Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 642517 |
| ensemblid | ENSG00000204172.12 |
| hgncid | 23463 |
| symbol | AGAP9 |
| name | ArfGAP with GTPase domain, ankyrin repeat and PH domain 9 |
| refseq_nuc | NM_001190810.1 |
| refseq_prot | NP_001177739.1 |
| ensembl_nuc | ENST00000452145.6 |
| ensembl_prot | ENSP00000392206.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 47501854 |
| end | 47523638 |
| strand | - |
| ver | v1.2 |
| region | chr10:47501854-47523638 |
| region5000 | chr10:47496854-47528638 |
| regionname0 | AGAP9_chr10_47501854_47523638 |
| regionname5000 | AGAP9_chr10_47496854_47528638 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 658 | 161 | 30 | 35 | 56 | 14 | 24 | 44 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0002 | 0/0 | 658 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0003 | 0/0 | 642 | 11 | 5 | 2 | 0 | 0 | 4 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(637): Show |
chr10 | 47496854 | 47528638 |
| a0004 | 0/0 | 11 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MTAQP others(6): Show |
chr10 | 47496854 | 47528638 |
| a0005 | 0/0 | 658 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0006 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(655): Show |
chr10 | 47496854 | 47528638 |
| a0007 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0008 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(655): Show |
chr10 | 47496854 | 47528638 |
| a0009 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0010 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0011 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(655): Show |
chr10 | 47496854 | 47528638 |
| a0012 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0013 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0014 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| a0015 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | MGNIL others(653): Show |
chr10 | 47496854 | 47528638 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1974 | 158 | 30 | 34 | 55 | 14 | 23 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0001c0015 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0001c0016 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0001c0017 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0002c0002 | 0/0 | 1974 | 14 | 12 | 2 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0002c0004 | 0/0 | 1974 | 5 | 5 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0003c0003 | 0/0 | 1980 | 11 | 5 | 2 | 0 | 0 | 4 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1975): Show |
chr10 | 47496854 | 47528638 | ||
| a0004c0005 | 0/0 | 1578 | 3 | 2 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | GTATC others(1573): Show |
chr10 | 47496854 | 47528638 | ||
| a0005c0006 | 0/0 | 1974 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0006c0008 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1976): Show |
chr10 | 47496854 | 47528638 | ||
| a0007c0018 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0008c0009 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1976): Show |
chr10 | 47496854 | 47528638 | ||
| a0009c0007 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0010c0012 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0011c0010 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1976): Show |
chr10 | 47496854 | 47528638 | ||
| a0012c0014 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0013c0011 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0014c0019 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 | ||
| a0015c0013 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | ATGGG others(1969): Show |
chr10 | 47496854 | 47528638 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2387 | 155 | 30 | 34 | 52 | 14 | 23 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0001c0001t0004 | 0/0 | 2387 | 3 | 0 | 0 | 3 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0001c0015t0001 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0001c0016t0001 | 0/0 | 2387 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0001c0017t0001 | 0/0 | 2387 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0002c0002t0001 | 0/0 | 2387 | 8 | 7 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0002c0002t0002 | 0/0 | 2387 | 6 | 5 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0002c0004t0003 | 0/0 | 2387 | 5 | 5 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0003c0003t0001 | 0/0 | 2393 | 11 | 5 | 2 | 0 | 0 | 4 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2388): Show |
chr10 | 47496854 | 47528638 |
| a0004c0005t0005 | 0/0 | 1879 | 3 | 2 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | GTATC others(1874): Show |
chr10 | 47496854 | 47528638 |
| a0005c0006t0001 | 0/0 | 2387 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0006c0008t0006 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2389): Show |
chr10 | 47496854 | 47528638 |
| a0007c0018t0001 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0008c0009t0001 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2389): Show |
chr10 | 47496854 | 47528638 |
| a0009c0007t0001 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0010c0012t0001 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0011c0010t0001 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2389): Show |
chr10 | 47496854 | 47528638 |
| a0012c0014t0001 | 0/0 | 2387 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0013c0011t0001 | 0/0 | 2387 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0014c0019t0001 | 0/0 | 2387 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| a0015c0013t0003 | 0/0 | 2387 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | AGCGG others(2382): Show |
chr10 | 47496854 | 47528638 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 8 | 11 | 1 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0002 | 0/0 | 11 | 3 | 1 | 3 | 2 | 2 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0003 | 0/0 | 8 | 3 | 0 | 3 | 0 | 2 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 1 | 3 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0005 | 0/0 | 7 | 1 | 1 | 3 | 1 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0006 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0007 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0010 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0015t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0016t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0001c0017t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0002c0004t0003g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0004c0005t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0004c0005t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0004c0005t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0005c0006t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0006c0008t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0007c0018t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0008c0009t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0009c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0010c0012t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0011c0010t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0012c0014t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0013c0011t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0014c0019t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| a0015c0013t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00741 | hp1 | a0005 | c0006 | t0001 | g0027 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01109 | hp1 | a0005 | c0006 | t0001 | g0027 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01175 | hp1 | a0001 | c0017 | t0001 | g0102 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01192 | hp1 | a0004 | c0005 | t0005 | g0106 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0095 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01884 | hp1 | a0006 | c0008 | t0006 | g0090 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01884 | hp2 | a0004 | c0005 | t0005 | g0105 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0101 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02280 | hp1 | a0007 | c0018 | t0001 | g0103 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02451 | hp1 | a0008 | c0009 | t0001 | g0097 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02622 | hp2 | a0002 | c0004 | t0003 | g0011 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0016 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02698 | hp2 | a0009 | c0007 | t0001 | g0051 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02723 | hp1 | a0010 | c0012 | t0001 | g0082 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02723 | hp2 | a0002 | c0004 | t0003 | g0011 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0092 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0015 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03041 | hp1 | a0002 | c0004 | t0003 | g0011 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03130 | hp1 | a0002 | c0004 | t0003 | g0011 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03209 | hp2 | a0004 | c0005 | t0005 | g0107 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0015 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0091 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0016 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0016 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03540 | hp2 | a0002 | c0004 | t0003 | g0011 | AFR | GWD | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03579 | hp2 | a0011 | c0010 | t0001 | g0093 | AFR | MSL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03927 | hp1 | a0001 | c0015 | t0001 | g0061 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04115 | hp2 | a0012 | c0014 | t0001 | g0033 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0094 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0015 | AFR | YRI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18953 | hp1 | a0013 | c0011 | t0001 | g0064 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18972 | hp1 | a0014 | c0019 | t0001 | g0053 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | LWK | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19043 | hp1 | a0015 | c0013 | t0003 | g0045 | AFR | LWK | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19054 | hp2 | a0001 | c0016 | t0001 | g0065 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ASW | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0104 | REF | REF | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0025 | REF | REF | AGAP9_chr10_47496854_47528638 | AGAP9 | chr10 | 47496854 | 47528638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:47502198 | G | GTACCAGA | 4 | a0003 a0006 a0008 others(1): Show |
