Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 728637 |
|---|---|
| ensemblid | ENSG00000239642.6 |
| hgncid | 51253 |
| symbol | MEIKIN |
| name | meiotic kinetochore factor |
| refseq_nuc | NM_001303622.2 |
| refseq_prot | NP_001290551.1 |
| ensembl_nuc | ENST00000442687.6 |
| ensembl_prot | ENSP00000488568.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 131806990 |
| end | 131945663 |
| strand | - |
| ver | v1.2 |
| region | chr5:131806990-131945663 |
| region5000 | chr5:131801990-131950663 |
| regionname0 | MEIKIN_chr5_131806990_131945663 |
| regionname5000 | MEIKIN_chr5_131801990_131950663 |
| 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 | 373 | 345 | 90 | 64 | 155 | 8 | 26 | 125 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0002 | 0/0 | 373 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| 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 | 1122 | 195 | 56 | 38 | 80 | 6 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0002 | 0/0 | 1122 | 136 | 20 | 26 | 75 | 2 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0003 | 0/0 | 1122 | 10 | 10 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0004 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0005 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| c0007 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| 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 | 405 | 303 | 56 | 56 | 155 | 8 | 26 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| t0002 | 0/0 | 405 | 40 | 32 | 8 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| t0003 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| t0004 | 0/0 | 405 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| t0005 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| 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 | 1122 | 195 | 56 | 38 | 80 | 6 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0002 | 0/0 | 1122 | 136 | 20 | 26 | 75 | 2 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0003 | 0/0 | 1122 | 10 | 10 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0004 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0007 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0002c0005 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1526 | 156 | 26 | 30 | 79 | 6 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0001t0002 | 0/0 | 1526 | 37 | 29 | 8 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0001t0003 | 0/0 | 1526 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0001t0004 | 0/0 | 1526 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0002t0001 | 0/0 | 1526 | 135 | 19 | 26 | 75 | 2 | 13 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0002t0005 | 0/0 | 1526 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0003t0001 | 0/0 | 1526 | 10 | 10 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0004t0002 | 0/0 | 1526 | 2 | 2 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0006t0002 | 0/0 | 1526 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0001c0007t0001 | 0/0 | 1526 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| a0002c0005t0001 | 0/0 | 1526 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | copy fasta | chr5 | 131801990 | 131950663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0002t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0001c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| a0002c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0340 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0336 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0329 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0232 | EUR | IBS | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0312 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01891 | hp2 | a0001 | c0007 | t0001 | g0201 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0325 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | CDX | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | CDX | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0309 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0306 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0310 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0193 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0342 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0308 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0314 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0311 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0295 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | BEB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0231 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | BEB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0315 | SAS | STU | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0307 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19080 | hp1 | a0002 | c0005 | t0001 | g0164 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ASW | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ASW | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0260 | EUR | TSI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | GIH | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0305 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0192 | AFR | ACB | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | USA | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA20300 | hp2 | a0001 | c0006 | t0002 | g0035 | AFR | USA | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0124 | REF | REF | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0058 | REF | REF | MEIKIN_chr5_131801990_131950663 | MEIKIN | chr5 | 131801990 | 131950663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131851283
|
T | C | 1 | a0002 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.956A>G | p.Gln319Arg | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/13 | 1114/1526 | 956/1122 | 319/373 | chr5 | 131851283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131818747
|
G | T | 1 | a0001c0003 | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1092C>A | p.Thr364Thr | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/13 | 1250/1526 | 1092/1122 | 364/373 | chr5 | 131818747 | ||
| chr5:131851369
|
T | C | 1 | a0001c0006 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.870A>G | p.Ser290Ser | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/13 | 1028/1526 | 870/1122 | 290/373 | chr5 | 131851369 | ||
| chr5:131933526
|
T | C | 1 | a0001c0004 | 2 | HG02559.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.465A>G | p.Lys155Lys | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/13 | 623/1526 | 465/1122 | 155/373 | chr5 | 131933526 | ||
| chr5:131933553
|
G | A | 1 | a0001c0007 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.438C>T | p.Ser146Ser | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/13 | 596/1526 | 438/1122 | 146/373 | chr5 | 131933553 | ||
| chr5:131945413
|
G | C | 2 | a0001c0002a0001c0003 | 146 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
synonymous_variant | LOW | c.93C>G | p.Ala31Ala | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 1/13 | 251/1526 | 93/1122 | 31/373 | chr5 | 131945413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131807002
|
T | C | 1 | a0001c0001t0004 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 13/13 | 234 | chr5 | 131807002 | |||||
| chr5:131807055
|
T | C | 3 | a0001c0001t0002a0001c0004t0002a0001c0006t0002 | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*181A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 13/13 | 181 | chr5 | 131807055 | |||||
| chr5:131807117
|
A | T | 1 | a0001c0001t0003 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 13/13 | 119 | chr5 | 131807117 | |||||
| chr5:131945577
|
G | A | 1 | a0001c0002t0005 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 1/13 | 72 | chr5 | 131945577 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131807287
|
C | T | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1100-29G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807287 | ||||||
| chr5:131807332
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-74G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807332 | ||||||
| chr5:131807556
|
C | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1100-298G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807556 | ||||||
| chr5:131807631
|
T | A | 275 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1100-373A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807631 | ||||||
| chr5:131807676
|
A | C | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1100-418T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807676 | ||||||
| chr5:131807714
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1100-456G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807714 | ||||||
| chr5:131807823
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1100-565G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807823 | ||||||
| chr5:131807966
|
T | C | 1 | a0001c0002t0001g0333 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1100-708A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131807966 | ||||||
| chr5:131808054
|
T | C | 16 | a0001c0002t0001g0323a0001c0002t0001g0325a0001c0002t0001g0326others(13): Show | 16 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1100-796A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808054 | ||||||
| chr5:131808161
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1100-903C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808161 | ||||||
| chr5:131808214
|
G | A | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1100-956C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808214 | ||||||
| chr5:131808629
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1100-1371T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808629 | ||||||
| chr5:131808874
|
G | A | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1100-1616C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808874 | ||||||
| chr5:131808912
|
C | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1100-1654G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808912 | ||||||
| chr5:131808912
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-1654G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131808912 | ||||||
| chr5:131809041
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1100-1783G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809041 | ||||||
| chr5:131809061
|
T | TCAAA | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1100-1807_1100-180 others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809061 | ||||||
| chr5:131809066
|
CAAACAA | C | 4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100-1814_1100-180 others(10): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809066 | ||||||
| chr5:131809267
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0163 | 2 | NA18940.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1100-2009A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809267 | ||||||
| chr5:131809307
|
C | A | 1 | a0001c0002t0001g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1100-2049G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809307 | ||||||
| chr5:131809504
|
A | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1100-2246T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809504 | ||||||
| chr5:131809517
|
C | T | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1100-2259G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809517 | ||||||
| chr5:131809547
|
G | A | 11 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0105others(8): Show | 11 | HG00408.hp1 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1100-2289C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809547 | ||||||
| chr5:131809798
|
A | T | 1 | a0001c0002t0001g0334 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1100-2540T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809798 | ||||||
| chr5:131809819
|
C | CA | 144 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1100-2562dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809819 | ||||||
| chr5:131809819
|
CA | C | 12 | a0001c0002t0001g0003a0001c0002t0001g0252a0001c0002t0001g0254others(9): Show | 13 | NA18945.hp2 NA18947.hp1 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.1100-2562delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809819 | ||||||
| chr5:131809822
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1100-2564T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809822 | ||||||
| chr5:131809833
|
C | A | 1 | a0001c0002t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1100-2575G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131809833 | ||||||
| chr5:131810021
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1100-2763G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810021 | ||||||
| chr5:131810044
|
A | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-2786T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810044 | ||||||
| chr5:131810108
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1100-2850C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810108 | ||||||
| chr5:131810326
|
A | T | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1100-3068T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810326 | ||||||
| chr5:131810329
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1100-3071T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810329 | ||||||
| chr5:131810491
|
G | C | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1100-3233C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131810491 | ||||||
| chr5:131811108
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1100-3850C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811108 | ||||||
| chr5:131811300
|
T | C | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1100-4042A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811300 | ||||||
| chr5:131811537
|
C | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0296 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1100-4279G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811537 | ||||||
| chr5:131811615
|
CT | C | 338 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1100-4358delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811615 | ||||||
| chr5:131811642
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1100-4384A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811642 | ||||||
| chr5:131811666
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1100-4408C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811666 | ||||||
| chr5:131811692
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1100-4434A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811692 | ||||||
| chr5:131811701
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1100-4443C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131811701 | ||||||
| chr5:131812088
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1100-4830G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131812088 | ||||||
| chr5:131812181
|
C | T | 1 | a0001c0002t0001g0244 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1100-4923G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131812181 | ||||||
| chr5:131812292
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1100-5034T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131812292 | ||||||
| chr5:131812515
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100-5257T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131812515 | ||||||
| chr5:131813257
|
T | C | 92 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(89): Show | 92 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1099+5483A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813257 | ||||||
| chr5:131813283
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1099+5457C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813283 | ||||||
| chr5:131813377
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099+5363G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813377 | ||||||
| chr5:131813387
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099+5353A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813387 | ||||||
| chr5:131813429
|
C | CT | 23 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(20): Show | 23 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1099+5310dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813429 | ||||||
| chr5:131813429
|
C | CTT | 131 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1099+5309_1099+531 others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813429 | ||||||
| chr5:131813429
|
C | CTTT | 9 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0044others(6): Show | 9 | HG00609.hp1 HG00621.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099+5308_1099+531 others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813429 | ||||||
| chr5:131813547
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1099+5193G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813547 | ||||||
| chr5:131813549
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0183 | 3 | HG01934.hp2 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1099+5191G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813549 | ||||||
| chr5:131813588
|
G | A | 1 | a0001c0002t0001g0335 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1099+5152C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813588 | ||||||
| chr5:131813674
|
G | T | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099+5066C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813674 | ||||||
| chr5:131813761
|
A | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1099+4979T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813761 | ||||||
| chr5:131813936
|
C | T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1099+4804G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131813936 | ||||||
| chr5:131814011
|
T | C | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1099+4729A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814011 | ||||||
| chr5:131814278
|
CT | C | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1099+4461delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814278 | ||||||
| chr5:131814406
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1099+4334A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814406 | ||||||
| chr5:131814574
|
C | G | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1099+4166G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814574 | ||||||
| chr5:131814900
|
G | T | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1099+3840C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814900 | ||||||
| chr5:131814987
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1099+3753G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131814987 | ||||||
| chr5:131815053
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01069.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1099+3687T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815053 | ||||||
| chr5:131815123
|
C | CATG | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1099+3616_1099+361 others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815123 | ||||||
| chr5:131815195
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1099+3545G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815195 | ||||||
| chr5:131815295
|
G | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1099+3445C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815295 | ||||||
| chr5:131815691
|
A | G | 1 | a0001c0002t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1099+3049T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815691 | ||||||
| chr5:131815752
|
C | T | 4 | a0001c0002t0001g0205a0001c0002t0001g0226a0001c0002t0001g0230others(1): Show | 4 | HG00733.hp1 HG01256.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+2988G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131815752 | ||||||
| chr5:131816178
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1099+2562G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816178 | ||||||
| chr5:131816418
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1099+2322A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816418 | ||||||
| chr5:131816486
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1099+2254A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816486 | ||||||
| chr5:131816561
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1099+2179T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816561 | ||||||
| chr5:131816595
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099+2145C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816595 | ||||||
| chr5:131816631
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1099+2109G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816631 | ||||||
| chr5:131816647
|
C | A | 1 | a0001c0002t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1099+2093G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816647 | ||||||
| chr5:131816681
|
G | C | 6 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099+2059C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816681 | ||||||
| chr5:131816699
|
T | A | 21 | a0001c0001t0001g0046a0001c0001t0001g0074a0001c0001t0001g0075others(18): Show | 21 | HG00544.hp1 HG02040.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099+2041A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816699 | ||||||
| chr5:131816805
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1099+1935G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816805 | ||||||
| chr5:131816837
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099+1903A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816837 | ||||||
| chr5:131816856
|
C | G | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1099+1884G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816856 | ||||||
| chr5:131816882
|
T | C | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1099+1858A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131816882 | ||||||
| chr5:131817108
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1099+1632C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817108 | ||||||
| chr5:131817161
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1099+1579G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817161 | ||||||
| chr5:131817345
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0110 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1099+1395G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817345 | ||||||
| chr5:131817573
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1099+1167C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817573 | ||||||
| chr5:131817594
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099+1146A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817594 | ||||||
| chr5:131817602
|
C | T | 162 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1099+1138G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817602 | ||||||
| chr5:131817613
|
C | CA | 195 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1099+1126dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817613 | ||||||
| chr5:131817613
|
C | CAA | 9 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0092others(6): Show | 9 | HG00733.hp2 HG01081.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099+1125_1099+112 others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817613 | ||||||
| chr5:131817734
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0183 | 3 | HG01934.hp2 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1099+1006C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817734 | ||||||
| chr5:131817872
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099+868T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131817872 | ||||||
| chr5:131818049
|
A | G | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1099+691T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131818049 | ||||||
| chr5:131818214
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1099+526C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131818214 | ||||||
| chr5:131818242
|
A | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0316 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1099+498T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131818242 | ||||||
| chr5:131818637
|
GAAT | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+100_1099+102d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 12/12 | chr5 | 131818637 | ||||||
| chr5:131818966
|
A | G | 1 | a0001c0002t0001g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.976-103T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131818966 | ||||||
| chr5:131819082
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.976-219G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819082 | ||||||
| chr5:131819327
|
C | T | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.976-464G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819327 | ||||||
| chr5:131819422
|
G | T | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.976-559C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819422 | ||||||
| chr5:131819439
|
A | AGAGGAGG others(15): Show |
4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-598_976-577dup others(22): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819439 | ||||||
| chr5:131819452
|
CA | C | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.976-590delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819452 | ||||||
| chr5:131819453
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.976-590T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819453 | ||||||
| chr5:131819469
|
A | G | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.976-606T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819469 | ||||||
| chr5:131819507
|
A | G | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.976-644T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819507 | ||||||
| chr5:131819586
|
T | C | 1 | a0001c0004t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.976-723A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819586 | ||||||
| chr5:131819590
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.976-727C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819590 | ||||||
| chr5:131819598
|
CT | C | 158 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.976-736delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819598 | ||||||
| chr5:131819615
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.976-752G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819615 | ||||||
| chr5:131819765
|
A | AT | 85 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0048others(82): Show | 85 | HG00438.hp2 HG00544.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.976-903dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATT | 6 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0075others(3): Show | 6 | HG02074.hp2 HG02148.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-904_976-903dup others(2): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(3): Show |
2 | a0001c0002t0001g0301a0001c0002t0001g0303 | 2 | HG01496.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.976-912_976-903dup others(10): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0002g0032a0001c0001t0002g0188 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.976-914_976-903dup others(12): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(6): Show |
1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.976-915_976-903dup others(13): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(7): Show |
1 | a0001c0004t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.976-916_976-903dup others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976-919_976-903dup others(17): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.976-922_976-903dup others(20): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0095 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.976-902T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
AT | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0094a0001c0001t0001g0100others(9): Show | 12 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.976-903delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
ATTTT | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.976-906_976-903del others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819765
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.976-913_976-903del others(11): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819765 | ||||||
| chr5:131819807
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-944C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819807 | ||||||
| chr5:131819807
|
G | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.976-944C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819807 | ||||||
| chr5:131819861
|
C | T | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.976-998G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819861 | ||||||
| chr5:131819901
|
A | G | 3 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0294 | 3 | HG01109.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.976-1038T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819901 | ||||||
| chr5:131819920
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1057G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819920 | ||||||
| chr5:131819925
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.976-1062C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819925 | ||||||
| chr5:131819951
|
A | T | 1 | a0001c0002t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.976-1088T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131819951 | ||||||
| chr5:131820074
|
C | CT | 224 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.976-1212dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820074 | ||||||
| chr5:131820074
|
C | CTT | 26 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0103others(23): Show | 26 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.976-1213_976-1212d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820074 | ||||||
| chr5:131820128
|
G | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.976-1265C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820128 | ||||||
| chr5:131820436
|
A | G | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.976-1573T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820436 | ||||||
| chr5:131820541
|
G | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-1678C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820541 | ||||||
| chr5:131820712
|
A | G | 2 | a0001c0002t0001g0215a0001c0002t0001g0216 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.976-1849T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820712 | ||||||
| chr5:131820714
|
A | G | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.976-1851T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820714 | ||||||
| chr5:131820769
|
A | C | 217 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.976-1906T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820769 | ||||||
| chr5:131820807
|
G | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.976-1944C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820807 | ||||||
| chr5:131820863
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2000G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820863 | ||||||
| chr5:131820915
|
C | A | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.976-2052G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131820915 | ||||||
| chr5:131821055
|
G | C | 2 | a0001c0002t0001g0268a0001c0002t0001g0271 | 2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.976-2192C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821055 | ||||||
| chr5:131821089
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.976-2226A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821089 | ||||||
| chr5:131821130
|
G | A | 2 | a0001c0002t0001g0268a0001c0002t0001g0271 | 2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.976-2267C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821130 | ||||||
| chr5:131821133
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-2270G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821133 | ||||||
| chr5:131821142
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.976-2279G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821142 | ||||||
| chr5:131821191
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.976-2328C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821191 | ||||||
| chr5:131821298
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.976-2435A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821298 | ||||||
| chr5:131821407
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.976-2544T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821407 | ||||||
| chr5:131821546
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0073others(2): Show | 5 | HG00609.hp2 NA18957.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-2683A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821546 | ||||||
| chr5:131821630
|
C | CT | 77 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(74): Show | 77 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.976-2768dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821630
|
C | CTT | 34 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0083others(31): Show | 35 | HG00408.hp1 HG00621.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.976-2769_976-2768d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821630
|
C | CTTT | 27 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0008others(24): Show | 27 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.976-2770_976-2768d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821630
|
C | CTTTT | 6 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0013others(3): Show | 6 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2771_976-2768d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821630
|
CT | C | 13 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0136others(10): Show | 13 | HG00738.hp2 HG01167.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.976-2768delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821630
|
CTT | C | 7 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.976-2769_976-2768d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821630 | ||||||
| chr5:131821663
|
C | A | 2 | a0001c0002t0001g0207a0001c0002t0001g0232 | 2 | HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.976-2800G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821663 | ||||||
| chr5:131821713
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.976-2850T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821713 | ||||||
| chr5:131821722
