Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3613 |
|---|---|
| ensemblid | ENSG00000141401.12 |
| hgncid | 6051 |
| symbol | IMPA2 |
| name | inositol monophosphatase 2 |
| refseq_nuc | NM_014214.3 |
| refseq_prot | NP_055029.1 |
| ensembl_nuc | ENST00000269159.8 |
| ensembl_prot | ENSP00000269159.3 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 11981507 |
| end | 12030877 |
| strand | + |
| ver | v1.2 |
| region | chr18:11981507-12030877 |
| region5000 | chr18:11976507-12035877 |
| regionname0 | IMPA2_chr18_11981507_12030877 |
| regionname5000 | IMPA2_chr18_11976507_12035877 |
| 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 | 288 | 356 | 94 | 68 | 145 | 14 | 33 | 99 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0002 | 0/0 | 288 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0003 | 0/0 | 288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0004 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0005 | 0/0 | 288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| 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 | 867 | 271 | 75 | 58 | 92 | 14 | 30 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0002 | 0/0 | 867 | 72 | 19 | 9 | 41 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0003 | 0/0 | 867 | 9 | 0 | 0 | 9 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0004 | 0/0 | 867 | 3 | 3 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0005 | 0/0 | 867 | 3 | 0 | 0 | 3 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0006 | 0/0 | 867 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0007 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0008 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0009 | 0/0 | 867 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| c0010 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| 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 | 583 | 352 | 89 | 67 | 146 | 14 | 34 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0002 | 0/0 | 583 | 6 | 6 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0003 | 0/0 | 583 | 2 | 1 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0004 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0005 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0006 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| t0007 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| 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 | 867 | 271 | 75 | 58 | 92 | 14 | 30 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002 | 0/0 | 867 | 72 | 19 | 9 | 41 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0003 | 0/0 | 867 | 9 | 0 | 0 | 9 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0006 | 0/0 | 867 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0007 | 0/0 | 867 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0009 | 0/0 | 867 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0002c0005 | 0/0 | 867 | 3 | 0 | 0 | 3 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0003c0004 | 0/0 | 867 | 3 | 3 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0004c0010 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0005c0008 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1449 | 264 | 69 | 57 | 92 | 14 | 30 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0001t0002 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0001t0003 | 0/0 | 1449 | 2 | 1 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0001t0005 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002t0001 | 0/0 | 1449 | 67 | 16 | 9 | 39 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002t0002 | 0/0 | 1449 | 2 | 2 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002t0004 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002t0006 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0002t0007 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0003t0001 | 0/0 | 1449 | 9 | 0 | 0 | 9 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0006t0001 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0007t0001 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0001c0009t0001 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0002c0005t0001 | 0/0 | 1449 | 3 | 0 | 0 | 3 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0003c0004t0001 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0004c0010t0001 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| a0005c0008t0001 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | copy fasta | chr18 | 11976507 | 12035877 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0009t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0004c0010t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0005c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0360 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0330 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01243 | hp1 | a0001 | c0009 | t0001 | g0124 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0357 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0284 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02129 | hp2 | a0001 | c0002 | t0007 | g0233 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0240 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02809 | hp1 | a0004 | c0010 | t0001 | g0062 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0027 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0070 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0061 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03710 | hp2 | a0005 | c0008 | t0001 | g0042 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0337 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18966 | hp1 | a0002 | c0005 | t0001 | g0096 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18971 | hp1 | a0002 | c0005 | t0001 | g0095 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0251 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19012 | hp1 | a0002 | c0005 | t0001 | g0024 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0332 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19086 | hp2 | a0001 | c0006 | t0001 | g0241 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19089 | hp1 | a0001 | c0007 | t0001 | g0252 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ASW | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12009914
|
G | A | 1 | a0003 | 3 | HG01884.hp1 HG03453.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.262G>A | p.Ala88Thr | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/8 | 425/1449 | 262/867 | 88/288 | chr18 | 12009914 | ||
| chr18:12009962
|
G | A | 1 | a0005 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.310G>A | p.Asp104Asn | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/8 | 473/1449 | 310/867 | 104/288 | chr18 | 12009962 | ||
| chr18:12014302
|
G | A | 1 | a0002 | 3 | NA18966.hp1 NA18971.hp1 NA19012.hp1 |
missense_variant | MODERATE | c.419G>A | p.Arg140Gln | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/8 | 582/1449 | 419/867 | 140/288 | chr18 | 12014302 | ||
| chr18:12014355
|
C | T | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.472C>T | p.Arg158Trp | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/8 | 635/1449 | 472/867 | 158/288 | chr18 | 12014355 | ||
| chr18:12030400
|
C | T | 1 | a0005 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.809C>T | p.Ala270Val | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 8/8 | 972/1449 | 809/867 | 270/288 | chr18 | 12030400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:11999116
|
T | C | 3 | a0001c0002a0001c0006a0001c0007 | 75 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(72): Show |
synonymous_variant | LOW | c.159T>C | p.Leu53Leu | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/8 | 322/1449 | 159/867 | 53/288 | chr18 | 11999116 | ||
| chr18:12014318
|
G | C | 1 | a0001c0007 | 1 | NA19089.hp1 | synonymous_variant | LOW | c.435G>C | p.Arg145Arg | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/8 | 598/1449 | 435/867 | 145/288 | chr18 | 12014318 | ||
| chr18:12028095
|
G | A | 1 | a0001c0009 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.543G>A | p.Ala181Ala | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/8 | 706/1449 | 543/867 | 181/288 | chr18 | 12028095 | ||
| chr18:12028110
|
C | T | 2 | a0001c0003a0001c0006 | 11 | HG00408.hp1 NA18948.hp1 NA18954.hp1 others(8): Show |
synonymous_variant | LOW | c.558C>T | p.Phe186Phe | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/8 | 721/1449 | 558/867 | 186/288 | chr18 | 12028110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:11981540
|
G | A | 1 | a0001c0002t0004 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/8 | 130 | chr18 | 11981540 | |||||
| chr18:11981653
|
G | A | 1 | a0001c0001t0003 | 2 | HG01167.hp1 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-17G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/8 | 17 | chr18 | 11981653 | |||||
| chr18:12030621
|
G | A | 2 | a0001c0001t0002a0001c0002t0002 | 6 | HG01891.hp1 HG01891.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*163G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 8/8 | 163 | chr18 | 12030621 | |||||
| chr18:12030673
|
C | A | 1 | a0001c0001t0005 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 8/8 | 215 | chr18 | 12030673 | |||||
| chr18:12030678
|
C | G | 1 | a0001c0002t0007 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 8/8 | 220 | chr18 | 12030678 | |||||
| chr18:12030822
|
C | T | 1 | a0001c0002t0006 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*364C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 8/8 | 364 | chr18 | 12030822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:11982133
|
C | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+368C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982133 | ||||||
| chr18:11982211
|
C | T | 21 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.96+446C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982211 | ||||||
| chr18:11982243
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 46 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.96+478G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982243 | ||||||
| chr18:11982418
|
T | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 47 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.96+653T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982418 | ||||||
| chr18:11982496
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.96+731C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982496 | ||||||
| chr18:11982501
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 48 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.96+736G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982501 | ||||||
| chr18:11982506
|
G | A | 2 | a0002c0005t0001g0095a0002c0005t0001g0096 | 2 | NA18966.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.96+741G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982506 | ||||||
| chr18:11982760
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96+995A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11982760 | ||||||
| chr18:11982793
|
CA | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.96+1045delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11982793 | |||||
| chr18:11982793
|
CAA | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0093others(21): Show | 26 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.96+1044_96+1045del others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11982793 | |||||
| chr18:11982793
|
CAAA | C | 51 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+1043_96+1045del others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11982793 | |||||
| chr18:11983013
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+1248A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983013 | ||||||
| chr18:11983015
|
C | T | 56 | a0001c0001t0001g0289a0001c0001t0001g0292a0001c0001t0001g0293others(53): Show | 56 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+1250C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983015 | ||||||
| chr18:11983036
|
T | TAATCTGC others(50): Show |
1 | a0001c0003t0001g0290 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.96+1308_96+1309ins others(57): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11983036 | |||||
| chr18:11983074
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(169): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.96+1309G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983074 | ||||||
| chr18:11983131
|
G | GAATT | 5 | a0001c0001t0001g0289a0001c0002t0001g0285a0001c0002t0001g0286others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1367_96+1370dup others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11983131 | |||||
| chr18:11983137
|
AAG | A | 52 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.96+1375_96+1376del others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11983137 | |||||
| chr18:11983311
|
A | T | 48 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.96+1546A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983311 | ||||||
| chr18:11983566
|
C | T | 53 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.96+1801C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983566 | ||||||
| chr18:11983606
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1841C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983606 | ||||||
| chr18:11983681
|
C | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.96+1916C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983681 | ||||||
| chr18:11983741
|
C | T | 1 | a0003c0004t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+1976C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983741 | ||||||
| chr18:11983803
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0002t0001g0272others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2038G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983803 | ||||||
| chr18:11983989
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.96+2224C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11983989 | ||||||
| chr18:11984008
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+2243A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984008 | ||||||
| chr18:11984014
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.96+2249C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984014 | ||||||
| chr18:11984016
|
A | G | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.96+2251A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984016 | ||||||
| chr18:11984070
|
G | A | 52 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.96+2305G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984070 | ||||||
| chr18:11984182
|
C | T | 1 | a0001c0002t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.96+2417C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984182 | ||||||
| chr18:11984197
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(81): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.96+2432T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984197 | ||||||
| chr18:11984206
|
CT | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0092others(1): Show | 4 | HG00639.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2443delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984206 | |||||
| chr18:11984212
|
T | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0092others(1): Show | 4 | HG00639.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2447T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984212 | ||||||
| chr18:11984213
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0092others(1): Show | 4 | HG00639.hp2 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2448G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984213 | ||||||
| chr18:11984243
|
C | T | 66 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0195others(63): Show | 66 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.96+2478C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984243 | ||||||
| chr18:11984277
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.96+2512C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984277 | ||||||
| chr18:11984278
|
C | T | 10 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(7): Show | 10 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+2513C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984278 | ||||||
| chr18:11984308
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+2543A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984308 | ||||||
| chr18:11984315
|
C | G | 1 | a0001c0001t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.96+2550C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984315 | ||||||
| chr18:11984524
|
A | G | 1 | a0003c0004t0001g0284 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+2759A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984524 | ||||||
| chr18:11984575
|
G | C | 90 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0077others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+2810G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984575 | ||||||
| chr18:11984622
|
C | G | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+2857C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984622 | ||||||
| chr18:11984673
|
A | G | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+2908A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984673 | ||||||
| chr18:11984755
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(2): Show | 5 | HG01891.hp1 HG01952.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+2990C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984755 | ||||||
| chr18:11984763
|
C | G | 63 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+2998C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984763 | ||||||
| chr18:11984778
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+3013T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984778 | ||||||
| chr18:11984783
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG01175.hp1 HG02109.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.96+3018C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984783 | ||||||
| chr18:11984803
|
TA | T | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3044delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984803 | |||||
| chr18:11984824
|
C | T | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3059C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984824 | ||||||
| chr18:11984837
|
G | A | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3072G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984837 | ||||||
| chr18:11984851
|
CCAG | C | 53 | a0001c0001t0001g0054a0001c0001t0001g0257a0001c0001t0001g0258others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.96+3088_96+3090del others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984851 | |||||
| chr18:11984861
|
A | G | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3096A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984861 | ||||||
| chr18:11984967
|
C | CA | 21 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0019others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3220dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984967 | |||||
| chr18:11984967
|
CA | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(85): Show | 90 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+3220delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984967 | |||||
| chr18:11984967
|
CAA | C | 14 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3219_96+3220del others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984967 | |||||
| chr18:11984981
|
AAAAAC | A | 60 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0243others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.96+3219_96+3223del others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11984981 | |||||
| chr18:11984987
|
A | T | 60 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.96+3222A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984987 | ||||||
| chr18:11985028
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0210 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.96+3263C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985028 | ||||||
| chr18:11985105
|
C | T | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3340C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985105 | ||||||
| chr18:11985131
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.96+3366G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985131 | ||||||
| chr18:11985147
|
C | CA | 8 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 8 | HG01175.hp2 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+3404dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.96+3404delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CAA | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG01515.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+3403_96+3404del others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CAAA | C | 18 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(15): Show | 18 | HG00408.hp2 HG01167.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+3402_96+3404del others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CAAAA | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(19): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.96+3401_96+3404del others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CAAAAA | C | 51 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 51 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.96+3400_96+3404del others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985147
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+3392_96+3404del others(13): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11985147 | |||||
| chr18:11985251
|
G | A | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3486G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985251 | ||||||
| chr18:11985273
|
T | C | 1 | a0001c0002t0006g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+3508T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985273 | ||||||
| chr18:11985276
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.96+3511C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985276 | ||||||
| chr18:11985305
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.96+3540C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985305 | ||||||