14 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
frameshift_variant | HIGH | c.1930_1931insTCTGGT others(1): Show |
p.Thr644fs | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 2042/2387 | 1930/1977 | 644/658 | chr10 | 47502198 | |||
| chr10:47502222 | T | C | 1 | a0011 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1907A>G | p.Asn636Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 2019/2387 | 1907/1977 | 636/658 | chr10 | 47502222 | |||
| chr10:47502280 | CG | C | 1 | a0003 | 11 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(8): Show |
frameshift_variant | HIGH | c.1848delC | p.Asn616fs | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1960/2387 | 1848/1977 | 616/658 | chr10 | 47502280 | |||
| chr10:47502343 | T | C | 3 | a0006 a0008 a0011 |
3 | HG01884.hp1 HG02451.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1786A>G | p.Thr596Ala | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1898/2387 | 1786/1977 | 596/658 | chr10 | 47502343 | |||
| chr10:47502436 | A | G | 2 | a0003 a0011 |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
missense_variant | MODERATE | c.1693T>C | p.Trp565Arg | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1805/2387 | 1693/1977 | 565/658 | chr10 | 47502436 | |||
| chr10:47502507 | T | C | 2 | a0005 a0010 |
3 | HG00741.hp1 HG01109.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1622A>G | p.Asn541Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1734/2387 | 1622/1977 | 541/658 | chr10 | 47502507 | |||
| chr10:47502579 | C | T | 2 | a0006 a0008 |
2 | HG01884.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.1550G>A | p.Arg517Gln | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1662/2387 | 1550/1977 | 517/658 | chr10 | 47502579 | |||
| chr10:47502604 | A | G | 5 | a0003 a0006 a0008 others(2): Show |
15 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(12): Show |
missense_variant | MODERATE | c.1525T>C | p.Phe509Leu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1637/2387 | 1525/1977 | 509/658 | chr10 | 47502604 | |||
| chr10:47502609 | C | T | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1520G>A | p.Arg507His | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1632/2387 | 1520/1977 | 507/658 | chr10 | 47502609 | |||
| chr10:47502650 | G | C | 2 | a0006 a0008 |
2 | HG01884.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.1479C>G | p.Asn493Lys | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1591/2387 | 1479/1977 | 493/658 | chr10 | 47502650 | |||
| chr10:47502781 | T | C | 4 | a0003 a0006 a0008 others(1): Show |
14 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
missense_variant | MODERATE | c.1348A>G | p.Lys450Glu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1460/2387 | 1348/1977 | 450/658 | chr10 | 47502781 | |||
| chr10:47502782 | G | C | 1 | a0015 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1347C>G | p.Cys449Trp | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1459/2387 | 1347/1977 | 449/658 | chr10 | 47502782 | |||
| chr10:47502841 | C | T | 1 | a0010 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1288G>A | p.Glu430Lys | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1400/2387 | 1288/1977 | 430/658 | chr10 | 47502841 | |||
| chr10:47502991 | C | T | 9 | a0002 a0003 a0004 others(6): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
missense_variant | MODERATE | c.1138G>A | p.Gly380Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1250/2387 | 1138/1977 | 380/658 | chr10 | 47502991 | |||
| chr10:47503195 | C | T | 1 | a0013 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.934G>A | p.Val312Met | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1046/2387 | 934/1977 | 312/658 | chr10 | 47503195 | |||
| chr10:47503383 | C | A | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.746G>T | p.Arg249Leu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 858/2387 | 746/1977 | 249/658 | chr10 | 47503383 | |||
| chr10:47503402 | C | T | 2 | a0003 a0011 |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
missense_variant | MODERATE | c.727G>A | p.Val243Ile | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 839/2387 | 727/1977 | 243/658 | chr10 | 47503402 | |||
| chr10:47503470 | G | A | 2 | a0006 a0008 |
2 | HG01884.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.659C>T | p.Pro220Leu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 771/2387 | 659/1977 | 220/658 | chr10 | 47503470 | |||
| chr10:47504200 | G | A | 1 | a0014 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.574C>T | p.His192Tyr | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/8 | 686/2387 | 574/1977 | 192/658 | chr10 | 47504200 | |||
| chr10:47510201 | A | C | 2 | a0006 a0008 |
2 | HG01884.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.467T>G | p.Ile156Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/8 | 579/2387 | 467/1977 | 156/658 | chr10 | 47510201 | |||
| chr10:47510267 | G | T | 1 | a0009 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.401C>A | p.Ser134Tyr | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/8 | 513/2387 | 401/1977 | 134/658 | chr10 | 47510267 | |||
| chr10:47515631 | ACTATGGC others(11078): Show |
A | 1 | a0004 | 3 | HG01192.hp1 HG01884.hp2 HG03209.hp2 |
exon_loss_variant | HIGH | c.-3190_396+2191del | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/8 | chr10 | 47515631 | |||||||
| chr10:47520553 | A | G | 2 | a0002 a0003 |
20 | HG00735.hp2 HG01192.hp2 HG01361.hp2 others(17): Show |
missense_variant | MODERATE | c.307T>C | p.Ser103Pro | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/8 | 419/2387 | 307/1977 | 103/658 | chr10 | 47520553 | |||
| chr10:47522880 | T | C | 1 | a0011 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.278A>G | p.Asn93Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/8 | 390/2387 | 278/1977 | 93/658 | chr10 | 47522880 | |||
| chr10:47522883 | C | T | 1 | a0001 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.275G>A | p.Arg92Lys | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/8 | 387/2387 | 275/1977 | 92/658 | chr10 | 47522883 | |||
| chr10:47522888 | G | T | 1 | a0003 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.270C>A | p.Phe90Leu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/8 | 382/2387 | 270/1977 | 90/658 | chr10 | 47522888 | |||
| chr10:47523329 | C | G | 1 | a0001 | 3 | HG02572.hp2 HG02602.hp2 NA18987.hp1 |
missense_variant | MODERATE | c.198G>C | p.Gln66His | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/8 | 310/2387 | 198/1977 | 66/658 | chr10 | 47523329 | |||
| chr10:47523435 | A | G | 1 | a0001 | 3 | HG02602.hp2 NA20805.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.92T>C | p.Ile31Thr | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/8 | 204/2387 | 92/1977 | 31/658 | chr10 | 47523435 | |||
| chr10:47523471 | T | TG | 2 | a0002 a0003 |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
frameshift_variant | HIGH | c.55dupC | p.Gln19fs | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/8 | 167/2387 | 55/1977 | 19/658 | chr10 | 47523471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:47502167 | C | T | 1 | a0001c0016 | 1 | NA19054.hp2 | synonymous_variant | LOW | c.1962G>A | p.Thr654Thr | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 2074/2387 | 1962/1977 | 654/658 | chr10 | 47502167 | |||
| chr10:47502371 | G | A | 1 | a0011c0010 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1758C>T | p.Ser586Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1870/2387 | 1758/1977 | 586/658 | chr10 | 47502371 | |||
| chr10:47502400 | G | A | 3 | a0002c0004 a0004c0005 a0015c0013 |
9 | HG01192.hp1 HG01884.hp2 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.1729C>T | p.Leu577Leu | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1841/2387 | 1729/1977 | 577/658 | chr10 | 47502400 | |||
| chr10:47502452 | C | T | 1 | a0001c0015 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1677G>A | p.Thr559Thr | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1789/2387 | 1677/1977 | 559/658 | chr10 | 47502452 | |||