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.976-2859G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821722 | ||||||
| chr5:131821738
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.976-2875A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821738 | ||||||
| chr5:131821998
|
T | A | 1 | a0001c0002t0001g0265 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.976-3135A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131821998 | ||||||
| chr5:131822221
|
T | C | 1 | a0001c0002t0001g0289 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.976-3358A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822221 | ||||||
| chr5:131822267
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0198 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.976-3404C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822267 | ||||||
| chr5:131822395
|
T | A | 1 | a0001c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.976-3532A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822395 | ||||||
| chr5:131822561
|
A | G | 3 | a0001c0002t0001g0260a0001c0002t0001g0290a0001c0002t0001g0291 | 3 | HG01070.hp1 HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.976-3698T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822561 | ||||||
| chr5:131822641
|
T | C | 1 | a0001c0002t0001g0339 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.976-3778A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822641 | ||||||
| chr5:131822794
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.976-3931A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822794 | ||||||
| chr5:131822801
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.976-3938C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822801 | ||||||
| chr5:131822814
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-3951G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822814 | ||||||
| chr5:131822867
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.976-4004C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822867 | ||||||
| chr5:131822869
|
G | A | 2 | a0001c0002t0001g0268a0001c0002t0001g0271 | 2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.976-4006C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822869 | ||||||
| chr5:131822934
|
A | AT | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0067others(22): Show | 25 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-4072dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822934 | ||||||
| chr5:131822934
|
AT | A | 134 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.976-4072delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822934 | ||||||
| chr5:131822934
|
ATT | A | 17 | a0001c0001t0001g0033a0001c0001t0001g0069a0001c0001t0001g0086others(14): Show | 18 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.976-4073_976-4072d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822934 | ||||||
| chr5:131822934
|
ATTTT | A | 9 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0308others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.976-4075_976-4072d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131822934 | ||||||
| chr5:131823074
|
C | T | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.976-4211G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823074 | ||||||
| chr5:131823396
|
CCTCT | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-4537_976-4534d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823396 | ||||||
| chr5:131823737
|
G | C | 1 | a0001c0002t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.976-4874C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823737 | ||||||
| chr5:131823763
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.976-4900A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823763 | ||||||
| chr5:131823830
|
T | C | 1 | a0001c0002t0001g0250 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.976-4967A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823830 | ||||||
| chr5:131823915
|
G | T | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.976-5052C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131823915 | ||||||
| chr5:131824195
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.976-5332T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824195 | ||||||
| chr5:131824307
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.976-5444C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824307 | ||||||
| chr5:131824344
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0094 | 2 | HG01993.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.976-5481C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824344 | ||||||
| chr5:131824412
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.976-5549G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824412 | ||||||
| chr5:131824494
|
T | G | 163 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.976-5631A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824494 | ||||||
| chr5:131824496
|
A | G | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.976-5633T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824496 | ||||||
| chr5:131824622
|
A | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-5759T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824622 | ||||||
| chr5:131824660
|
A | G | 2 | a0001c0002t0001g0330a0001c0002t0001g0331 | 2 | NA18998.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.976-5797T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824660 | ||||||
| chr5:131824843
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.976-5980C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824843 | ||||||
| chr5:131824916
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.976-6053A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824916 | ||||||
| chr5:131824953
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.976-6090T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824953 | ||||||
| chr5:131824955
|
G | T | 1 | a0001c0002t0001g0334 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.976-6092C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131824955 | ||||||
| chr5:131825030
|
A | AAAG | 9 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0308others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.976-6170_976-6168d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825030 | ||||||
| chr5:131825063
|
G | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-6200C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825063 | ||||||
| chr5:131825090
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-6227G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825090 | ||||||
| chr5:131825600
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.976-6737G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825600 | ||||||
| chr5:131825742
|
C | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-6879G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825742 | ||||||
| chr5:131825961
|
G | A | 1 | a0001c0001t0002g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.976-7098C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131825961 | ||||||
| chr5:131826086
|
C | CT | 6 | a0001c0001t0002g0018a0001c0002t0001g0202a0001c0002t0001g0203others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-7224dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826086 | ||||||
| chr5:131826086
|
CT | C | 172 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.976-7224delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826086 | ||||||
| chr5:131826086
|
CTT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0160a0001c0002t0001g0300others(4): Show | 7 | HG01496.hp1 HG01943.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-7225_976-7224d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826086 | ||||||
| chr5:131826106
|
T | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.976-7243A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826106 | ||||||
| chr5:131826148
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-7285C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826148 | ||||||
| chr5:131826431
|
C | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.976-7568G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826431 | ||||||
| chr5:131826449
|
C | T | 1 | a0001c0002t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.976-7586G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826449 | ||||||
| chr5:131826757
|
CA | C | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 38 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.976-7895delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131826757 | ||||||
| chr5:131827004
|
A | T | 16 | a0001c0002t0001g0323a0001c0002t0001g0325a0001c0002t0001g0326others(13): Show | 16 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.976-8141T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131827004 | ||||||
| chr5:131827329
|
G | A | 163 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.976-8466C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131827329 | ||||||
| chr5:131827946
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.976-9083C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131827946 | ||||||
| chr5:131828001
|
C | T | 7 | a0001c0001t0001g0066a0001c0001t0001g0087a0001c0001t0001g0090others(4): Show | 7 | HG01934.hp2 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.976-9138G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131828001 | ||||||
| chr5:131828038
|
C | CA | 16 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(13): Show | 16 | HG01192.hp2 HG01261.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.976-9176dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131828038 | ||||||
| chr5:131828815
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-9952T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131828815 | ||||||
| chr5:131828977
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.976-10114A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131828977 | ||||||
| chr5:131829066
|
T | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.976-10203A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829066 | ||||||
| chr5:131829278
|
T | G | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0172others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-10415A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829278 | ||||||
| chr5:131829313
|
C | T | 208 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.976-10450G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829313 | ||||||
| chr5:131829461
|
T | C | 1 | a0001c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.976-10598A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829461 | ||||||
| chr5:131829501
|
G | T | 1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.976-10638C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829501 | ||||||
| chr5:131829523
|
T | G | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.976-10660A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829523 | ||||||
| chr5:131829797
|
C | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.976-10934G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131829797 | ||||||
| chr5:131830045
|
G | A | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.976-11182C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830045 | ||||||
| chr5:131830321
|
T | C | 207 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.976-11458A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830321 | ||||||
| chr5:131830335
|
T | A | 3 | a0001c0001t0002g0191a0001c0004t0002g0192a0001c0004t0002g0193 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.976-11472A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830335 | ||||||
| chr5:131830361
|
C | A | 1 | a0001c0001t0001g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.976-11498G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830361 | ||||||
| chr5:131830497
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.976-11634C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830497 | ||||||
| chr5:131830562
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.976-11699G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830562 | ||||||
| chr5:131830576
|
T | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(33): Show | 37 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.976-11713A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830576 | ||||||
| chr5:131830883
|
C | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.976-12020G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830883 | ||||||
| chr5:131830903
|
G | GT | 13 | a0001c0001t0001g0062a0001c0002t0001g0203a0001c0002t0001g0330others(10): Show | 13 | HG00642.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.976-12041dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131830903 | ||||||
| chr5:131831073
|
T | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0031 | 2 | HG00642.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.976-12210A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831073 | ||||||
| chr5:131831393
|
A | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.976-12530T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831393 | ||||||
| chr5:131831530
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.976-12667C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831530 | ||||||
| chr5:131831548
|
C | T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.976-12685G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831548 | ||||||
| chr5:131831553
|
C | CTCAA | 18 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0047others(15): Show | 18 | HG00609.hp2 HG01978.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.976-12694_976-1269 others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831553 | ||||||
| chr5:131831627
|
T | C | 1 | a0001c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.976-12764A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831627 | ||||||
| chr5:131831691
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.976-12828C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831691 | ||||||
| chr5:131831849
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.976-12986T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831849 | ||||||
| chr5:131831994
|
A | G | 1 | a0001c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.976-13131T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131831994 | ||||||
| chr5:131832007
|
C | T | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.976-13144G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832007 | ||||||
| chr5:131832071
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-13208G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832071 | ||||||
| chr5:131832142
|
G | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.976-13279C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832142 | ||||||
| chr5:131832238
|
T | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.976-13375A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832238 | ||||||
| chr5:131832412
|
G | A | 6 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-13549C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832412 | ||||||
| chr5:131832429
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-13566A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832429 | ||||||
| chr5:131832674
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.976-13811T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832674 | ||||||
| chr5:131832730
|
C | A | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.976-13867G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131832730 | ||||||
| chr5:131833244
|
C | T | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.976-14381G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131833244 | ||||||
| chr5:131833425
|
G | A | 111 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.976-14562C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131833425 | ||||||
| chr5:131833488
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.976-14625G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131833488 | ||||||
| chr5:131833674
|
T | TTATTCAC others(9): Show |
1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.976-14827_976-1481 others(20): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131833674 | ||||||
| chr5:131834118
|
G | A | 1 | a0001c0002t0001g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.976-15255C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131834118 | ||||||
| chr5:131834458
|
A | T | 1 | a0001c0001t0002g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.976-15595T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131834458 | ||||||
| chr5:131834596
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0110 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.976-15733C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131834596 | ||||||
| chr5:131835131
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.975+16133A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835131 | ||||||
| chr5:131835157
|
T | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.975+16107A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835157 | ||||||
| chr5:131835176
|
A | G | 3 | a0001c0001t0002g0191a0001c0004t0002g0192a0001c0004t0002g0193 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.975+16088T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835176 | ||||||
| chr5:131835192
|
G | GTGTGTAT others(21): Show |
39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.975+16071_975+1607 others(32): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835192 | ||||||
| chr5:131835198
|
G | A | 217 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.975+16066C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835198 | ||||||
| chr5:131835206
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.975+16058T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835206 | ||||||
| chr5:131835212
|
G | T | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.975+16052C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835212 | ||||||
| chr5:131835249
|
TATATG | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+16010_975+1601 others(9): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835249 | ||||||
| chr5:131835315
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.975+15949C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835315 | ||||||
| chr5:131835327
|
T | A | 2 | a0001c0002t0001g0261a0001c0002t0001g0279 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.975+15937A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835327 | ||||||
| chr5:131835415
|
G | A | 1 | a0001c0002t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.975+15849C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835415 | ||||||
| chr5:131835500
|
G | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+15764C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835500 | ||||||
| chr5:131835558
|
G | A | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.975+15706C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835558 | ||||||
| chr5:131835625
|
G | A | 1 | a0001c0002t0001g0264 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.975+15639C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835625 | ||||||
| chr5:131835831
|
G | C | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.975+15433C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835831 | ||||||
| chr5:131835912
|
T | A | 2 | a0001c0002t0001g0215a0001c0002t0001g0216 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+15352A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835912 | ||||||
| chr5:131835940
|
T | A | 1 | a0001c0003t0001g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.975+15324A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835940 | ||||||
| chr5:131835960
|
A | G | 217 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.975+15304T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835960 | ||||||
| chr5:131835969
|
G | T | 1 | a0001c0002t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.975+15295C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131835969 | ||||||
| chr5:131836079
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.975+15185A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836079 | ||||||
| chr5:131836128
|
T | A | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+15136A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836128 | ||||||
| chr5:131836231
|
C | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.975+15033G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836231 | ||||||
| chr5:131836450
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+14814A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836450 | ||||||
| chr5:131836468
|
G | T | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.975+14796C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836468 | ||||||
| chr5:131836503
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0174 | 2 | HG01167.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.975+14761G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836503 | ||||||
| chr5:131836548
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.975+14716G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836548 | ||||||
| chr5:131836725
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.975+14539G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836725 | ||||||
| chr5:131836740
|
GT | G | 12 | a0001c0001t0002g0007a0001c0001t0002g0188a0001c0002t0001g0214others(9): Show | 12 | HG02258.hp1 NA18947.hp1 NA18988.hp2 others(9): Show |
intron_variant | MODIFIER | c.975+14523delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836740 | ||||||
| chr5:131836774
|
G | C | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.975+14490C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836774 | ||||||
| chr5:131836788
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+14476T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836788 | ||||||
| chr5:131836903
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.975+14361T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836903 | ||||||
| chr5:131836999
|
T | C | 1 | a0001c0003t0001g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.975+14265A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131836999 | ||||||
| chr5:131837086
|
A | C | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+14178T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837086 | ||||||
| chr5:131837110
|
C | A | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.975+14154G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837110 | ||||||
| chr5:131837142
|
C | G | 1 | a0001c0002t0001g0298 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.975+14122G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837142 | ||||||
| chr5:131837193
|
T | C | 207 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.975+14071A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837193 | ||||||
| chr5:131837413
|
C | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.975+13851G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837413 | ||||||
| chr5:131837469
|
T | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.975+13795A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837469 | ||||||
| chr5:131837684
|
T | C | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+13580A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131837684 | ||||||
| chr5:131838051
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.975+13213T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838051 | ||||||
| chr5:131838199
|
A | G | 1 | a0001c0002t0001g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.975+13065T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838199 | ||||||
| chr5:131838255
|
C | T | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.975+13009G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838255 | ||||||
| chr5:131838359
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0043 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.975+12905G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838359 | ||||||
| chr5:131838360
|
G | A | 1 | a0001c0002t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.975+12904C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838360 | ||||||
| chr5:131838408
|
T | A | 41 | a0001c0001t0001g0084a0001c0001t0001g0121a0001c0001t0002g0002others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.975+12856A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838408 | ||||||
| chr5:131838522
|
A | G | 163 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.975+12742T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838522 | ||||||
| chr5:131838574
|
G | GT | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.975+12689dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838574 | ||||||
| chr5:131838659
|
T | C | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0172others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+12605A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838659 | ||||||
| chr5:131838777
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+12487A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838777 | ||||||
| chr5:131838807
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+12457G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131838807 | ||||||
| chr5:131839156
|
T | C | 1 | a0001c0002t0001g0335 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.975+12108A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131839156 | ||||||
| chr5:131839565
|
G | A | 162 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.975+11699C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131839565 | ||||||
| chr5:131839885
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+11379C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131839885 | ||||||
| chr5:131839885
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.975+11379C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131839885 | ||||||
| chr5:131839891
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0198 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.975+11373T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131839891 | ||||||
| chr5:131840020
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.975+11244C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840020 | ||||||
| chr5:131840268
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+10996G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840268 | ||||||
| chr5:131840363
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.975+10901A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840363 | ||||||
| chr5:131840608
|
C | CT | 16 | a0001c0002t0001g0323a0001c0002t0001g0325a0001c0002t0001g0326others(13): Show | 16 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.975+10655dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840608 | ||||||
| chr5:131840634
|
A | G | 1 | a0001c0002t0001g0252 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.975+10630T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840634 | ||||||
| chr5:131840764
|
C | A | 1 | a0001c0003t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.975+10500G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840764 | ||||||
| chr5:131840800
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.975+10464G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840800 | ||||||
| chr5:131840951
|
C | T | 217 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.975+10313G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131840951 | ||||||
| chr5:131841209
|
T | C | 272 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.975+10055A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131841209 | ||||||
| chr5:131841224
|
A | G | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.975+10040T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131841224 | ||||||
| chr5:131841337
|
T | G | 9 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.975+9927A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131841337 | ||||||
| chr5:131841412
|
C | T | 18 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0047others(15): Show | 18 | HG00609.hp2 HG01978.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.975+9852G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131841412 | ||||||
| chr5:131841977
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.975+9287T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131841977 | ||||||
| chr5:131842145
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 34 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.975+9119A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842145 | ||||||
| chr5:131842201
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.975+9063C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842201 | ||||||
| chr5:131842251
|
C | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+9013G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842251 | ||||||
| chr5:131842339
|
T | C | 1 | a0001c0002t0001g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.975+8925A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842339 | ||||||
| chr5:131842415
|
T | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.975+8849A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842415 | ||||||
| chr5:131842459
|
T | G | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.975+8805A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842459 | ||||||
| chr5:131842559
|
C | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.975+8705G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842559 | ||||||
| chr5:131842613
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975+8651A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842613 | ||||||
| chr5:131842617
|
G | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0190 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.975+8647C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842617 | ||||||
| chr5:131842763
|
T | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+8501A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842763 | ||||||
| chr5:131842782
|
C | G | 1 | a0001c0002t0001g0264 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.975+8482G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842782 | ||||||
| chr5:131842887
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.975+8377A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842887 | ||||||
| chr5:131842960
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+8304G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131842960 | ||||||
| chr5:131843369
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.975+7895G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843369 | ||||||
| chr5:131843496
|
C | T | 160 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.975+7768G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843496 | ||||||
| chr5:131843719
|
G | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0024 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.975+7545C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843719 | ||||||
| chr5:131843777
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0155 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.975+7487A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843777 | ||||||
| chr5:131843783
|
G | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.975+7481C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843783 | ||||||
| chr5:131843834
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.975+7430A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131843834 | ||||||
| chr5:131844007
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.975+7257C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844007 | ||||||
| chr5:131844028
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0001g0146others(2): Show | 5 | HG00733.hp2 HG01070.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+7236C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844028 | ||||||
| chr5:131844093
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+7171C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844093 | ||||||
| chr5:131844103
|
C | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.975+7161G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844103 | ||||||
| chr5:131844119
|
T | A | 1 | a0001c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.975+7145A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844119 | ||||||
| chr5:131844212
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+7052C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844212 | ||||||
| chr5:131844548
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.975+6716C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844548 | ||||||
| chr5:131844654
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.975+6610A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131844654 | ||||||
| chr5:131845121
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.975+6143A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845121 | ||||||
| chr5:131845136
|
C | G | 340 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(337): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.975+6128G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845136 | ||||||
| chr5:131845142
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.975+6122G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845142 | ||||||
| chr5:131845163
|
C | G | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.975+6101G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845163 | ||||||
| chr5:131845242
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.975+6022G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845242 | ||||||
| chr5:131845260
|
A | G | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.975+6004T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845260 | ||||||
| chr5:131845268
|
G | A | 9 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.975+5996C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845268 | ||||||
| chr5:131845271
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+5993A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845271 | ||||||
| chr5:131845272
|
T | TA | 35 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0064others(32): Show | 35 | HG00733.hp2 HG01175.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.975+5991dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAA | 6 | a0001c0001t0001g0049a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+5989_975+5991d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(1): Show |
