Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr9 | 131855112 | 132084867 |
| a0002 | 0/0 | 311 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 936 | 273 | 94 | 52 | 101 | 4 | 20 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| c0002 | 0/0 | 936 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 450 | 217 | 80 | 43 | 74 | 4 | 14 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| t0002 | 0/0 | 450 | 57 | 14 | 9 | 28 | 0 | 6 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 936 | 273 | 94 | 52 | 101 | 4 | 20 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| a0002c0002 | 0/0 | 936 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | 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 | copy fasta | chr9 | 131855112 | 132084867 |
| a0001c0001t0002 | 0/0 | 1385 | 57 | 14 | 9 | 28 | 0 | 6 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| a0002c0002t0001 | 0/0 | 1385 | 1 | 0 | 0 | 1 | 0 | 0 | MED27_chr9_131855112_132084867 | MED27 | copy fasta | chr9 | 131855112 | 132084867 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 0/0 | 1 | 1 | 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 | 1/0 | 1 | 0 | 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 |
| a0001c0001t0001g0094 | 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 |
| a0001c0001t0002g0093 | 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 | g0094 | 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 | g0105 | 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 | g0006 | 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 | g0107 | 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 | g0093 | 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 | g0005 | 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 | g0106 | 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 | g0117 | 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 | g0118 | 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 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | MED27_chr9_131855112_132084867 | MED27 | chr9 | 131855112 | 132084867 |
| 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 |
| 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 |
|---|
| 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 |
| 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | 107 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0015others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(104): 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 | a0001c0001t0001g0182a0001c0001t0001g0209 | 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(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 | a0001c0001t0002g0074a0001c0001t0002g0125a0001c0001t0002g0143 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0040others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0084a0001c0001t0002g0200 | 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 | 83 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(80): 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 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0040others(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 | a0001c0001t0002g0092a0001c0001t0002g0123a0001c0001t0002g0129others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(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 | 91 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(88): 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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0073others(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 | a0001c0001t0001g0113a0001c0001t0001g0234a0001c0001t0001g0235others(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 | 90 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(87): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0013a0001c0001t0001g0216 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0002g0076a0001c0001t0002g0077 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0072a0001c0001t0001g0230a0001c0001t0001g0249others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0160a0001c0001t0001g0161 | 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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0081a0001c0001t0001g0172a0001c0001t0001g0173others(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 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(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 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0078others(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 | 162 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(159): 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 | a0001c0001t0001g0014a0001c0001t0001g0079a0001c0001t0001g0081others(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 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(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 | a0001c0001t0001g0170a0001c0001t0001g0212a0001c0001t0002g0217 | 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 | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(222): 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 | a0001c0001t0001g0012a0001c0001t0001g0222a0001c0001t0001g0231 | 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 | a0001c0001t0001g0073a0001c0001t0001g0184a0001c0001t0001g0250others(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 | a0001c0001t0002g0076a0001c0001t0002g0077 | 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 | a0001c0001t0001g0184a0001c0001t0002g0217 | 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 | a0001c0001t0001g0005 | 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 | 208 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(205): 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0017a0001c0001t0001g0270 | 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 | a0001c0001t0001g0017a0001c0001t0001g0270 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | 213 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0016a0001c0001t0001g0196a0001c0001t0001g0197others(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 | a0001c0001t0001g0085a0001c0001t0001g0199 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0040others(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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0268a0001c0001t0001g0269 | 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 | a0001c0001t0001g0184a0001c0001t0001g0219a0001c0001t0002g0217 | 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 | 13 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0088others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG01346.hp2 others(10): 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0002g0244a0001c0001t0002g0245 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): 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 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0166others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0016a0001c0001t0001g0073a0001c0001t0001g0169others(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 | a0001c0001t0001g0081a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0254others(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 | a0001c0001t0001g0072a0001c0001t0001g0170a0001c0001t0001g0212others(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 | a0001c0001t0001g0157a0001c0001t0001g0229a0001c0001t0001g0251 | 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 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0113others(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 | 89 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(86): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0068a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | a0001c0001t0001g0012a0001c0001t0001g0073a0001c0001t0001g0201others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0002g0074a0001c0001t0002g0125a0001c0001t0002g0143 | 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 | a0001c0001t0001g0081a0001c0001t0001g0172 | 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 | a0001c0001t0002g0021a0001c0001t0002g0119a0001c0001t0002g0120others(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 | a0001c0001t0001g0184a0001c0001t0001g0219a0001c0001t0002g0021others(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 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0213others(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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(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 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0172others(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 | a0001c0001t0001g0004a0001c0001t0001g0081a0001c0001t0001g0169others(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 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0082others(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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): 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 | a0001c0001t0001g0048a0001c0001t0001g0061a0001c0001t0001g0088others(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 | a0001c0001t0001g0101a0001c0001t0001g0241 | 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 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0052others(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 | a0001c0001t0001g0184a0001c0001t0002g0217 | 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0170others(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 | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0068a0001c0001t0001g0201a0001c0001t0001g0223others(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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0230others(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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0230others(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 | a0001c0001t0001g0113a0001c0001t0001g0237 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0066others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | 2 | a0001c0001t0001g0104a0001c0001t0001g0136 | 2 | HG01358.