| chr10:47502743 | A | G | 2 | a0006c0008 a0008c0009 |
2 | HG01884.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.1386T>C | p.Ser462Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1498/2387 | 1386/1977 | 462/658 | chr10 | 47502743 | |||
| chr10:47502950 | G | A | 1 | a0013c0011 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.1179C>T | p.Pro393Pro | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1291/2387 | 1179/1977 | 393/658 | chr10 | 47502950 | |||
| chr10:47502956 | C | T | 3 | a0003c0003 a0004c0005 a0011c0010 |
15 | HG00735.hp2 HG01192.hp1 HG01361.hp2 others(12): Show |
synonymous_variant | LOW | c.1173G>A | p.Pro391Pro | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 1285/2387 | 1173/1977 | 391/658 | chr10 | 47502956 | |||
| chr10:47503247 | T | C | 4 | a0003c0003 a0006c0008 a0008c0009 others(1): Show |
14 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
synonymous_variant | LOW | c.882A>G | p.Gly294Gly | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 994/2387 | 882/1977 | 294/658 | chr10 | 47503247 | |||
| chr10:47503295 | G | A | 1 | a0001c0017 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.834C>T | p.Ser278Ser | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 946/2387 | 834/1977 | 278/658 | chr10 | 47503295 | |||
| chr10:47523380 | T | C | 4 | a0002c0002 a0002c0004 a0011c0010 others(1): Show |
10 | HG01123.hp1 HG02055.hp1 HG02622.hp2 others(7): Show |
synonymous_variant | LOW | c.147A>G | p.Val49Val | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/8 | 259/2387 | 147/1977 | 49/658 | chr10 | 47523380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:47501948 | G | A | 1 | a0001c0001t0004 | 3 | NA18944.hp1 NA18953.hp2 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*204C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 204 | chr10 | 47501948 | ||||||
| chr10:47502054 | T | C | 1 | a0002c0002t0002 | 6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*98A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 98 | chr10 | 47502054 | ||||||
| chr10:47502090 | G | A | 2 | a0002c0004t0003 a0015c0013t0003 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*62C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 62 | chr10 | 47502090 | ||||||
| chr10:47502138 | C | T | 1 | a0006c0008t0006 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 8/8 | 14 | chr10 | 47502138 | ||||||
| chr10:47523542 | T | C | 10 | a0001c0001t0001 a0002c0002t0001 a0002c0002t0002 others(7): Show |
37 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/8 | 16 | chr10 | 47523542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:47503601 | T | C | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-58A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503601 | |||||||
| chr10:47503726 | C | T | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.586-183G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503726 | |||||||
| chr10:47503760 | CA | C | 8 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.586-218delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503760 | |||||||
| chr10:47503936 | TCAAAAAA others(4): Show |
T | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.585+242_585+252del others(11): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503936 | |||||||
| chr10:47503937 | C | CA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(6): Show |
12 | HG00280.hp2 HG01515.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.585+251dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.585+242_585+251dup others(10): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0030 |
2 | HG01123.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.585+237_585+251dup others(15): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0007 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.585+236_585+251dup others(16): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.585+233_585+251dup others(19): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0088 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.585+232_585+251dup others(20): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0035 a0013c0011t0001g0064 |
2 | NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.585+230_585+251dup others(22): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.585+229_585+251dup others(23): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0067 |
2 | HG02615.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.585+228_585+251dup others(24): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.585+225_585+251dup others(27): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.585+251_585+252ins others(33): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | CA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(5): Show |
8 | HG01517.hp2 HG02004.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+251delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | CAAA | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(5): Show |
9 | HG01109.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+249_585+251del others(3): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | CAAAAAAA | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
82 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.585+245_585+251del others(7): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | CAAAAAAA others(3): Show |
C | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+242_585+251del others(10): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47503937 | CAAAAAAA others(7): Show |
C | 8 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.585+238_585+251del others(14): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47503937 | |||||||
| chr10:47504004 | C | T | 10 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(7): Show |
14 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+185G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47504004 | |||||||
| chr10:47504080 | T | C | 1 | a0002c0002t0001g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.585+109A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 7/7 | chr10 | 47504080 | |||||||
| chr10:47504307 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.534-67T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504307 | |||||||
| chr10:47504358 | A | G | 10 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(7): Show |
14 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.534-118T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504358 | |||||||
| chr10:47504524 | C | G | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.534-284G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504524 | |||||||
| chr10:47504608 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.534-368A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504608 | |||||||
| chr10:47504700 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.534-460A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504700 | |||||||
| chr10:47504806 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.534-566G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504806 | |||||||
| chr10:47504845 | TC | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.534-606delG | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504845 | |||||||
| chr10:47504846 | C | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0055 |
2 | HG01258.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.534-606G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504846 | |||||||
| chr10:47504846 | C | CT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(19): Show |
29 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.534-607dupA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504846 | |||||||
| chr10:47504846 | CT | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(10): Show |
13 | HG00741.hp1 HG01070.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-607delA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504846 | |||||||
| chr10:47504846 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.534-620_534-607del others(14): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504846 | |||||||
| chr10:47504847 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.534-607A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504847 | |||||||
| chr10:47504902 | G | A | 1 | a0010c0012t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.534-662C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47504902 | |||||||
| chr10:47505000 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.534-760C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505000 | |||||||
| chr10:47505194 | G | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0074 |
2 | NA18747.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.534-954C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505194 | |||||||
| chr10:47505642 | A | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.534-1402T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505642 | |||||||
| chr10:47505666 | T | C | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.534-1426A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505666 | |||||||
| chr10:47505949 | G | C | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533+1599C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505949 | |||||||