12 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0019others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.975+5984_975+5991d others(10): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(2): Show |
10 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(7): Show | 11 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.975+5983_975+5991d others(11): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0016others(1): Show | 4 | HG02258.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+5982_975+5991d others(12): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(4): Show |
5 | a0001c0001t0002g0190a0001c0003t0001g0305a0001c0003t0001g0306others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+5981_975+5991d others(13): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(5): Show |
5 | a0001c0001t0002g0032a0001c0001t0002g0187a0001c0001t0002g0188others(2): Show | 5 | HG02258.hp1 HG03195.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+5980_975+5991d others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(6): Show |
1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+5979_975+5991d others(15): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0177a0001c0001t0002g0189a0001c0001t0002g0191others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+5976_975+5991d others(18): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0194 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.975+5975_975+5991d others(19): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(11): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0002g0186 | 3 | HG02109.hp1 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.975+5974_975+5991d others(20): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.975+5973_975+5991d others(21): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(15): Show |
1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.975+5970_975+5991d others(24): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(19): Show |
2 | a0001c0001t0001g0184a0001c0001t0003g0106 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.975+5966_975+5991d others(28): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
T | TAAAAAAA others(26): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.975+5991_975+5992i others(35): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
TA | T | 20 | a0001c0001t0001g0046a0001c0001t0001g0059a0001c0001t0001g0061others(17): Show | 20 | HG01168.hp1 HG01168.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.975+5991delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845272
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.975+5980_975+5991d others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845272 | ||||||
| chr5:131845340
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+5924G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845340 | ||||||
| chr5:131845419
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+5845A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845419 | ||||||
| chr5:131845587
|
C | T | 220 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.975+5677G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845587 | ||||||
| chr5:131845612
|
C | CA | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.975+5651dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845612 | ||||||
| chr5:131845612
|
C | CAA | 6 | a0001c0001t0001g0153a0001c0001t0002g0026a0001c0001t0002g0188others(3): Show | 6 | HG01884.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+5650_975+5651d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845612 | ||||||
| chr5:131845624
|
C | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.975+5640G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845624 | ||||||
| chr5:131845643
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.975+5621A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845643 | ||||||
| chr5:131845699
|
G | T | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.975+5565C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131845699 | ||||||
| chr5:131846043
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+5221G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846043 | ||||||
| chr5:131846135
|
A | C | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+5129T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846135 | ||||||
| chr5:131846177
|
C | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0061others(3): Show | 6 | NA18944.hp1 NA19010.hp2 NA19060.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+5087G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846177 | ||||||
| chr5:131846208
|
C | G | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.975+5056G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846208 | ||||||
| chr5:131846893
|
A | AGGCAGAG others(2): Show |
216 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.975+4370_975+4371i others(11): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846893 | ||||||
| chr5:131846966
|
T | C | 45 | a0001c0002t0001g0001a0001c0002t0001g0204a0001c0002t0001g0205others(42): Show | 47 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.975+4298A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131846966 | ||||||
| chr5:131847492
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975+3772T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131847492 | ||||||
| chr5:131847940
|
T | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+3324A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131847940 | ||||||
| chr5:131847991
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.975+3273G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131847991 | ||||||
| chr5:131848007
|
C | T | 1 | a0001c0002t0001g0326 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.975+3257G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848007 | ||||||
| chr5:131848051
|
C | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.975+3213G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848051 | ||||||
| chr5:131848094
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+3170G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848094 | ||||||
| chr5:131848186
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.975+3078G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848186 | ||||||
| chr5:131848204
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.975+3060A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848204 | ||||||
| chr5:131848424
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.975+2840C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848424 | ||||||
| chr5:131848746
|
C | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.975+2518G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848746 | ||||||
| chr5:131848754
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.975+2510A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848754 | ||||||
| chr5:131848771
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.975+2493T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848771 | ||||||
| chr5:131848843
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.975+2421C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848843 | ||||||
| chr5:131848901
|
C | T | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.975+2363G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131848901 | ||||||
| chr5:131849019
|
G | C | 1 | a0001c0001t0002g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.975+2245C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849019 | ||||||
| chr5:131849154
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+2110C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849154 | ||||||
| chr5:131849156
|
G | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+2108C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849156 | ||||||
| chr5:131849356
|
G | GAACCTCT others(20): Show |
96 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0041others(93): Show | 96 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.975+1881_975+1907d others(29): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
G | GAACCTCT others(47): Show |
31 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0059others(28): Show | 33 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.975+1854_975+1907d others(56): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
G | GAACCTCT others(74): Show |
9 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0131others(6): Show | 9 | HG00438.hp1 HG02071.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.975+1827_975+1907d others(83): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
G | GAACCTCT others(101): Show |
1 | a0001c0001t0001g0171 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.975+1800_975+1907d others(110): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
GAACCTCT others(20): Show |
G | 41 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0082others(38): Show | 41 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.975+1881_975+1907d others(29): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
GAACCTCT others(47): Show |
G | 68 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0053others(65): Show | 69 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.975+1854_975+1907d others(56): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
GAACCTCT others(74): Show |
G | 30 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0050others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.975+1827_975+1907d others(83): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
GAACCTCT others(101): Show |
G | 36 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0055others(33): Show | 37 | HG00621.hp2 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.975+1800_975+1907d others(2): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849356
|
GAACCTCT others(128): Show |
G | 3 | a0001c0001t0002g0014a0001c0001t0003g0106a0001c0003t0001g0314 | 3 | HG03225.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.975+1773_975+1907d others(2): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849356 | ||||||
| chr5:131849394
|
C | T | 1 | a0001c0002t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.975+1870G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849394 | ||||||
| chr5:131849472
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1792A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849472 | ||||||
| chr5:131849477
|
TTATATAT others(51): Show |
T | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.975+1729_975+1786d others(60): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849477 | ||||||
| chr5:131849499
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1765A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849499 | ||||||
| chr5:131849517
|
G | C | 6 | a0001c0001t0002g0015a0001c0001t0002g0026a0001c0001t0002g0027others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+1747C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849517 | ||||||
| chr5:131849526
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1738A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849526 | ||||||
| chr5:131849544
|
G | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(19): Show | 23 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.975+1720C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849544 | ||||||
| chr5:131849553
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1711A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849553 | ||||||
| chr5:131849571
|
G | C | 1 | a0001c0001t0002g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.975+1693C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849571 | ||||||
| chr5:131849580
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1684A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849580 | ||||||
| chr5:131849607
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1657A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849607 | ||||||
| chr5:131849653
|
G | C | 6 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+1611C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849653 | ||||||
| chr5:131849689
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.975+1575G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849689 | ||||||
| chr5:131849833
|
G | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.975+1431C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849833 | ||||||
| chr5:131849932
|
T | G | 2 | a0001c0001t0001g0127a0001c0002t0001g0315 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.975+1332A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131849932 | ||||||
| chr5:131850005
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.975+1259A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850005 | ||||||
| chr5:131850057
|
C | CA | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.975+1206dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850057 | ||||||
| chr5:131850082
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.975+1182A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850082 | ||||||
| chr5:131850363
|
C | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+901G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850363 | ||||||
| chr5:131850602
|
C | T | 1 | a0001c0002t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.975+662G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850602 | ||||||
| chr5:131850619
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.975+645G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850619 | ||||||
| chr5:131850894
|
G | C | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.975+370C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850894 | ||||||
| chr5:131850912
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.975+352G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131850912 | ||||||
| chr5:131851053
|
T | C | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.975+211A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131851053 | ||||||
| chr5:131851218
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.975+46T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 11/12 | chr5 | 131851218 | ||||||
| chr5:131851489
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.856-106A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131851489 | ||||||
| chr5:131852048
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.856-665G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852048 | ||||||
| chr5:131852069
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.856-686G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852069 | ||||||
| chr5:131852133
|
T | C | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.856-750A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852133 | ||||||
| chr5:131852157
|
C | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.856-774G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852157 | ||||||
| chr5:131852189
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.856-806G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852189 | ||||||
| chr5:131852387
|
G | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0165others(9): Show | 12 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.856-1004C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852387 | ||||||
| chr5:131852567
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.856-1184G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852567 | ||||||
| chr5:131852743
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.856-1360G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852743 | ||||||
| chr5:131852754
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.856-1371A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852754 | ||||||
| chr5:131852810
|
C | A | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.856-1427G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852810 | ||||||
| chr5:131852874
|
GA | G | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.856-1492delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852874 | ||||||
| chr5:131852952
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.856-1569C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131852952 | ||||||
| chr5:131853134
|
T | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+1620A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853134 | ||||||
| chr5:131853369
|
G | A | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.855+1385C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853369 | ||||||
| chr5:131853413
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.855+1341A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853413 | ||||||
| chr5:131853514
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0177a0001c0001t0002g0188 | 3 | HG02280.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.855+1240T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853514 | ||||||
| chr5:131853645
|
C | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.855+1109G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853645 | ||||||
| chr5:131853716
|
A | G | 3 | a0001c0001t0002g0017a0001c0001t0002g0025a0001c0001t0002g0031 | 3 | HG00642.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.855+1038T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853716 | ||||||
| chr5:131853998
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.855+756G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131853998 | ||||||
| chr5:131854104
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.855+650A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131854104 | ||||||
| chr5:131854140
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.855+614G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131854140 | ||||||
| chr5:131854368
|
T | C | 1 | a0002c0005t0001g0164 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.855+386A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 10/12 | chr5 | 131854368 | ||||||
| chr5:131854913
|
A | C | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-79T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131854913 | ||||||
| chr5:131854944
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775-110A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131854944 | ||||||
| chr5:131854993
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-159T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131854993 | ||||||
| chr5:131855795
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.775-961T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131855795 | ||||||
| chr5:131855914
|
A | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-1080T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131855914 | ||||||
| chr5:131855979
|
G | A | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.775-1145C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131855979 | ||||||
| chr5:131856090
|
G | C | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.775-1256C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856090 | ||||||
| chr5:131856097
|
A | C | 3 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0303 | 3 | HG01496.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.775-1263T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856097 | ||||||
| chr5:131856158
|
C | G | 6 | a0001c0001t0002g0029a0001c0002t0001g0300a0001c0002t0001g0301others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-1324G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856158 | ||||||
| chr5:131856476
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-1642T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856476 | ||||||
| chr5:131856887
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.775-2053A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856887 | ||||||
| chr5:131856942
|
T | A | 2 | a0001c0002t0001g0237a0001c0002t0001g0238 | 2 | HG03927.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.775-2108A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131856942 | ||||||
| chr5:131857143
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-2309C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857143 | ||||||
| chr5:131857377
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.775-2543G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857377 | ||||||
| chr5:131857539
|
C | A | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.775-2705G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857539 | ||||||
| chr5:131857626
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-2792G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857626 | ||||||
| chr5:131857875
|
C | T | 1 | a0001c0001t0002g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.775-3041G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857875 | ||||||
| chr5:131857978
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.775-3144C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131857978 | ||||||
| chr5:131858103
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.775-3269C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858103 | ||||||
| chr5:131858140
|
G | T | 1 | a0001c0002t0001g0333 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.775-3306C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858140 | ||||||
| chr5:131858283
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-3449G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858283 | ||||||
| chr5:131858306
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.775-3472G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858306 | ||||||
| chr5:131858376
|
G | T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.775-3542C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858376 | ||||||
| chr5:131858409
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.775-3575G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858409 | ||||||
| chr5:131858592
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775-3758A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858592 | ||||||
| chr5:131858593
|
T | G | 11 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0105others(8): Show | 11 | HG00408.hp1 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.775-3759A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858593 | ||||||
| chr5:131858665
|
A | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-3831T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858665 | ||||||
| chr5:131858686
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG01993.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-3852G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858686 | ||||||
| chr5:131858687
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.775-3853C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858687 | ||||||
| chr5:131858793
|
A | C | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.775-3959T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858793 | ||||||
| chr5:131858817
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-3983C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858817 | ||||||
| chr5:131858864
|
A | C | 1 | a0001c0003t0001g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.775-4030T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858864 | ||||||
| chr5:131858902
|
T | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.775-4068A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131858902 | ||||||
| chr5:131859000
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.775-4166C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859000 | ||||||
| chr5:131859263
|
C | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.775-4429G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859263 | ||||||
| chr5:131859309
|
C | T | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.775-4475G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859309 | ||||||
| chr5:131859334
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.775-4500C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859334 | ||||||
| chr5:131859487
|
C | T | 1 | a0001c0003t0001g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.775-4653G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859487 | ||||||
| chr5:131859766
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-4932G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859766 | ||||||
| chr5:131859857
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01069.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.775-5023C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131859857 | ||||||
| chr5:131860064
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0247 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.775-5230G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860064 | ||||||
| chr5:131860250
|
T | A | 1 | a0001c0002t0001g0320 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.775-5416A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860250 | ||||||
| chr5:131860280
|
G | GT | 9 | a0001c0001t0001g0049a0001c0001t0001g0076a0001c0001t0001g0079others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-5447dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860280 | ||||||
| chr5:131860280
|
G | GTT | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 34 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.775-5448_775-5447d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860280 | ||||||
| chr5:131860280
|
GT | G | 10 | a0001c0001t0001g0097a0001c0002t0001g0239a0001c0002t0001g0268others(7): Show | 10 | HG01496.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.775-5447delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860280 | ||||||
| chr5:131860347
|
A | AT | 185 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.775-5514dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860347 | ||||||
| chr5:131860347
|
A | ATT | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.775-5515_775-5514d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860347 | ||||||
| chr5:131860406
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.775-5572G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860406 | ||||||
| chr5:131860440
|
G | GT | 13 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0165others(10): Show | 13 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.775-5607dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860440 | ||||||
| chr5:131860449
|
G | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-5615C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860449 | ||||||
| chr5:131860611
|
A | AT | 56 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 57 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.775-5778dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860611 | ||||||
| chr5:131860618
|
T | TA | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.775-5785_775-5784i others(3): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860618 | ||||||
| chr5:131860623
|
A | T | 1 | a0001c0001t0002g0011 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.775-5789T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860623 | ||||||
| chr5:131860673
|
T | C | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-5839A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860673 | ||||||
| chr5:131860754
|
C | CT | 169 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.775-5921dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860754 | ||||||
| chr5:131860754
|
C | CTT | 42 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0037others(39): Show | 42 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.775-5922_775-5921d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860754 | ||||||
| chr5:131860754
|
C | CTTT | 6 | a0001c0001t0001g0062a0001c0001t0001g0075a0001c0001t0001g0159others(3): Show | 6 | HG00642.hp1 HG02040.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-5923_775-5921d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860754 | ||||||
| chr5:131860754
|
CT | C | 9 | a0001c0001t0002g0023a0001c0001t0002g0027a0001c0001t0002g0191others(6): Show | 9 | HG01069.hp1 HG01496.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-5921delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860754 | ||||||
| chr5:131860792
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775-5958A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860792 | ||||||
| chr5:131860805
|
A | G | 1 | a0001c0002t0001g0318 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.775-5971T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131860805 | ||||||
| chr5:131861107
|
T | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775-6273A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861107 | ||||||
| chr5:131861204
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.775-6370G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861204 | ||||||
| chr5:131861533
|
C | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-6699G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861533 | ||||||
| chr5:131861605
|
T | C | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.775-6771A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861605 | ||||||
| chr5:131861713
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-6879A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861713 | ||||||
| chr5:131861778
|
T | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-6944A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861778 | ||||||
| chr5:131861961
|
G | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(30): Show | 34 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.775-7127C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131861961 | ||||||
| chr5:131862015
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-7181T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862015 | ||||||
| chr5:131862319
|
A | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0016others(4): Show | 7 | HG00642.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-7485T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862319 | ||||||
| chr5:131862425
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.775-7591T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862425 | ||||||
| chr5:131862452
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-7618C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862452 | ||||||
| chr5:131862655
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.775-7821A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862655 | ||||||
| chr5:131862661
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.775-7827G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862661 | ||||||
| chr5:131862959
|
C | A | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.775-8125G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862959 | ||||||
| chr5:131862970
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775-8136T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862970 | ||||||
| chr5:131862971
|
T | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-8137A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131862971 | ||||||
| chr5:131863084
|
C | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.775-8250G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863084 | ||||||
| chr5:131863087
|
T | C | 163 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.775-8253A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863087 | ||||||
| chr5:131863167
|
G | A | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.775-8333C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863167 | ||||||
| chr5:131863405
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.775-8571G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863405 | ||||||
| chr5:131863424
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.775-8590G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863424 | ||||||
| chr5:131863557
|
C | CT | 15 | a0001c0001t0002g0032a0001c0002t0001g0203a0001c0002t0001g0260others(12): Show | 15 | HG01261.hp1 HG01496.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.775-8724dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
C | CTT | 9 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0191others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-8725_775-8724d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
C | CTTT | 6 | a0001c0002t0001g0202a0001c0002t0001g0302a0001c0003t0001g0312others(3): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-8726_775-8724d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
C | CTTTTT | 22 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0006others(19): Show | 23 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.775-8728_775-8724d others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
CT | C | 58 | a0001c0001t0001g0089a0001c0002t0001g0001a0001c0002t0001g0204others(55): Show | 60 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.775-8724delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
CTT | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0064others(9): Show | 12 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.775-8725_775-8724d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
CTTT | C | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.775-8726_775-8724d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863557
|
CTTTT | C | 9 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 9 | HG00438.hp2 HG01256.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-8727_775-8724d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863557 | ||||||
| chr5:131863765
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.775-8931A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863765 | ||||||
| chr5:131863815
|
G | A | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.775-8981C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863815 | ||||||
| chr5:131863941
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.775-9107G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863941 | ||||||
| chr5:131863988
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-9154C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131863988 | ||||||
| chr5:131864076
|
G | C | 5 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-9242C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864076 | ||||||
| chr5:131864088
|
T | G | 2 | a0001c0002t0001g0235a0001c0002t0001g0236 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.775-9254A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864088 | ||||||
| chr5:131864178
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.775-9344A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864178 | ||||||
| chr5:131864204
|
T | G | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0172others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-9370A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864204 | ||||||
| chr5:131864338