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0111others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): 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 | a0001c0001t0001g0145a0001c0001t0001g0247 | 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 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0249others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | 213 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): 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 | a0001c0001t0001g0110a0001c0001t0001g0231 | 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 | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): 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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0157a0001c0001t0001g0229a0001c0001t0001g0251 | 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 | a0001c0001t0001g0013a0001c0001t0001g0216 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.682-3230C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 5/7 | chr9 | 131887329 | ||||||
| chr9:131887407
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(89): 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | 2 | a0001c0001t0001g0104a0001c0001t0001g0136 | 2 | HG01358.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0170a0001c0001t0001g0212a0001c0001t0001g0268others(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 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0194others(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 | 85 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(82): 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0166 | 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 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0166 | 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 | 84 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0081others(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 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0194others(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 | a0001c0001t0001g0135a0001c0001t0001g0178 | 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0144a0001c0001t0001g0230a0001c0001t0001g0231others(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 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0053 | 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 | a0001c0001t0002g0105 | 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 | a0001c0001t0001g0111a0001c0001t0001g0183 | 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0079a0001c0001t0001g0096 | 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 | a0001c0001t0002g0074a0001c0001t0002g0125a0001c0001t0002g0143 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0085others(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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(215): 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(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 | 88 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.574-1913dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131895904 | ||||||
| chr9:131895968
|
G | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0073a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0068a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | a0001c0001t0001g0182a0001c0001t0001g0209 | 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 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0249others(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 | a0001c0001t0001g0068a0001c0001t0001g0208a0001c0001t0001g0259others(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 | a0001c0001t0001g0157a0001c0001t0001g0229a0001c0001t0001g0251 | 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 | 215 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(212): 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 | a0001c0001t0001g0157a0001c0001t0001g0229a0001c0001t0001g0251 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0223others(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 | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.574-4273A>G | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131898265 | ||||||
| chr9:131898272
|
T | C | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): 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 | a0001c0001t0001g0012a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0079others(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 | a0001c0001t0001g0013a0001c0001t0001g0216 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0166 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(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 | a0001c0001t0001g0075a0001c0001t0001g0139a0001c0001t0001g0167 | 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 | a0001c0001t0001g0026a0001c0001t0001g0222a0001c0001t0002g0217 | 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 | a0001c0001t0002g0132a0001c0001t0002g0133 | 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 | a0001c0001t0001g0073a0001c0001t0001g0250a0001c0001t0001g0252others(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 | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): 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 | a0001c0001t0001g0073a0001c0001t0001g0081a0001c0001t0001g0169others(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 | 99 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(96): 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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): 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 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0079others(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 | 193 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.574-9900delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131903891 | ||||||
| chr9:131903907
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0194others(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 | a0001c0001t0001g0100a0001c0001t0001g0102 | 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 | a0001c0001t0001g0100a0001c0001t0001g0102 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | 199 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(196): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0068others(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 | 44 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0043others(41): Show | 44 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(41): 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(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 | a0001c0001t0001g0184a0001c0001t0002g0217 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | a0001c0001t0002g0022a0001c0001t0002g0032a0001c0001t0002g0126others(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 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0054others(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 | a0001c0001t0001g0081a0001c0001t0001g0104a0001c0001t0001g0169others(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 | a0001c0001t0001g0073a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0141 | 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 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0088others(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 | 77 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0044others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(74): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0159others(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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0001g0161others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0150others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 166 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): 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 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0194others(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 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(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 | 198 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): 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 | 198 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): 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 | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): 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 | a0001c0001t0001g0015a0001c0001t0001g0060a0001c0001t0001g0134 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 198 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0254 | 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 | a0001c0001t0001g0073a0001c0001t0001g0081a0001c0001t0001g0169others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 118 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(115): 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 | a0001c0001t0001g0046a0001c0001t0001g0071a0001c0001t0001g0210others(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 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(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 | 44 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0043others(41): Show | 44 | HG00140.hp2 HG00609.hp2 HG00741.hp2 others(41): 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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.574-14152dupC | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908143 | ||||||