| chr18:11985314
|
A | G | 62 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3549A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985314 | ||||||
| chr18:11985443
|
T | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.96+3678T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985443 | ||||||
| chr18:11985595
|
C | T | 2 | a0001c0001t0003g0112a0001c0001t0003g0113 | 2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.96+3830C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985595 | ||||||
| chr18:11985599
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.96+3834C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985599 | ||||||
| chr18:11985663
|
T | C | 61 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0094others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.96+3898T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985663 | ||||||
| chr18:11985769
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+4004G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985769 | ||||||
| chr18:11985869
|
C | T | 13 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(10): Show | 13 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4104C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985869 | ||||||
| chr18:11985873
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+4108G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11985873 | ||||||
| chr18:11986061
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG00280.hp2 HG01069.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4296C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986061 | ||||||
| chr18:11986142
|
G | A | 13 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(10): Show | 13 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4377G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986142 | ||||||
| chr18:11986151
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.96+4386C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986151 | ||||||
| chr18:11986246
|
C | G | 8 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(5): Show | 8 | HG02027.hp1 NA18948.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+4481C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986246 | ||||||
| chr18:11986278
|
T | C | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+4513T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986278 | ||||||
| chr18:11986283
|
T | C | 62 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+4518T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986283 | ||||||
| chr18:11986327
|
G | C | 62 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+4562G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986327 | ||||||
| chr18:11986439
|
G | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(3): Show | 7 | HG02615.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+4674G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986439 | ||||||
| chr18:11986558
|
C | T | 76 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0048others(73): Show | 77 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.96+4793C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986558 | ||||||
| chr18:11986634
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0048others(18): Show | 22 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+4869C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986634 | ||||||
| chr18:11986657
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.96+4892C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986657 | ||||||
| chr18:11986707
|
C | T | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+4942C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986707 | ||||||
| chr18:11986709
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96+4944C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986709 | ||||||
| chr18:11986728
|
G | A | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+4963G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986728 | ||||||
| chr18:11986740
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.96+4975C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986740 | ||||||
| chr18:11986752
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.96+4987A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986752 | ||||||
| chr18:11986916
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.96+5151A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986916 | ||||||
| chr18:11986919
|
C | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0093others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+5154C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986919 | ||||||
| chr18:11986946
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.96+5181G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11986946 | ||||||
| chr18:11986969
|
ATGTTT | A | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+5217_96+5221del others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11986969 | |||||
| chr18:11987086
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0029 | 2 | NA18956.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.96+5321G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987086 | ||||||
| chr18:11987162
|
C | T | 1 | a0004c0010t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+5397C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987162 | ||||||
| chr18:11987165
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0002g0012 | 3 | HG01891.hp1 HG01952.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.96+5400C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987165 | ||||||
| chr18:11987273
|
C | T | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+5508C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987273 | ||||||
| chr18:11987356
|
C | T | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+5591C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987356 | ||||||
| chr18:11987369
|
C | T | 1 | a0001c0002t0001g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.96+5604C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987369 | ||||||
| chr18:11987416
|
T | C | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+5651T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987416 | ||||||
| chr18:11987459
|
C | T | 63 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.96+5694C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987459 | ||||||
| chr18:11987477
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+5712T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987477 | ||||||
| chr18:11987522
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+5757C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987522 | ||||||
| chr18:11987529
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+5764C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987529 | ||||||
| chr18:11987577
|
C | T | 1 | a0001c0002t0001g0253 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.96+5812C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987577 | ||||||
| chr18:11987584
|
G | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02109.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.96+5819G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987584 | ||||||
| chr18:11987670
|
A | G | 64 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0064others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.96+5905A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987670 | ||||||
| chr18:11987711
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+5946G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987711 | ||||||
| chr18:11987768
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0048others(19): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+6003G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987768 | ||||||
| chr18:11987769
|
CT | C | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(7): Show | 10 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+6005delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987769 | ||||||
| chr18:11987818
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(7): Show | 10 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+6053G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987818 | ||||||
| chr18:11987869
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.96+6104G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987869 | ||||||
| chr18:11987930
|
T | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(106): Show | 111 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.96+6165T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987930 | ||||||
| chr18:11987958
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0051others(8): Show | 11 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+6193G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987958 | ||||||
| chr18:11987989
|
C | A | 75 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0060others(72): Show | 76 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+6224C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11987989 | ||||||
| chr18:11988000
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.96+6235G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988000 | ||||||
| chr18:11988001
|
C | CT | 229 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.96+6258dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11988001 | |||||
| chr18:11988001
|
C | CTT | 36 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(33): Show | 36 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.96+6257_96+6258dup others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11988001 | |||||
| chr18:11988001
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.96+6236C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988001 | ||||||
| chr18:11988001
|
CTTTTTT | C | 64 | a0001c0001t0001g0046a0001c0001t0001g0060a0001c0001t0001g0090others(61): Show | 65 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.96+6253_96+6258del others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11988001 | |||||
| chr18:11988036
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.96+6271T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988036 | ||||||
| chr18:11988069
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.96+6304G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988069 | ||||||
| chr18:11988098
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.96+6333C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988098 | ||||||
| chr18:11988099
|
G | C | 75 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0060others(72): Show | 76 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+6334G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988099 | ||||||
| chr18:11988511
|
A | G | 1 | a0001c0002t0001g0171 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.96+6746A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988511 | ||||||
| chr18:11988518
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0046others(84): Show | 89 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.96+6753T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988518 | ||||||
| chr18:11988610
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+6845G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988610 | ||||||
| chr18:11988638
|
A | G | 75 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0060others(72): Show | 76 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+6873A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988638 | ||||||
| chr18:11988686
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.96+6921A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988686 | ||||||
| chr18:11988801
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00423.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.96+7036T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988801 | ||||||
| chr18:11988856
|
G | A | 75 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0060others(72): Show | 76 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+7091G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988856 | ||||||
| chr18:11988917
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(2): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+7152G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11988917 | ||||||
| chr18:11989017
|
G | A | 6 | a0001c0001t0001g0063a0001c0001t0001g0276a0001c0002t0001g0133others(3): Show | 6 | HG00639.hp2 HG02083.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+7252G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989017 | ||||||
| chr18:11989019
|
G | T | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+7254G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989019 | ||||||
| chr18:11989026
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0092others(2): Show | 5 | HG00408.hp2 HG01884.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7261C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989026 | ||||||
| chr18:11989129
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.96+7364G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989129 | ||||||
| chr18:11989267
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0092others(2): Show | 5 | HG00408.hp2 HG01884.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7502T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989267 | ||||||
| chr18:11989362
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+7597C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989362 | ||||||
| chr18:11989363
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0255a0003c0004t0001g0070 | 3 | HG03453.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.96+7598G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989363 | ||||||
| chr18:11989374
|
A | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0060others(79): Show | 83 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.96+7609A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989374 | ||||||
| chr18:11989380
|
A | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+7615A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989380 | ||||||
| chr18:11989395
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+7630C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989395 | ||||||
| chr18:11989417
|
G | A | 102 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(99): Show | 103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.96+7652G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989417 | ||||||
| chr18:11989436
|
A | G | 105 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(102): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.96+7671A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989436 | ||||||
| chr18:11989437
|
A | C | 105 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(102): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.96+7672A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989437 | ||||||
| chr18:11989532
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0092others(2): Show | 5 | HG00408.hp2 HG01884.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7767T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989532 | ||||||
| chr18:11989558
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(8): Show | 11 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+7793C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989558 | ||||||
| chr18:11989593
|
T | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+7828T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989593 | ||||||
| chr18:11989634
|
G | C | 1 | a0001c0002t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.96+7869G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989634 | ||||||
| chr18:11989793
|
C | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0092others(2): Show | 5 | HG00408.hp2 HG01884.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+8028C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989793 | ||||||
| chr18:11989824
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+8059C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989824 | ||||||
| chr18:11989970
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+8205G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11989970 | ||||||
| chr18:11990000
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.96+8235C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990000 | ||||||
| chr18:11990201
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+8436G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990201 | ||||||
| chr18:11990228
|
T | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+8463T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990228 | ||||||
| chr18:11990292
|
G | T | 1 | a0001c0002t0001g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.96+8527G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990292 | ||||||
| chr18:11990347
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02109.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.96+8582G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990347 | ||||||
| chr18:11990358
|
A | AG | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+8593_96+8594ins others(1): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990358 | ||||||
| chr18:11990359
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+8594A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990359 | ||||||
| chr18:11990382
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(183): Show | 188 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.96+8617G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990382 | ||||||
| chr18:11990429
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-8625G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990429 | ||||||
| chr18:11990471
|
T | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8583T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990471 | ||||||
| chr18:11990484
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.97-8570C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990484 | ||||||
| chr18:11990506
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8548A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990506 | ||||||
| chr18:11990540
|
C | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8514C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990540 | ||||||
| chr18:11990699
|
C | G | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-8355C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990699 | ||||||
| chr18:11990731
|
AG | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8320delG | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11990731 | |||||
| chr18:11990776
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-8278G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990776 | ||||||
| chr18:11990829
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8225A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990829 | ||||||
| chr18:11990874
|
T | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8180T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990874 | ||||||
| chr18:11990899
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.97-8155G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990899 | ||||||
| chr18:11990921
|
C | T | 130 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0060others(127): Show | 131 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.97-8133C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11990921 | ||||||
| chr18:11991126
|
G | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-7928G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991126 | ||||||
| chr18:11991133
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-7921G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991133 | ||||||
| chr18:11991159
|
A | C | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.97-7895A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991159 | ||||||
| chr18:11991170
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97-7884G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991170 | ||||||
| chr18:11991272
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-7782C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991272 | ||||||
| chr18:11991314
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.97-7740G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991314 | ||||||
| chr18:11991365
|
G | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-7689G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991365 | ||||||
| chr18:11991420
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-7634A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991420 | ||||||
| chr18:11991508
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97-7546C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991508 | ||||||
| chr18:11991568
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.97-7486C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991568 | ||||||
| chr18:11991621
|
G | A | 2 | a0001c0001t0003g0112a0001c0001t0003g0113 | 2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.97-7433G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991621 | ||||||
| chr18:11991652
|
C | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.97-7402C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991652 | ||||||
| chr18:11991702
|
G | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 171 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.97-7352G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991702 | ||||||
| chr18:11991775
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.97-7279T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991775 | ||||||
| chr18:11991799
|
A | G | 1 | a0001c0002t0001g0249 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.97-7255A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991799 | ||||||
| chr18:11991844
|
C | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 32 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-7210C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991844 | ||||||
| chr18:11991846
|
A | AT | 13 | a0001c0001t0001g0028a0001c0001t0001g0063a0001c0001t0001g0093others(10): Show | 13 | HG00639.hp2 HG02055.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.97-7193dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11991846 | |||||