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | NA18965.hp1 NA18971.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-9504C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864338 | ||||||
| chr5:131864432
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-9598C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864432 | ||||||
| chr5:131864444
|
T | C | 1 | a0001c0002t0001g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.775-9610A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864444 | ||||||
| chr5:131864539
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.775-9705A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864539 | ||||||
| chr5:131864665
|
T | C | 6 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-9831A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864665 | ||||||
| chr5:131864671
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-9837C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864671 | ||||||
| chr5:131864844
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.775-10010T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864844 | ||||||
| chr5:131864864
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.775-10030C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131864864 | ||||||
| chr5:131865224
|
AT | A | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.775-10391delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865224 | ||||||
| chr5:131865258
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.775-10424G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865258 | ||||||
| chr5:131865306
|
G | A | 2 | a0001c0002t0001g0260a0001c0002t0001g0335 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.775-10472C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865306 | ||||||
| chr5:131865313
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.775-10479G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865313 | ||||||
| chr5:131865314
|
G | A | 11 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0105others(8): Show | 11 | HG00408.hp1 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.775-10480C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865314 | ||||||
| chr5:131865364
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0247 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.775-10530G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865364 | ||||||
| chr5:131865366
|
T | C | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.775-10532A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865366 | ||||||
| chr5:131865375
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775-10541T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865375 | ||||||
| chr5:131865386
|
A | AT | 54 | a0001c0002t0001g0001a0001c0002t0001g0203a0001c0002t0001g0204others(51): Show | 56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.775-10553dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865386 | ||||||
| chr5:131865424
|
T | C | 1 | a0001c0002t0001g0334 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775-10590A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865424 | ||||||
| chr5:131865486
|
C | T | 204 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.775-10652G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865486 | ||||||
| chr5:131865504
|
C | A | 140 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.775-10670G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865504 | ||||||
| chr5:131865657
|
AT | A | 7 | a0001c0002t0001g0263a0001c0002t0001g0273a0001c0002t0001g0274others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-10824delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865657 | ||||||
| chr5:131865663
|
T | C | 3 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0332 | 3 | HG01261.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.775-10829A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865663 | ||||||
| chr5:131865818
|
T | C | 1 | a0001c0002t0001g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.775-10984A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865818 | ||||||
| chr5:131865874
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-11040G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131865874 | ||||||
| chr5:131866205
|
C | T | 1 | a0001c0002t0001g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.775-11371G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866205 | ||||||
| chr5:131866255
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-11421A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866255 | ||||||
| chr5:131866417
|
C | T | 2 | a0001c0002t0001g0296a0001c0002t0005g0342 | 2 | HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.775-11583G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866417 | ||||||
| chr5:131866468
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0176 | 2 | NA18945.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.775-11634C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866468 | ||||||
| chr5:131866608
|
T | C | 1 | a0001c0003t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.775-11774A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866608 | ||||||
| chr5:131866691
|
G | GGAGGGAG others(15): Show |
1 | a0001c0001t0001g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.775-11879_775-1185 others(26): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866691 | ||||||
| chr5:131866764
|
G | A | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.775-11930C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866764 | ||||||
| chr5:131866813
|
T | C | 4 | a0001c0002t0001g0205a0001c0002t0001g0226a0001c0002t0001g0230others(1): Show | 4 | HG00733.hp1 HG01256.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-11979A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866813 | ||||||
| chr5:131866932
|
T | C | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.774+12046A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131866932 | ||||||
| chr5:131867108
|
T | C | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.774+11870A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867108 | ||||||
| chr5:131867160
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.774+11818A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867160 | ||||||
| chr5:131867231
|
T | G | 2 | a0001c0002t0001g0263a0001c0002t0001g0275 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.774+11747A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867231 | ||||||
| chr5:131867536
|
C | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+11442G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867536 | ||||||
| chr5:131867594
|
T | G | 12 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0016others(9): Show | 12 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.774+11384A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867594 | ||||||
| chr5:131867678
|
C | T | 3 | a0001c0001t0001g0123a0001c0002t0001g0208a0001c0002t0001g0239 | 3 | NA18981.hp2 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.774+11300G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867678 | ||||||
| chr5:131867721
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.774+11257G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867721 | ||||||
| chr5:131867722
|
T | C | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.774+11256A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131867722 | ||||||
| chr5:131868068
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02165.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.774+10910A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868068 | ||||||
| chr5:131868165
|
T | A | 1 | a0001c0001t0002g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.774+10813A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868165 | ||||||
| chr5:131868229
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+10749T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868229 | ||||||
| chr5:131868239
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+10739T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868239 | ||||||
| chr5:131868333
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+10645G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868333 | ||||||
| chr5:131868496
|
G | C | 1 | a0001c0002t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.774+10482C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868496 | ||||||
| chr5:131868717
|
C | CA | 13 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(10): Show | 13 | HG00438.hp1 HG01123.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.774+10260dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868717 | ||||||
| chr5:131868717
|
CA | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(4): Show | 8 | HG01167.hp1 HG01169.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.774+10260delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868717 | ||||||
| chr5:131868816
|
G | A | 53 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 54 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.774+10162C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868816 | ||||||
| chr5:131868901
|
G | A | 4 | a0001c0002t0001g0206a0001c0002t0001g0212a0001c0002t0001g0227others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+10077C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868901 | ||||||
| chr5:131868966
|
A | G | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.774+10012T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131868966 | ||||||
| chr5:131869237
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.774+9741G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869237 | ||||||
| chr5:131869285
|
T | C | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.774+9693A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869285 | ||||||
| chr5:131869333
|
C | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+9645G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869333 | ||||||
| chr5:131869598
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+9380C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869598 | ||||||
| chr5:131869651
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+9327C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869651 | ||||||
| chr5:131869850
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+9128C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131869850 | ||||||
| chr5:131870093
|
A | C | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 33 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.774+8885T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870093 | ||||||
| chr5:131870142
|
AT | A | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.774+8835delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870142 | ||||||
| chr5:131870195
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.774+8783A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870195 | ||||||
| chr5:131870258
|
C | A | 1 | a0001c0001t0002g0015 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.774+8720G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870258 | ||||||
| chr5:131870260
|
A | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.774+8718T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870260 | ||||||
| chr5:131870291
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0183 | 3 | HG01934.hp2 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.774+8687G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870291 | ||||||
| chr5:131870490
|
C | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+8488G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870490 | ||||||
| chr5:131870719
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.774+8259G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870719 | ||||||
| chr5:131870769
|
C | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+8209G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870769 | ||||||
| chr5:131870789
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.774+8189T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870789 | ||||||
| chr5:131870860
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.774+8118G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870860 | ||||||
| chr5:131870868
|
T | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+8110A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870868 | ||||||
| chr5:131870901
|
A | C | 199 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.774+8077T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870901 | ||||||
| chr5:131870903
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.774+8075A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870903 | ||||||
| chr5:131870931
|
C | T | 159 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.774+8047G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131870931 | ||||||
| chr5:131871085
|
C | T | 5 | a0001c0002t0001g0202a0001c0002t0001g0206a0001c0002t0001g0212others(2): Show | 5 | HG02486.hp2 HG02602.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+7893G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871085 | ||||||
| chr5:131871144
|
T | G | 159 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.774+7834A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871144 | ||||||
| chr5:131871155
|
G | A | 38 | a0001c0002t0001g0003a0001c0002t0001g0252a0001c0002t0001g0253others(35): Show | 39 | HG02135.hp1 HG02155.hp2 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.774+7823C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871155 | ||||||
| chr5:131871169
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.774+7809C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871169 | ||||||
| chr5:131871186
|
C | T | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.774+7792G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871186 | ||||||
| chr5:131871197
|
A | G | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.774+7781T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871197 | ||||||
| chr5:131871201
|
A | T | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.774+7777T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871201 | ||||||
| chr5:131871209
|
C | T | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.774+7769G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871209 | ||||||
| chr5:131871241
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.774+7737G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871241 | ||||||
| chr5:131871270
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.774+7708G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871270 | ||||||
| chr5:131871271
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+7707C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871271 | ||||||
| chr5:131871295
|
C | T | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.774+7683G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871295 | ||||||
| chr5:131871356
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0122 | 2 | NA18948.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.774+7622G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871356 | ||||||
| chr5:131871412
|
A | T | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.774+7566T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871412 | ||||||
| chr5:131871492
|
C | A | 159 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.774+7486G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871492 | ||||||
| chr5:131871503
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.774+7475G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871503 | ||||||
| chr5:131871508
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+7470T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871508 | ||||||
| chr5:131871617
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.774+7361T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871617 | ||||||
| chr5:131871665
|
C | T | 90 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(87): Show | 90 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.774+7313G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871665 | ||||||
| chr5:131871666
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.774+7312C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871666 | ||||||
| chr5:131871767
|
C | G | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.774+7211G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871767 | ||||||
| chr5:131871829
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.774+7149A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871829 | ||||||
| chr5:131871832
|
C | A | 141 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.774+7146G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871832 | ||||||
| chr5:131871842
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0080 | 2 | HG02523.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.774+7136T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871842 | ||||||
| chr5:131871846
|
C | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.774+7132G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871846 | ||||||
| chr5:131871848
|
G | A | 15 | a0001c0002t0001g0001a0001c0002t0001g0208a0001c0002t0001g0224others(12): Show | 17 | HG00408.hp2 HG01978.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.774+7130C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871848 | ||||||
| chr5:131871864
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.774+7114G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131871864 | ||||||
| chr5:131872160
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+6818G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872160 | ||||||
| chr5:131872199
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.774+6779G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872199 | ||||||
| chr5:131872232
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774+6746T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872232 | ||||||
| chr5:131872248
|
G | GA | 215 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.774+6729dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872248 | ||||||
| chr5:131872320
|
A | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+6658T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872320 | ||||||
| chr5:131872409
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+6569G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872409 | ||||||
| chr5:131872513
|
A | T | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.774+6465T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872513 | ||||||
| chr5:131872542
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+6436C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872542 | ||||||
| chr5:131872580
|
T | C | 1 | a0001c0004t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.774+6398A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872580 | ||||||
| chr5:131872590
|
G | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+6388C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872590 | ||||||
| chr5:131872614
|
C | A | 4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+6364G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872614 | ||||||
| chr5:131872761
|
A | G | 3 | a0001c0001t0002g0191a0001c0004t0002g0192a0001c0004t0002g0193 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.774+6217T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872761 | ||||||
| chr5:131872768
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.774+6210T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872768 | ||||||
| chr5:131872857
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0095 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+6121C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872857 | ||||||
| chr5:131872988
|
C | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+5990G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872988 | ||||||
| chr5:131872995
|
G | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+5983C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131872995 | ||||||
| chr5:131873018
|
C | A | 162 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.774+5960G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873018 | ||||||
| chr5:131873059
|
G | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+5919C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873059 | ||||||
| chr5:131873090
|
C | A | 161 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.774+5888G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873090 | ||||||
| chr5:131873094
|
C | T | 3 | a0001c0002t0001g0205a0001c0002t0001g0226a0001c0002t0001g0231 | 3 | HG00733.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.774+5884G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873094 | ||||||
| chr5:131873141
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.774+5837A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873141 | ||||||
| chr5:131873182
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+5796G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873182 | ||||||
| chr5:131873234
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.774+5744C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873234 | ||||||
| chr5:131873363
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.774+5615T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873363 | ||||||
| chr5:131873444
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.774+5534T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873444 | ||||||
| chr5:131873586
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.774+5392A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873586 | ||||||
| chr5:131873590
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.774+5388A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873590 | ||||||
| chr5:131873591
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.774+5387C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873591 | ||||||
| chr5:131873622
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+5356A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873622 | ||||||
| chr5:131873645
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.774+5333C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873645 | ||||||
| chr5:131873681
|
A | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+5297T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873681 | ||||||
| chr5:131873751
|
A | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+5227T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873751 | ||||||
| chr5:131873774
|
C | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+5204G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873774 | ||||||
| chr5:131873774
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.774+5204G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873774 | ||||||
| chr5:131873947
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0005g0342 | 2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.774+5031C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131873947 | ||||||
| chr5:131874016
|
G | GC | 3 | a0001c0001t0001g0055a0001c0001t0001g0097a0001c0001t0004g0057 | 3 | HG00621.hp2 HG02523.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.774+4961dupG | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874016 | ||||||
| chr5:131874082
|
T | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+4896A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874082 | ||||||
| chr5:131874100
|
C | A | 1 | a0001c0004t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.774+4878G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874100 | ||||||
| chr5:131874128
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+4850T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874128 | ||||||
| chr5:131874323
|
G | A | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 38 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.774+4655C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874323 | ||||||
| chr5:131874470
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774+4508G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874470 | ||||||
| chr5:131874529
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.774+4449C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874529 | ||||||
| chr5:131874531
|
A | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+4447T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874531 | ||||||
| chr5:131874550
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0107others(3): Show | 6 | HG02109.hp1 HG02145.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+4428C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874550 | ||||||
| chr5:131874556
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.774+4422A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874556 | ||||||
| chr5:131874839
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+4139G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874839 | ||||||
| chr5:131874987
|
C | T | 1 | a0001c0002t0001g0238 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.774+3991G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131874987 | ||||||
| chr5:131875033
|
TATC | T | 20 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0104others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.774+3942_774+3944d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875033 | ||||||
| chr5:131875052
|
A | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+3926T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875052 | ||||||
| chr5:131875078
|
T | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+3900A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875078 | ||||||
| chr5:131875090
|
G | C | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.774+3888C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875090 | ||||||
| chr5:131875112
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02165.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.774+3866G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875112 | ||||||
| chr5:131875171
|
G | C | 1 | a0001c0002t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.774+3807C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875171 | ||||||
| chr5:131875189
|
AGAG | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0115others(7): Show | 10 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.774+3786_774+3788d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875189 | ||||||
| chr5:131875284
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.774+3694A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875284 | ||||||
| chr5:131875288
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+3690G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875288 | ||||||
| chr5:131875318
|
A | G | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.774+3660T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875318 | ||||||
| chr5:131875439
|
G | T | 1 | a0001c0002t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.774+3539C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875439 | ||||||
| chr5:131875441
|
C | T | 7 | a0001c0002t0001g0236a0001c0003t0001g0305a0001c0003t0001g0306others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+3537G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875441 | ||||||
| chr5:131875483
|
T | G | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.774+3495A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875483 | ||||||
| chr5:131875495
|
G | A | 4 | a0001c0002t0001g0263a0001c0002t0001g0273a0001c0002t0001g0274others(1): Show | 4 | HG01099.hp2 HG01168.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+3483C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875495 | ||||||
| chr5:131875524
|
G | C | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.774+3454C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875524 | ||||||
| chr5:131875539
|
T | G | 164 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.774+3439A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875539 | ||||||
| chr5:131875571
|
C | A | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.774+3407G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875571 | ||||||
| chr5:131875645
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.774+3333A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875645 | ||||||
| chr5:131875806
|
T | A | 1 | a0001c0002t0001g0252 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.774+3172A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875806 | ||||||
| chr5:131875839
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.774+3139G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875839 | ||||||
| chr5:131875903
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+3075C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875903 | ||||||
| chr5:131875960
|
G | T | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.774+3018C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875960 | ||||||
| chr5:131875981
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.774+2997A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131875981 | ||||||
| chr5:131876107
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.774+2871T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876107 | ||||||
| chr5:131876166
|
G | C | 1 | a0001c0002t0001g0204 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.774+2812C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876166 | ||||||
| chr5:131876167
|
A | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0108a0001c0001t0001g0122 | 3 | HG00099.hp1 NA18948.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.774+2811T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876167 | ||||||
| chr5:131876168
|
T | C | 1 | a0001c0002t0001g0333 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+2810A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876168 | ||||||
| chr5:131876171
|
G | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0108a0001c0001t0001g0122 | 3 | HG00099.hp1 NA18948.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.774+2807C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876171 | ||||||
| chr5:131876278
|
T | C | 200 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.774+2700A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876278 | ||||||
| chr5:131876374
|
G | A | 8 | a0001c0001t0001g0051a0001c0001t0002g0014a0001c0001t0002g0015others(5): Show | 8 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+2604C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876374 | ||||||
| chr5:131876412
|
T | C | 218 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.774+2566A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876412 | ||||||
| chr5:131876432
|
A | G | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+2546T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876432 | ||||||
| chr5:131876478
|
T | C | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0172others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+2500A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876478 | ||||||
| chr5:131876491
|
AAAC | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+2484_774+2486d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876491 | ||||||
| chr5:131876523
|
T | C | 4 | a0001c0002t0001g0209a0001c0002t0001g0240a0001c0002t0001g0241others(1): Show | 4 | NA18966.hp1 NA18978.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+2455A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876523 | ||||||
| chr5:131876623
|
T | C | 163 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.774+2355A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876623 | ||||||
| chr5:131876662
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+2316A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876662 | ||||||
| chr5:131876786
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.774+2192G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131876786 | ||||||
| chr5:131877014
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.774+1964G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877014 | ||||||
| chr5:131877112
|
C | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.774+1866G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877112 | ||||||
| chr5:131877162
|
A | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+1816T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877162 | ||||||
| chr5:131877171
|
A | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+1807T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877171 | ||||||
| chr5:131877422
|
C | T | 5 | a0001c0001t0001g0105a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00408.hp1 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+1556G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877422 | ||||||
| chr5:131877426
|
T | G | 1 | a0001c0001t0002g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.774+1552A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877426 | ||||||
| chr5:131877763
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0169 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.774+1215C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877763 | ||||||
| chr5:131877984
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.774+994A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131877984 | ||||||
| chr5:131878055
|
T | C | 1 | a0001c0002t0001g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.774+923A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878055 | ||||||
| chr5:131878120
|
C | T | 1 | a0001c0002t0001g0321 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.774+858G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878120 | ||||||
| chr5:131878201
|
TG | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.774+776delC | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878201 | ||||||
| chr5:131878334
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0005g0342 | 2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.774+644C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878334 | ||||||
| chr5:131878338
|
C | T | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.774+640G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878338 | ||||||
| chr5:131878428
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+550G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878428 | ||||||
| chr5:131878443
|
C | T | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.774+535G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878443 | ||||||
| chr5:131878444
|
G | A | 2 | a0001c0002t0001g0326a0001c0002t0001g0329 | 2 | HG01261.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.774+534C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878444 | ||||||
| chr5:131878511
|
G | A | 160 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.774+467C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878511 | ||||||