| chr10:47505997 | C | G | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533+1551G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47505997 | |||||||
| chr10:47506011 | C | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.533+1537G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506011 | |||||||
| chr10:47506052 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.533+1496C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506052 | |||||||
| chr10:47506059 | T | C | 5 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(2): Show |
7 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.533+1489A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506059 | |||||||
| chr10:47506092 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.533+1456A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506092 | |||||||
| chr10:47506116 | T | G | 7 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(4): Show |
8 | HG01123.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.533+1432A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506116 | |||||||
| chr10:47506117 | G | T | 7 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(4): Show |
8 | HG01123.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.533+1431C>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506117 | |||||||
| chr10:47506161 | T | G | 1 | a0001c0001t0001g0023 | 2 | HG02040.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.533+1387A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506161 | |||||||
| chr10:47506238 | A | C | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.533+1310T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506238 | |||||||
| chr10:47506392 | A | G | 3 | a0001c0001t0001g0063 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG00741.hp2 HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.533+1156T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506392 | |||||||
| chr10:47506433 | T | C | 18 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(15): Show |
25 | HG01123.hp1 HG01192.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.533+1115A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506433 | |||||||
| chr10:47506581 | T | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.533+967A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506581 | |||||||
| chr10:47506703 | G | C | 3 | a0006c0008t0006g0090 a0008c0009t0001g0097 a0011c0010t0001g0093 |
3 | HG01884.hp1 HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.533+845C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506703 | |||||||
| chr10:47506725 | C | T | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.533+823G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506725 | |||||||
| chr10:47506829 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.533+719G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506829 | |||||||
| chr10:47506837 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(18): Show |
49 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.533+711G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506837 | |||||||
| chr10:47506840 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
87 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.533+708G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506840 | |||||||
| chr10:47506905 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.533+643G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506905 | |||||||
| chr10:47506979 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.533+569C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47506979 | |||||||
| chr10:47507083 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.533+465G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507083 | |||||||
| chr10:47507140 | A | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.533+408T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507140 | |||||||
| chr10:47507183 | T | C | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+365A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507183 | |||||||
| chr10:47507236 | T | G | 1 | a0010c0012t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.533+312A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507236 | |||||||
| chr10:47507271 | G | A | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+277C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507271 | |||||||
| chr10:47507347 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.533+201A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 6/7 | chr10 | 47507347 | |||||||
| chr10:47507598 | C | A | 12 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(9): Show |
17 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-15G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507598 | |||||||
| chr10:47507637 | C | A | 12 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(9): Show |
17 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-54G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507637 | |||||||
| chr10:47507787 | G | A | 3 | a0004c0005t0005g0105 a0004c0005t0005g0106 a0004c0005t0005g0107 |
3 | HG01192.hp1 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.498-204C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507787 | |||||||
| chr10:47507842 | C | T | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-259G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507842 | |||||||
| chr10:47507844 | T | G | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-261A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507844 | |||||||
| chr10:47507862 | G | C | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-279C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507862 | |||||||
| chr10:47507864 | T | C | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-281A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47507864 | |||||||
| chr10:47508094 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.498-511G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508094 | |||||||
| chr10:47508095 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.498-512C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508095 | |||||||
| chr10:47508143 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.498-560G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508143 | |||||||
| chr10:47508218 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.498-635G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508218 | |||||||
| chr10:47508222 | A | C | 2 | a0005c0006t0001g0027 a0010c0012t0001g0082 |
3 | HG00741.hp1 HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.498-639T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508222 | |||||||
| chr10:47508307 | A | C | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-724T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508307 | |||||||
| chr10:47508460 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.498-877A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508460 | |||||||
| chr10:47508532 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.498-949C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508532 | |||||||
| chr10:47508585 | G | A | 8 | a0001c0001t0001g0020 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
13 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-1002C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508585 | |||||||
| chr10:47508793 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.498-1210C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508793 | |||||||
| chr10:47508966 | T | A | 29 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(26): Show |
41 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.497+1205A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47508966 | |||||||
| chr10:47509044 | T | C | 3 | a0003c0003t0001g0095 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01361.hp2 HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+1127A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509044 | |||||||
| chr10:47509056 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+1115A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509056 | |||||||
| chr10:47509077 | T | C | 1 | a0003c0003t0001g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.497+1094A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509077 | |||||||
| chr10:47509132 | C | T | 26 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(23): Show |
38 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.497+1039G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509132 | |||||||
| chr10:47509133 | A | G | 28 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(25): Show |
40 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.497+1038T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509133 | |||||||
| chr10:47509259 | A | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+912T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509259 | |||||||
| chr10:47509509 | C | T | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+662G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509509 | |||||||
| chr10:47509535 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.497+636A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509535 | |||||||
| chr10:47509686 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.497+485T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509686 | |||||||
