072651 | A | C | 1 | a0001c0001t0002g0074 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.348+4791T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072651 | |||||||
| chr9:132072666 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348+4776C>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072666 | |||||||
| chr9:132072724 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.348+4718C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072724 | |||||||
| chr9:132072765 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.348+4677C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072765 | |||||||
| chr9:132072842 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+4600C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132072842 | |||||||
| chr9:132073026 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.348+4416G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073026 | |||||||
| chr9:132073241 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+4201G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073241 | |||||||
| chr9:132073281 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.348+4161A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073281 | |||||||
| chr9:132073296 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.348+4146T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073296 | |||||||
| chr9:132073319 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.348+4123C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073319 | |||||||
| chr9:132073408 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.348+4034T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073408 | |||||||
| chr9:132073476 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+3966G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073476 | |||||||
| chr9:132073650 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+3792A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073650 | |||||||
| chr9:132073768 | G | GA | 13 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(10): Show |
13 | HG00621.hp1 HG00621.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+3673dupT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073768 | |||||||
| chr9:132073820 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348+3622G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073820 | |||||||
| chr9:132073830 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0208 a0001c0001t0001g0218 |
3 | HG02451.hp2 HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.348+3612C>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073830 | |||||||
| chr9:132073877 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+3565G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073877 | |||||||
| chr9:132073878 | G | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0200 |
3 | HG02258.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348+3564C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132073878 | |||||||
| chr9:132074279 | AT | A | 21 | a0001c0001t0001g0201 a0001c0001t0001g0223 a0001c0001t0001g0224 others(18): Show |
21 | HG00558.hp2 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.348+3162delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074279 | |||||||
| chr9:132074485 | T | G | 1 | a0001c0001t0002g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.348+2957A>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074485 | |||||||
| chr9:132074616 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.348+2826T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074616 | |||||||
| chr9:132074720 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.348+2722A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074720 | |||||||
| chr9:132074732 | T | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02451.hp1 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.348+2710A>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074732 | |||||||
| chr9:132074955 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+2487G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132074955 | |||||||
| chr9:132075178 | A | C | 1 | a0001c0001t0002g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.348+2264T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132075178 | |||||||
| chr9:132075197 | C | G | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.348+2245G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132075197 | |||||||
| chr9:132075299 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.348+2143G>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132075299 | |||||||
| chr9:132075569 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.348+1873A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132075569 | |||||||
| chr9:132075857 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+1585G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132075857 | |||||||
| chr9:132076057 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.348+1385G>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132076057 | |||||||
| chr9:132076265 | C | CT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0209 a0001c0001t0001g0223 others(4): Show |
7 | HG01109.hp2 HG01256.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1176dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132076265 | |||||||
| chr9:132076797 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.348+645C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132076797 | |||||||
| chr9:132076816 | TTC | T | 3 | a0001c0001t0001g0222 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02886.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+624_348+625del others(2): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132076816 | |||||||
| chr9:132077176 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+266C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132077176 | |||||||
| chr9:132077356 | A | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+86T>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132077356 | |||||||
| chr9:132077403 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(260): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.348+39A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132077403 | |||||||
| chr9:132077421 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.348+21G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132077421 | |||||||
| chr9:132077422 | G | A | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+20C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132077422 | |||||||
| chr9:132077712 | T | C | 53 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 others(50): Show |
53 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-126A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 1/7 | chr9 | 132077712 | |||||||
| chr9:132078735 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0003 |
2 | NA18964.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.203+907G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 1/7 | chr9 | 132078735 | |||||||
| chr9:132079155 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG00639.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.203+487G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 1/7 | chr9 | 132079155 | |||||||
| chr9:132079234 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.203+408C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 1/7 | chr9 | 132079234 |