| chr5:131878522
|
A | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.774+456T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878522 | ||||||
| chr5:131878546
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.774+432C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878546 | ||||||
| chr5:131878626
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.774+352A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878626 | ||||||
| chr5:131878661
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+317A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878661 | ||||||
| chr5:131878876
|
T | TA | 25 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0002t0001g0001others(22): Show | 27 | HG00408.hp2 HG01243.hp2 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.774+101dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878876 | ||||||
| chr5:131878876
|
TA | T | 162 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.774+101delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878876 | ||||||
| chr5:131878876
|
TAA | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0120others(4): Show | 7 | HG01081.hp2 HG01516.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+100_774+101del others(2): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878876 | ||||||
| chr5:131878927
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.774+51A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 9/12 | chr5 | 131878927 | ||||||
| chr5:131879135
|
A | C | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.704-87T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879135 | ||||||
| chr5:131879152
|
G | C | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-104C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879152 | ||||||
| chr5:131879154
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704-106T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879154 | ||||||
| chr5:131879247
|
C | A | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-199G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879247 | ||||||
| chr5:131879322
|
T | C | 1 | a0001c0002t0001g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.704-274A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879322 | ||||||
| chr5:131879419
|
A | G | 2 | a0001c0003t0001g0313a0001c0003t0001g0314 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-371T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879419 | ||||||
| chr5:131879735
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-687A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879735 | ||||||
| chr5:131879929
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.704-881A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131879929 | ||||||
| chr5:131880183
|
G | A | 11 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(8): Show | 11 | HG00438.hp1 HG00544.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.704-1135C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880183 | ||||||
| chr5:131880193
|
G | A | 2 | a0001c0002t0001g0328a0001c0002t0001g0332 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.704-1145C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880193 | ||||||
| chr5:131880206
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704-1158G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880206 | ||||||
| chr5:131880264
|
A | AT | 154 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.704-1217dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880264 | ||||||
| chr5:131880264
|
A | ATT | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0052others(5): Show | 8 | HG00621.hp1 HG01123.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-1218_704-1217d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880264 | ||||||
| chr5:131880264
|
AT | A | 18 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0016others(15): Show | 18 | HG00642.hp2 HG01081.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.704-1217delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880264 | ||||||
| chr5:131880264
|
ATT | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.704-1218_704-1217d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880264 | ||||||
| chr5:131880334
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.704-1286G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880334 | ||||||
| chr5:131880404
|
AT | A | 212 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.704-1357delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880404 | ||||||
| chr5:131880461
|
C | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-1413G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880461 | ||||||
| chr5:131880484
|
C | T | 1 | a0001c0003t0001g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.704-1436G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880484 | ||||||
| chr5:131880734
|
G | T | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.704-1686C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880734 | ||||||
| chr5:131880909
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-1861G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880909 | ||||||
| chr5:131880943
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.704-1895A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131880943 | ||||||
| chr5:131881044
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.704-1996C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881044 | ||||||
| chr5:131881251
|
G | C | 219 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.704-2203C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881251 | ||||||
| chr5:131881337
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.704-2289G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881337 | ||||||
| chr5:131881441
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.704-2393C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881441 | ||||||
| chr5:131881682
|
T | C | 1 | a0001c0002t0001g0329 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.704-2634A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881682 | ||||||
| chr5:131881723
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-2675A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881723 | ||||||
| chr5:131881780
|
T | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.704-2732A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881780 | ||||||
| chr5:131881780
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-2732A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881780 | ||||||
| chr5:131881816
|
C | A | 1 | a0001c0002t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.704-2768G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881816 | ||||||
| chr5:131881906
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-2858A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881906 | ||||||
| chr5:131881958
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-2910T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131881958 | ||||||
| chr5:131882116
|
G | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0030 | 2 | HG00639.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.704-3068C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882116 | ||||||
| chr5:131882295
|
T | C | 162 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.704-3247A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882295 | ||||||
| chr5:131882331
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.704-3283C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882331 | ||||||
| chr5:131882424
|
T | G | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-3376A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882424 | ||||||
| chr5:131882507
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007 | 4 | HG01167.hp1 HG01169.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-3459A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882507 | ||||||
| chr5:131882536
|
T | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-3488A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882536 | ||||||
| chr5:131882569
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-3521G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882569 | ||||||
| chr5:131882788
|
C | A | 1 | a0001c0003t0001g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.704-3740G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131882788 | ||||||
| chr5:131883026
|
G | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-3978C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883026 | ||||||
| chr5:131883112
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-4064C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883112 | ||||||
| chr5:131883551
|
T | C | 1 | a0001c0002t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.704-4503A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883551 | ||||||
| chr5:131883563
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.704-4515A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883563 | ||||||
| chr5:131883718
|
T | C | 17 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0047others(14): Show | 17 | HG00609.hp2 HG01978.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-4670A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883718 | ||||||
| chr5:131883835
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.704-4787A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131883835 | ||||||
| chr5:131884121
|
C | T | 12 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-5073G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884121 | ||||||
| chr5:131884317
|
C | A | 12 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-5269G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884317 | ||||||
| chr5:131884317
|
C | G | 264 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.704-5269G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884317 | ||||||
| chr5:131884370
|
G | A | 55 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 56 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.704-5322C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884370 | ||||||
| chr5:131884458
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.704-5410C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884458 | ||||||
| chr5:131884541
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.704-5493A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884541 | ||||||
| chr5:131884560
|
G | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-5512C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884560 | ||||||
| chr5:131884744
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.704-5696G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884744 | ||||||
| chr5:131884841
|
C | T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-5793G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884841 | ||||||
| chr5:131884864
|
T | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-5816A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131884864 | ||||||
| chr5:131885040
|
G | A | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.704-5992C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885040 | ||||||
| chr5:131885156
|
T | C | 2 | a0001c0002t0001g0229a0001c0002t0001g0316 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.704-6108A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885156 | ||||||
| chr5:131885315
|
C | T | 4 | a0001c0002t0001g0206a0001c0002t0001g0212a0001c0002t0001g0227others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-6267G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885315 | ||||||
| chr5:131885338
|
TGAAAGAG others(13): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.704-6310_704-6291d others(22): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885338 | ||||||
| chr5:131885340
|
AAAGAGAG others(4): Show |
A | 2 | a0001c0001t0001g0105a0001c0001t0001g0146 | 2 | HG01070.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.704-6303_704-6293d others(13): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885340 | ||||||
| chr5:131885340
|
AAAGAGAG others(8): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.704-6307_704-6293d others(17): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885340 | ||||||
| chr5:131885340
|
AAAGAGAG others(10): Show |
A | 4 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0091others(1): Show | 4 | HG02165.hp2 HG03688.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-6309_704-6293d others(19): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885340 | ||||||
| chr5:131885340
|
AAAGAGAG others(22): Show |
A | 2 | a0001c0002t0001g0207a0001c0002t0001g0330 | 2 | HG02738.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.704-6321_704-6293d others(31): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885340 | ||||||
| chr5:131885341
|
A | AAGAGAGA others(3): Show |
1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-6303_704-6294d others(12): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
A | AAGAGAGA others(13): Show |
1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-6313_704-6294d others(22): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
A | AAGAGAGA others(35): Show |
1 | a0001c0001t0001g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.704-6335_704-6294d others(44): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAG | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0104a0001c0001t0001g0108others(2): Show | 5 | HG00099.hp1 HG00621.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-6295_704-6294d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAG | A | 8 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0084others(5): Show | 8 | HG00438.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-6297_704-6294d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAG | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0054others(4): Show | 7 | HG00609.hp1 HG00639.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-6299_704-6294d others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(1): Show |
A | 12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0102others(9): Show | 12 | HG01099.hp1 HG01167.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.704-6301_704-6294d others(10): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(3): Show |
A | 16 | a0001c0001t0001g0039a0001c0001t0001g0071a0001c0001t0001g0090others(13): Show | 16 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.704-6303_704-6294d others(12): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(5): Show |
A | 22 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0073others(19): Show | 22 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-6305_704-6294d others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(7): Show |
A | 22 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0056others(19): Show | 22 | HG00642.hp1 HG00733.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-6307_704-6294d others(16): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(9): Show |
A | 28 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0066others(25): Show | 28 | HG01496.hp1 HG01943.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.704-6309_704-6294d others(18): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(11): Show |
A | 15 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0059others(12): Show | 15 | HG00408.hp1 HG02015.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.704-6311_704-6294d others(20): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(13): Show |
A | 19 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0078others(16): Show | 20 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.704-6313_704-6294d others(22): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(15): Show |
A | 8 | a0001c0001t0001g0070a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 8 | HG00621.hp1 HG01496.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-6315_704-6294d others(24): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(17): Show |
A | 24 | a0001c0001t0001g0156a0001c0001t0002g0004a0001c0001t0002g0005others(21): Show | 24 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.704-6317_704-6294d others(26): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(19): Show |
A | 6 | a0001c0001t0001g0060a0001c0001t0001g0122a0001c0001t0002g0187others(3): Show | 6 | HG01978.hp2 HG02145.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-6319_704-6294d others(28): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(21): Show |
A | 17 | a0001c0002t0001g0001a0001c0002t0001g0203a0001c0002t0001g0231others(14): Show | 19 | HG00408.hp2 HG01981.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.704-6321_704-6294d others(30): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(23): Show |
A | 97 | a0001c0002t0001g0003a0001c0002t0001g0204a0001c0002t0001g0205others(94): Show | 98 | HG00438.hp1 HG00733.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.704-6323_704-6294d others(32): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(25): Show |
A | 1 | a0001c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.704-6325_704-6294d others(34): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885341
|
AAGAGAGA others(27): Show |
A | 3 | a0001c0002t0001g0211a0001c0002t0001g0229a0001c0002t0001g0316 | 3 | HG00544.hp2 HG02040.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.704-6327_704-6294d others(36): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885341 | ||||||
| chr5:131885364
|
AGAGAGAG others(6): Show |
A | 1 | a0001c0003t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-6329_704-6317d others(15): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885364 | ||||||
| chr5:131885364
|
AGAGAGAG others(8): Show |
A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.704-6331_704-6317d others(17): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885364 | ||||||
| chr5:131885365
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0097others(1): Show | 4 | HG01123.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-6317C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885365 | ||||||
| chr5:131885366
|
AGAGAGAG others(22): Show |
A | 1 | a0001c0002t0001g0279 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.704-6347_704-6319d others(31): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885366 | ||||||
| chr5:131885367
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0108a0001c0001t0004g0057 | 3 | HG00099.hp1 HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.704-6319C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885367 | ||||||
| chr5:131885369
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0096others(1): Show | 4 | HG00438.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-6321C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885369 | ||||||
| chr5:131885371
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0101others(1): Show | 4 | HG00609.hp1 HG01243.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-6323C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885371 | ||||||
| chr5:131885373
|
G | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0102a0001c0001t0001g0107others(5): Show | 8 | HG01167.hp2 HG01516.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-6325C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885373 | ||||||
| chr5:131885375
|
G | A | 8 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0172others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-6327C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885375 | ||||||
| chr5:131885377
|
G | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0099others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-6329C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885377 | ||||||
| chr5:131885379
|
G | A | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0056others(7): Show | 10 | HG02572.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-6331C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885379 | ||||||
| chr5:131885381
|
G | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0002g0008others(6): Show | 9 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-6333C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885381 | ||||||
| chr5:131885383
|
G | A | 1 | a0001c0003t0001g0308 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-6335C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885383 | ||||||
| chr5:131885385
|
G | A | 11 | a0001c0001t0001g0177a0001c0001t0002g0002a0001c0001t0002g0006others(8): Show | 12 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.704-6337C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885385 | ||||||
| chr5:131885387
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0032a0001c0001t0002g0189 | 3 | HG02630.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.704-6339C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885387 | ||||||
| chr5:131885389
|
G | A | 23 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0009others(20): Show | 23 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.704-6341C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885389 | ||||||
| chr5:131885391
|
G | A | 3 | a0001c0001t0002g0187a0001c0001t0002g0190a0001c0002t0001g0249 | 3 | HG01978.hp2 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-6343C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885391 | ||||||
| chr5:131885393
|
G | A | 15 | a0001c0002t0001g0001a0001c0002t0001g0203a0001c0002t0001g0233others(12): Show | 17 | HG00408.hp2 HG01981.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.704-6345C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885393 | ||||||
| chr5:131885395
|
G | A | 102 | a0001c0002t0001g0003a0001c0002t0001g0204a0001c0002t0001g0205others(99): Show | 103 | HG00438.hp1 HG00733.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.704-6347C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885395 | ||||||
| chr5:131885397
|
G | A | 1 | a0001c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.704-6349C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885397 | ||||||
| chr5:131885399
|
G | A | 3 | a0001c0002t0001g0211a0001c0002t0001g0229a0001c0002t0001g0316 | 3 | HG00544.hp2 HG02040.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.704-6351C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885399 | ||||||
| chr5:131885425
|
T | G | 1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-6377A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885425 | ||||||
| chr5:131885426
|
T | A | 1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-6378A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885426 | ||||||
| chr5:131885695
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.704-6647C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885695 | ||||||
| chr5:131885778
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.704-6730C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885778 | ||||||
| chr5:131885830
|
C | T | 9 | a0001c0002t0001g0253a0001c0002t0001g0256a0001c0002t0001g0276others(6): Show | 9 | HG02135.hp1 HG02165.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-6782G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131885830 | ||||||
| chr5:131886002
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.704-6954T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886002 | ||||||
| chr5:131886019
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-6971C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886019 | ||||||
| chr5:131886144
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0094 | 3 | HG01993.hp2 HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.704-7096G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886144 | ||||||
| chr5:131886178
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-7130C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886178 | ||||||
| chr5:131886356
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-7308C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886356 | ||||||
| chr5:131886529
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-7481G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886529 | ||||||
| chr5:131886691
|
G | C | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.704-7643C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886691 | ||||||
| chr5:131886717
|
C | T | 2 | a0001c0002t0001g0261a0001c0002t0001g0279 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.704-7669G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886717 | ||||||
| chr5:131886989
|
C | G | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.704-7941G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131886989 | ||||||
| chr5:131887135
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0167 | 2 | NA18979.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.704-8087G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887135 | ||||||
| chr5:131887156
|
T | C | 1 | a0001c0003t0001g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.704-8108A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887156 | ||||||
| chr5:131887172
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.704-8124A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887172 | ||||||
| chr5:131887191
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.704-8143T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887191 | ||||||
| chr5:131887201
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-8153A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887201 | ||||||
| chr5:131887231
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.704-8183A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887231 | ||||||
| chr5:131887320
|
T | C | 1 | a0001c0002t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704-8272A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887320 | ||||||
| chr5:131887329
|
G | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-8281C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887329 | ||||||
| chr5:131887358
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.704-8310A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887358 | ||||||
| chr5:131887517
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-8469T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887517 | ||||||
| chr5:131887589
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.704-8541C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887589 | ||||||
| chr5:131887708
|
T | A | 2 | a0001c0002t0001g0208a0001c0002t0001g0239 | 2 | NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.704-8660A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887708 | ||||||
| chr5:131887709
|
T | A | 124 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(121): Show | 127 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.704-8661A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887709 | ||||||
| chr5:131887844
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-8796C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887844 | ||||||
| chr5:131887854
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.704-8806T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887854 | ||||||
| chr5:131887951
|
C | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.704-8903G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887951 | ||||||
| chr5:131887955
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.704-8907G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887955 | ||||||
| chr5:131887956
|
G | A | 1 | a0001c0003t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-8908C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887956 | ||||||
| chr5:131887978
|
T | C | 229 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0040others(226): Show | 233 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.704-8930A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131887978 | ||||||
| chr5:131888061
|
A | C | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.704-9013T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888061 | ||||||
| chr5:131888078
|
A | G | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.704-9030T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888078 | ||||||
| chr5:131888106
|
T | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0020 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.704-9058A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888106 | ||||||
| chr5:131888206
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-9158C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888206 | ||||||
| chr5:131888209
|
C | A | 1 | a0001c0001t0002g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.704-9161G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888209 | ||||||
| chr5:131888245
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-9197T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888245 | ||||||
| chr5:131888280
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0198 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.704-9232C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888280 | ||||||
| chr5:131888369
|
CTGT | C | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.704-9324_704-9322d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888369 | ||||||
| chr5:131888395
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0184 | 3 | HG01175.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.704-9347G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888395 | ||||||
| chr5:131888436
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704-9388G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888436 | ||||||
| chr5:131888494
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.704-9446A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888494 | ||||||
| chr5:131888590
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.704-9542T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888590 | ||||||
| chr5:131888649
|
A | G | 5 | a0001c0002t0001g0253a0001c0002t0001g0276a0001c0002t0001g0278others(2): Show | 5 | NA18941.hp2 NA18946.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-9601T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888649 | ||||||
| chr5:131888697
|
A | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | NA18944.hp1 NA19010.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-9649T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888697 | ||||||
| chr5:131888701
|
G | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | NA18944.hp1 NA19010.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-9653C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888701 | ||||||
| chr5:131888794
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.704-9746C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888794 | ||||||
| chr5:131888841
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.704-9793A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888841 | ||||||
| chr5:131888910
|
G | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-9862C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888910 | ||||||
| chr5:131888935
|
C | G | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(45): Show | 49 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.704-9887G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888935 | ||||||
| chr5:131888986
|
G | A | 3 | a0001c0002t0001g0317a0001c0002t0001g0321a0001c0002t0001g0322 | 3 | NA18949.hp2 NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.704-9938C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131888986 | ||||||
| chr5:131889025
|
A | C | 1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-9977T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889025 | ||||||
| chr5:131889026
|
A | T | 176 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(173): Show | 180 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.704-9978T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889026 | ||||||
| chr5:131889055
|
G | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704-10007C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889055 | ||||||
| chr5:131889111
|
T | C | 120 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(117): Show | 123 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.704-10063A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889111 | ||||||
| chr5:131889139
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-10091A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889139 | ||||||
| chr5:131889192
|
A | G | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0026others(4): Show | 7 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-10144T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889192 | ||||||
| chr5:131889205
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.704-10157C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889205 | ||||||
| chr5:131889353
|
T | A | 1 | a0001c0001t0001g0124 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.704-10305A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889353 | ||||||
| chr5:131889688
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.704-10640A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889688 | ||||||
| chr5:131889697
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-10649C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889697 | ||||||
| chr5:131889697
|
G | C | 16 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0001g0257others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.704-10649C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889697 | ||||||
| chr5:131889923
|
G | C | 2 | a0001c0002t0001g0224a0001c0002t0001g0225 | 2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.704-10875C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889923 | ||||||
| chr5:131889998
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-10950T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131889998 | ||||||
| chr5:131890026
|
G | A | 2 | a0001c0002t0001g0208a0001c0002t0001g0239 | 2 | NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.704-10978C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890026 | ||||||
| chr5:131890093
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-11045C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890093 | ||||||
| chr5:131890107
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.704-11059T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890107 | ||||||
| chr5:131890138
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-11090C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890138 | ||||||
| chr5:131890159
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.704-11111G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890159 | ||||||
| chr5:131890282
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-11234G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890282 | ||||||