| chr10:47509732 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+439G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509732 | |||||||
| chr10:47509892 | T | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+279A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509892 | |||||||
| chr10:47509937 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.497+234G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509937 | |||||||
| chr10:47509944 | A | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+227T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509944 | |||||||
| chr10:47509956 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.497+215G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509956 | |||||||
| chr10:47509983 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.497+188G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47509983 | |||||||
| chr10:47510045 | C | G | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+126G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47510045 | |||||||
| chr10:47510054 | A | G | 18 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(15): Show |
25 | HG01123.hp1 HG01192.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.497+117T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47510054 | |||||||
| chr10:47510129 | C | T | 1 | a0007c0018t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.497+42G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 5/7 | chr10 | 47510129 | |||||||
| chr10:47510400 | A | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-129T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510400 | |||||||
| chr10:47510537 | A | G | 1 | a0007c0018t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397-266T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510537 | |||||||
| chr10:47510626 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.397-355G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510626 | |||||||
| chr10:47510646 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.397-375A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510646 | |||||||
| chr10:47510657 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-386G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510657 | |||||||
| chr10:47510686 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-415G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510686 | |||||||
| chr10:47510748 | C | T | 29 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(26): Show |
41 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.397-477G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510748 | |||||||
| chr10:47510805 | G | A | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-534C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510805 | |||||||
| chr10:47510829 | C | CA | 18 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0049 others(15): Show |
24 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.397-559dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510829 | |||||||
| chr10:47510877 | AT | A | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-607delA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510877 | |||||||
| chr10:47510912 | TTCTA | T | 3 | a0004c0005t0005g0105 a0004c0005t0005g0106 a0004c0005t0005g0107 |
3 | HG01192.hp1 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.397-645_397-642del others(4): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510912 | |||||||
| chr10:47510915 | TATTA | T | 2 | a0001c0001t0001g0003 a0005c0006t0001g0027 |
3 | HG00741.hp1 HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.397-648_397-645del others(4): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510915 | |||||||
| chr10:47510919 | A | T | 3 | a0004c0005t0005g0105 a0004c0005t0005g0106 a0004c0005t0005g0107 |
3 | HG01192.hp1 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.397-648T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510919 | |||||||
| chr10:47510927 | A | T | 1 | a0002c0002t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.397-656T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510927 | |||||||
| chr10:47510931 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0044 others(8): Show |
18 | HG01106.hp2 HG01175.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.397-660T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510931 | |||||||
| chr10:47510935 | A | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(45): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.397-664T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510935 | |||||||
| chr10:47510935 | AATTT | A | 4 | a0002c0004t0003g0011 a0006c0008t0006g0090 a0010c0012t0001g0082 others(1): Show |
8 | HG01884.hp1 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.397-668_397-665del others(4): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510935 | |||||||
| chr10:47510939 | T | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0031 others(15): Show |
22 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.397-668A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510939 | |||||||
| chr10:47510943 | T | A | 5 | a0001c0001t0001g0070 a0003c0003t0001g0096 a0006c0008t0006g0090 others(2): Show |
5 | HG00735.hp2 HG01884.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-672A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510943 | |||||||
| chr10:47510947 | T | A | 1 | a0011c0010t0001g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.397-676A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510947 | |||||||
| chr10:47510967 | G | A | 1 | a0007c0018t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397-696C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47510967 | |||||||
| chr10:47511034 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.397-763G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511034 | |||||||
| chr10:47511093 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
177 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.397-822T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511093 | |||||||
| chr10:47511180 | T | C | 29 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(26): Show |
41 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.397-909A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511180 | |||||||
| chr10:47511181 | G | A | 11 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(8): Show |
14 | HG01123.hp1 HG01192.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.397-910C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511181 | |||||||
| chr10:47511241 | T | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-970A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511241 | |||||||
| chr10:47511304 | C | T | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-1033G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511304 | |||||||
| chr10:47511357 | C | T | 7 | a0002c0004t0003g0011 a0004c0005t0005g0105 a0004c0005t0005g0106 others(4): Show |
11 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.397-1086G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511357 | |||||||
| chr10:47511588 | T | C | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397-1317A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511588 | |||||||
| chr10:47511606 | T | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-1335A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511606 | |||||||
| chr10:47511662 | T | C | 1 | a0006c0008t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397-1391A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511662 | |||||||
| chr10:47511668 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.397-1397C>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511668 | |||||||
| chr10:47511849 | C | G | 3 | a0001c0001t0001g0044 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.397-1578G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511849 | |||||||
| chr10:47511966 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.397-1695G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47511966 | |||||||
| chr10:47512205 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.397-1934C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512205 | |||||||
| chr10:47512337 | G | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0100 |
2 | NA18984.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.397-2066C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512337 | |||||||
| chr10:47512370 | G | C | 1 | a0002c0002t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.397-2099C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512370 | |||||||
| chr10:47512385 | G | C | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-2114C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512385 | |||||||
| chr10:47512391 | C | T | 3 | a0001c0001t0001g0100 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.397-2120G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512391 | |||||||
| chr10:47512396 | T | G | 3 | a0001c0001t0001g0100 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.397-2125A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512396 | |||||||
| chr10:47512401 | T | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-2130A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512401 | |||||||