| chr9:131908147
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | ||||||
| chr9:131908193
|
G | GC | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.574-14202dupG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908193 | ||||||
| chr9:131908225
|
G | A | 116 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.574-14233C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131908225 | ||||||
| chr9:131908237
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(115): 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181 | 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 | 212 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(209): 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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0072others(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 | 95 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0015others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(92): 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0170others(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 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0141 | 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 | a0001c0001t0001g0068a0001c0001t0001g0150a0001c0001t0001g0201others(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 | 80 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(77): 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 | a0001c0001t0001g0170a0001c0001t0001g0212 | 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 | 199 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(196): 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 | a0001c0001t0001g0081a0001c0001t0001g0169a0001c0001t0001g0171others(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 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0192others(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 | a0001c0001t0001g0184a0001c0001t0001g0219 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0031others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0024a0001c0001t0001g0078a0001c0001t0001g0113others(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 | a0001c0001t0001g0005a0001c0001t0001g0006 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0075others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0145a0001c0001t0001g0247 | 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 | 65 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0060others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(62): 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0124others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0014a0001c0001t0001g0073a0001c0001t0001g0208others(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 | a0001c0001t0001g0024a0001c0001t0001g0080a0001c0001t0001g0083others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0075others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0068others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0054others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0061others(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 | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): 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 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0075others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | 86 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(83): Show | 86 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(83): 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 | a0001c0001t0001g0061a0001c0001t0001g0124a0001c0001t0002g0002others(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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0068others(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 | 94 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(91): Show | 94 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.573+19569dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131919811 | ||||||
| chr9:131919811
|
C | CTT | 33 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0024a0001c0001t0001g0080a0001c0001t0001g0083others(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 | a0001c0001t0001g0012a0001c0001t0001g0016 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(217): 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 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0031others(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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(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 | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(172): 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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195others(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 | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(210): 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0157a0001c0001t0001g0229a0001c0001t0001g0251 | 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 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0001g0248 | 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 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0001g0248 | 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 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0124others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | 76 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(73): Show | 76 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(73): 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 | a0001c0001t0001g0078a0001c0001t0001g0086 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0089others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(152): 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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0181others(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 | a0001c0001t0001g0072a0001c0001t0001g0073 | 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 | a0001c0001t0001g0067a0001c0001t0001g0070 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(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 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0001g0248 | 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 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0174others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0111others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0037others(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 | a0001c0001t0001g0020a0001c0001t0001g0114a0001c0001t0001g0239others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0014a0001c0001t0001g0075a0001c0001t0001g0208others(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 | a0001c0001t0002g0105 | 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 | a0001c0001t0001g0019a0001c0001t0001g0071 | 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 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0058others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0002g0189a0001c0001t0002g0258 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0232others(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 | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.573+7072delT | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 4/7 | chr9 | 131932308 | ||||||
| chr9:131932382
|
G | GA | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(209): 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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0185a0001c0001t0001g0207 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0262others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0096others(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 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0065others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0072others(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 | 58 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0098others(55): Show | 58 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(55): 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 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0094others(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 | a0001c0001t0001g0233a0001c0001t0002g0022 | 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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0184a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(190): 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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0072others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(190): 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0046others(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 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0086others(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 | a0001c0001t0001g0010a0001c0001t0001g0075a0001c0001t0001g0117others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0097others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0002g0217 | 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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | ||||||