| chr5:131890310
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.704-11262C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890310 | ||||||
| chr5:131890523
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.704-11475A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890523 | ||||||
| chr5:131890539
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.704-11491T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890539 | ||||||
| chr5:131890572
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.704-11524A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890572 | ||||||
| chr5:131890664
|
C | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-11616G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890664 | ||||||
| chr5:131890782
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.704-11734G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890782 | ||||||
| chr5:131890956
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0121 | 2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.704-11908C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131890956 | ||||||
| chr5:131891024
|
G | A | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.704-11976C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891024 | ||||||
| chr5:131891102
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.704-12054A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891102 | ||||||
| chr5:131891148
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-12100T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891148 | ||||||
| chr5:131891353
|
A | C | 1 | a0001c0002t0001g0297 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.704-12305T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891353 | ||||||
| chr5:131891571
|
T | G | 2 | a0001c0002t0001g0214a0001c0002t0001g0247 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.704-12523A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891571 | ||||||
| chr5:131891662
|
T | G | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-12614A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891662 | ||||||
| chr5:131891706
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.704-12658G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891706 | ||||||
| chr5:131891847
|
A | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-12799T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891847 | ||||||
| chr5:131891855
|
G | A | 4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-12807C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891855 | ||||||
| chr5:131891872
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-12824A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891872 | ||||||
| chr5:131891884
|
C | T | 53 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 54 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.704-12836G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891884 | ||||||
| chr5:131891959
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG02809.hp1 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.704-12911A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131891959 | ||||||
| chr5:131892000
|
G | T | 53 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 54 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.704-12952C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892000 | ||||||
| chr5:131892020
|
G | C | 177 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(174): Show | 181 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.704-12972C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892020 | ||||||
| chr5:131892046
|
C | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG00408.hp1 HG02040.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-12998G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892046 | ||||||
| chr5:131892076
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-13028T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892076 | ||||||
| chr5:131892096
|
C | G | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-13048G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892096 | ||||||
| chr5:131892102
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.704-13054G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892102 | ||||||
| chr5:131892103
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-13055C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892103 | ||||||
| chr5:131892129
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.704-13081G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892129 | ||||||
| chr5:131892322
|
G | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704-13274C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892322 | ||||||
| chr5:131892348
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-13300A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892348 | ||||||
| chr5:131892416
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-13368A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892416 | ||||||
| chr5:131892428
|
T | C | 1 | a0001c0003t0001g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.704-13380A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892428 | ||||||
| chr5:131892478
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.704-13430G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892478 | ||||||
| chr5:131892544
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-13496C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892544 | ||||||
| chr5:131892549
|
G | A | 1 | a0001c0002t0001g0321 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.704-13501C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892549 | ||||||
| chr5:131892631
|
G | T | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704-13583C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892631 | ||||||
| chr5:131892639
|
A | G | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0026others(4): Show | 7 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-13591T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892639 | ||||||
| chr5:131892728
|
G | C | 141 | a0001c0001t0001g0185a0001c0002t0001g0001a0001c0002t0001g0003others(138): Show | 144 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.704-13680C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892728 | ||||||
| chr5:131892850
|
C | G | 2 | a0001c0002t0001g0336a0001c0002t0001g0337 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.704-13802G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892850 | ||||||
| chr5:131892884
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.704-13836A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892884 | ||||||
| chr5:131892908
|
A | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.704-13860T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892908 | ||||||
| chr5:131892943
|
C | G | 1 | a0001c0007t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-13895G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892943 | ||||||
| chr5:131892975
|
G | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-13927C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892975 | ||||||
| chr5:131892977
|
T | C | 140 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(137): Show | 143 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.704-13929A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892977 | ||||||
| chr5:131892987
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-13939G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131892987 | ||||||
| chr5:131893130
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.704-14082C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893130 | ||||||
| chr5:131893154
|
G | C | 1 | a0001c0002t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.704-14106C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893154 | ||||||
| chr5:131893160
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-14112A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893160 | ||||||
| chr5:131893166
|
TTGTC | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0040others(19): Show | 22 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-14122_704-1411 others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893166 | ||||||
| chr5:131893175
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704-14127G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893175 | ||||||
| chr5:131893263
|
TG | T | 123 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(120): Show | 126 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.704-14216delC | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893263 | ||||||
| chr5:131893308
|
G | A | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(29): Show | 33 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.704-14260C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893308 | ||||||
| chr5:131893374
|
G | A | 5 | a0001c0002t0001g0203a0001c0002t0001g0215a0001c0002t0001g0216others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-14326C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893374 | ||||||
| chr5:131893445
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.704-14397G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893445 | ||||||
| chr5:131893557
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.704-14509C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893557 | ||||||
| chr5:131893574
|
G | A | 2 | a0001c0001t0002g0188a0001c0003t0001g0311 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.704-14526C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893574 | ||||||
| chr5:131893693
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.704-14645G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893693 | ||||||
| chr5:131893696
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-14648C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893696 | ||||||
| chr5:131893909
|
C | A | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.704-14861G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893909 | ||||||
| chr5:131893913
|
T | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.704-14865A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131893913 | ||||||
| chr5:131894183
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.704-15135T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894183 | ||||||
| chr5:131894299
|
T | C | 9 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-15251A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894299 | ||||||
| chr5:131894456
|
C | G | 1 | a0001c0002t0001g0233 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.704-15408G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894456 | ||||||
| chr5:131894656
|
T | C | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-15608A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894656 | ||||||
| chr5:131894677
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.704-15629G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894677 | ||||||
| chr5:131894690
|
G | A | 3 | a0001c0002t0001g0205a0001c0002t0001g0226a0001c0002t0001g0231 | 3 | HG00733.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.704-15642C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894690 | ||||||
| chr5:131894854
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.704-15806T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131894854 | ||||||
| chr5:131895078
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.704-16030A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895078 | ||||||
| chr5:131895130
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.704-16082G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895130 | ||||||
| chr5:131895175
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.704-16127A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895175 | ||||||
| chr5:131895334
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-16286A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895334 | ||||||
| chr5:131895441
|
G | T | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.703+16374C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895441 | ||||||
| chr5:131895653
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+16162A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895653 | ||||||
| chr5:131895842
|
T | C | 141 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(138): Show | 144 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.703+15973A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895842 | ||||||
| chr5:131895843
|
G | A | 4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+15972C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895843 | ||||||
| chr5:131895998
|
C | T | 177 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(174): Show | 181 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.703+15817G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131895998 | ||||||
| chr5:131896010
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703+15805G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896010 | ||||||
| chr5:131896098
|
T | C | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.703+15717A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896098 | ||||||
| chr5:131896142
|
T | C | 4 | a0001c0002t0001g0206a0001c0002t0001g0212a0001c0002t0001g0227others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+15673A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896142 | ||||||
| chr5:131896209
|
T | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+15606A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896209 | ||||||
| chr5:131896268
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.703+15547C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896268 | ||||||
| chr5:131896299
|
T | C | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.703+15516A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896299 | ||||||
| chr5:131896336
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+15479G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896336 | ||||||
| chr5:131896391
|
G | T | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703+15424C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896391 | ||||||
| chr5:131896394
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703+15421C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896394 | ||||||
| chr5:131896402
|
T | C | 4 | a0001c0002t0001g0206a0001c0002t0001g0212a0001c0002t0001g0227others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+15413A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896402 | ||||||
| chr5:131896407
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.703+15408C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896407 | ||||||
| chr5:131896522
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0168 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.703+15293G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896522 | ||||||
| chr5:131896577
|
C | A | 1 | a0001c0002t0001g0220 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.703+15238G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896577 | ||||||
| chr5:131896628
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.703+15187A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896628 | ||||||
| chr5:131896645
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.703+15170A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896645 | ||||||
| chr5:131896883
|
T | A | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+14932A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131896883 | ||||||
| chr5:131897006
|
T | C | 2 | a0001c0002t0001g0290a0001c0002t0001g0291 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.703+14809A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897006 | ||||||
| chr5:131897010
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.703+14805C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897010 | ||||||
| chr5:131897068
|
G | C | 1 | a0001c0002t0001g0221 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.703+14747C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897068 | ||||||
| chr5:131897266
|
G | A | 120 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(117): Show | 123 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.703+14549C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897266 | ||||||
| chr5:131897390
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.703+14425G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897390 | ||||||
| chr5:131897396
|
G | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+14419C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897396 | ||||||
| chr5:131897516
|
G | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+14299C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897516 | ||||||
| chr5:131897532
|
G | A | 122 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(119): Show | 125 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.703+14283C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897532 | ||||||
| chr5:131897577
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.703+14238A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897577 | ||||||
| chr5:131897679
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+14136G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897679 | ||||||
| chr5:131897722
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+14093A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897722 | ||||||
| chr5:131897748
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+14067A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897748 | ||||||
| chr5:131897785
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.703+14030G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897785 | ||||||
| chr5:131897811
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.703+14004C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897811 | ||||||
| chr5:131897885
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.703+13930G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897885 | ||||||
| chr5:131897928
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.703+13887G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131897928 | ||||||
| chr5:131898066
|
G | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+13749C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898066 | ||||||
| chr5:131898169
|
G | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0046others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.703+13646C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898169 | ||||||
| chr5:131898176
|
T | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+13639A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898176 | ||||||
| chr5:131898227
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+13588G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898227 | ||||||
| chr5:131898239
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703+13576G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898239 | ||||||
| chr5:131898262
|
A | G | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.703+13553T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898262 | ||||||
| chr5:131898302
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+13513G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898302 | ||||||
| chr5:131898410
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0168 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.703+13405T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898410 | ||||||
| chr5:131898546
|
C | A | 1 | a0001c0002t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.703+13269G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898546 | ||||||
| chr5:131898569
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.703+13246C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898569 | ||||||
| chr5:131898583
|
A | G | 1 | a0001c0003t0001g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.703+13232T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898583 | ||||||
| chr5:131898634
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.703+13181C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898634 | ||||||
| chr5:131898731
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.703+13084G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898731 | ||||||
| chr5:131898831
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.703+12984G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898831 | ||||||
| chr5:131898953
|
A | G | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.703+12862T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131898953 | ||||||
| chr5:131899009
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+12806C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899009 | ||||||
| chr5:131899193
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703+12622A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899193 | ||||||
| chr5:131899335
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+12480G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899335 | ||||||
| chr5:131899404
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+12411G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899404 | ||||||
| chr5:131899538
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+12277C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899538 | ||||||
| chr5:131899542
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.703+12273A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899542 | ||||||
| chr5:131899542
|
T | TA | 23 | a0001c0001t0001g0060a0001c0001t0001g0122a0001c0001t0002g0005others(20): Show | 23 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.703+12272dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899542 | ||||||
| chr5:131899542
|
TA | T | 15 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp1 HG01167.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+12272delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899542 | ||||||
| chr5:131899578
|
G | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.703+12237C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899578 | ||||||
| chr5:131899581
|
T | G | 139 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(136): Show | 142 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.703+12234A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899581 | ||||||
| chr5:131899582
|
T | C | 139 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(136): Show | 142 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.703+12233A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899582 | ||||||
| chr5:131899606
|
T | G | 7 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+12209A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899606 | ||||||
| chr5:131899789
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+12026G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899789 | ||||||
| chr5:131899878
|
G | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+11937C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131899878 | ||||||
| chr5:131900203
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.703+11612T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900203 | ||||||
| chr5:131900231
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.703+11584G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900231 | ||||||
| chr5:131900237
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.703+11578C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900237 | ||||||
| chr5:131900555
|
T | A | 2 | a0001c0002t0001g0202a0001c0002t0005g0342 | 2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.703+11260A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900555 | ||||||
| chr5:131900577
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.703+11238G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900577 | ||||||
| chr5:131900652
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+11163T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900652 | ||||||
| chr5:131900844
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703+10971C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900844 | ||||||
| chr5:131900865
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.703+10950C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900865 | ||||||
| chr5:131900887
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.703+10928G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900887 | ||||||
| chr5:131900977
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | NA18939.hp2 NA18946.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+10838A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131900977 | ||||||
| chr5:131901069
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.703+10746G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901069 | ||||||
| chr5:131901171
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+10644T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901171 | ||||||
| chr5:131901176
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.703+10639G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901176 | ||||||
| chr5:131901352
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.703+10463G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901352 | ||||||
| chr5:131901374
|
T | C | 2 | a0001c0002t0001g0209a0001c0002t0001g0242 | 2 | NA18978.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.703+10441A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901374 | ||||||
| chr5:131901584
|
C | G | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.703+10231G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901584 | ||||||
| chr5:131901701
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.703+10114A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901701 | ||||||
| chr5:131901729
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0095 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.703+10086A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901729 | ||||||
| chr5:131901797
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.703+10018C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901797 | ||||||
| chr5:131901854
|
T | C | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.703+9961A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901854 | ||||||
| chr5:131901906
|
A | G | 179 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(176): Show | 183 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.703+9909T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131901906 | ||||||
| chr5:131902058
|
T | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184 | 3 | HG02572.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.703+9757A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902058 | ||||||
| chr5:131902066
|
C | T | 65 | a0001c0002t0001g0003a0001c0002t0001g0252a0001c0002t0001g0253others(62): Show | 66 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.703+9749G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902066 | ||||||
| chr5:131902120
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+9695G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902120 | ||||||
| chr5:131902490
|
T | TTCTTGTA others(2): Show |
200 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(197): Show | 204 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.703+9316_703+9324d others(11): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902490 | ||||||
| chr5:131902634
|
T | C | 1 | a0001c0002t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+9181A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902634 | ||||||
| chr5:131902674
|
T | C | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+9141A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902674 | ||||||
| chr5:131902858
|
C | T | 2 | a0001c0001t0002g0189a0001c0002t0001g0276 | 2 | HG02630.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.703+8957G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131902858 | ||||||
| chr5:131903060
|
G | C | 1 | a0001c0002t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+8755C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903060 | ||||||
| chr5:131903177
|
T | C | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.703+8638A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903177 | ||||||
| chr5:131903224
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+8591T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903224 | ||||||
| chr5:131903428
|
T | C | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.703+8387A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903428 | ||||||
| chr5:131903487
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.703+8328C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903487 | ||||||
| chr5:131903759
|
G | A | 1 | a0001c0002t0001g0334 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.703+8056C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903759 | ||||||
| chr5:131903870
|
C | T | 52 | a0001c0002t0001g0001a0001c0002t0001g0203a0001c0002t0001g0204others(49): Show | 54 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.703+7945G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903870 | ||||||
| chr5:131903994
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+7821T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131903994 | ||||||
| chr5:131904454
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.703+7361G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131904454 | ||||||
| chr5:131904621
|
T | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(177): Show | 184 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.703+7194A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131904621 | ||||||
| chr5:131904697
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.703+7118G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131904697 | ||||||
| chr5:131904701
|
T | C | 1 | a0001c0002t0001g0270 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.703+7114A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131904701 | ||||||
| chr5:131904729
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+7086A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131904729 | ||||||
| chr5:131905028
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0020 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.703+6787A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905028 | ||||||
| chr5:131905042
|
G | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+6773C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905042 | ||||||
| chr5:131905069
|
T | G | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+6746A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905069 | ||||||
| chr5:131905150
|
C | A | 128 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(125): Show | 131 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.703+6665G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905150 | ||||||
| chr5:131905167
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+6648C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905167 | ||||||
| chr5:131905192
|
C | T | 141 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(138): Show | 144 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.703+6623G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905192 | ||||||
| chr5:131905373
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+6442G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905373 | ||||||
| chr5:131905402
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+6413G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905402 | ||||||
| chr5:131905502
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+6313G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905502 | ||||||
| chr5:131905570
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.703+6245A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905570 | ||||||
| chr5:131905764
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+6051T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905764 | ||||||
| chr5:131905894
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(10): Show | 13 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+5921G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905894 | ||||||
| chr5:131905994
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+5821T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131905994 | ||||||
| chr5:131906085
|
T | C | 180 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(177): Show | 184 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.703+5730A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906085 | ||||||
| chr5:131906250
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+5565G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906250 | ||||||
| chr5:131906362
|
G | A | 178 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 182 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.703+5453C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906362 | ||||||
| chr5:131906437
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.703+5378G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906437 | ||||||
| chr5:131906525
|
T | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(176): Show | 183 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.703+5290A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906525 | ||||||
| chr5:131906539
|
T | TA | 70 | a0001c0002t0001g0003a0001c0002t0001g0252a0001c0002t0001g0253others(67): Show | 71 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.703+5275dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906539 | ||||||
| chr5:131906613
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+5202G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906613 | ||||||
| chr5:131906646
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.703+5169T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906646 | ||||||
| chr5:131906676
|
C | T | 53 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 54 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.703+5139G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906676 | ||||||
| chr5:131906813
|
A | T | 122 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(119): Show | 125 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.703+5002T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906813 | ||||||
| chr5:131906825
|
T | C | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0172others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+4990A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906825 | ||||||
| chr5:131906924
|
G | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0026others(4): Show | 7 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+4891C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131906924 | ||||||
| chr5:131907002
