Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MKPSG others(283): Show |
chr18 | 11976507 | 12035877 |
| a0002 | 0/0 | 288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | MKPSG others(283): Show |
chr18 | 11976507 | 12035877 |
| a0003 | 0/0 | 288 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | MKPSG others(283): Show |
chr18 | 11976507 | 12035877 |
| a0004 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | MKPSG others(283): Show |
chr18 | 11976507 | 12035877 |
| a0005 | 0/0 | 288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | MKPSG others(283): Show |
chr18 | 11976507 | 12035877 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 864 | 271 | 75 | 58 | 92 | 14 | 30 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0001c0002 | 0/0 | 864 | 72 | 19 | 9 | 41 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0001c0003 | 0/0 | 864 | 9 | 0 | 0 | 9 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0001c0006 | 0/0 | 864 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0001c0007 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0001c0009 | 0/0 | 864 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0002c0004 | 0/0 | 864 | 3 | 3 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0003c0005 | 0/0 | 864 | 3 | 0 | 0 | 3 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0004c0010 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
chr18 | 11976507 | 12035877 | ||
| a0005c0008 | 0/0 | 864 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | ATGAA others(859): Show |
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 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0001t0002 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0001t0003 | 0/0 | 1449 | 2 | 1 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0001t0005 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0002t0001 | 0/0 | 1449 | 67 | 16 | 9 | 39 | 0 | 3 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0002t0002 | 0/0 | 1449 | 2 | 2 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0002t0004 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0002t0006 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0002t0007 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0003t0001 | 0/0 | 1449 | 9 | 0 | 0 | 9 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0006t0001 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0007t0001 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0001c0009t0001 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0002c0004t0001 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0003c0005t0001 | 0/0 | 1449 | 3 | 0 | 0 | 3 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0004c0010t0001 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| a0005c0008t0001 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | TGCCC others(1444): Show |
chr18 | 11976507 | 12035877 |
| actghapid | grch38/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 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0006 | 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 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0036 | 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 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0047 | 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 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0091 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0136 | 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 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0156 | 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 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0171 | 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 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0206 | 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 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0212 | 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 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0333 | 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 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0001t0005g0048 | 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 |
| a0001c0002t0001g0019 | 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 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0074 | 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 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0120 | 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 |
| a0001c0002t0001g0135 | 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 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0186 | 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 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0222 | 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 | 1 | 0 | 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 |
| 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 |
| a0001c0002t0001g0233 | 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 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0001g0292 | 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 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0002t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0003t0001g0331 | 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 |
| a0001c0003t0001g0335 | 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 |
| a0001c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0006t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0001c0009t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0002c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0003c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0004c0010t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| a0005c0008t0001g0043 | 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 | g0104 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0359 | 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 | g0329 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0107 | 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 | g0105 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0114 | 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 | g0303 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0358 | 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 | g0351 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01243 | hp1 | a0001 | c0009 | t0001 | g0125 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0285 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0007 | 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 | g0034 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0360 | 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 | g0352 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0165 | 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 | g0333 | 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 | g0171 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02129 | hp2 | a0001 | c0002 | t0007 | g0230 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0055 | 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 | g0019 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0273 | 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 | g0115 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0236 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | 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 | g0151 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02809 | hp1 | a0004 | c0010 | t0001 | g0063 | 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 | g0208 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0340 | 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 | g0113 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0070 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0062 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03710 | hp2 | a0005 | c0008 | t0001 | g0043 | SAS | PJL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CHB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0136 | 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 | g0257 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0129 | 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 | g0156 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0332 | 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 | g0079 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0137 | 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 | g0195 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0020 | 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 | g0336 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18966 | hp1 | a0003 | c0005 | t0001 | g0097 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18971 | hp1 | a0003 | c0005 | t0001 | g0096 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0252 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0160 | 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 | g0120 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0157 | 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 | g0037 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0235 | 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 | g0058 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0315 | 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 | g0140 | 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 | g0117 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19012 | hp1 | a0003 | c0005 | t0001 | g0025 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0335 | 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 | g0173 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0139 | 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 | g0135 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0331 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0172 | 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 | g0334 | 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 | g0030 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0152 | 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 | g0337 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19086 | hp2 | a0001 | c0006 | t0001 | g0240 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19089 | hp1 | a0001 | c0007 | t0001 | g0253 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ASW | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0183 | 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 | g0147 | AMR | CLM | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0282 | 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 | g0046 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | MSL | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | USA | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | LWK | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0130 | REF | REF | IMPA2_chr18_11976507_12035877 | IMPA2 | chr18 | 11976507 | 12035877 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12009914 | G | A | 1 | a0002 | 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 | a0003 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:11999116 | T | C | 3 | a0001c0002 a0001c0006 a0001c0007 |