| chr18:11991846
|
A | ATT | 96 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(93): Show | 98 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.97-7194_97-7193dup others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11991846 | |||||
| chr18:11991846
|
A | ATTT | 57 | a0001c0001t0001g0046a0001c0001t0001g0060a0001c0001t0001g0090others(54): Show | 57 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.97-7195_97-7193dup others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11991846 | |||||
| chr18:11991869
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-7185A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991869 | ||||||
| chr18:11991904
|
C | T | 169 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 171 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.97-7150C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991904 | ||||||
| chr18:11991921
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 32 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-7133G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11991921 | ||||||
| chr18:11992082
|
G | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(8): Show | 11 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-6972G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992082 | ||||||
| chr18:11992087
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-6967G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992087 | ||||||
| chr18:11992176
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-6878G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992176 | ||||||
| chr18:11992262
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97-6792G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992262 | ||||||
| chr18:11992266
|
C | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(164): Show | 169 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.97-6788C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992266 | ||||||
| chr18:11992341
|
A | G | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-6713A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992341 | ||||||
| chr18:11992360
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-6694G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992360 | ||||||
| chr18:11992480
|
G | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 171 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.97-6574G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992480 | ||||||
| chr18:11992520
|
A | G | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 12 | HG00140.hp2 HG00280.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-6534A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992520 | ||||||
| chr18:11992547
|
C | G | 140 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0060others(137): Show | 141 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.97-6507C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992547 | ||||||
| chr18:11992589
|
CCCATATT others(20): Show |
C | 5 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(2): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-6464_97-6438del others(27): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992589 | ||||||
| chr18:11992666
|
T | C | 11 | a0001c0001t0001g0046a0001c0002t0001g0002a0001c0002t0001g0044others(8): Show | 12 | HG01167.hp2 HG01169.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-6388T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992666 | ||||||
| chr18:11992679
|
A | G | 2 | a0001c0002t0001g0248a0001c0007t0001g0252 | 2 | NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.97-6375A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992679 | ||||||
| chr18:11992693
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0186 | 3 | NA19005.hp1 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.97-6361A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992693 | ||||||
| chr18:11992723
|
T | C | 13 | a0001c0001t0001g0058a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.97-6331T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992723 | ||||||
| chr18:11992726
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.97-6328T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992726 | ||||||
| chr18:11992741
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.97-6313G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992741 | ||||||
| chr18:11992817
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0261 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-6237G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992817 | ||||||
| chr18:11992908
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.97-6146T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992908 | ||||||
| chr18:11992972
|
A | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.97-6082A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992972 | ||||||
| chr18:11992982
|
T | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0174others(1): Show | 4 | HG00558.hp1 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-6072T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11992982 | ||||||
| chr18:11993039
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.97-6015A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993039 | ||||||
| chr18:11993075
|
AACTGAT | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-5974_97-5969del others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11993075 | |||||
| chr18:11993097
|
T | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-5957T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993097 | ||||||
| chr18:11993123
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0094 | 3 | HG02055.hp1 NA19030.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-5931C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993123 | ||||||
| chr18:11993135
|
A | G | 2 | a0001c0002t0001g0246a0001c0002t0001g0247 | 2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.97-5919A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993135 | ||||||
| chr18:11993139
|
C | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-5915C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993139 | ||||||
| chr18:11993176
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(176): Show | 181 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.97-5878C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993176 | ||||||
| chr18:11993219
|
A | G | 1 | a0001c0002t0001g0245 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.97-5835A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993219 | ||||||
| chr18:11993282
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0187 | 3 | NA18990.hp2 NA19012.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.97-5772A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993282 | ||||||
| chr18:11993319
|
G | A | 1 | a0001c0003t0001g0136 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.97-5735G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993319 | ||||||
| chr18:11993323
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-5731G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993323 | ||||||
| chr18:11993429
|
G | A | 1 | a0004c0010t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97-5625G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993429 | ||||||
| chr18:11993669
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97-5385C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993669 | ||||||
| chr18:11993673
|
G | A | 28 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(25): Show | 28 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.97-5381G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993673 | ||||||
| chr18:11993676
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG00639.hp2 HG02055.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5378C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993676 | ||||||
| chr18:11993741
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(27): Show | 31 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-5313A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993741 | ||||||
| chr18:11993749
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-5305A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993749 | ||||||
| chr18:11993890
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-5164T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993890 | ||||||
| chr18:11993960
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.97-5094T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993960 | ||||||
| chr18:11993995
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-5059C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11993995 | ||||||
| chr18:11994006
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.97-5048C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994006 | ||||||
| chr18:11994014
|
CAAAG | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(2): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-5035_97-5032del others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11994014 | |||||
| chr18:11994130
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-4924T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994130 | ||||||
| chr18:11994164
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-4890T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994164 | ||||||
| chr18:11994254
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-4800T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994254 | ||||||
| chr18:11994259
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-4795G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994259 | ||||||
| chr18:11994266
|
C | G | 1 | a0001c0002t0001g0217 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.97-4788C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994266 | ||||||
| chr18:11994268
|
G | T | 1 | a0001c0001t0001g0325 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.97-4786G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994268 | ||||||
| chr18:11994346
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0299 | 2 | HG02080.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.97-4708A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994346 | ||||||
| chr18:11994390
|
A | G | 1 | a0001c0002t0001g0291 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.97-4664A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994390 | ||||||
| chr18:11994415
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.97-4639C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994415 | ||||||
| chr18:11994449
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 25 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-4605C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994449 | ||||||
| chr18:11994481
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-4573A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994481 | ||||||
| chr18:11994569
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.97-4485A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994569 | ||||||
| chr18:11994599
|
C | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.97-4455C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994599 | ||||||
| chr18:11994600
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0092 | 3 | HG01884.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.97-4454G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994600 | ||||||
| chr18:11994687
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(27): Show | 31 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-4367T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994687 | ||||||
| chr18:11994778
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-4276G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11994778 | ||||||
| chr18:11995042
|
C | CGGAGG | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-3997_97-3993dup others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11995042 | |||||
| chr18:11995087
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0087 | 2 | HG00140.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.97-3967G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995087 | ||||||
| chr18:11995186
|
C | T | 1 | a0001c0002t0006g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-3868C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995186 | ||||||
| chr18:11995273
|
T | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0060a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-3781T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995273 | ||||||
| chr18:11995287
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG00280.hp1 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3767A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995287 | ||||||
| chr18:11995403
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.97-3651A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995403 | ||||||
| chr18:11995410
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.97-3644C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995410 | ||||||
| chr18:11995452
|
A | G | 84 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(81): Show | 84 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.97-3602A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995452 | ||||||
| chr18:11995454
|
T | C | 1 | a0001c0002t0001g0057 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.97-3600T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995454 | ||||||
| chr18:11995543
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.97-3511T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995543 | ||||||
| chr18:11995615
|
C | T | 1 | a0001c0002t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.97-3439C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995615 | ||||||
| chr18:11995626
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0094others(1): Show | 4 | HG02055.hp1 HG03098.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3428C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995626 | ||||||
| chr18:11995662
|
G | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(34): Show | 38 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-3392G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995662 | ||||||
| chr18:11995704
|
C | T | 56 | a0001c0001t0001g0243a0001c0001t0001g0271a0001c0002t0001g0018others(53): Show | 56 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.97-3350C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995704 | ||||||
| chr18:11995744
|
CAACAGGG others(10): Show |
C | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.97-3304_97-3288del others(17): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11995744 | |||||
| chr18:11995808
|
T | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(18): Show | 22 | HG01167.hp1 HG01884.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-3246T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995808 | ||||||
| chr18:11995817
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-3237C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11995817 | ||||||
| chr18:11996085
|
A | G | 1 | a0004c0010t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97-2969A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996085 | ||||||
| chr18:11996338
|
G | A | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(200): Show | 205 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.97-2716G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996338 | ||||||
| chr18:11996608
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | NA18995.hp1 NA19064.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.97-2446C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996608 | ||||||
| chr18:11996609
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-2445G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996609 | ||||||
| chr18:11996630
|
C | G | 69 | a0001c0001t0001g0243a0001c0001t0001g0271a0001c0002t0001g0002others(66): Show | 70 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.97-2424C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996630 | ||||||
| chr18:11996938
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97-2116C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11996938 | ||||||
| chr18:11996999
|
A | AAC | 8 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 8 | HG01981.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-2039_97-2038dup others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11996999 | |||||
| chr18:11997069
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0261 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-1985C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997069 | ||||||
| chr18:11997162
|
T | A | 3 | a0001c0001t0001g0331a0001c0003t0001g0290a0001c0003t0001g0336 | 3 | NA18963.hp1 NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.97-1892T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997162 | ||||||
| chr18:11997184
|
A | G | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.97-1870A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997184 | ||||||
| chr18:11997198
|
C | T | 69 | a0001c0001t0001g0243a0001c0001t0001g0271a0001c0002t0001g0002others(66): Show | 70 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.97-1856C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997198 | ||||||
| chr18:11997238
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.97-1816C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997238 | ||||||
| chr18:11997293
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97-1761T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997293 | ||||||
| chr18:11997333
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.97-1721C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997333 | ||||||
| chr18:11997351
|
A | G | 156 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(153): Show | 157 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.97-1703A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997351 | ||||||
| chr18:11997398
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97-1656G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997398 | ||||||
| chr18:11997426
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.97-1628G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997426 | ||||||
| chr18:11997484
|
G | GT | 86 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.97-1562dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11997484 | |||||
| chr18:11997631
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.97-1423C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997631 | ||||||
| chr18:11997905
|
C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 39 | HG00280.hp2 HG01167.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.97-1149C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11997905 | ||||||
| chr18:11998096
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.97-958G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998096 | ||||||
| chr18:11998303
|
C | T | 69 | a0001c0001t0001g0243a0001c0001t0001g0271a0001c0002t0001g0002others(66): Show | 70 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.97-751C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998303 | ||||||
| chr18:11998556
|
A | T | 2 | a0001c0001t0001g0354a0001c0001t0001g0355 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.97-498A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998556 | ||||||
| chr18:11998689
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.97-365C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998689 | ||||||
| chr18:11998735
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(30): Show | 34 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.97-319G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998735 | ||||||
| chr18:11998922
|
CCCG | C | 64 | a0001c0001t0001g0010a0001c0002t0001g0002a0001c0002t0001g0018others(61): Show | 65 | HG00438.hp1 HG00673.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.97-126_97-124delGC others(1): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998922 | |||||
| chr18:11998923
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97-131C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998923 | ||||||
| chr18:11998923
|
CCG | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0078others(8): Show | 11 | HG00280.hp1 HG01346.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-129_97-128delGC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998923 | |||||
| chr18:11998925
|
G | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG01496.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.97-129G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998925 | ||||||
| chr18:11998925
|
GCCGCCC | G | 15 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0179others(12): Show | 15 | HG00408.hp1 HG00597.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-126_97-121delGC others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998925 | |||||
| chr18:11998925
|
GCCGCCCC | G | 44 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(41): Show | 44 | HG00639.hp2 HG00673.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.97-126_97-120delGC others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998925 | |||||
| chr18:11998925
|
GCCGCCCC others(1): Show |
G | 23 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0051others(20): Show | 24 | HG00741.hp1 HG01167.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-126_97-119delGC others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998925 | |||||
| chr18:11998925
|
GCCGCCCC others(3): Show |
G | 3 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02109.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.97-126_97-117delGC others(8): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998925 | |||||
| chr18:11998926
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.97-128C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998926 | ||||||
| chr18:11998927
|
C | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0089 | 2 | HG00140.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.97-127C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998927 | ||||||
| chr18:11998928
|
G | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0089others(3): Show | 6 | HG00140.hp2 HG00408.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-126G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998928 | ||||||