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+4813G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907002 | ||||||
| chr5:131907033
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.703+4782C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907033 | ||||||
| chr5:131907347
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+4468C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907347 | ||||||
| chr5:131907390
|
G | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.703+4425C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907390 | ||||||
| chr5:131907488
|
T | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+4327A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907488 | ||||||
| chr5:131907565
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.703+4250G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907565 | ||||||
| chr5:131907584
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+4231T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907584 | ||||||
| chr5:131907596
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0121a0001c0001t0001g0165others(1): Show | 4 | HG02056.hp2 HG02135.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+4219G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907596 | ||||||
| chr5:131907648
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703+4167G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907648 | ||||||
| chr5:131907649
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.703+4166C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907649 | ||||||
| chr5:131907670
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.703+4145C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131907670 | ||||||
| chr5:131908166
|
A | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+3649T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908166 | ||||||
| chr5:131908171
|
T | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0152 | 2 | HG00621.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.703+3644A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908171 | ||||||
| chr5:131908182
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.703+3633A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908182 | ||||||
| chr5:131908260
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+3555G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908260 | ||||||
| chr5:131908261
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.703+3554C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908261 | ||||||
| chr5:131908295
|
A | G | 1 | a0001c0002t0001g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.703+3520T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908295 | ||||||
| chr5:131908381
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.703+3434C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908381 | ||||||
| chr5:131908413
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.703+3402G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908413 | ||||||
| chr5:131908485
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3330C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908485 | ||||||
| chr5:131908534
|
A | T | 1 | a0001c0002t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.703+3281T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908534 | ||||||
| chr5:131908554
|
A | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+3261T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908554 | ||||||
| chr5:131908647
|
T | G | 1 | a0001c0002t0001g0341 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.703+3168A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908647 | ||||||
| chr5:131908767
|
C | T | 7 | a0001c0001t0001g0066a0001c0001t0001g0087a0001c0001t0001g0090others(4): Show | 7 | HG01934.hp2 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+3048G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908767 | ||||||
| chr5:131908894
|
A | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+2921T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908894 | ||||||
| chr5:131908929
|
A | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+2886T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908929 | ||||||
| chr5:131908980
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0107 | 3 | NA18612.hp1 NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.703+2835A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131908980 | ||||||
| chr5:131909016
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.703+2799C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909016 | ||||||
| chr5:131909035
|
A | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+2780T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909035 | ||||||
| chr5:131909052
|
C | A | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.703+2763G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909052 | ||||||
| chr5:131909057
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+2758A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909057 | ||||||
| chr5:131909252
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703+2563A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909252 | ||||||
| chr5:131909275
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+2540G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909275 | ||||||
| chr5:131909276
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.703+2539C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909276 | ||||||
| chr5:131909532
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+2283G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909532 | ||||||
| chr5:131909597
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+2218G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909597 | ||||||
| chr5:131909815
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+2000T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909815 | ||||||
| chr5:131909897
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703+1918C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909897 | ||||||
| chr5:131909926
|
C | T | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.703+1889G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909926 | ||||||
| chr5:131909938
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703+1877C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909938 | ||||||
| chr5:131909956
|
G | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+1859C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131909956 | ||||||
| chr5:131910019
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.703+1796C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910019 | ||||||
| chr5:131910045
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.703+1770G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910045 | ||||||
| chr5:131910069
|
T | G | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1746A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910069 | ||||||
| chr5:131910113
|
G | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+1702C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910113 | ||||||
| chr5:131910293
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.703+1522A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910293 | ||||||
| chr5:131910384
|
T | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1431A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910384 | ||||||
| chr5:131910787
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.703+1028C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910787 | ||||||
| chr5:131910899
|
C | A | 1 | a0001c0002t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+916G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910899 | ||||||
| chr5:131910959
|
C | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+856G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131910959 | ||||||
| chr5:131911003
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 41 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.703+812G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911003 | ||||||
| chr5:131911039
|
C | G | 3 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0332 | 3 | HG01261.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.703+776G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911039 | ||||||
| chr5:131911190
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+625G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911190 | ||||||
| chr5:131911248
|
A | T | 178 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 182 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.703+567T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911248 | ||||||
| chr5:131911422
|
T | C | 1 | a0001c0002t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+393A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911422 | ||||||
| chr5:131911525
|
G | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.703+290C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911525 | ||||||
| chr5:131911811
|
T | A | 1 | a0001c0002t0001g0271 | 1 | NA18945.hp2 | splice_region_variant&intron_variant | LOW | c.703+4A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 8/12 | chr5 | 131911811 | ||||||
| chr5:131911899
|
T | G | 316 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.639-20A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131911899 | ||||||
| chr5:131912028
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.639-149A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912028 | ||||||
| chr5:131912042
|
T | C | 2 | a0001c0001t0002g0187a0001c0001t0002g0190 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.639-163A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912042 | ||||||
| chr5:131912097
|
G | A | 20 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0104others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.639-218C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912097 | ||||||
| chr5:131912098
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-219A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912098 | ||||||
| chr5:131912664
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.639-785C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912664 | ||||||
| chr5:131912732
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.639-853G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912732 | ||||||
| chr5:131912897
|
T | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.639-1018A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912897 | ||||||
| chr5:131912907
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0198 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.639-1028A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131912907 | ||||||
| chr5:131913076
|
C | T | 316 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.639-1197G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913076 | ||||||
| chr5:131913201
|
G | A | 178 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 182 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.639-1322C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913201 | ||||||
| chr5:131913227
|
G | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.639-1348C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913227 | ||||||
| chr5:131913309
|
T | C | 2 | a0001c0002t0001g0252a0001c0002t0001g0272 | 2 | NA18988.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.639-1430A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913309 | ||||||
| chr5:131913534
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.639-1655C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913534 | ||||||
| chr5:131913600
|
C | G | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-1721G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913600 | ||||||
| chr5:131913770
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.639-1891A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913770 | ||||||
| chr5:131913871
|
C | T | 1 | a0001c0002t0001g0330 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.639-1992G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913871 | ||||||
| chr5:131913939
|
A | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(34): Show | 38 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.639-2060T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913939 | ||||||
| chr5:131913940
|
T | C | 1 | a0001c0002t0001g0316 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.639-2061A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131913940 | ||||||
| chr5:131914057
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.639-2178G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914057 | ||||||
| chr5:131914097
|
C | G | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-2218G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914097 | ||||||
| chr5:131914310
|
G | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-2431C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914310 | ||||||
| chr5:131914383
|
CA | C | 190 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(187): Show | 194 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(191): Show |
intron_variant | MODIFIER | c.638+2502delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914383 | ||||||
| chr5:131914557
|
AGGGAAGG others(22): Show |
A | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.638+2300_638+2328d others(31): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914557 | ||||||
| chr5:131914592
|
G | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.638+2294C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914592 | ||||||
| chr5:131914592
|
GAAGGGAA others(13): Show |
G | 2 | a0001c0002t0001g0235a0001c0002t0001g0236 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.638+2274_638+2293d others(22): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914592 | ||||||
| chr5:131914597
|
GAAGGGAA others(8): Show |
G | 134 | a0001c0001t0001g0166a0001c0001t0002g0032a0001c0001t0002g0188others(131): Show | 137 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.638+2274_638+2288d others(17): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914597 | ||||||
| chr5:131914602
|
GAAGGGAA others(3): Show |
G | 188 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.638+2274_638+2283d others(12): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914602 | ||||||
| chr5:131914607
|
GAAGGA | G | 13 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0084others(10): Show | 13 | HG01167.hp2 HG01243.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.638+2274_638+2278d others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914607 | ||||||
| chr5:131914612
|
A | G | 4 | a0001c0001t0003g0106a0001c0002t0001g0298a0001c0002t0001g0299others(1): Show | 4 | HG02615.hp1 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+2274T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914612 | ||||||
| chr5:131914617
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.638+2269C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914617 | ||||||
| chr5:131914664
|
G | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.638+2222C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914664 | ||||||
| chr5:131914893
|
G | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.638+1993C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131914893 | ||||||
| chr5:131915501
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01069.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.638+1385A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131915501 | ||||||
| chr5:131915509
|
C | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0026others(4): Show | 7 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+1377G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131915509 | ||||||
| chr5:131915803
|
A | T | 1 | a0001c0003t0001g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638+1083T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131915803 | ||||||
| chr5:131915949
|
T | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.638+937A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131915949 | ||||||
| chr5:131916168
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.638+718T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916168 | ||||||
| chr5:131916185
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+701C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916185 | ||||||
| chr5:131916373
|
T | G | 1 | a0001c0002t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.638+513A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916373 | ||||||
| chr5:131916393
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+493G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916393 | ||||||
| chr5:131916492
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.638+394C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916492 | ||||||
| chr5:131916511
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+375T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916511 | ||||||
| chr5:131916607
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+279T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916607 | ||||||
| chr5:131916703
|
C | T | 139 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0202others(136): Show | 142 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.638+183G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916703 | ||||||
| chr5:131916730
|
A | G | 1 | a0001c0002t0001g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.638+156T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916730 | ||||||
| chr5:131916734
|
C | T | 4 | a0001c0002t0001g0326a0001c0002t0001g0327a0001c0002t0001g0330others(1): Show | 4 | NA18939.hp1 NA18998.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+152G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916734 | ||||||
| chr5:131916812
|
A | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+74T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916812 | ||||||
| chr5:131916861
|
C | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.638+25G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 7/12 | chr5 | 131916861 | ||||||
| chr5:131916946
|
A | C | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.599-21T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131916946 | ||||||
| chr5:131917123
|
G | A | 1 | a0001c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.599-198C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917123 | ||||||
| chr5:131917211
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599-286A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917211 | ||||||
| chr5:131917236
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.599-311G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917236 | ||||||
| chr5:131917287
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-362G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917287 | ||||||
| chr5:131917332
|
G | A | 2 | a0001c0001t0002g0004a0001c0002t0001g0304 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.599-407C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917332 | ||||||
| chr5:131917427
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0005g0342 | 2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.599-502C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917427 | ||||||
| chr5:131917563
|
C | CA | 26 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0097others(23): Show | 26 | HG01496.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.599-639dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917563 | ||||||
| chr5:131917563
|
CA | C | 115 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0052others(112): Show | 118 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.599-639delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917563 | ||||||
| chr5:131917782
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.599-857A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917782 | ||||||
| chr5:131917795
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.599-870A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917795 | ||||||
| chr5:131917937
|
T | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.599-1012A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917937 | ||||||
| chr5:131917990
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.599-1065G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131917990 | ||||||
| chr5:131919010
|
C | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-2085G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919010 | ||||||
| chr5:131919088
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.599-2163G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919088 | ||||||
| chr5:131919110
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0115others(7): Show | 10 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.599-2185T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919110 | ||||||
| chr5:131919218
|
T | C | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.599-2293A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919218 | ||||||
| chr5:131919417
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.598+2405T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919417 | ||||||
| chr5:131919525
|
G | C | 1 | a0001c0001t0002g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.598+2297C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919525 | ||||||
| chr5:131919637
|
A | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.598+2185T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919637 | ||||||
| chr5:131919793
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.598+2029T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919793 | ||||||
| chr5:131919912
|
C | T | 8 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+1910G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131919912 | ||||||
| chr5:131920051
|
C | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0296 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.598+1771G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920051 | ||||||
| chr5:131920173
|
G | T | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.598+1649C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920173 | ||||||
| chr5:131920239
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.598+1583C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920239 | ||||||
| chr5:131920290
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.598+1532T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920290 | ||||||
| chr5:131920305
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.598+1517G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920305 | ||||||
| chr5:131920459
|
T | A | 1 | a0001c0002t0001g0264 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.598+1363A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920459 | ||||||
| chr5:131920522
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.598+1300C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920522 | ||||||
| chr5:131920604
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.598+1218C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920604 | ||||||
| chr5:131920697
|
A | AT | 6 | a0001c0001t0001g0086a0001c0002t0001g0300a0001c0002t0001g0301others(3): Show | 6 | HG01496.hp1 HG01934.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+1124dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920697 | ||||||
| chr5:131920697
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.598+1125T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920697 | ||||||
| chr5:131920697
|
AT | A | 52 | a0001c0001t0001g0051a0001c0001t0001g0102a0001c0001t0001g0154others(49): Show | 53 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.598+1124delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920697 | ||||||
| chr5:131920745
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.598+1077C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920745 | ||||||
| chr5:131920767
|
C | G | 12 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0165others(9): Show | 12 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+1055G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920767 | ||||||
| chr5:131920993
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598+829G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131920993 | ||||||
| chr5:131921321
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.598+501C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921321 | ||||||
| chr5:131921333
|
G | A | 1 | a0001c0002t0001g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.598+489C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921333 | ||||||
| chr5:131921334
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.598+488T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921334 | ||||||
| chr5:131921483
|
C | T | 1 | a0001c0002t0001g0247 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.598+339G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921483 | ||||||
| chr5:131921678
|
T | G | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.598+144A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921678 | ||||||
| chr5:131921776
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.598+46G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 6/12 | chr5 | 131921776 | ||||||
| chr5:131922013
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.479-72G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922013 | ||||||
| chr5:131922071
|
G | A | 1 | a0001c0002t0001g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.479-130C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922071 | ||||||
| chr5:131922224
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479-283A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922224 | ||||||
| chr5:131922597
|
A | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.479-656T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922597 | ||||||
| chr5:131922613
|
G | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-672C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922613 | ||||||
| chr5:131922685
|
A | C | 200 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(197): Show | 204 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.479-744T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922685 | ||||||
| chr5:131922860
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.479-919G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922860 | ||||||
| chr5:131922939
|
T | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.479-998A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922939 | ||||||
| chr5:131922998
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.479-1057A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131922998 | ||||||
| chr5:131923033
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.479-1092T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923033 | ||||||
| chr5:131923080
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.479-1139C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923080 | ||||||
| chr5:131923206
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.479-1265A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923206 | ||||||
| chr5:131923422
|
T | C | 1 | a0001c0002t0001g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.479-1481A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923422 | ||||||
| chr5:131923439
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.479-1498C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923439 | ||||||
| chr5:131923668
|
C | T | 12 | a0001c0002t0001g0003a0001c0002t0001g0252a0001c0002t0001g0254others(9): Show | 13 | NA18945.hp2 NA18947.hp1 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.479-1727G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923668 | ||||||
| chr5:131923669
|
G | A | 2 | a0001c0001t0001g0174a0001c0002t0005g0342 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.479-1728C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923669 | ||||||
| chr5:131923809
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0177 | 2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.479-1868A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923809 | ||||||
| chr5:131923834
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.479-1893C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131923834 | ||||||
| chr5:131924088
|
C | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479-2147G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924088 | ||||||
| chr5:131924265
|
G | C | 4 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0002g0025others(1): Show | 4 | HG00642.hp2 HG02897.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-2324C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924265 | ||||||
| chr5:131924369
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.479-2428G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924369 | ||||||
| chr5:131924627
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.479-2686C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924627 | ||||||
| chr5:131924673
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.479-2732A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924673 | ||||||
| chr5:131924716
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.479-2775G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924716 | ||||||
| chr5:131924759
|
C | A | 178 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 182 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.479-2818G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924759 | ||||||
| chr5:131924923
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.479-2982T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924923 | ||||||
| chr5:131924995
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.479-3054C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131924995 | ||||||
| chr5:131925125
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.479-3184C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925125 | ||||||
| chr5:131925469
|
G | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.479-3528C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925469 | ||||||
| chr5:131925482
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0107 | 3 | NA18612.hp1 NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.479-3541G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925482 | ||||||
| chr5:131925486
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.479-3545A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925486 | ||||||
| chr5:131925630
|
A | G | 2 | a0001c0003t0001g0313a0001c0003t0001g0314 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.479-3689T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925630 | ||||||
| chr5:131925760
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.479-3819G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925760 | ||||||
| chr5:131925848
|
A | T | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.479-3907T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925848 | ||||||
| chr5:131925873
|
G | C | 1 | a0001c0002t0001g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.479-3932C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925873 | ||||||
| chr5:131925916
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479-3975G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925916 | ||||||
| chr5:131925966
|
C | T | 9 | a0001c0002t0001g0204a0001c0002t0001g0210a0001c0002t0001g0217others(6): Show | 9 | HG00438.hp1 HG01192.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.479-4025G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925966 | ||||||
| chr5:131925994
|
A | G | 5 | a0001c0002t0001g0203a0001c0002t0001g0215a0001c0002t0001g0216others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-4053T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131925994 | ||||||
| chr5:131926069
|
A | G | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.479-4128T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926069 | ||||||
| chr5:131926152
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-4211G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926152 | ||||||
| chr5:131926197
|
A | G | 39 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(36): Show | 40 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.479-4256T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926197 | ||||||
| chr5:131926280
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-4339A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926280 | ||||||
| chr5:131926384
|
C | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.479-4443G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926384 | ||||||
| chr5:131926385
|
G | A | 10 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0165others(7): Show | 10 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-4444C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926385 | ||||||
| chr5:131926398
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.479-4457C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926398 | ||||||
| chr5:131926399
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.479-4458C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926399 | ||||||
| chr5:131926400
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.479-4459A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926400 | ||||||
| chr5:131926428
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.479-4487A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926428 | ||||||
| chr5:131926482
|
T | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-4541A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926482 | ||||||
| chr5:131926820
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-4879A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926820 | ||||||
| chr5:131926864
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.479-4923A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131926864 | ||||||
| chr5:131927174
|
T | TTGTGC | 123 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(120): Show | 126 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.479-5238_479-5234d others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927174 | ||||||
| chr5:131927212
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.479-5271A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927212 | ||||||
| chr5:131927458
|
T | C | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.479-5517A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927458 | ||||||
| chr5:131927467
|
T | C | 3 | a0001c0001t0002g0191a0001c0004t0002g0192a0001c0004t0002g0193 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.479-5526A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927467 | ||||||
