Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79796 |
| ensemblid | ENSG00000086848.15 |
| hgncid | 15672 |
| symbol | ALG9 |
| name | ALG9 alpha-1,2-mannosyltransferase |
| refseq_nuc | NM_024740.2 |
| refseq_prot | NP_079016.2 |
| ensembl_nuc | ENST00000616540.5 |
| ensembl_prot | ENSP00000482437.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 111782195 |
| end | 111871581 |
| strand | - |
| ver | v1.2 |
| region | chr11:111782195-111871581 |
| region5000 | chr11:111777195-111876581 |
| regionname0 | ALG9_chr11_111782195_111871581 |
| regionname5000 | ALG9_chr11_111777195_111876581 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 618 | 203 | 65 | 44 | 62 | 11 | 19 | 49 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0002 | 0/0 | 618 | 97 | 15 | 16 | 50 | 1 | 15 | 38 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0003 | 0/0 | 618 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0004 | 0/0 | 618 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0005 | 0/0 | 618 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0006 | 0/0 | 618 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| a0007 | 0/0 | 618 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | MASRG others(613): Show |
chr11 | 111777195 | 111876581 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1854 | 198 | 62 | 44 | 60 | 11 | 19 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0001c0005 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0001c0006 | 0/0 | 1854 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0001c0010 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0002c0002 | 0/0 | 1854 | 97 | 15 | 16 | 50 | 1 | 15 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0003c0003 | 0/0 | 1854 | 6 | 6 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0004c0004 | 0/0 | 1854 | 4 | 0 | 0 | 4 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0005c0007 | 0/0 | 1854 | 2 | 1 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0006c0008 | 0/0 | 1854 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 | ||
| a0007c0009 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | ATGGC others(1849): Show |
chr11 | 111777195 | 111876581 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6158 | 6 | 5 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0002 | 1/1 | 6158 | 71 | 5 | 17 | 31 | 3 | 13 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0003 | 0/0 | 6145 | 62 | 12 | 17 | 23 | 5 | 5 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6140): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0004 | 0/0 | 6157 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6152): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0005 | 0/0 | 6159 | 16 | 12 | 4 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6154): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0006 | 0/0 | 6158 | 4 | 4 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0007 | 0/0 | 6145 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6140): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0008 | 0/0 | 6144 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6139): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0009 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0010 | 0/0 | 6159 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6154): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0011 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0012 | 0/0 | 6158 | 3 | 3 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0013 | 0/0 | 6158 | 2 | 0 | 0 | 0 | 1 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0014 | 0/0 | 6144 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6139): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0015 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0016 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0017 | 0/0 | 6145 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6140): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0018 | 0/0 | 6158 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0019 | 0/0 | 6145 | 2 | 0 | 1 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6140): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0020 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0022 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0023 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6139): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0024 | 0/0 | 6158 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0025 | 0/0 | 6158 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0027 | 0/0 | 6159 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6154): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0028 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0030 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0001t0031 | 0/0 | 6159 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6154): Show |
chr11 | 111777195 | 111876581 |
| a0001c0005t0011 | 0/0 | 6158 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0001c0006t0003 | 0/0 | 6145 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6140): Show |
chr11 | 111777195 | 111876581 |
| a0001c0010t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0002c0002t0001 | 0/0 | 6158 | 74 | 2 | 15 | 42 | 1 | 14 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0002c0002t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0002c0002t0004 | 0/0 | 6157 | 19 | 12 | 1 | 6 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6152): Show |
chr11 | 111777195 | 111876581 |
| a0002c0002t0021 | 0/0 | 6158 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0002c0002t0029 | 0/0 | 6158 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0003c0003t0001 | 0/0 | 6158 | 4 | 4 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0003c0003t0004 | 0/0 | 6157 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6152): Show |
chr11 | 111777195 | 111876581 |
| a0003c0003t0026 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0004c0004t0001 | 0/0 | 6158 | 4 | 0 | 0 | 4 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0005c0007t0009 | 0/0 | 6158 | 2 | 1 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0006c0008t0001 | 0/0 | 6158 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| a0007c0009t0002 | 0/0 | 6158 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | GTCTT others(6153): Show |
chr11 | 111777195 | 111876581 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0014g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0016g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0017g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0017g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0018g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0018g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0019g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0019g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0023g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0024g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0027g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0030g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0001t0031g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0005t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0005t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0006t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0006t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0001c0010t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0021g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0002c0002t0029g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0003c0003t0026g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0004c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0004c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0004c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0004c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0005c0007t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0005c0007t0009g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0006c0008t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| a0007c0009t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0013 | g0163 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0257 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0210 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00597 | hp1 | a0004 | c0004 | t0001 | g0099 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00621 | hp2 | a0002 | c0002 | t0021 | g0068 | EAS | CHS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0302 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00735 | hp1 | a0001 | c0001 | t0017 | g0234 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00735 | hp2 | a0006 | c0008 | t0001 | g0057 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0301 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0121 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01256 | hp2 | a0001 | c0001 | t0014 | g0225 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0243 | EUR | IBS | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0124 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0106 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0231 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01952 | hp1 | a0005 | c0007 | t0009 | g0286 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01978 | hp1 | a0001 | c0001 | t0019 | g0220 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01993 | hp1 | a0002 | c0002 | t0004 | g0075 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0148 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0264 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02145 | hp2 | a0001 | c0005 | t0011 | g0200 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | CDX | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02257 | hp2 | a0002 | c0002 | t0004 | g0100 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0126 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02300 | hp1 | a0001 | c0001 | t0014 | g0224 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0081 | AMR | PEL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02523 | hp1 | a0001 | c0001 | t0025 | g0133 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0108 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0101 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02630 | hp1 | a0001 | c0005 | t0011 | g0130 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02630 | hp2 | a0001 | c0001 | t0031 | g0112 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0104 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0146 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0086 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0197 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0127 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02976 | hp1 | a0003 | c0003 | t0004 | g0122 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0128 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03130 | hp1 | a0001 | c0001 | t0020 | g0107 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03130 | hp2 | a0001 | c0001 | t0027 | g0113 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03139 | hp1 | a0007 | c0009 | t0002 | g0132 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0087 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0140 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03516 | hp1 | a0005 | c0007 | t0009 | g0284 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03579 | hp2 | a0001 | c0001 | t0030 | g0109 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03834 | hp1 | a0002 | c0002 | t0029 | g0082 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0255 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0151 | SAS | BEB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | STU | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18943 | hp1 | a0001 | c0006 | t0003 | g0258 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18954 | hp2 | a0002 | c0002 | t0004 | g0059 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18968 | hp2 | a0004 | c0004 | t0001 | g0098 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18969 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18974 | hp2 | a0001 | c0001 | t0008 | g0265 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18978 | hp1 | a0002 | c0002 | t0021 | g0011 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18982 | hp2 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18985 | hp2 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18989 | hp2 | a0004 | c0004 | t0001 | g0096 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19000 | hp1 | a0001 | c0006 | t0003 | g0262 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19002 | hp2 | a0001 | c0001 | t0019 | g0244 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19010 | hp1 | a0002 | c0002 | t0004 | g0054 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19043 | hp1 | a0003 | c0003 | t0026 | g0141 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19076 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19084 | hp2 | a0004 | c0004 | t0001 | g0097 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0125 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ASW | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20129 | hp2 | a0001 | c0010 | t0002 | g0206 | AFR | ASW | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20752 | hp2 | a0001 | c0001 | t0017 | g0272 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0273 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02109 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0102 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0105 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | ACB | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03471 | hp1 | a0001 | c0001 | t0028 | g0012 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0123 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | USA | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA21309 | hp1 | a0001 | c0001 | t0023 | g0270 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0300 | AFR | LWK | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0204 | REF | REF | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0136 | REF | REF | ALG9_chr11_111777195_111876581 | ALG9 | chr11 | 111777195 | 111876581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111786462 | A | G | 1 | a0007 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1792T>C | p.Tyr598His | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1891/6158 | 1792/1857 | 598/618 | chr11 | 111786462 | |||
| chr11:111809772 | A | C | 1 | a0004 | 4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1604T>G | p.Ile535Ser | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/15 | 1703/6158 | 1604/1857 | 535/618 | chr11 | 111809772 | |||
| chr11:111836229 | G | A | 1 | a0006 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1538C>T | p.Pro513Leu | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/15 | 1637/6158 | 1538/1857 | 513/618 | chr11 | 111836229 | |||
| chr11:111853410 | C | T | 3 | a0002 a0004 a0006 |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
missense_variant | MODERATE | c.865G>A | p.Val289Ile | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/15 | 964/6158 | 865/1857 | 289/618 | chr11 | 111853410 | |||