| chr18:11998928
|
G | GC | 61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-108dupC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998928 | |||||
| chr18:11998928
|
G | GCC | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(27): Show | 30 | HG00621.hp1 HG00642.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.97-109_97-108dupCC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998928 | |||||
| chr18:11998928
|
GC | G | 33 | a0001c0001t0001g0032a0001c0001t0001g0115a0001c0001t0001g0127others(30): Show | 33 | HG00438.hp1 HG00673.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-108delC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998928 | |||||
| chr18:11998928
|
GCC | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0097others(14): Show | 18 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-109_97-108delCC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998928 | |||||
| chr18:11998937
|
C | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0210a0001c0001t0001g0273others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-117C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998937 | ||||||
| chr18:11998938
|
C | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 7 | HG01346.hp2 HG02074.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-116C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998938 | ||||||
| chr18:11998940
|
C | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0329 | 2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.97-114C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998940 | ||||||
| chr18:11998942
|
C | A | 1 | a0001c0001t0001g0340 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.97-112C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998942 | ||||||
| chr18:11998942
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.97-112C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998942 | ||||||
| chr18:11998947
|
A | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 40 | HG00140.hp2 HG01081.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-107A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998947 | ||||||
| chr18:11998948
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97-106C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11998948 | ||||||
| chr18:11999039
|
G | A | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(70): Show | 73 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.97-15G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11999039 | ||||||
| chr18:11999260
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.230+73G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999260 | ||||||
| chr18:11999326
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+139C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999326 | ||||||
| chr18:11999327
|
G | A | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(70): Show | 73 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.230+140G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999327 | ||||||
| chr18:11999396
|
TCACGTCA others(25): Show |
T | 1 | a0001c0002t0001g0217 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230+212_230+243del others(32): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 11999396 | |||||
| chr18:11999483
|
C | T | 1 | a0004c0010t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.230+296C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999483 | ||||||
| chr18:11999557
|
G | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(100): Show | 104 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.230+370G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999557 | ||||||
| chr18:11999640
|
C | T | 2 | a0001c0002t0001g0193a0001c0002t0001g0194 | 2 | NA18956.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.230+453C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999640 | ||||||
| chr18:11999698
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+511G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999698 | ||||||
| chr18:11999725
|
G | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(101): Show | 105 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.230+538G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999725 | ||||||
| chr18:11999774
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.230+587G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 11999774 | ||||||
| chr18:12000140
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+953A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000140 | ||||||
| chr18:12000279
|
C | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(80): Show | 83 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.230+1092C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000279 | ||||||
| chr18:12000334
|
C | CT | 10 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0041others(7): Show | 10 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.230+1167dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000334 | |||||
| chr18:12000334
|
CT | C | 94 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(91): Show | 94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.230+1167delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000334 | |||||
| chr18:12000334
|
CTT | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 110 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.230+1166_230+1167d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000334 | |||||
| chr18:12000354
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(9): Show | 12 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.230+1167T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000354 | ||||||
| chr18:12000407
|
CT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(101): Show | 105 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.230+1229delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000407 | |||||
| chr18:12000535
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 15 | HG01891.hp1 HG01952.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.230+1348A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000535 | ||||||
| chr18:12000615
|
A | AT | 144 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 145 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.230+1446dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000615 | |||||
| chr18:12000615
|
A | ATT | 21 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(18): Show | 21 | HG00280.hp1 HG01167.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.230+1445_230+1446d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000615 | |||||
| chr18:12000615
|
A | ATTT | 21 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 21 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.230+1444_230+1446d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000615 | |||||
| chr18:12000678
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(102): Show | 106 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.230+1491T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000678 | ||||||
| chr18:12000684
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.230+1497T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000684 | ||||||
| chr18:12000706
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0003g0112a0001c0001t0003g0113 | 3 | HG01167.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.230+1519C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000706 | ||||||
| chr18:12000745
|
A | C | 1 | a0001c0002t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.230+1558A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12000745 | ||||||
| chr18:12000931
|
T | TTAAAAAG others(3227): Show |
1 | a0001c0001t0001g0265 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.230+1757_230+1758i others(3236): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12000931 | |||||
| chr18:12001007
|
G | A | 13 | a0001c0001t0001g0064a0001c0002t0001g0002a0001c0002t0001g0044others(10): Show | 14 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.230+1820G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001007 | ||||||
| chr18:12001013
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 27 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.230+1826C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001013 | ||||||
| chr18:12001065
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.230+1878C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001065 | ||||||
| chr18:12001102
|
G | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(192): Show | 197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.230+1915G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001102 | ||||||
| chr18:12001160
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.230+1973C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001160 | ||||||
| chr18:12001161
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.230+1974G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001161 | ||||||
| chr18:12001189
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.230+2002A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001189 | ||||||
| chr18:12001259
|
C | A | 58 | a0001c0001t0001g0116a0001c0001t0001g0168a0001c0001t0001g0197others(55): Show | 58 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.230+2072C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001259 | ||||||
| chr18:12001321
|
C | T | 8 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(5): Show | 8 | HG02027.hp1 NA18948.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.230+2134C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001321 | ||||||
| chr18:12001327
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.230+2140G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001327 | ||||||
| chr18:12001420
|
C | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(193): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.230+2233C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001420 | ||||||
| chr18:12001460
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+2273G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001460 | ||||||
| chr18:12001484
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.230+2297G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001484 | ||||||
| chr18:12001596
|
C | T | 1 | a0001c0002t0001g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.230+2409C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001596 | ||||||
| chr18:12001708
|
G | T | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(194): Show | 199 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.230+2521G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001708 | ||||||
| chr18:12001768
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.230+2581C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001768 | ||||||
| chr18:12001854
|
G | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+2667G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001854 | ||||||
| chr18:12001887
|
T | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+2700T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001887 | ||||||
| chr18:12001972
|
C | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(193): Show | 198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.230+2785C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12001972 | ||||||
| chr18:12002160
|
A | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(2): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+2973A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002160 | ||||||
| chr18:12002279
|
G | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+3092G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002279 | ||||||
| chr18:12002309
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.230+3122G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002309 | ||||||
| chr18:12002475
|
G | A | 4 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0172others(1): Show | 4 | HG02083.hp1 HG02135.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+3288G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002475 | ||||||
| chr18:12002496
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.230+3309G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002496 | ||||||
| chr18:12002537
|
C | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3350C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002537 | ||||||
| chr18:12002552
|
T | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0255others(1): Show | 4 | HG02622.hp1 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+3365T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002552 | ||||||
| chr18:12002690
|
G | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3503G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002690 | ||||||
| chr18:12002708
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.230+3521G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002708 | ||||||
| chr18:12002763
|
C | CA | 146 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.230+3594dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12002763 | |||||
| chr18:12002763
|
CAAAA | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(194): Show | 199 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.230+3591_230+3594d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12002763 | |||||
| chr18:12002889
|
C | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3702C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002889 | ||||||
| chr18:12002918
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.230+3731C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002918 | ||||||
| chr18:12002923
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3736T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002923 | ||||||
| chr18:12002928
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3741T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002928 | ||||||
| chr18:12002941
|
C | T | 4 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0172others(1): Show | 4 | HG02083.hp1 HG02135.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+3754C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002941 | ||||||
| chr18:12002958
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.230+3771C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002958 | ||||||
| chr18:12002964
|
G | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3777G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12002964 | ||||||
| chr18:12003100
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.230+3913C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003100 | ||||||
| chr18:12003101
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+3914A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003101 | ||||||
| chr18:12003109
|
C | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 34 | HG00280.hp1 HG01346.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.230+3922C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003109 | ||||||
| chr18:12003260
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.230+4073C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003260 | ||||||
| chr18:12003279
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+4092C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003279 | ||||||
| chr18:12003384
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(264): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.230+4197A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003384 | ||||||
| chr18:12003465
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.230+4278A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003465 | ||||||
| chr18:12003472
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.230+4285C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003472 | ||||||
| chr18:12003593
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+4406G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003593 | ||||||
| chr18:12003650
|
T | TA | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.230+4477dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003650 | |||||
| chr18:12003650
|
TA | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0082others(5): Show | 8 | HG00280.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.230+4477delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003650 | |||||
| chr18:12003658
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.230+4471A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003658 | ||||||
| chr18:12003663
|
AAGAAAAG others(1): Show |
A | 11 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(8): Show | 11 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.230+4478_230+4485d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003663 | |||||
| chr18:12003664
|
AG | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(15): Show | 18 | HG01891.hp1 HG01952.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.230+4478delG | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003664 | ||||||
| chr18:12003664
|
AGAAAAG | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0168others(4): Show | 8 | HG00544.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.230+4483_230+4488d others(8): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003664 | |||||
| chr18:12003664
|
AGAAAAGG | A | 65 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0094others(62): Show | 65 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.230+4478_230+4484d others(9): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003664 | ||||||
| chr18:12003665
|
G | A | 86 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(83): Show | 87 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.230+4478G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003665 | ||||||
| chr18:12003670
|
GGAAAA | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(25): Show | 28 | HG00280.hp1 HG01346.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.230+4484_230+4488d others(7): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003670 | ||||||
| chr18:12003670
|
GGAAAAA | G | 83 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(80): Show | 84 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.230+4484_230+4489d others(8): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003670 | ||||||
| chr18:12003671
|
G | A | 2 | a0001c0001t0001g0168a0001c0006t0001g0251 | 2 | HG00544.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.230+4484G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003671 | ||||||
| chr18:12003671
|
GA | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.230+4499delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003671 | |||||
| chr18:12003671
|
GAA | G | 23 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0173others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.230+4498_230+4499d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12003671 | |||||
| chr18:12003675
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0211others(2): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+4488A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003675 | ||||||
| chr18:12003676
|
A | G | 8 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0315others(5): Show | 8 | HG00673.hp2 HG02027.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.230+4489A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003676 | ||||||
| chr18:12003677
|
A | G | 61 | a0001c0001t0001g0116a0001c0001t0001g0168a0001c0002t0001g0018others(58): Show | 61 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.230+4490A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003677 | ||||||
| chr18:12003761
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+4574T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003761 | ||||||
| chr18:12003860
|
T | A | 78 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(75): Show | 78 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.230+4673T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003860 | ||||||
| chr18:12003861
|
C | T | 57 | a0001c0001t0001g0116a0001c0001t0001g0168a0001c0002t0001g0018others(54): Show | 57 | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.230+4674C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003861 | ||||||
| chr18:12003864
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(196): Show | 201 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.230+4677T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003864 | ||||||
| chr18:12003917
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.230+4730G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003917 | ||||||
| chr18:12003954
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+4767T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12003954 | ||||||
| chr18:12004047
|
G | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+4860G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004047 | ||||||
| chr18:12004091
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+4904A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004091 | ||||||
| chr18:12004165
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.230+4978C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004165 | ||||||
| chr18:12004247
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.230+5060A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004247 | ||||||
| chr18:12004314
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(197): Show | 202 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.230+5127C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004314 | ||||||
| chr18:12004349
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.230+5162T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004349 | ||||||
| chr18:12004388
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.230+5201G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004388 | ||||||
| chr18:12004469
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.230+5282G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004469 | ||||||
| chr18:12004534
|
G | GT | 22 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0021others(19): Show | 22 | HG01106.hp2 HG01243.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.231-5335dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12004534 | |||||