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 | a0001c0003 a0001c0006 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002 a0001c0002t0002 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:11982133 | C | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0003c0005t0001g0096 a0003c0005t0001g0097 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0094 others(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 | 50 | a0001c0001t0001g0004 a0001c0001t0001g0293 a0001c0001t0001g0294 others(47): 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 | a0001c0001t0001g0261 | 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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0290 a0001c0001t0001g0293 others(52): 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 | a0001c0003t0001g0291 | 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 | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): 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 | a0001c0001t0001g0290 a0001c0002t0001g0286 a0001c0002t0001g0287 others(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 | 51 | a0001c0001t0001g0004 a0001c0001t0001g0293 a0001c0001t0001g0294 others(48): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | 52 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0259 others(49): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(177): 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 | a0002c0004t0001g0285 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0002t0001g0273 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | 51 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0259 others(48): 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 | a0001c0002t0001g0056 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0196 others(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 | a0001c0002t0001g0257 | 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 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+2543A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | chr18 | 11984308 | |||||||
| chr18:11984524 | A | G | 1 | a0002c0004t0001g0285 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | 52 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0258 others(49): 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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(84): 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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): 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 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0002t0006g0028 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0356 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(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 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0330 a0001c0001t0001g0333 a0001c0001t0001g0334 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | 75 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0047 others(72): 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 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0030 |
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 | a0004c0010t0001g0063 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0002g0013 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0002t0001g0255 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0191 | 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 | a0001c0002t0001g0254 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0129 | 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 | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(225): 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 | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(32): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0061 others(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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0277 a0001c0002t0001g0134 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0256 a0002c0004t0001g0070 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | a0001c0001t0001g0119 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | a0001c0002t0001g0135 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(182): 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 | a0001c0002t0001g0286 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | a0001c0002t0001g0186 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | a0001c0001t0001g0279 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | a0001c0001t0001g0023 | 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(172): 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 | 129 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(126): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): 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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0094 others(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 | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): 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 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0072 | 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 | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0264 | 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 | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): 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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): 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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | 139 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0055 others(136): 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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0047 a0001c0002t0001g0002 a0001c0002t0001g0045 others(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 | a0001c0002t0001g0248 a0001c0007t0001g0253 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0262 |
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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): 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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0175 others(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 | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0095 |
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 | a0001c0002t0001g0246 a0001c0002t0001g0247 |
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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): 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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0188 |
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 | a0001c0003t0001g0137 | 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 | a0001c0001t0001g0072 | 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 | a0004c0010t0001g0063 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0339 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | a0001c0001t0001g0296 a0001c0001t0001g0300 |
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 | a0001c0002t0001g0292 | 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): 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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0093 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0088 |
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 | a0001c0002t0006g0028 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0061 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0002t0001g0257 | 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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0051 others(80): 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 | a0001c0002t0001g0058 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0272 a0001c0002t0001g0019 others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0060 | 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 | a0004c0010t0001g0063 | 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 | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): 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 | a0001c0001t0001g0297 a0001c0001t0001g0323 a0001c0001t0001g0324 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0272 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0330 a0001c0003t0001g0291 a0001c0003t0001g0335 |
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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0272 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0181 | 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 | 155 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0051 others(152): 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 | a0001c0001t0001g0138 | 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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | 85 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0272 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0353 a0001c0001t0001g0354 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0011 a0001c0002t0001g0002 a0001c0002t0001g0019 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0086 |
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 | GCCGCC | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0094 others(11): Show |
14 | HG00438.hp2 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-126_97-122delGC others(3): Show |
IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 11998925 | ||||||
| chr18:11998925 | GCCGCCC | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0090 others(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 | 60 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0023 others(57): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0211 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0301 a0001c0001t0001g0328 |
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 | a0001c0001t0001g0339 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0029 | 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 | 72 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0051 others(69): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0029 | 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 | 72 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0051 others(69): 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 | a0004c0010t0001g0063 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0033 others(79): 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 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0042 others(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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0033 others(90): 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(140): 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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0052 a0001c0001t0003g0113 a0001c0001t0003g0114 |
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 | a0001c0002t0001g0235 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0065 a0001c0002t0001g0002 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0095 | 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 | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0330 a0001c0001t0001g0333 a0001c0001t0001g0334 others(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 | a0001c0001t0001g0052 | 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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0002t0001g0255 | 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 | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): 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 | a0001c0001t0001g0026 a0001c0001t0001g0032 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): 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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0091 | 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 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0173 others(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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0256 others(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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0002t0001g0227 | 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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): 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 | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0191 | 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0173 others(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 | a0001c0001t0001g0131 | 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0340 | 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0001g0225 | 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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0095 others(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 | 85 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0033 others(82): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | 82 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0033 others(79): 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 | a0001c0001t0001g0169 a0001c0006t0001g0252 |
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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): 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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0317 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0002t0001g0019 others(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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | 77 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0033 others(74): 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 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0002t0001g0019 others(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 | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): 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 | a0001c0001t0001g0029 | 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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | a0001c0001t0001g0026 a0001c0001t0001g0032 |
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 | a0001c0001t0001g0057 | 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 | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(196): 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 | a0001c0001t0001g0093 | 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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0109 a0001c0009t0001g0125 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0209 |
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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): 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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): 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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0002g0007 a0002c0004t0001g0062 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0117 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0095 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | a0003c0005t0001g0096 a0003c0005t0001g0097 |
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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0061 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0061 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0350 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0005g0048 a0002c0004t0001g0285 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0099 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0099 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0002t0001g0019 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0208 a0001c0001t0002g0207 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0197 a0001c0001t0003g0114 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0208 a0001c0001t0002g0207 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0075 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0321 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0309 others(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 | a0001c0001t0001g0330 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0088 a0001c0001t0001g0100 others(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 | 36 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0081 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(33): 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 | a0001c0001t0001g0104 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0183 a0001c0002t0001g0002 |
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 | a0001c0001t0001g0065 a0001c0002t0001g0045 a0001c0002t0001g0046 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0145 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0263 a0001c0001t0001g0265 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0002g0013 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0264 a0001c0001t0001g0266 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0099 a0001c0001t0001g0106 others(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 | 1 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0065 a0001c0002t0001g0002 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0173 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0351 a0001c0001t0001g0358 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0015 a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0015 a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0015 a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0015 a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0256 a0001c0002t0001g0046 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0042 |
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 | a0001c0002t0002g0221 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | 77 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0023 others(74): 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0078 a0001c0001t0001g0085 others(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 | 140 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0032 others(137): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): 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 | a0001c0001t0003g0114 | 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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0143 a0001c0001t0001g0152 others(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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | 340 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(337): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.381+243A>C | IMPA2 | ENSG00000141401.12 | transcript | ENST00000269159.8 | protein_coding | 4/7 | chr18 | 12012458 | |||||||
| chr18:12012468 | A | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0023 others(74): 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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | 77 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0023 others(74): 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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0032 |
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 | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): 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 | a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | 83 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(80): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): 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 | a0001c0002t0001g0092 | 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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0001t0001g0061 a0001c0001t0002g0207 a0001c0001t0002g0281 |