| chr5:131927497
|
C | G | 1 | a0001c0002t0001g0329 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.479-5556G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927497 | ||||||
| chr5:131927691
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0247 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.479-5750G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927691 | ||||||
| chr5:131927787
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.478+5726A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927787 | ||||||
| chr5:131927873
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0168 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.478+5640G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927873 | ||||||
| chr5:131927956
|
T | C | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.478+5557A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927956 | ||||||
| chr5:131927973
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.478+5540C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131927973 | ||||||
| chr5:131928006
|
C | T | 200 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(197): Show | 204 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.478+5507G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928006 | ||||||
| chr5:131928036
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.478+5477G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928036 | ||||||
| chr5:131928069
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.478+5444C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928069 | ||||||
| chr5:131928118
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+5395A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928118 | ||||||
| chr5:131928130
|
C | A | 1 | a0001c0002t0001g0335 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.478+5383G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928130 | ||||||
| chr5:131928130
|
C | T | 2 | a0001c0002t0001g0257a0001c0002t0001g0258 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.478+5383G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928130 | ||||||
| chr5:131928131
|
A | G | 178 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(175): Show | 182 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.478+5382T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928131 | ||||||
| chr5:131928143
|
C | CA | 124 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0087others(121): Show | 127 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.478+5369dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928143 | ||||||
| chr5:131928143
|
CA | C | 40 | a0001c0001t0001g0061a0001c0001t0001g0113a0001c0001t0001g0172others(37): Show | 41 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.478+5369delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928143 | ||||||
| chr5:131928353
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG00140.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.478+5160G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928353 | ||||||
| chr5:131928454
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+5059G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928454 | ||||||
| chr5:131928538
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.478+4975G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928538 | ||||||
| chr5:131928744
|
A | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+4769T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928744 | ||||||
| chr5:131928952
|
C | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+4561G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131928952 | ||||||
| chr5:131929114
|
A | G | 4 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0002g0025others(1): Show | 4 | HG00642.hp2 HG02897.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+4399T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929114 | ||||||
| chr5:131929155
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.478+4358T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929155 | ||||||
| chr5:131929167
|
A | C | 1 | a0001c0003t0001g0313 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.478+4346T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929167 | ||||||
| chr5:131929225
|
C | T | 9 | a0001c0002t0001g0001a0001c0002t0001g0233a0001c0002t0001g0234others(6): Show | 11 | HG00408.hp2 HG01978.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.478+4288G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929225 | ||||||
| chr5:131929320
|
T | G | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.478+4193A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929320 | ||||||
| chr5:131929452
|
C | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+4061G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929452 | ||||||
| chr5:131929797
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.478+3716G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929797 | ||||||
| chr5:131929846
|
T | C | 9 | a0001c0002t0001g0001a0001c0002t0001g0233a0001c0002t0001g0234others(6): Show | 11 | HG00408.hp2 HG01978.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.478+3667A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929846 | ||||||
| chr5:131929909
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.478+3604G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131929909 | ||||||
| chr5:131930080
|
T | C | 1 | a0001c0002t0001g0247 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.478+3433A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930080 | ||||||
| chr5:131930116
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478+3397G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930116 | ||||||
| chr5:131930156
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.478+3357A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930156 | ||||||
| chr5:131930201
|
G | T | 2 | a0001c0004t0002g0192a0001c0004t0002g0193 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.478+3312C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930201 | ||||||
| chr5:131930341
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+3172C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930341 | ||||||
| chr5:131930669
|
T | C | 201 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(198): Show | 205 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.478+2844A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930669 | ||||||
| chr5:131930734
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.478+2779A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930734 | ||||||
| chr5:131930760
|
T | C | 2 | a0001c0002t0001g0235a0001c0002t0001g0236 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.478+2753A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930760 | ||||||
| chr5:131930908
|
T | C | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.478+2605A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930908 | ||||||
| chr5:131930968
|
G | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+2545C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131930968 | ||||||
| chr5:131931061
|
A | G | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.478+2452T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931061 | ||||||
| chr5:131931238
|
T | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+2275A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931238 | ||||||
| chr5:131931262
|
T | A | 1 | a0001c0002t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478+2251A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931262 | ||||||
| chr5:131931322
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.478+2191G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931322 | ||||||
| chr5:131931406
|
G | T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.478+2107C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931406 | ||||||
| chr5:131931481
|
C | G | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.478+2032G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931481 | ||||||
| chr5:131931713
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.478+1800T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931713 | ||||||
| chr5:131931766
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.478+1747A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931766 | ||||||
| chr5:131931916
|
G | A | 179 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(176): Show | 183 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.478+1597C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931916 | ||||||
| chr5:131931971
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | NA18965.hp1 NA18971.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+1542G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131931971 | ||||||
| chr5:131932014
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.478+1499A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932014 | ||||||
| chr5:131932108
|
A | T | 1 | a0001c0002t0001g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.478+1405T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932108 | ||||||
| chr5:131932404
|
G | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+1109C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932404 | ||||||
| chr5:131932480
|
C | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+1033G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932480 | ||||||
| chr5:131932533
|
TA | T | 122 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(119): Show | 125 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.478+979delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932533 | ||||||
| chr5:131932843
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.478+670T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932843 | ||||||
| chr5:131932985
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+528G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131932985 | ||||||
| chr5:131933250
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.478+263C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131933250 | ||||||
| chr5:131933392
|
G | A | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.478+121C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 5/12 | chr5 | 131933392 | ||||||
| chr5:131933760
|
G | A | 177 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(174): Show | 181 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.350-119C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131933760 | ||||||
| chr5:131933992
|
G | T | 2 | a0001c0002t0001g0326a0001c0002t0001g0327 | 2 | NA18939.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.350-351C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131933992 | ||||||
| chr5:131933995
|
G | A | 1 | a0001c0002t0001g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.350-354C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131933995 | ||||||
| chr5:131934111
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02976.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.350-470A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934111 | ||||||
| chr5:131934332
|
T | C | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0190 | 3 | HG02109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.350-691A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934332 | ||||||
| chr5:131934443
|
T | C | 122 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(119): Show | 125 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.350-802A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934443 | ||||||
| chr5:131934529
|
A | T | 121 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.350-888T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934529 | ||||||
| chr5:131934655
|
T | A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.350-1014A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934655 | ||||||
| chr5:131934854
|
G | C | 2 | a0001c0001t0001g0088a0002c0005t0001g0164 | 2 | NA18995.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.350-1213C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934854 | ||||||
| chr5:131934861
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.350-1220A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131934861 | ||||||
| chr5:131935053
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.350-1412G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935053 | ||||||
| chr5:131935161
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.350-1520A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935161 | ||||||
| chr5:131935263
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.350-1622A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935263 | ||||||
| chr5:131935267
|
C | CA | 49 | a0001c0001t0001g0039a0001c0001t0001g0090a0001c0001t0001g0091others(46): Show | 51 | HG00408.hp2 HG00639.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.350-1627dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935267 | ||||||
| chr5:131935267
|
CA | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0168a0001c0001t0002g0016others(7): Show | 10 | HG01167.hp2 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1627delT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935267 | ||||||
| chr5:131935286
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0094 | 3 | HG01993.hp2 HG02602.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.350-1645T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935286 | ||||||
| chr5:131935315
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0095 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.350-1674T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935315 | ||||||
| chr5:131935329
|
T | G | 112 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.350-1688A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935329 | ||||||
| chr5:131935524
|
G | A | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1883C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935524 | ||||||
| chr5:131935835
|
G | C | 201 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0092others(198): Show | 205 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.350-2194C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935835 | ||||||
| chr5:131935889
|
C | CA | 123 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0203others(120): Show | 126 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.350-2249dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935889 | ||||||
| chr5:131935990
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.350-2349A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131935990 | ||||||
| chr5:131936051
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.350-2410A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936051 | ||||||
| chr5:131936126
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.350-2485G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936126 | ||||||
| chr5:131936230
|
C | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.350-2589G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936230 | ||||||
| chr5:131936235
|
T | C | 1 | a0001c0002t0001g0249 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.350-2594A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936235 | ||||||
| chr5:131936282
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-2641A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936282 | ||||||
| chr5:131936453
|
G | A | 1 | a0001c0003t0001g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-2812C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936453 | ||||||
| chr5:131936618
|
G | A | 2 | a0001c0002t0001g0336a0001c0002t0001g0337 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.350-2977C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936618 | ||||||
| chr5:131936705
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.350-3064G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936705 | ||||||
| chr5:131936713
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.350-3072C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936713 | ||||||
| chr5:131936809
|
A | C | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.350-3168T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131936809 | ||||||
| chr5:131937580
|
C | A | 7 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0184others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-3939G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131937580 | ||||||
| chr5:131937629
|
A | T | 1 | a0001c0002t0001g0341 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.350-3988T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131937629 | ||||||
| chr5:131937883
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.350-4242C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131937883 | ||||||
| chr5:131938141
|
G | A | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+4494C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938141 | ||||||
| chr5:131938165
|
C | CT | 9 | a0001c0001t0001g0051a0001c0001t0001g0105a0001c0001t0002g0032others(6): Show | 9 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+4469dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938165 | ||||||
| chr5:131938165
|
CT | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0168others(9): Show | 12 | HG00738.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+4469delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938165 | ||||||
| chr5:131938165
|
CTT | C | 121 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0002t0001g0001others(118): Show | 124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.349+4468_349+4469d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938165 | ||||||
| chr5:131938293
|
G | A | 4 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+4342C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938293 | ||||||
| chr5:131938368
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.349+4267C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938368 | ||||||
| chr5:131938387
|
C | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+4248G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938387 | ||||||
| chr5:131938437
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.349+4198C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938437 | ||||||
| chr5:131938438
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.349+4197C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938438 | ||||||
| chr5:131938522
|
T | C | 1 | a0001c0002t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.349+4113A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938522 | ||||||
| chr5:131938524
|
G | C | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+4111C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938524 | ||||||
| chr5:131938542
|
T | C | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0026others(4): Show | 7 | HG00639.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+4093A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938542 | ||||||
| chr5:131938581
|
T | G | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.349+4054A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938581 | ||||||
| chr5:131938637
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+3998A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938637 | ||||||
| chr5:131938638
|
A | G | 1 | a0001c0002t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.349+3997T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938638 | ||||||
| chr5:131938651
|
A | C | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+3984T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938651 | ||||||
| chr5:131938691
|
C | A | 2 | a0001c0003t0001g0313a0001c0003t0001g0314 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.349+3944G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938691 | ||||||
| chr5:131938693
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+3942G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938693 | ||||||
| chr5:131938735
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349+3900A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938735 | ||||||
| chr5:131938856
|
C | T | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+3779G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131938856 | ||||||
| chr5:131939353
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0169 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.349+3282A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939353 | ||||||
| chr5:131939394
|
T | G | 3 | a0001c0001t0002g0191a0001c0004t0002g0192a0001c0004t0002g0193 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.349+3241A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939394 | ||||||
| chr5:131939396
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+3239C>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939396 | ||||||
| chr5:131939403
|
T | C | 1 | a0001c0002t0001g0338 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.349+3232A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939403 | ||||||
| chr5:131939496
|
C | T | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+3139G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939496 | ||||||
| chr5:131939583
|
C | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+3052G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939583 | ||||||
| chr5:131939762
|
C | T | 1 | a0001c0003t0001g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+2873G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939762 | ||||||
| chr5:131939764
|
A | T | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+2871T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939764 | ||||||
| chr5:131939816
|
G | A | 180 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0002others(177): Show | 184 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.349+2819C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939816 | ||||||
| chr5:131939833
|
C | A | 1 | a0001c0001t0002g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349+2802G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939833 | ||||||
| chr5:131939975
|
A | C | 10 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+2660T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939975 | ||||||
| chr5:131939976
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02165.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.349+2659A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131939976 | ||||||
| chr5:131940057
|
T | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+2578A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940057 | ||||||
| chr5:131940079
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.349+2556G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940079 | ||||||
| chr5:131940102
|
T | C | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.349+2533A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940102 | ||||||
| chr5:131940230
|
A | G | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+2405T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940230 | ||||||
| chr5:131940379
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.349+2256C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940379 | ||||||
| chr5:131940382
|
T | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349+2253A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940382 | ||||||
| chr5:131940463
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+2172G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940463 | ||||||
| chr5:131940923
|
C | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+1712G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940923 | ||||||
| chr5:131940968
|
C | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+1667G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940968 | ||||||
| chr5:131940973
|
C | A | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1662G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131940973 | ||||||
| chr5:131941109
|
C | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1526G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941109 | ||||||
| chr5:131941142
|
C | CT | 25 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(22): Show | 25 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.349+1492dupA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
C | CTT | 17 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 17 | HG01433.hp1 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+1491_349+1492d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
C | CTTT | 8 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+1490_349+1492d others(5): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CT | C | 80 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0103others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.349+1492delA | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTT | C | 10 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+1491_349+1492d others(4): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTT | C | 19 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0205others(16): Show | 19 | HG01433.hp2 HG01934.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.349+1489_349+1492d others(6): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTT | C | 102 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0002t0001g0001others(99): Show | 105 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.349+1488_349+1492d others(7): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTTT | C | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | NA18956.hp2 NA18957.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+1487_349+1492d others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.349+1481_349+1492d others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.349+1480_349+1492d others(15): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0003t0001g0312a0001c0003t0001g0313a0001c0003t0001g0314 | 3 | HG01884.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.349+1478_349+1492d others(17): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941142
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+1475_349+1492d others(20): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941142 | ||||||
| chr5:131941182
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+1453T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941182 | ||||||
| chr5:131941217
|
G | GGCTCAAA others(67): Show |
6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1417_349+1418i others(76): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941217 | ||||||
| chr5:131941218
|
A | G | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1417T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941218 | ||||||
| chr5:131941222
|
A | G | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1413T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941222 | ||||||
| chr5:131941225
|
C | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1410G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941225 | ||||||
| chr5:131941236
|
G | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1399C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941236 | ||||||
| chr5:131941245
|
G | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+1390C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941245 | ||||||
| chr5:131941253
|
G | GGTCCCA | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1381_349+1382i others(8): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941253 | ||||||
| chr5:131941262
|
G | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1373C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941262 | ||||||
| chr5:131941269
|
T | C | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1366A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941269 | ||||||
| chr5:131941272
|
T | C | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1363A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941272 | ||||||
| chr5:131941283
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.349+1352G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941283 | ||||||
| chr5:131941303
|
C | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1332G>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941303 | ||||||
| chr5:131941304
|
G | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1331C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941304 | ||||||
| chr5:131941305
|
C | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1330G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941305 | ||||||
| chr5:131941306
|
C | G | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1329G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941306 | ||||||
| chr5:131941309
|
C | T | 50 | a0001c0002t0001g0001a0001c0002t0001g0203a0001c0002t0001g0204others(47): Show | 52 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.349+1326G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941309 | ||||||
| chr5:131941314
|
AC | A | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1320delG | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941314 | ||||||
| chr5:131941316
|
G | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1319C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941316 | ||||||
| chr5:131941326
|
A | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1309T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941326 | ||||||
| chr5:131941327
|
T | TATTTTTT others(5): Show |
6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1307_349+1308i others(14): Show |
MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941327 | ||||||
| chr5:131941331
|
G | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1304C>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941331 | ||||||
| chr5:131941333
|
A | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1302T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941333 | ||||||
| chr5:131941355
|
C | T | 6 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1280G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941355 | ||||||
| chr5:131941456
|
GC | G | 180 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0002others(177): Show | 184 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.349+1178delG | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941456 | ||||||
| chr5:131941674
|
A | G | 1 | a0001c0002t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.349+961T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941674 | ||||||
| chr5:131941742
|
A | T | 1 | a0001c0002t0001g0340 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+893T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941742 | ||||||
| chr5:131941955
|
A | G | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+680T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941955 | ||||||
| chr5:131941957
|
T | C | 1 | a0001c0002t0001g0339 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.349+678A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941957 | ||||||
| chr5:131941989
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.349+646G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131941989 | ||||||
| chr5:131942342
|
A | C | 5 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+293T>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131942342 | ||||||
| chr5:131942574
|
T | C | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+61A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 4/12 | chr5 | 131942574 | ||||||
| chr5:131942825
|
T | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.289-130A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131942825 | ||||||
| chr5:131943135
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.289-440C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943135 | ||||||
| chr5:131943207
|
T | A | 1 | a0001c0002t0005g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.289-512A>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943207 | ||||||
| chr5:131943293
|
C | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.289-598G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943293 | ||||||
| chr5:131943472
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 41 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.289-777A>G | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943472 | ||||||
| chr5:131943527
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.289-832T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943527 | ||||||
| chr5:131943559
|
C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.289-864G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943559 | ||||||
| chr5:131943727
|
C | G | 123 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0002t0001g0001others(120): Show | 126 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.288+938G>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943727 | ||||||
| chr5:131943819
|
A | T | 1 | a0001c0001t0002g0032 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.288+846T>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943819 | ||||||
| chr5:131943844
|
G | A | 6 | a0001c0002t0001g0317a0001c0002t0001g0318a0001c0002t0001g0319others(3): Show | 6 | NA18949.hp2 NA18951.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+821C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131943844 | ||||||
| chr5:131944111
|
C | CA | 18 | a0001c0002t0001g0323a0001c0002t0001g0324a0001c0002t0001g0325others(15): Show | 18 | HG00738.hp1 HG01081.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+553dupT | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131944111 | ||||||
| chr5:131944254
|
C | T | 29 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(26): Show | 30 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.288+411G>A | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131944254 | ||||||
| chr5:131944355
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.288+310T>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131944355 | ||||||
| chr5:131944476
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02257.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+189C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 3/12 | chr5 | 131944476 | ||||||
| chr5:131945024
|
G | A | 1 | a0001c0002t0001g0341 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.200+132C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 2/12 | chr5 | 131945024 | ||||||
| chr5:131945117
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.200+39A>C | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 2/12 | chr5 | 131945117 | ||||||
| chr5:131945144
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0007t0001g0201 | 3 | HG00140.hp2 HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.200+12C>T | MEIKIN | ENSG00000239642.6 | transcript | ENST00000442687.6 | protein_coding | 2/12 | chr5 | 131945144 |