| chr18:12004697
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.231-5186A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12004697 | ||||||
| chr18:12005068
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.231-4815C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005068 | ||||||
| chr18:12005102
|
C | T | 2 | a0001c0001t0001g0108a0001c0009t0001g0124 | 2 | HG01243.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.231-4781C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005102 | ||||||
| chr18:12005103
|
G | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 26 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.231-4780G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005103 | ||||||
| chr18:12005144
|
C | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-4739C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005144 | ||||||
| chr18:12005346
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.231-4537G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005346 | ||||||
| chr18:12005391
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0205 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.231-4492A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005391 | ||||||
| chr18:12005439
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(199): Show | 204 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.231-4444T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005439 | ||||||
| chr18:12005488
|
GA | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(193): Show | 198 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.231-4381delA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12005488 | |||||
| chr18:12005502
|
A | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(23): Show | 27 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.231-4381A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005502 | ||||||
| chr18:12005592
|
A | C | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG00280.hp1 HG01261.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-4291A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005592 | ||||||
| chr18:12005696
|
G | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.231-4187G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005696 | ||||||
| chr18:12005766
|
C | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-4117C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005766 | ||||||
| chr18:12005826
|
C | T | 2 | a0001c0001t0002g0006a0003c0004t0001g0061 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.231-4057C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005826 | ||||||
| chr18:12005827
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-4056A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005827 | ||||||
| chr18:12005930
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-3953A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005930 | ||||||
| chr18:12005934
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3949A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005934 | ||||||
| chr18:12005969
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.231-3914C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12005969 | ||||||
| chr18:12006036
|
G | A | 65 | a0001c0001t0001g0094a0001c0001t0001g0116a0001c0001t0001g0131others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.231-3847G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006036 | ||||||
| chr18:12006039
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.231-3844T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006039 | ||||||
| chr18:12006060
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.231-3823G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006060 | ||||||
| chr18:12006120
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.231-3763G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006120 | ||||||
| chr18:12006149
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.231-3734T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006149 | ||||||
| chr18:12006172
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3711A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006172 | ||||||
| chr18:12006176
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3707C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006176 | ||||||
| chr18:12006197
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.231-3686C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006197 | ||||||
| chr18:12006253
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.231-3630C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006253 | ||||||
| chr18:12006318
|
T | G | 66 | a0001c0001t0001g0028a0001c0001t0001g0094a0001c0001t0001g0116others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.231-3565T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006318 | ||||||
| chr18:12006387
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3496A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006387 | ||||||
| chr18:12006413
|
C | T | 60 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0132others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.231-3470C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006413 | ||||||
| chr18:12006440
|
C | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3443C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006440 | ||||||
| chr18:12006665
|
G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(24): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.231-3218G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006665 | ||||||
| chr18:12006699
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-3184A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006699 | ||||||
| chr18:12006852
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00741.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.231-3031C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006852 | ||||||
| chr18:12006939
|
G | A | 2 | a0002c0005t0001g0095a0002c0005t0001g0096 | 2 | NA18966.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.231-2944G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006939 | ||||||
| chr18:12006940
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.231-2943G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12006940 | ||||||
| chr18:12007023
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2860A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007023 | ||||||
| chr18:12007044
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2839T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007044 | ||||||
| chr18:12007054
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2829C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007054 | ||||||
| chr18:12007104
|
TGGGCGAC others(1): Show |
T | 7 | a0001c0001t0001g0021a0001c0001t0001g0060a0001c0001t0001g0067others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-2772_231-2765d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007104 | |||||
| chr18:12007108
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183 | 3 | HG00280.hp2 HG01069.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.231-2775C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007108 | ||||||
| chr18:12007209
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231-2674G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007209 | ||||||
| chr18:12007265
|
G | T | 62 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0132others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.231-2618G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007265 | ||||||
| chr18:12007271
|
C | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0060a0001c0001t0001g0067others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-2612C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007271 | ||||||
| chr18:12007303
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.231-2580C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007303 | ||||||
| chr18:12007346
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.231-2537G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007346 | ||||||
| chr18:12007425
|
C | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2458C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007425 | ||||||
| chr18:12007436
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2447C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007436 | ||||||
| chr18:12007453
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(25): Show | 29 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.231-2430T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007453 | ||||||
| chr18:12007485
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-2398C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007485 | ||||||
| chr18:12007543
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.231-2340A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007543 | ||||||
| chr18:12007547
|
T | C | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0351others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2336T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007547 | ||||||
| chr18:12007553
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.231-2330G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007553 | ||||||
| chr18:12007557
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.231-2326C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007557 | ||||||
| chr18:12007578
|
CTTTCT | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.231-2292_231-2288d others(7): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007578 | |||||
| chr18:12007586
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231-2297T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007586 | ||||||
| chr18:12007587
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231-2296C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007587 | ||||||
| chr18:12007588
|
T | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 27 | HG00280.hp1 HG01261.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.231-2295T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007588 | ||||||
| chr18:12007590
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231-2293T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007590 | ||||||
| chr18:12007590
|
TTCTTTCT others(7): Show |
T | 2 | a0001c0001t0005g0047a0003c0004t0001g0284 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.231-2277_231-2264d others(16): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007590 | |||||
| chr18:12007602
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0098a0001c0001t0001g0110others(7): Show | 10 | HG01109.hp1 HG01258.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-2281T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007602 | ||||||
| chr18:12007604
|
C | T | 10 | a0001c0001t0001g0050a0001c0001t0001g0098a0001c0001t0001g0110others(7): Show | 10 | HG01109.hp1 HG01258.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-2279C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007604 | ||||||
| chr18:12007606
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(9): Show | 12 | HG01167.hp1 HG02056.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.231-2277C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007606 | ||||||
| chr18:12007607
|
T | TTTCTTTC others(10): Show |
1 | a0001c0002t0001g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.231-2266_231-2265i others(19): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007607 | |||||
| chr18:12007610
|
C | CTTTCTT | 3 | a0001c0001t0001g0050a0001c0001t0001g0207a0001c0001t0002g0206 | 3 | HG02818.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.231-2271_231-2266d others(8): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007610 | |||||
| chr18:12007614
|
C | CTT | 4 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0197others(1): Show | 4 | HG01109.hp1 HG01975.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2267_231-2266d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007614 | |||||
| chr18:12007614
|
CTTTCTTT | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0196a0001c0001t0003g0113 | 3 | HG01167.hp1 HG02056.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.231-2266_231-2260d others(9): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007614 | |||||
| chr18:12007615
|
TTTC | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0051others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2265_231-2263d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007615 | |||||
| chr18:12007616
|
T | TC | 4 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0210others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2267_231-2266i others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007616 | ||||||
| chr18:12007618
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0198others(4): Show | 7 | HG01258.hp1 HG01361.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-2265C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007618 | ||||||
| chr18:12007620
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(8): Show | 11 | HG01258.hp1 HG01361.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.231-2263T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007620 | ||||||
| chr18:12007620
|
T | TC | 3 | a0001c0001t0001g0050a0001c0001t0001g0207a0001c0001t0002g0206 | 3 | HG02818.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.231-2263_231-2262i others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007620 | ||||||
| chr18:12007620
|
T | TTTCTTCT others(14): Show |
1 | a0001c0001t0001g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.231-2261_231-2260i others(23): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007620 | |||||
| chr18:12007620
|
TTTTCTTT others(4): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.231-2252_231-2242d others(13): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007620 | |||||
| chr18:12007620
|
TTTTCTTT others(8): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.231-2252_231-2238d others(17): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007620 | |||||
| chr18:12007621
|
T | TC | 4 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0197others(1): Show | 4 | HG01109.hp1 HG01975.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2262_231-2261i others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007621 | ||||||
| chr18:12007621
|
TTTCTTTC | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.231-2252_231-2246d others(9): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007621 | |||||
| chr18:12007625
|
TTTC | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0196others(1): Show | 4 | HG01167.hp1 HG02056.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2252_231-2250d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007625 | |||||
| chr18:12007627
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0205 | 3 | HG01258.hp1 HG01361.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.231-2256T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007627 | ||||||
| chr18:12007628
|
C | CT | 30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 30 | HG01109.hp1 HG01891.hp2 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.231-2253dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCT | 22 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0032others(19): Show | 23 | HG00673.hp2 HG01168.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.231-2207_231-2204d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTCT others(8): Show |
1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.231-2250_231-2249i others(17): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(1): Show |
30 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0078others(27): Show | 30 | HG00280.hp1 HG00673.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.231-2211_231-2204d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(5): Show |
40 | a0001c0001t0001g0067a0001c0001t0001g0083a0001c0001t0001g0111others(37): Show | 40 | HG00438.hp1 HG00544.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.231-2215_231-2204d others(14): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(9): Show |
31 | a0001c0001t0001g0021a0001c0001t0001g0074a0001c0001t0001g0079others(28): Show | 31 | HG00423.hp1 HG00597.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.231-2219_231-2204d others(18): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(13): Show |
11 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0317others(8): Show | 11 | HG02083.hp2 HG02165.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.231-2223_231-2204d others(22): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(17): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0314others(1): Show | 4 | HG02559.hp2 HG04115.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2227_231-2204d others(26): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | CTTCTTTC others(21): Show |
1 | a0001c0001t0001g0331 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.231-2231_231-2204d others(30): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0205 | 3 | HG01258.hp1 HG01361.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.231-2255C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007628 | ||||||
| chr18:12007628
|
CTTCT | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0087a0001c0001t0001g0099others(19): Show | 22 | HG00408.hp1 HG00558.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.231-2207_231-2204d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
CTTCTTTC others(1): Show |
C | 37 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0080others(34): Show | 37 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.231-2211_231-2204d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
CTTCTTTC others(5): Show |
C | 19 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0115others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.231-2215_231-2204d others(14): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
CTTCTTTC others(9): Show |
C | 3 | a0001c0001t0001g0094a0001c0001t0001g0182a0001c0002t0001g0002 | 4 | HG01167.hp2 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2219_231-2204d others(18): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
CTTCTTTC others(13): Show |
C | 12 | a0001c0001t0001g0064a0001c0002t0001g0044a0001c0002t0001g0045others(9): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.231-2223_231-2204d others(22): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007628
|
CTTCTTTC others(17): Show |
C | 5 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0001g0161others(2): Show | 5 | HG00544.hp1 HG02015.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-2227_231-2204d others(26): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007628 | |||||
| chr18:12007636
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.231-2247T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007636 | ||||||
| chr18:12007641
|
TTC | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.231-2240_231-2239d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007641 | |||||
| chr18:12007649
|
TTC | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.231-2232_231-2231d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007649 | |||||
| chr18:12007651
|
CT | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.231-2229delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007651 | |||||
| chr18:12007659
|
CT | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.231-2221delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007659 | |||||
| chr18:12007662
|
TCTTTCTT others(10): Show |
T | 2 | a0001c0001t0001g0262a0001c0001t0001g0264 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.231-2211_231-2195d others(19): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007662 | |||||
| chr18:12007670
|
T | TCTTTCTT others(6): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0002g0012 | 3 | HG01891.hp1 HG01952.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.231-2204_231-2203i others(15): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007670 | |||||
| chr18:12007674
|
TCTTTC | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0263a0001c0001t0001g0265others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-2203_231-2199d others(7): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007674 | |||||
| chr18:12007678
|
TC | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231-2203delC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007678 | |||||
| chr18:12007679
|
C | CTTTCTTT others(12): Show |
1 | a0001c0001t0001g0305 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.231-2204_231-2203i others(21): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007679 | ||||||
| chr18:12007714
|
CCTT | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-2165_231-2163d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007714 | |||||
| chr18:12007724
|
TTCTC | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.231-2150_231-2147d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12007724 | |||||
| chr18:12007728
|
C | T | 11 | a0001c0001t0001g0050a0001c0001t0001g0098a0001c0001t0001g0104others(8): Show | 11 | HG00735.hp2 HG01109.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.231-2155C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007728 | ||||||
| chr18:12007822
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.231-2061G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007822 | ||||||
| chr18:12007834
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.231-2049A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007834 | ||||||
| chr18:12007846
|
C | T | 13 | a0001c0001t0001g0064a0001c0002t0001g0002a0001c0002t0001g0044others(10): Show | 14 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.231-2037C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007846 | ||||||
| chr18:12007899
|
T | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.231-1984T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12007899 | ||||||
| chr18:12008019
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231-1864C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008019 | ||||||
| chr18:12008020
|