| chr9:131941801
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.480-2327T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131941801 | ||||||
| chr9:131941817
|
A | AT | 56 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0025others(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 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(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 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0209others(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 | a0001c0001t0001g0015a0001c0001t0001g0094a0001c0001t0001g0184others(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 | a0001c0001t0001g0075a0001c0001t0001g0249a0001c0001t0001g0254others(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 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0161others(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 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0160others(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 | a0001c0001t0001g0096a0001c0001t0001g0163a0001c0001t0001g0182others(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 | a0001c0001t0001g0013a0001c0001t0001g0169 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0181others(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 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0070others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0094others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0124a0001c0001t0002g0092a0001c0001t0002g0123others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0075a0001c0001t0001g0104a0001c0001t0001g0124others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0254 | 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 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0001g0254 | 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 | a0001c0001t0001g0078a0001c0001t0001g0144a0001c0001t0001g0157others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0096others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0094others(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 | a0001c0001t0001g0075a0001c0001t0001g0104a0001c0001t0001g0124others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0075a0001c0001t0001g0104a0001c0001t0001g0124others(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 | a0001c0001t0001g0014a0001c0001t0001g0250 | 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 | a0001c0001t0001g0096a0001c0001t0001g0191a0001c0001t0001g0192others(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 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0199others(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 | a0001c0001t0002g0132a0001c0001t0002g0133 | 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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0073a0001c0001t0001g0233 | 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 | a0001c0001t0001g0012a0001c0001t0001g0271a0001c0001t0002g0108others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0014a0001c0001t0001g0208a0001c0001t0001g0211others(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 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0002g0217 | 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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0072others(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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0051others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0141 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0065others(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 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0159others(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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0094others(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 | a0001c0001t0001g0096a0001c0001t0001g0191a0001c0001t0001g0192others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0096others(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 | a0001c0001t0001g0012a0001c0001t0001g0209a0001c0001t0001g0213others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0096others(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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0072others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0124others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097 | 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 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0199others(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 | ||||||
| chr9:131959300
|
T | TA | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.480-19827_480-1982 others(5): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131959300 | ||||||
| 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 | a0001c0001t0001g0094a0001c0001t0001g0097 | 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 | a0001c0001t0002g0244a0001c0001t0002g0245 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0183 | 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 | a0001c0001t0001g0054a0001c0001t0001g0210a0001c0001t0002g0076others(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 | a0001c0001t0001g0017a0001c0001t0001g0072 | 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 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0075others(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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0002g0108a0001c0001t0002g0128 | 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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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(727): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 108 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(105): 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(724): Show |
46 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0098others(43): Show | 46 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(43): 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 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0075others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0184others(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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0232others(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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0170others(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 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0104others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0002g0091 | 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 | a0001c0001t0001g0101a0001c0001t0001g0114a0001c0001t0001g0115others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0016others(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 | a0001c0001t0001g0024a0001c0001t0001g0176a0001c0001t0001g0178others(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 | a0001c0001t0001g0023a0001c0001t0001g0175a0001c0001t0001g0177others(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 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0148others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0139others(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 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0086others(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 | a0001c0001t0001g0073a0001c0001t0001g0261 | 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 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0029a0001c0001t0001g0056a0001c0001t0001g0067others(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 | a0001c0001t0001g0066a0001c0001t0001g0137a0001c0001t0001g0191others(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 | a0001c0001t0001g0135a0001c0001t0001g0150a0001c0001t0001g0222others(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 |