| chr10:47512411 | T | G | 2 | a0006c0008t0006g0090 a0008c0009t0001g0097 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.397-2140A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512411 | |||||||
| chr10:47512493 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.397-2222A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512493 | |||||||
| chr10:47512734 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18984.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.397-2463C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512734 | |||||||
| chr10:47512746 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.397-2475C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512746 | |||||||
| chr10:47512767 | TC | T | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-2497delG | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512767 | |||||||
| chr10:47512787 | TG | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0046 |
3 | HG02897.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397-2517delC | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512787 | |||||||
| chr10:47512795 | G | C | 5 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(2): Show |
6 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-2524C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512795 | |||||||
| chr10:47512995 | G | A | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.397-2724C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47512995 | |||||||
| chr10:47513063 | T | C | 19 | a0001c0001t0001g0032 a0002c0002t0001g0018 a0002c0002t0001g0019 others(16): Show |
26 | HG01123.hp1 HG01192.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.397-2792A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513063 | |||||||
| chr10:47513127 | G | A | 2 | a0005c0006t0001g0027 a0010c0012t0001g0082 |
3 | HG00741.hp1 HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.397-2856C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513127 | |||||||
| chr10:47513195 | C | A | 4 | a0003c0003t0001g0016 a0003c0003t0001g0094 a0003c0003t0001g0095 others(1): Show |
6 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.397-2924G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513195 | |||||||
| chr10:47513232 | A | G | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.397-2961T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513232 | |||||||
| chr10:47513374 | G | T | 1 | a0008c0009t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.397-3103C>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513374 | |||||||
| chr10:47513375 | C | T | 1 | a0015c0013t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397-3104G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513375 | |||||||
| chr10:47513411 | A | AC | 3 | a0001c0001t0001g0035 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.397-3141dupG | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513411 | |||||||
| chr10:47513486 | C | T | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-3215G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513486 | |||||||
| chr10:47513536 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0083 others(2): Show |
10 | HG01884.hp1 HG02451.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-3265C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513536 | |||||||
| chr10:47513539 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0083 others(2): Show |
10 | HG01884.hp1 HG02451.hp1 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.397-3268A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513539 | |||||||
| chr10:47513651 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.397-3380T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513651 | |||||||
| chr10:47513667 | C | T | 7 | a0001c0001t0001g0043 a0002c0002t0002g0017 a0002c0002t0002g0029 others(4): Show |
8 | HG01123.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.397-3396G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513667 | |||||||
| chr10:47513705 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG01261.hp2 HG01884.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-3434A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513705 | |||||||
| chr10:47513835 | T | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.397-3564A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513835 | |||||||
| chr10:47513838 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.397-3567C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513838 | |||||||
| chr10:47513868 | C | G | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-3597G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513868 | |||||||
| chr10:47513870 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.397-3599A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47513870 | |||||||
| chr10:47514074 | A | G | 3 | a0001c0001t0001g0035 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.396+3749T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514074 | |||||||
| chr10:47514134 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.396+3689T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514134 | |||||||
| chr10:47514252 | T | TTA | 3 | a0001c0001t0001g0035 a0002c0002t0002g0098 a0008c0009t0001g0097 |
3 | HG02451.hp1 HG02976.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.396+3569_396+3570d others(4): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514252 | |||||||
| chr10:47514333 | T | C | 13 | a0001c0001t0001g0035 a0002c0002t0002g0098 a0003c0003t0001g0015 others(10): Show |
17 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.396+3490A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514333 | |||||||
| chr10:47514363 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.396+3460C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514363 | |||||||
| chr10:47514394 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.396+3429G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514394 | |||||||
| chr10:47514407 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.396+3416T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514407 | |||||||
| chr10:47514468 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0099 |
3 | HG00642.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.396+3355C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514468 | |||||||
| chr10:47514480 | G | A | 1 | a0004c0005t0005g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.396+3343C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514480 | |||||||
| chr10:47514581 | C | G | 4 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0036 others(1): Show |
5 | HG01123.hp1 HG02055.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+3242G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514581 | |||||||
| chr10:47514688 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.396+3135A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514688 | |||||||
| chr10:47514707 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.396+3116G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514707 | |||||||
| chr10:47514761 | G | A | 1 | a0001c0017t0001g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.396+3062C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514761 | |||||||
| chr10:47514773 | C | G | 1 | a0001c0001t0001g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.396+3050G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514773 | |||||||
| chr10:47514839 | C | CTGCAG | 3 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0012c0014t0001g0033 |
5 | HG02055.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.396+2983_396+2984i others(7): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514839 | |||||||
| chr10:47514841 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0012c0014t0001g0033 |
5 | HG02055.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.396+2982G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514841 | |||||||
| chr10:47514886 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.396+2937G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514886 | |||||||
| chr10:47514970 | C | CAAATCTT others(13): Show |
1 | a0001c0001t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.396+2833_396+2852d others(22): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47514970 | |||||||
| chr10:47515096 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.396+2727G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515096 | |||||||
| chr10:47515171 | C | T | 1 | a0002c0002t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.396+2652G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515171 | |||||||
| chr10:47515196 | G | A | 1 | a0007c0018t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.396+2627C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515196 | |||||||
| chr10:47515694 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0010 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.396+2129A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515694 | |||||||
| chr10:47515710 | CCTTTCCA others(12): Show |
C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0002c0002t0002g0036 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.396+2094_396+2112d others(21): Show |
AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515710 | |||||||
| chr10:47515999 | TA | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0035 others(11): Show |