G | A | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG00280.hp1 HG01261.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-1863G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008020 | ||||||
| chr18:12008022
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.231-1861T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008022 | ||||||
| chr18:12008074
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.231-1809C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008074 | ||||||
| chr18:12008140
|
C | T | 4 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0172others(1): Show | 4 | HG02083.hp1 HG02135.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-1743C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008140 | ||||||
| chr18:12008392
|
C | T | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG00280.hp1 HG01261.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-1491C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008392 | ||||||
| chr18:12008848
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(181): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.231-1035A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12008848 | ||||||
| chr18:12009007
|
G | GGGGCAGG others(3): Show |
69 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0031others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.231-868_231-867ins others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12009007 | |||||
| chr18:12009017
|
G | A | 69 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0031others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.231-866G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009017 | ||||||
| chr18:12009128
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0059others(3): Show | 6 | HG00408.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-755C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009128 | ||||||
| chr18:12009132
|
C | A | 2 | a0001c0001t0001g0352a0001c0001t0001g0359 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.231-751C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009132 | ||||||
| chr18:12009247
|
G | GC | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0059others(3): Show | 6 | HG00408.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-635dupC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12009247 | |||||
| chr18:12009289
|
C | CAAA | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0059others(3): Show | 6 | HG00408.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.231-589_231-587dup others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 12009289 | |||||
| chr18:12009349
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.231-534C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009349 | ||||||
| chr18:12009390
|
G | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0103others(4): Show | 7 | HG00323.hp2 HG00741.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-493G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009390 | ||||||
| chr18:12009448
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0048others(7): Show | 10 | HG01167.hp1 HG01952.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.231-435C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009448 | ||||||
| chr18:12009600
|
C | T | 3 | a0001c0001t0001g0014a0001c0002t0001g0282a0001c0002t0001g0283 | 3 | HG00408.hp2 HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.231-283C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009600 | ||||||
| chr18:12009629
|
AATTCC | A | 3 | a0001c0001t0001g0014a0001c0002t0001g0282a0001c0002t0001g0283 | 3 | HG00408.hp2 HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.231-253_231-249del others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009629 | ||||||
| chr18:12009653
|
G | T | 3 | a0001c0001t0001g0014a0001c0002t0001g0282a0001c0002t0001g0283 | 3 | HG00408.hp2 HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.231-230G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009653 | ||||||
| chr18:12009654
|
C | T | 3 | a0001c0001t0001g0014a0001c0002t0001g0282a0001c0002t0001g0283 | 3 | HG00408.hp2 HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.231-229C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009654 | ||||||
| chr18:12009770
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.231-113T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009770 | ||||||
| chr18:12009799
|
T | C | 2 | a0001c0001t0001g0255a0001c0002t0001g0045 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.231-84T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009799 | ||||||
| chr18:12009876
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.231-7A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 2/7 | chr18 | 12009876 | ||||||
| chr18:12010163
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.335+176G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010163 | ||||||
| chr18:12010475
|
G | T | 12 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.335+488G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010475 | ||||||
| chr18:12010506
|
G | A | 14 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.335+519G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010506 | ||||||
| chr18:12010579
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(9): Show | 13 | HG01884.hp1 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.335+592G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010579 | ||||||
| chr18:12010647
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.335+660G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010647 | ||||||
| chr18:12010830
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0041 | 3 | HG00621.hp2 NA18986.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.335+843A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010830 | ||||||
| chr18:12010839
|
T | C | 1 | a0001c0002t0002g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.335+852T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010839 | ||||||
| chr18:12010911
|
T | G | 14 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.335+924T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12010911 | ||||||
| chr18:12011084
|
T | C | 14 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.336-1086T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011084 | ||||||
| chr18:12011100
|
G | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.336-1070G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011100 | ||||||
| chr18:12011128
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.336-1042C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011128 | ||||||
| chr18:12011155
|
T | C | 15 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0084others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.336-1015T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011155 | ||||||
| chr18:12011206
|
G | A | 141 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0031others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.336-964G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011206 | ||||||
| chr18:12011227
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.336-943G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011227 | ||||||
| chr18:12011278
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.336-892G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011278 | ||||||
| chr18:12011290
|
G | A | 14 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.336-880G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011290 | ||||||
| chr18:12011295
|
T | C | 14 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0093others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.336-875T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011295 | ||||||
| chr18:12011324
|
C | G | 1 | a0001c0002t0001g0171 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.336-846C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011324 | ||||||
| chr18:12011420
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0098others(7): Show | 10 | HG00735.hp2 HG01109.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.336-750C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011420 | ||||||
| chr18:12011438
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.336-732G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011438 | ||||||
| chr18:12011478
|
C | G | 2 | a0001c0001t0002g0206a0001c0001t0002g0280 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.336-692C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011478 | ||||||
| chr18:12011479
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.336-691A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011479 | ||||||
| chr18:12011669
|
G | C | 1 | a0001c0001t0003g0113 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.336-501G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011669 | ||||||
| chr18:12011790
|
G | T | 1 | a0001c0002t0001g0249 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.336-380G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011790 | ||||||
| chr18:12011805
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0209 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.336-365C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011805 | ||||||
| chr18:12011851
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.336-319C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011851 | ||||||
| chr18:12011862
|
T | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0084a0001c0001t0001g0093others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.336-308T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011862 | ||||||
| chr18:12011980
|
A | G | 15 | a0001c0001t0001g0060a0001c0001t0001g0077a0001c0001t0001g0084others(12): Show | 15 | HG01261.hp2 HG01346.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.336-190A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12011980 | ||||||
| chr18:12012073
|
A | C | 20 | a0001c0001t0001g0034a0001c0001t0001g0142a0001c0001t0001g0151others(17): Show | 20 | HG00423.hp2 HG02132.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.336-97A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 3/7 | chr18 | 12012073 | ||||||
| chr18:12012365
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.381+150G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012365 | ||||||
| chr18:12012421
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+206T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012421 | ||||||
| chr18:12012452
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.381+237G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012452 | ||||||
| chr18:12012458
|
A | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.381+243A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012458 | ||||||
| chr18:12012468
|
A | C | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.381+253A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012468 | ||||||
| chr18:12012488
|
A | G | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.381+273A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012488 | ||||||
| chr18:12012517
|
G | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.381+302G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012517 | ||||||
| chr18:12012688
|
T | A | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+473T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012688 | ||||||
| chr18:12012739
|
A | G | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(353): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.381+524A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012739 | ||||||
| chr18:12012745
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.381+530C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012745 | ||||||
| chr18:12012804
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.381+589T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012804 | ||||||
| chr18:12013020
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.381+805G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013020 | ||||||
| chr18:12013023
|
G | T | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(353): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.381+808G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013023 | ||||||
| chr18:12013112
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+897T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013112 | ||||||
| chr18:12013161
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+946T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013161 | ||||||
| chr18:12013183
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+968A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013183 | ||||||
| chr18:12013222
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0280 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+1007G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013222 | ||||||
| chr18:12013385
|
T | C | 84 | a0001c0001t0001g0034a0001c0001t0001g0079a0001c0001t0001g0080others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.382-880T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013385 | ||||||
| chr18:12013410
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.382-855G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013410 | ||||||
| chr18:12013452
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-813G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013452 | ||||||
| chr18:12013513
|
G | T | 59 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0031others(56): Show | 59 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.382-752G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013513 | ||||||
| chr18:12013595
|
G | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0110others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-670G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013595 | ||||||
| chr18:12013634
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-631C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013634 | ||||||
| chr18:12013640
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-625C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013640 | ||||||
| chr18:12013742
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-523A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013742 | ||||||
| chr18:12013786
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0002g0206a0001c0001t0002g0280 | 3 | HG02622.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-479G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013786 | ||||||
| chr18:12013920
|
A | G | 6 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0090others(3): Show | 6 | HG02622.hp1 HG03225.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-345A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12013920 | ||||||
| chr18:12014169
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.382-96C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12014169 | ||||||
| chr18:12014221
|
G | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.382-44G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12014221 | ||||||
| chr18:12014384
|
C | CA | 30 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(27): Show | 31 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.490+13dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12014384 | |||||
| chr18:12014387
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+14C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014387 | ||||||
| chr18:12014412
|
T | G | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(353): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.490+39T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014412 | ||||||
| chr18:12014446
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490+73G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014446 | ||||||
| chr18:12014559
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG02135.hp1 HG04228.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+186C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014559 | ||||||
| chr18:12014596
|
C | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.490+223C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014596 | ||||||
| chr18:12014622
|
A | G | 80 | a0001c0001t0001g0034a0001c0001t0001g0079a0001c0001t0001g0080others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.490+249A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014622 | ||||||
| chr18:12014876
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0093others(4): Show | 8 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+503C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014876 | ||||||
| chr18:12014965
|
C | G | 1 | a0001c0001t0001g0334 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490+592C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12014965 | ||||||
| chr18:12015150
|
G | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0028others(52): Show | 56 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.490+777G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015150 | ||||||
| chr18:12015220
|
A | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 64 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.490+847A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015220 | ||||||
| chr18:12015299
|
C | G | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.490+926C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015299 | ||||||
| chr18:12015364
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.490+991A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015364 | ||||||
| chr18:12015426
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.490+1053C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015426 | ||||||
| chr18:12015435
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.490+1062C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015435 | ||||||
| chr18:12015469
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0261 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.490+1096C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015469 | ||||||
| chr18:12015523
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.490+1150G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015523 | ||||||
| chr18:12015661
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.490+1288C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015661 | ||||||
| chr18:12015824
|
C | T | 89 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.490+1451C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015824 | ||||||
| chr18:12015836
|
G | A | 86 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(83): Show | 86 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.490+1463G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015836 | ||||||
| chr18:12015888
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.490+1515A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015888 | ||||||
| chr18:12015916
|
G | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.490+1543G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015916 | ||||||
| chr18:12015990
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0002g0012a0001c0001t0003g0113others(1): Show | 4 | HG01167.hp1 HG01891.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1617G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12015990 | ||||||
| chr18:12016265
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.490+1892C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016265 | ||||||
| chr18:12016298
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.490+1925C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016298 | ||||||
| chr18:12016424
|
G | GC | 13 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0065others(10): Show | 13 | HG00408.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+2052dupC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12016424 | |||||
| chr18:12016488
|
C | A | 2 | a0001c0001t0001g0350a0001c0001t0001g0356 | 2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.490+2115C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016488 | ||||||
| chr18:12016567
|
G | A | 2 | a0001c0002t0001g0215a0001c0002t0001g0226 | 2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.490+2194G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016567 | ||||||
| chr18:12016656
|
T | C | 1 | a0001c0002t0001g0291 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.490+2283T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016656 | ||||||
| chr18:12016671
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490+2298G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016671 | ||||||
| chr18:12016718
|
C | T | 82 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.490+2345C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016718 | ||||||
| chr18:12016719
|
G | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0059others(10): Show | 13 | HG00408.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+2346G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016719 | ||||||
| chr18:12016952
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0051others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+2579C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016952 | ||||||
| chr18:12016990
|
C | G | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.490+2617C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12016990 | ||||||
| chr18:12017010
|
A | ATC | 8 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0197others(5): Show | 9 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+2647_490+2648d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12017010 | |||||
| chr18:12017034
|
C | G | 1 | a0003c0004t0001g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.490+2661C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017034 | ||||||
| chr18:12017172
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+2799A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017172 | ||||||
| chr18:12017263
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG02145.hp2 HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+2890C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017263 | ||||||
| chr18:12017264
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.490+2891G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017264 | ||||||
| chr18:12017344
|
A | G | 85 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.490+2971A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017344 | ||||||