7 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0136others(4): Show | 7 | HG01175.hp1 HG02257.hp1 HG02922.hp1 others(4): 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 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0042others(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 | a0001c0001t0001g0037a0001c0001t0001g0142a0001c0001t0001g0170others(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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0103others(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 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0210others(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 | a0001c0001t0001g0201a0001c0001t0001g0209a0001c0001t0001g0234others(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 | a0001c0001t0001g0046a0001c0001t0001g0247a0001c0001t0001g0269 | 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 | a0001c0001t0001g0055a0001c0001t0001g0182a0001c0001t0001g0216others(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 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0028a0001c0001t0001g0049 | 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 | a0001c0001t0001g0031a0001c0001t0001g0054 | 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 | a0001c0001t0001g0034a0001c0001t0001g0214 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0169others(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 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0233others(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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0016a0001c0001t0001g0072a0001c0001t0001g0075others(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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0170others(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 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0109others(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 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0016a0001c0001t0001g0072a0001c0001t0001g0094others(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 | a0001c0001t0001g0070a0001c0001t0001g0257a0001c0001t0001g0259others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0155others(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 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0139others(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 | a0001c0001t0001g0013a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0173a0001c0001t0001g0209 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0088a0001c0001t0001g0219a0001c0001t0001g0228others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0072others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0219others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0222others(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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0182others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0124a0001c0001t0002g0092a0001c0001t0002g0123others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0148others(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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0147a0001c0001t0001g0149 | 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 | a0001c0001t0001g0012a0001c0001t0001g0014 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0268a0001c0001t0001g0269 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0046others(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 | a0001c0001t0001g0070a0001c0001t0001g0223a0001c0001t0001g0224others(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 | a0001c0001t0001g0015a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 87 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(84): Show | 87 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(84): 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 | a0001c0001t0001g0104a0001c0001t0001g0147a0001c0001t0001g0185others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(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 |
66 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(63): Show | 66 | HG00140.hp2 HG00609.hp1 HG00741.hp2 others(63): 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 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 94 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0075others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(91): 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | 258 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): 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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0169others(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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.479+31242G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131983095 | ||||||
| chr9:131983127
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0071others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | 266 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(264): 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 | 112 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(109): Show | 113 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.479+27337dupA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131986999 | ||||||
| chr9:131986999
|
A | ATT | 27 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0031others(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 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0058others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0085others(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 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0017others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | 229 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.479+25450delG | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131988886 | ||||||
| chr9:131988995
|
T | C | 104 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0002g0002a0001c0001t0002g0003 | 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.479+23909T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 131990428 | ||||||
| chr9:131990504
|
G | A | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(98): Show | 101 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(98): 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 | a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(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 | 150 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 150 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(147): 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 | 129 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(126): Show | 129 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(126): 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0088a0001c0001t0001g0219a0001c0001t0001g0228others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0046others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 118 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(115): Show | 118 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(115): 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 | a0001c0001t0002g0074a0001c0001t0002g0125a0001c0001t0002g0143 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | 110 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0072others(107): Show | 110 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(107): 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 | 132 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(129): Show | 132 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(129): 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 | a0001c0001t0001g0048a0001c0001t0001g0223a0001c0001t0001g0224others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | 265 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): 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 | 94 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(91): 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 | a0001c0001t0001g0225a0001c0001t0001g0226 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0199others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0163a0001c0001t0001g0190a0001c0001t0002g0186others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0169others(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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0169others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0169others(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 | 5 | a0001c0001t0001g0103a0001c0001t0001g0136a0001c0001t0001g0157others(2): Show | 5 | HG01361.hp2 HG01981.hp1 HG02055.hp2 others(2): 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 102 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(99): Show | 102 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(99): 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 | a0001c0001t0002g0130a0001c0001t0002g0188 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0065a0001c0001t0001g0078a0002c0002t0001g0273 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0052a0001c0001t0001g0061a0001c0001t0002g0099others(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 | a0001c0001t0001g0063a0001c0001t0001g0181a0001c0001t0001g0201others(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 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0199others(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 | 104 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(101): 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 | 116 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(113): Show | 116 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(113): 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | a0001c0001t0001g0242a0001c0001t0001g0243 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0043others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 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 | 85 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(82): Show | 85 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(82): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0103others(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 | 123 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(120): Show | 123 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.479+11408C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132002929 | ||||||