18 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.396+1823delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47515999 | |||||||
| chr10:47516112 | G | C | 9 | a0001c0001t0001g0085 a0002c0002t0002g0098 a0003c0003t0001g0015 others(6): Show |
13 | HG00735.hp2 HG01361.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.396+1711C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516112 | |||||||
| chr10:47516568 | A | C | 3 | a0001c0001t0001g0035 a0002c0002t0002g0036 a0002c0002t0002g0098 |
3 | HG02976.hp1 HG03130.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.396+1255T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516568 | |||||||
| chr10:47516640 | T | C | 11 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0036 others(8): Show |
16 | HG00735.hp2 HG01123.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.396+1183A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516640 | |||||||
| chr10:47516663 | G | A | 1 | a0010c0012t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.396+1160C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516663 | |||||||
| chr10:47516805 | A | G | 25 | a0001c0001t0001g0035 a0002c0002t0001g0018 a0002c0002t0001g0019 others(22): Show |
37 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.396+1018T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516805 | |||||||
| chr10:47516826 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.396+997A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516826 | |||||||
| chr10:47516955 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.396+868A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47516955 | |||||||
| chr10:47517115 | G | A | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.396+708C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517115 | |||||||
| chr10:47517164 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.396+659G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517164 | |||||||
| chr10:47517165 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.396+658C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517165 | |||||||
| chr10:47517268 | C | CT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(6): Show |
13 | HG01175.hp2 HG02055.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.396+554dupA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517268 | |||||||
| chr10:47517268 | CT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(8): Show |
16 | HG00741.hp1 HG01109.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.396+554delA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517268 | |||||||
| chr10:47517485 | T | C | 9 | a0001c0001t0001g0035 a0002c0002t0002g0036 a0003c0003t0001g0015 others(6): Show |
13 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.396+338A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517485 | |||||||
| chr10:47517551 | C | T | 1 | a0002c0002t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.396+272G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517551 | |||||||
| chr10:47517663 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.396+160C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 4/7 | chr10 | 47517663 | |||||||
| chr10:47517865 | T | TA | 6 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0029 others(3): Show |
7 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.362-9dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47517865 | |||||||
| chr10:47517876 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.362-19T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47517876 | |||||||
| chr10:47517879 | A | C | 1 | a0001c0001t0001g0008 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.362-22T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47517879 | |||||||
| chr10:47518336 | T | C | 1 | a0005c0006t0001g0027 | 2 | HG00741.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.362-479A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518336 | |||||||
| chr10:47518411 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0024 |
2 | HG01070.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.362-554A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518411 | |||||||
| chr10:47518461 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
9 | HG00642.hp2 HG01106.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.362-604C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518461 | |||||||
| chr10:47518498 | A | G | 13 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0029 others(10): Show |
18 | HG00735.hp2 HG01123.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.362-641T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518498 | |||||||
| chr10:47518581 | T | G | 7 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(4): Show |
11 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-724A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518581 | |||||||
| chr10:47518765 | A | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0075 a0002c0002t0002g0017 others(11): Show |
19 | HG00735.hp2 HG01123.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.362-908T>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47518765 | |||||||
| chr10:47519088 | A | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0060 others(15): Show |
24 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.362-1231T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519088 | |||||||
| chr10:47519092 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.362-1235C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519092 | |||||||
| chr10:47519175 | G | A | 13 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0029 others(10): Show |
18 | HG00735.hp2 HG01123.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.362-1318C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519175 | |||||||
| chr10:47519239 | G | A | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+1260C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519239 | |||||||
| chr10:47519280 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.361+1219A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519280 | |||||||
| chr10:47519361 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.361+1138C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519361 | |||||||
| chr10:47519372 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.361+1127C>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519372 | |||||||
| chr10:47519422 | T | C | 14 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0029 others(11): Show |
19 | HG00735.hp2 HG00741.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.361+1077A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519422 | |||||||
| chr10:47519440 | T | C | 13 | a0001c0001t0001g0035 a0002c0002t0002g0017 a0002c0002t0002g0029 others(10): Show |
18 | HG00735.hp2 HG01123.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.361+1059A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519440 | |||||||
| chr10:47519467 | C | CA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0100 a0001c0016t0001g0065 others(2): Show |
5 | HG00741.hp1 HG02723.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+1031dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519467 | |||||||
| chr10:47519467 | CA | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0026 others(13): Show |
21 | HG00735.hp2 HG01074.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.361+1031delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519467 | |||||||
| chr10:47519529 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.361+970C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519529 | |||||||
| chr10:47519612 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.361+887A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519612 | |||||||
| chr10:47519841 | T | C | 1 | a0002c0002t0002g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.361+658A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519841 | |||||||
| chr10:47519888 | C | T | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+611G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47519888 | |||||||
| chr10:47520083 | A | G | 1 | a0003c0003t0001g0094 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.361+416T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520083 | |||||||
| chr10:47520088 | T | C | 2 | a0001c0001t0001g0002 a0009c0007t0001g0051 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.361+411A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520088 | |||||||
| chr10:47520091 | T | A | 1 | a0001c0001t0001g0004 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.361+408A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520091 | |||||||
| chr10:47520098 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.361+401A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520098 | |||||||
| chr10:47520239 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361+260C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520239 | |||||||
| chr10:47520314 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 |
7 | NA18980.hp1 NA18980.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+185C>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520314 | |||||||
| chr10:47520328 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0070 |
3 | HG02602.hp2 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.361+171G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 3/7 | chr10 | 47520328 | |||||||