| chr18:12017533
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.490+3160G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017533 | ||||||
| chr18:12017651
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490+3278C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017651 | ||||||
| chr18:12017677
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3304A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017677 | ||||||
| chr18:12017702
|
C | T | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.490+3329C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017702 | ||||||
| chr18:12017790
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.490+3417C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017790 | ||||||
| chr18:12017792
|
A | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.490+3419A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017792 | ||||||
| chr18:12017898
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3525T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017898 | ||||||
| chr18:12017932
|
T | G | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.490+3559T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017932 | ||||||
| chr18:12017945
|
GT | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.490+3583delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12017945 | |||||
| chr18:12017998
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(20): Show | 24 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+3625A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12017998 | ||||||
| chr18:12018011
|
G | A | 84 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0064others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.490+3638G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018011 | ||||||
| chr18:12018041
|
A | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.490+3668A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018041 | ||||||
| chr18:12018074
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0030others(9): Show | 13 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+3701G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018074 | ||||||
| chr18:12018085
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.490+3712C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018085 | ||||||
| chr18:12018088
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.490+3715A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018088 | ||||||
| chr18:12018127
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3754G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018127 | ||||||
| chr18:12018132
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3759G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018132 | ||||||
| chr18:12018192
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.490+3819G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018192 | ||||||
| chr18:12018194
|
G | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0021others(16): Show | 20 | HG00408.hp2 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.490+3821G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018194 | ||||||
| chr18:12018299
|
A | G | 81 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(78): Show | 81 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.490+3926A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018299 | ||||||
| chr18:12018351
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3978G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018351 | ||||||
| chr18:12018353
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+3980T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018353 | ||||||
| chr18:12018399
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0006 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490+4026C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018399 | ||||||
| chr18:12018454
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.490+4081C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018454 | ||||||
| chr18:12018615
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0048others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+4242A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018615 | ||||||
| chr18:12018660
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490+4287T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018660 | ||||||
| chr18:12018666
|
C | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.490+4293C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018666 | ||||||
| chr18:12018714
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.490+4341A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018714 | ||||||
| chr18:12018810
|
G | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.490+4437G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018810 | ||||||
| chr18:12018823
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.490+4450T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018823 | ||||||
| chr18:12018959
|
G | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0030others(8): Show | 12 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.490+4586G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12018959 | ||||||
| chr18:12019040
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.490+4667G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019040 | ||||||
| chr18:12019167
|
G | T | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG00408.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.490+4794G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019167 | ||||||
| chr18:12019373
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0209 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.490+5000G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019373 | ||||||
| chr18:12019420
|
A | AT | 21 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0028others(18): Show | 22 | HG01243.hp1 HG02135.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.490+5066dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12019420 | |||||
| chr18:12019489
|
A | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0030others(9): Show | 13 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+5116A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019489 | ||||||
| chr18:12019664
|
A | C | 2 | a0001c0001t0001g0069a0001c0001t0002g0006 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490+5291A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019664 | ||||||
| chr18:12019882
|
AT | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0067others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+5510delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019882 | ||||||
| chr18:12019883
|
T | A | 83 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0034others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.490+5510T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019883 | ||||||
| chr18:12019986
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490+5613C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12019986 | ||||||
| chr18:12020000
|
T | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.490+5627T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020000 | ||||||
| chr18:12020123
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.490+5750G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020123 | ||||||
| chr18:12020172
|
C | CTTTA | 11 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0030others(8): Show | 12 | HG01243.hp2 HG01361.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.490+5806_490+5809d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020172 | |||||
| chr18:12020172
|
C | CTTTATTT others(1): Show |
5 | a0001c0001t0001g0065a0001c0001t0001g0269a0001c0002t0001g0282others(2): Show | 5 | HG00408.hp2 HG02735.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+5802_490+5809d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020172 | |||||
| chr18:12020172
|
C | CTTTATTT others(5): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0067others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+5809_490+5810i others(14): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020172 | |||||
| chr18:12020179
|
T | G | 2 | a0001c0001t0001g0102a0001c0002t0001g0171 | 2 | HG00099.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.490+5806T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020179 | ||||||
| chr18:12020179
|
T | TATTG | 6 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0098others(3): Show | 6 | HG01109.hp1 HG01975.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+5836_490+5839d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020179 | |||||
| chr18:12020179
|
TATTG | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(45): Show | 50 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.490+5836_490+5839d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020179 | |||||
| chr18:12020183
|
G | T | 10 | a0001c0001t0001g0021a0001c0001t0001g0063a0001c0001t0001g0067others(7): Show | 10 | HG00639.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.490+5810G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020183 | ||||||
| chr18:12020274
|
A | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.490+5901A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020274 | ||||||
| chr18:12020361
|
TTTGGTAT others(17): Show |
T | 1 | a0001c0001t0001g0326 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.490+5991_490+6014d others(26): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020361 | |||||
| chr18:12020439
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490+6066C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020439 | ||||||
| chr18:12020471
|
G | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG02135.hp1 HG04228.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+6098G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020471 | ||||||
| chr18:12020531
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490+6158G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020531 | ||||||
| chr18:12020675
|
CTT | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.490+6306_490+6307d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12020675 | |||||
| chr18:12020751
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0051others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+6378T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020751 | ||||||
| chr18:12020751
|
T | G | 1 | a0001c0002t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490+6378T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020751 | ||||||
| chr18:12020823
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0269a0004c0010t0001g0062 | 3 | HG02809.hp1 NA18522.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.490+6450G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12020823 | ||||||
| chr18:12021006
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0083 | 2 | NA18953.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.490+6633G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021006 | ||||||
| chr18:12021016
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0059a0001c0001t0001g0067others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+6643C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021016 | ||||||
| chr18:12021031
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0030others(8): Show | 12 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.490+6658C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021031 | ||||||
| chr18:12021222
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.491-6821A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021222 | ||||||
| chr18:12021239
|
A | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG02135.hp1 HG04228.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-6804A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021239 | ||||||
| chr18:12021301
|
GAGTTCAA others(9): Show |
G | 1 | a0001c0001t0001g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.491-6723_491-6708d others(18): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12021301 | |||||
| chr18:12021382
|
C | CAGGCT | 18 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0021others(15): Show | 19 | HG00408.hp2 HG02109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-6661_491-6660i others(7): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021382 | ||||||
| chr18:12021383
|
T | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0021others(15): Show | 19 | HG00408.hp2 HG02109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-6660T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021383 | ||||||
| chr18:12021463
|
G | GC | 245 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.491-6578dupC | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12021463 | |||||
| chr18:12021510
|
T | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.491-6533T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021510 | ||||||
| chr18:12021519
|
G | A | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.491-6524G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021519 | ||||||
| chr18:12021565
|
C | CT | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.491-6477dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12021565 | |||||
| chr18:12021587
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG02145.hp2 HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-6456G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021587 | ||||||
| chr18:12021641
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.491-6402C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021641 | ||||||
| chr18:12021644
|
C | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.491-6399C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021644 | ||||||
| chr18:12021676
|
C | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0069others(3): Show | 6 | HG00639.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-6367C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021676 | ||||||
| chr18:12021724
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0267others(1): Show | 4 | HG01243.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-6319C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021724 | ||||||
| chr18:12021760
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.491-6283G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021760 | ||||||
| chr18:12021826
|
C | T | 79 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(76): Show | 79 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.491-6217C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021826 | ||||||
| chr18:12021869
|
G | A | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.491-6174G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021869 | ||||||
| chr18:12021894
|
C | G | 6 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0069others(3): Show | 6 | HG00639.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-6149C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12021894 | ||||||
| chr18:12022002
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-6041A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022002 | ||||||
| chr18:12022068
|
T | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.491-5975T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022068 | ||||||
| chr18:12022079
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG01952.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-5964A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022079 | ||||||
| chr18:12022082
|
CCATT | C | 79 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(76): Show | 79 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.491-5958_491-5955d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022082 | |||||
| chr18:12022133
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.491-5910T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022133 | ||||||
| chr18:12022259
|
C | T | 140 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0031others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.491-5784C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022259 | ||||||
| chr18:12022298
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.491-5745G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022298 | ||||||
| chr18:12022319
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.491-5724G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022319 | ||||||
| chr18:12022330
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.491-5713G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022330 | ||||||
| chr18:12022358
|
C | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0069others(2): Show | 5 | HG00639.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-5685C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022358 | ||||||
| chr18:12022527
|
G | GA | 3 | a0001c0001t0001g0014a0001c0001t0001g0269a0001c0002t0001g0214 | 3 | HG02602.hp1 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.491-5514dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022527 | |||||
| chr18:12022528
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0289 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.491-5514_491-5513i others(20): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAAATATA others(13): Show |
1 | a0003c0004t0001g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.491-5514_491-5513i others(22): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAAATATA others(15): Show |
1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.491-5514_491-5513i others(24): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAAATATA others(19): Show |
2 | a0001c0001t0001g0063a0001c0001t0002g0006 | 2 | HG00639.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.491-5514_491-5513i others(28): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAAT | 7 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0077others(4): Show | 7 | HG01261.hp2 HG01346.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT | 7 | a0001c0001t0001g0203a0001c0002t0001g0018a0001c0002t0001g0171others(4): Show | 7 | HG00438.hp1 HG02257.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(9): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(4): Show |
26 | a0001c0001t0001g0034a0001c0001t0001g0097a0001c0001t0001g0099others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(13): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(6): Show |
30 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0053others(27): Show | 30 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(15): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(8): Show |
28 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0089others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(17): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(10): Show |
17 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0117others(14): Show | 17 | HG00544.hp1 HG00639.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(19): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(12): Show |
8 | a0001c0001t0001g0088a0001c0001t0001g0150a0001c0001t0001g0168others(5): Show | 8 | HG00544.hp2 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(21): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(14): Show |
11 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0149others(8): Show | 11 | HG00408.hp2 HG01175.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.491-5514_491-5513i others(23): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(18): Show |
3 | a0001c0001t0001g0118a0001c0001t0001g0188a0001c0002t0001g0283 | 3 | HG02109.hp1 HG02735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.491-5514_491-5513i others(27): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(20): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0114 | 3 | HG02109.hp2 HG02602.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.491-5514_491-5513i others(29): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(22): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0068 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.491-5514_491-5513i others(31): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAATATAT others(26): Show |
1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.491-5514_491-5513i others(35): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AAT | 5 | a0001c0001t0001g0026a0001c0001t0001g0122a0001c0002t0001g0091others(2): Show | 5 | HG00140.hp1 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-5488_491-5487d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AATATAT | 10 | a0001c0001t0001g0015a0001c0002t0001g0002a0001c0002t0001g0044others(7): Show | 11 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.491-5492_491-5487d others(8): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AATATATA others(1): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0261a0001c0002t0001g0076 | 3 | HG02486.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.491-5494_491-5487d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0208a0001c0002t0001g0052a0001c0002t0006g0027 | 3 | HG02486.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.491-5496_491-5487d others(12): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
A | AATATATA others(11): Show |
1 | a0001c0002t0001g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-5504_491-5487d others(20): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
AAT | A | 10 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(7): Show | 10 | HG00673.hp2 HG02027.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-5488_491-5487d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
AATAT | A | 74 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(71): Show | 74 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.491-5490_491-5487d others(6): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022528
|
AATATATA others(1): Show |
A | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.491-5494_491-5487d others(10): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022528 | |||||
| chr18:12022529
|
AT | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0207others(4): Show | 8 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-5513delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022529 | ||||||