| chr9:132003050
|
G | A | 123 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0072others(120): Show | 123 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(120): 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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(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 | 94 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(91): 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0028a0001c0001t0001g0053 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 121 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(118): Show | 121 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(118): 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | 96 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): 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 | a0001c0001t0002g0106 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.479+8532T>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005805 | ||||||
| chr9:132005821
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.479+8516T>C | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | 132005821 | ||||||
| chr9:132005903
|
G | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 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 | 118 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(115): Show | 118 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(115): 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0002g0002a0001c0001t0002g0003 | 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 | a0001c0001t0002g0106 | 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 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 | 121 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(118): Show | 121 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(118): 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 | 269 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(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 | 104 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0169others(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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0056 | 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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0159others(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 | 130 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(127): Show | 130 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(127): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0259others(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 | 118 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(115): Show | 118 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(115): 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0169others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 99 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(96): Show | 99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): 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 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 103 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(100): Show | 103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.349-1834G>A | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132016301 | ||||||
| chr9:132016477
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(262): Show | 266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): 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 | 106 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 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 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0056 | 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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0174a0001c0001t0001g0175 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | 93 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(90): 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(98): Show | 101 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(98): 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 | 269 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | 229 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(227): 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 | a0001c0001t0001g0072a0001c0001t0001g0194a0001c0001t0001g0195others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0002g0244a0001c0001t0002g0245 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0232others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0159a0001c0001t0001g0163 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 251 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(248): Show | 252 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(249): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | ||||||
| chr9:132024814
|
G | A | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.349-10347C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132024814 | ||||||
| chr9:132025033
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0014 | 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 | 221 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(219): 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 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0250others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0184a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | 96 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.349-11370C>T | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132025837 | ||||||
| chr9:132025994
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): 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 | 97 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(94): Show | 97 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(94): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 110 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(107): 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0213others(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 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0002g0076a0001c0001t0002g0077 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0073others(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 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0109others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0150a0001c0001t0001g0201a0001c0001t0001g0223others(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 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | 117 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(114): Show | 117 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(114): 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0073 | 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 | 103 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(100): Show | 103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0185a0001c0001t0001g0207 | 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 | a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | 123 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(120): Show | 123 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(120): 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0088a0001c0001t0001g0219a0001c0001t0001g0228others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(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 | 229 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(227): 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 96 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0075others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): 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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0124a0001c0001t0001g0154a0001c0001t0002g0002others(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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0020others(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 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0232others(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 | a0001c0001t0001g0060a0001c0001t0002g0032 | 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 91 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0098others(88): Show | 91 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(88): 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(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 | 103 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(100): Show | 103 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(100): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0185a0001c0001t0001g0207 | 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 | a0001c0001t0001g0065a0002c0002t0001g0273 | 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 | a0001c0001t0001g0016a0001c0001t0001g0259a0001c0001t0002g0099others(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 | a0001c0001t0001g0216a0001c0001t0002g0217 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | 96 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0190a0001c0001t0002g0186a0001c0001t0002g0187others(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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0012a0001c0001t0001g0014 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0213others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(46): Show | 49 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(46): 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0184others(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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0002g0107 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | 97 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(94): Show | 97 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(94): 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 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(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 | 269 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0088a0001c0001t0001g0219a0001c0001t0001g0228others(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 | a0001c0001t0001g0015a0001c0001t0001g0101a0001c0001t0001g0109others(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 | 151 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0064others(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 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0075others(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 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0199others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0012a0001c0001t0001g0016 | 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 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0144others(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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0259others(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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0216a0001c0001t0002g0217 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0016a0001c0001t0001g0256a0001c0001t0001g0257others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(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 | 259 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): 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 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0216a0001c0001t0002g0217 | 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0157others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | 133 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 133 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(130): 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | 254 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): 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 | a0001c0001t0001g0160a0001c0001t0001g0161 | 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 | a0001c0001t0001g0229a0001c0001t0001g0250 | 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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0169others(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 | a0001c0001t0001g0150a0001c0001t0001g0201a0001c0001t0001g0223others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0001g0164a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0098a0001c0001t0001g0101a0001c0001t0001g0102others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0001g0088others(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 | a0001c0001t0001g0017a0001c0001t0001g0198a0001c0001t0001g0199others(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 | a0001c0001t0001g0072a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | 100 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(97): 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 | 101 | a0001c0001t0001g0015a0001c0001t0001g0073a0001c0001t0001g0075others(98): Show | 101 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(98): 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 | a0001c0001t0001g0184a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | 256 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(254): 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 | a0001c0001t0001g0208a0001c0001t0001g0211a0001c0001t0001g0218 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | 96 | a0001c0001t0001g0015a0001c0001t0001g0094a0001c0001t0001g0096others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(93): 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0208a0001c0001t0001g0218 | 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 | 259 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0001t0001g0165others(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 | a0001c0001t0001g0088a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0080a0001c0001t0001g0272 | 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 | a0001c0001t0002g0099a0001c0001t0002g0151 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0198a0001c0001t0001g0199 | 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 | a0001c0001t0001g0184a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0216a0001c0001t0002g0217 | 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 | a0001c0001t0001g0012a0001c0001t0001g0014 | 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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0002g0002a0001c0001t0002g0003 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | 129 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(126): Show | 129 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.348+14825delA | MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 2/7 | chr9 | 132062616 | ||||||
| chr9:132062616
|
ATT | A | 6 | a0001c0001t0001g0154a0001c0001t0002g0095a0001c0001t0002g0152others(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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0012a0001c0001t0001g0014 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0016a0001c0001t0001g0073 | 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0001g0065a0002c0002t0001g0273 | 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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0078a0001c0001t0001g0219a0001c0001t0001g0228others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0014a0001c0001t0001g0208a0001c0001t0001g0211others(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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | 263 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(260): Show | 264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): 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 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(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 | 99 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0094others(96): Show | 99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 109 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0075others(106): Show | 109 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(106): 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 | 109 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0075others(106): Show | 109 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(106): 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0216a0001c0001t0002g0217 | 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 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(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 | 107 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0075others(104): Show | 107 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(104): 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 134 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(131): Show | 134 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(131): 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 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(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 | 259 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): 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 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(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 | a0001c0001t0001g0016a0001c0001t0001g0208a0001c0001t0001g0218 | 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 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0200 | 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 | a0001c0001t0001g0201a0001c0001t0001g0223a0001c0001t0001g0224others(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 | a0001c0001t0001g0223a0001c0001t0001g0224 | 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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0013a0001c0001t0001g0209a0001c0001t0001g0223others(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 | a0001c0001t0001g0222a0001c0001t0002g0220a0001c0001t0002g0221 | 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 | 264 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(261): Show | 265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(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 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0001t0002g0002a0001c0001t0002g0003 | 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 |