| chr10:47520577 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
9 | HG00642.hp2 HG01106.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-10A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520577 | |||||||
| chr10:47520629 | G | A | 4 | a0005c0006t0001g0027 a0007c0018t0001g0103 a0010c0012t0001g0082 others(1): Show |
5 | HG00741.hp1 HG01109.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-62C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520629 | |||||||
| chr10:47520677 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.293-110A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520677 | |||||||
| chr10:47520759 | G | A | 1 | a0002c0004t0003g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.293-192C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520759 | |||||||
| chr10:47520838 | T | TA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0002c0002t0001g0018 others(10): Show |
21 | HG01109.hp2 HG01123.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.293-272dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520838 | |||||||
| chr10:47520838 | TA | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(12): Show |
18 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-272delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520838 | |||||||
| chr10:47520839 | A | T | 1 | a0013c0011t0001g0064 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.293-272T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520839 | |||||||
| chr10:47520861 | AG | A | 7 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(4): Show |
9 | HG00735.hp2 HG01361.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-295delC | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520861 | |||||||
| chr10:47520862 | G | A | 16 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(13): Show |
24 | HG00741.hp1 HG01109.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-295C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520862 | |||||||
| chr10:47520870 | G | A | 4 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0098 others(1): Show |
5 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-303C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47520870 | |||||||
| chr10:47521100 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.293-533T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521100 | |||||||
| chr10:47521240 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-673G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521240 | |||||||
| chr10:47521288 | A | G | 24 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(21): Show |
36 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-721T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521288 | |||||||
| chr10:47521292 | A | T | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-725T>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521292 | |||||||
| chr10:47521306 | T | C | 3 | a0005c0006t0001g0027 a0010c0012t0001g0082 a0011c0010t0001g0093 |
4 | HG00741.hp1 HG01109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-739A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521306 | |||||||
| chr10:47521366 | C | T | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-799G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521366 | |||||||
| chr10:47521450 | A | G | 1 | a0001c0001t0001g0003 | 2 | NA19066.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.293-883T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521450 | |||||||
| chr10:47521491 | A | G | 2 | a0005c0006t0001g0027 a0010c0012t0001g0082 |
3 | HG00741.hp1 HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.293-924T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521491 | |||||||
| chr10:47521532 | G | C | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-965C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521532 | |||||||
| chr10:47521719 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292+1147C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521719 | |||||||
| chr10:47521786 | C | CT | 4 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0030 others(1): Show |
6 | HG01123.hp2 HG01515.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+1079dupA | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521786 | |||||||
| chr10:47521979 | G | A | 2 | a0001c0001t0001g0006 a0002c0002t0002g0029 |
2 | HG01106.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.292+887C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47521979 | |||||||
| chr10:47522007 | GA | G | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+858delT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522007 | |||||||
| chr10:47522053 | C | T | 1 | a0001c0017t0001g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.292+813G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522053 | |||||||
| chr10:47522067 | G | A | 4 | a0002c0002t0002g0017 a0002c0002t0002g0029 a0002c0002t0002g0098 others(1): Show |
5 | HG01123.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+799C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522067 | |||||||
| chr10:47522156 | C | T | 7 | a0003c0003t0001g0015 a0003c0003t0001g0016 a0003c0003t0001g0091 others(4): Show |
11 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+710G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522156 | |||||||
| chr10:47522180 | A | AG | 5 | a0002c0002t0002g0036 a0005c0006t0001g0027 a0007c0018t0001g0103 others(2): Show |
6 | HG00741.hp1 HG01109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+685dupC | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522180 | |||||||
| chr10:47522210 | T | C | 1 | a0002c0002t0002g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.292+656A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522210 | |||||||
| chr10:47522229 | G | A | 10 | a0001c0001t0001g0001 a0001c0015t0001g0061 a0002c0002t0002g0036 others(7): Show |
14 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.292+637C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522229 | |||||||
| chr10:47522234 | C | A | 5 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(2): Show |
7 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+632G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522234 | |||||||
| chr10:47522244 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.292+622G>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522244 | |||||||
| chr10:47522441 | C | T | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+425G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522441 | |||||||
| chr10:47522495 | T | C | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+371A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522495 | |||||||
| chr10:47522638 | G | GA | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+227dupT | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522638 | |||||||
| chr10:47522641 | T | A | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+225A>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522641 | |||||||
| chr10:47522819 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.292+47T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522819 | |||||||
| chr10:47522837 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.292+29T>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522837 | |||||||
| chr10:47522850 | G | A | 2 | a0002c0004t0003g0011 a0015c0013t0003g0045 |
6 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+16C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 2/7 | chr10 | 47522850 | |||||||
| chr10:47523018 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(3): Show |
14 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-84C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523018 | |||||||
| chr10:47523111 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.224-177G>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523111 | |||||||
| chr10:47523136 | T | G | 1 | a0002c0002t0002g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.223+168A>C | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523136 | |||||||
| chr10:47523144 | G | A | 3 | a0001c0001t0001g0031 a0006c0008t0006g0090 a0008c0009t0001g0097 |
3 | HG01884.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.223+160C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523144 | |||||||
| chr10:47523184 | C | T | 6 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0039 others(3): Show |
8 | HG01192.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+120G>A | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523184 | |||||||
| chr10:47523225 | G | A | 8 | a0002c0002t0002g0036 a0003c0003t0001g0015 a0003c0003t0001g0016 others(5): Show |
12 | HG00735.hp2 HG01361.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.223+79C>T | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523225 | |||||||
| chr10:47523276 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0089 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.223+28C>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523276 | |||||||
| chr10:47523301 | T | C | 2 | a0001c0001t0001g0070 a0010c0012t0001g0082 |
2 | HG02602.hp2 HG02723.hp1 |
splice_region_variant&intron_variant | LOW | c.223+3A>G | AGAP9 | ENSG00000204172.12 | transcript | ENST00000452145.6 | protein_coding | 1/7 | chr10 | 47523301 |