| chr18:12022538
|
T | A | 52 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.491-5505T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022538 | ||||||
| chr18:12022609
|
G | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0030others(8): Show | 12 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.491-5434G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022609 | ||||||
| chr18:12022628
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491-5415C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12022628 | ||||||
| chr18:12022782
|
C | CT | 159 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(156): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.491-5249dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022782 | |||||
| chr18:12022941
|
A | AT | 85 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0058others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.491-5077dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022941 | |||||
| chr18:12022941
|
A | ATT | 94 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0023others(91): Show | 94 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.491-5078_491-5077d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022941 | |||||
| chr18:12022941
|
A | ATTT | 13 | a0001c0001t0001g0041a0001c0001t0001g0083a0001c0001t0001g0094others(10): Show | 13 | HG00621.hp1 HG00621.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-5079_491-5077d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022941 | |||||
| chr18:12022941
|
AT | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 46 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.491-5077delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022941 | |||||
| chr18:12022941
|
ATTTTTTT others(3): Show |
A | 16 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0021others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.491-5086_491-5077d others(12): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12022941 | |||||
| chr18:12023073
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0002g0006 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.491-4970G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023073 | ||||||
| chr18:12023118
|
T | A | 78 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(75): Show | 78 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.491-4925T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023118 | ||||||
| chr18:12023362
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0063 | 2 | HG00639.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.491-4681C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023362 | ||||||
| chr18:12023423
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.491-4620C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023423 | ||||||
| chr18:12023562
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.491-4481G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023562 | ||||||
| chr18:12023581
|
C | T | 77 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0032others(74): Show | 77 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.491-4462C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023581 | ||||||
| chr18:12023658
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.491-4385G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023658 | ||||||
| chr18:12023660
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.491-4383A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023660 | ||||||
| chr18:12023747
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.491-4296C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12023747 | ||||||
| chr18:12024141
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.491-3902G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024141 | ||||||
| chr18:12024192
|
A | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG00558.hp2 HG00597.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-3851A>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024192 | ||||||
| chr18:12024257
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.491-3786G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024257 | ||||||
| chr18:12024345
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.491-3698A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024345 | ||||||
| chr18:12024369
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0335 | 2 | HG02132.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.491-3674C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024369 | ||||||
| chr18:12024389
|
CAA | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(20): Show | 23 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.491-3653_491-3652d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024389 | ||||||
| chr18:12024483
|
C | CA | 18 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0090others(15): Show | 19 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.491-3553dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12024483 | |||||
| chr18:12024585
|
C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-3458C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024585 | ||||||
| chr18:12024663
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0165 | 2 | HG00735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.491-3380C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024663 | ||||||
| chr18:12024673
|
T | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(17): Show | 21 | HG01167.hp1 HG02145.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.491-3370T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024673 | ||||||
| chr18:12024845
|
C | G | 2 | a0001c0003t0001g0290a0001c0003t0001g0336 | 2 | NA18963.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.491-3198C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024845 | ||||||
| chr18:12024854
|
C | CT | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG02717.hp2 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-3189_491-3188i others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12024854 | ||||||
| chr18:12024915
|
CATT | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0093a0001c0001t0001g0120others(2): Show | 5 | HG01952.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-3122_491-3120d others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12024915 | |||||
| chr18:12025007
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0123a0001c0001t0001g0263others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-3036G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025007 | ||||||
| chr18:12025120
|
T | TGG | 57 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0082others(54): Show | 57 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.491-2922_491-2921d others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12025120 | |||||
| chr18:12025143
|
T | C | 54 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0082others(51): Show | 54 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.491-2900T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025143 | ||||||
| chr18:12025296
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.491-2747C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025296 | ||||||
| chr18:12025721
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0001g0123others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-2322A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025721 | ||||||
| chr18:12025727
|
G | A | 2 | a0001c0001t0001g0293a0001c0002t0001g0057 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.491-2316G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025727 | ||||||
| chr18:12025849
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.491-2194C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025849 | ||||||
| chr18:12025875
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0071others(2): Show | 5 | HG01952.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-2168C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12025875 | ||||||
| chr18:12026034
|
AT | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(332): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.491-1992delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12026034 | |||||
| chr18:12026104
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0003g0112a0001c0002t0001g0091 | 3 | HG02970.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.491-1939G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026104 | ||||||
| chr18:12026156
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.491-1887T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026156 | ||||||
| chr18:12026233
|
A | G | 140 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(137): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.491-1810A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026233 | ||||||
| chr18:12026504
|
C | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 184 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.491-1539C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026504 | ||||||
| chr18:12026784
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0003g0113 | 2 | HG01167.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.491-1259G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026784 | ||||||
| chr18:12026856
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.491-1187C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026856 | ||||||
| chr18:12026875
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0003g0113 | 3 | HG01167.hp1 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.491-1168C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12026875 | ||||||
| chr18:12027029
|
C | T | 138 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(135): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.491-1014C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027029 | ||||||
| chr18:12027066
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0066a0001c0001t0001g0261others(1): Show | 4 | HG02055.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-977T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027066 | ||||||
| chr18:12027151
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.491-892G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027151 | ||||||
| chr18:12027159
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.491-884C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027159 | ||||||
| chr18:12027206
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.491-837G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027206 | ||||||
| chr18:12027343
|
G | C | 1 | a0001c0001t0001g0022 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-700G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027343 | ||||||
| chr18:12027357
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.491-686G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027357 | ||||||
| chr18:12027362
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.491-681G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027362 | ||||||
| chr18:12027519
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0122others(3): Show | 6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-524T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027519 | ||||||
| chr18:12027567
|
A | ATT | 57 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.491-454_491-453dup others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027567 | |||||
| chr18:12027567
|
A | ATTT | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 68 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.491-455_491-453dup others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027567 | |||||
| chr18:12027567
|
A | ATTTT | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0032others(72): Show | 76 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.491-456_491-453dup others(4): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027567 | |||||
| chr18:12027567
|
A | ATTTTT | 10 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0077others(7): Show | 10 | HG01346.hp2 HG01361.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-457_491-453dup others(5): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027567 | |||||
| chr18:12027567
|
A | ATTTTTTT | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-459_491-453dup others(7): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027567 | |||||
| chr18:12027590
|
T | A | 1 | a0001c0003t0001g0336 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.491-453T>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027590 | ||||||
| chr18:12027590
|
T | TA | 13 | a0001c0001t0001g0022a0001c0001t0001g0105a0001c0001t0001g0145others(10): Show | 13 | HG01069.hp2 HG01074.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-450dupA | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027590 | |||||
| chr18:12027590
|
T | TTA | 120 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.491-453_491-452ins others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027590 | ||||||
| chr18:12027590
|
T | TTTA | 7 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0158others(4): Show | 7 | HG00597.hp1 HG02300.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-453_491-452ins others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027590 | ||||||
| chr18:12027606
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02109.hp2 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.491-437T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027606 | ||||||
| chr18:12027640
|
A | G | 1 | a0001c0006t0001g0251 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.491-403A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027640 | ||||||
| chr18:12027689
|
C | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-354C>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027689 | ||||||
| chr18:12027748
|
AT | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-281delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 12027748 | |||||
| chr18:12027894
|
T | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-149T>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027894 | ||||||
| chr18:12027942
|
AT | A | 141 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(138): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.491-100delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 5/7 | chr18 | 12027942 | ||||||
| chr18:12028168
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0211a0001c0001t0001g0275 | 3 | HG02615.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.599+17G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028168 | ||||||
| chr18:12028199
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.599+48C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028199 | ||||||
| chr18:12028225
|
CT | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0107a0001c0001t0001g0146others(3): Show | 6 | HG00639.hp1 HG01070.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+75delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028225 | ||||||
| chr18:12028248
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.599+97A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028248 | ||||||
| chr18:12028250
|
G | A | 134 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(131): Show | 134 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.599+99G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028250 | ||||||
| chr18:12028297
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0013others(8): Show | 11 | HG01952.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.599+146T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028297 | ||||||
| chr18:12028362
|
G | A | 1 | a0001c0002t0001g0242 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.599+211G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028362 | ||||||
| chr18:12028393
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.599+242C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028393 | ||||||
| chr18:12028581
|
A | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.600-261A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028581 | ||||||
| chr18:12028660
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.600-182C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028660 | ||||||
| chr18:12028750
|
T | C | 1 | a0001c0002t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.600-92T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028750 | ||||||
| chr18:12028768
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0205 | 2 | HG01952.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.600-74G>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028768 | ||||||
| chr18:12028810
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.600-32G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 6/7 | chr18 | 12028810 | ||||||
| chr18:12029076
|
C | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 38 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.751+83C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029076 | ||||||
| chr18:12029108
|
G | GT | 73 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 75 | HG00438.hp1 HG01070.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.751+140dupT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029108 | |||||
| chr18:12029108
|
G | GTT | 9 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0150others(6): Show | 9 | HG01167.hp1 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.751+139_751+140dup others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029108 | |||||
| chr18:12029108
|
GT | G | 20 | a0001c0001t0001g0054a0001c0001t0001g0128a0001c0001t0001g0131others(17): Show | 20 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.751+140delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029108 | |||||
| chr18:12029108
|
GTT | G | 58 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(55): Show | 58 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.751+139_751+140del others(2): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029108 | |||||
| chr18:12029150
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.751+157G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029150 | ||||||
| chr18:12029208
|
G | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.751+215G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029208 | ||||||
| chr18:12029251
|
A | G | 9 | a0001c0001t0001g0164a0001c0001t0001g0297a0001c0001t0001g0303others(6): Show | 9 | HG02027.hp2 NA18942.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.751+258A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029251 | ||||||
| chr18:12029272
|
G | GCCTGGCT others(1294): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.751+293_751+294ins others(1301): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029272 | |||||
| chr18:12029305
|
G | A | 148 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.751+312G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029305 | ||||||
| chr18:12029430
|
CT | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.751+447delT | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 12029430 | |||||
| chr18:12029536
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.751+543C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029536 | ||||||
| chr18:12029562
|
A | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(147): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.751+569A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029562 | ||||||
| chr18:12029593
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.751+600G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029593 | ||||||
| chr18:12029696
|
C | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0262a0001c0001t0001g0264others(3): Show | 6 | HG00639.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-647C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029696 | ||||||
| chr18:12029783
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-560C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029783 | ||||||
| chr18:12029792
|
A | C | 1 | a0001c0002t0001g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.752-551A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029792 | ||||||
| chr18:12029856
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-487T>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029856 | ||||||
| chr18:12029858
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(288): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.752-485A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029858 | ||||||
| chr18:12029889
|
C | T | 2 | a0001c0001t0001g0101a0001c0002t0001g0239 | 2 | HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.752-454C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029889 | ||||||
| chr18:12029985
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.752-358G>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12029985 | ||||||
| chr18:12030024
|
C | T | 3 | a0001c0001t0001g0294a0002c0005t0001g0095a0002c0005t0001g0096 | 3 | NA18966.hp1 NA18971.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.752-319C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030024 | ||||||
| chr18:12030060
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-283A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030060 | ||||||
| chr18:12030086
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-257C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030086 | ||||||
| chr18:12030141
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-202C>T | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030141 | ||||||
| chr18:12030145
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.752-198G>A | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030145 | ||||||
| chr18:12030184
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.752-159A>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030184 | ||||||
| chr18:12030327
|
C | G | 1 | a0001c0002t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.752-16C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030327 | ||||||
| chr18:12030339
|
C | G | 2 | a0001c0001t0001g0101a0001c0002t0001g0239 | 2 | HG02698.hp1 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.752-4C>G | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 7/7 | chr18 | 12030339 |