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 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0151 | 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 | 77 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0023 others(74): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0055 | 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 | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | 79 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): 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 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(80): 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 | a0001c0001t0001g0198 | 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 | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(220): 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0023 | 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 | 88 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0023 others(85): 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 | 85 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0023 others(82): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0052 a0001c0001t0002g0013 a0001c0001t0003g0114 others(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 | a0001c0001t0001g0181 | 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 | a0001c0002t0001g0135 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0349 a0001c0001t0001g0355 |
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 | a0001c0002t0001g0215 a0001c0002t0001g0225 |
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 | a0001c0002t0001g0292 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0052 others(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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(77): 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 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0198 others(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 | a0002c0004t0001g0070 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0059 | 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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(77): 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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(226): 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 | a0001c0001t0001g0059 | 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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(77): 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 | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(222): 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 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0022 others(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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(77): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0071 a0001c0001t0002g0007 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0060 | 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 | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): 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 | a0001c0001t0001g0339 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0002t0001g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0071 a0001c0001t0002g0007 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0270 a0001c0002t0001g0283 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0104 a0001c0002t0001g0172 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0064 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0320 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0052 others(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 | a0001c0002t0001g0077 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0270 a0004c0010t0001g0063 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0022 others(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 | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(241): 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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0075 | 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 | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0299 | 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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(75): 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 | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(75): 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 | a0001c0001t0001g0185 | 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 | 139 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0032 others(136): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0270 a0001c0002t0001g0214 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0290 |
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 | a0002c0004t0001g0070 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0064 a0001c0001t0002g0007 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0204 a0001c0002t0001g0019 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0151 a0001c0001t0001g0169 others(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 |
10 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0001g0146 others(7): Show |
10 | HG00408.hp2 HG01175.hp1 HG02300.hp1 others(7): 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 | a0001c0001t0001g0119 a0001c0001t0001g0189 a0001c0002t0001g0283 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0115 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0123 a0001c0002t0001g0092 others(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 | a0001c0001t0001g0016 a0001c0002t0001g0002 a0001c0002t0001g0045 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0262 a0001c0002t0001g0077 |
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 | a0001c0001t0001g0206 a0001c0002t0001g0053 a0001c0002t0006g0028 |
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 | a0001c0002t0001g0255 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | 73 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(70): 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0016 | 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 | 158 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(155): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): 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 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0059 others(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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0023 others(90): 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 | a0001c0001t0001g0042 a0001c0001t0001g0084 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0071 a0001c0001t0002g0007 |
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 | 77 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(74): 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0197 | 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 | 76 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(73): 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0005g0048 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0334 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0017 others(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 | a0001c0003t0001g0291 a0001c0003t0001g0335 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0094 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0264 others(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 | 56 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0083 others(53): Show |
56 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(53): 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 | 53 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0083 others(50): Show |
53 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(50): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0295 a0001c0002t0001g0058 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0072 others(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 | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): 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 | a0001c0001t0001g0290 a0001c0001t0003g0113 a0001c0002t0001g0092 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0075 a0001c0001t0003g0114 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0003g0114 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0262 others(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 | a0001c0002t0001g0076 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0123 others(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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(53): 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 | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
67 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(64): 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0003t0001g0335 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0069 |
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 | a0001c0006t0001g0252 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0212 a0001c0001t0001g0276 |
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 | a0001c0001t0002g0007 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0109 | 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 | a0001c0002t0001g0194 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0298 a0001c0001t0001g0306 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0002t0001g0076 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0002t0001g0076 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0263 a0001c0001t0001g0265 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0002t0001g0076 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0102 a0001c0002t0001g0236 |
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 | a0001c0001t0002g0013 | 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 | a0001c0001t0001g0294 a0003c0005t0001g0096 a0003c0005t0001g0097 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0002g0281 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0102 a0001c0002t0001g0236 |
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 |