| chr11:111853460 | T | C | 1 | a0005 | 2 | HG01952.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.815A>G | p.Tyr272Cys | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/15 | 914/6158 | 815/1857 | 272/618 | chr11 | 111853460 | |||
| chr11:111853674 | G | A | 1 | a0003 | 6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.764C>T | p.Ser255Leu | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/15 | 863/6158 | 764/1857 | 255/618 | chr11 | 111853674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111786460 | G | A | 1 | a0001c0005 | 2 | HG02145.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.1794C>T | p.Tyr598Tyr | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1893/6158 | 1794/1857 | 598/618 | chr11 | 111786460 | |||
| chr11:111809717 | G | A | 1 | a0001c0006 | 2 | NA18943.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.1659C>T | p.Pro553Pro | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/15 | 1758/6158 | 1659/1857 | 553/618 | chr11 | 111809717 | |||
| chr11:111837557 | G | A | 1 | a0001c0010 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1383C>T | p.Thr461Thr | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/15 | 1482/6158 | 1383/1857 | 461/618 | chr11 | 111837557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111782432 | C | T | 1 | a0001c0001t0015 | 2 | HG02886.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3965G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3965 | chr11 | 111782432 | ||||||
| chr11:111782647 | T | G | 2 | a0001c0001t0009 a0005c0007t0009 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3750A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3750 | chr11 | 111782647 | ||||||
| chr11:111782899 | C | T | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3498 | chr11 | 111782899 | ||||||
| chr11:111782900 | G | A | 1 | a0001c0001t0025 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3497C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3497 | chr11 | 111782900 | ||||||
| chr11:111782926 | T | C | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3471A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3471 | chr11 | 111782926 | ||||||
| chr11:111782974 | A | G | 1 | a0003c0003t0026 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3423T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3423 | chr11 | 111782974 | ||||||
| chr11:111783054 | T | C | 1 | a0001c0001t0027 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3343A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 3343 | chr11 | 111783054 | ||||||
| chr11:111783505 | C | T | 1 | a0001c0001t0028 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2892G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2892 | chr11 | 111783505 | ||||||
| chr11:111783657 | C | G | 1 | a0001c0001t0028 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2740G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2740 | chr11 | 111783657 | ||||||
| chr11:111783896 | CTATAT | C | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(5): Show |
77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2500delATAT others(1): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2496 | chr11 | 111783896 | ||||||
| chr11:111783917 | GT | G | 3 | a0001c0001t0004 a0002c0002t0004 a0003c0003t0004 |
21 | HG01891.hp1 HG01993.hp1 HG02055.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2479delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2479 | chr11 | 111783917 | ||||||
| chr11:111783922 | T | A | 1 | a0001c0001t0016 | 2 | HG02922.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2475A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2475 | chr11 | 111783922 | ||||||
| chr11:111783923 | T | A | 7 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0016 others(4): Show |
11 | HG00733.hp2 HG01099.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2474A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2474 | chr11 | 111783923 | ||||||
| chr11:111783923 | T | TA | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(3): Show |
74 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2473_*2474insT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2473 | chr11 | 111783923 | ||||||
| chr11:111783924 | T | A | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(28): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2473A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2473 | chr11 | 111783924 | ||||||
| chr11:111783940 | C | A | 1 | a0002c0002t0004 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2457G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2457 | chr11 | 111783940 | ||||||
| chr11:111783945 | TGACAAAA others(2): Show |
T | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(5): Show |
77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2443_*2451delTGTT others(5): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2443 | chr11 | 111783945 | ||||||
| chr11:111784167 | T | G | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2230A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 2230 | chr11 | 111784167 | ||||||
| chr11:111784457 | C | T | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1940G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1940 | chr11 | 111784457 | ||||||
| chr11:111784549 | C | T | 1 | a0001c0001t0013 | 2 | HG00099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1848 | chr11 | 111784549 | ||||||
| chr11:111784717 | C | A | 1 | a0001c0001t0017 | 2 | HG00735.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1680G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1680 | chr11 | 111784717 | ||||||
| chr11:111784717 | C | CA | 3 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0031 |
18 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1679dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1679 | chr11 | 111784717 | ||||||
| chr11:111784726 | A | G | 1 | a0001c0001t0007 | 3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1671 | chr11 | 111784726 | ||||||
| chr11:111784773 | T | G | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1624A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1624 | chr11 | 111784773 | ||||||
| chr11:111784790 | G | A | 2 | a0001c0001t0018 a0001c0001t0028 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1607C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1607 | chr11 | 111784790 | ||||||
| chr11:111784977 | G | C | 1 | a0001c0001t0019 | 2 | HG01978.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1420C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1420 | chr11 | 111784977 | ||||||
| chr11:111784995 | A | G | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1402T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1402 | chr11 | 111784995 | ||||||
| chr11:111785056 | C | T | 1 | a0001c0001t0022 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1341 | chr11 | 111785056 | ||||||
| chr11:111785177 | G | A | 3 | a0001c0001t0006 a0001c0001t0020 a0001c0001t0030 |
7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1220C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 1220 | chr11 | 111785177 | ||||||
| chr11:111785426 | G | A | 1 | a0002c0002t0021 | 2 | HG00621.hp2 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*971C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 971 | chr11 | 111785426 | ||||||
| chr11:111785609 | T | C | 1 | a0002c0002t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 788 | chr11 | 111785609 | ||||||
| chr11:111785728 | G | T | 1 | a0001c0001t0006 | 4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*669C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 669 | chr11 | 111785728 | ||||||
| chr11:111786074 | T | C | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 323 | chr11 | 111786074 | ||||||
| chr11:111786388 | G | A | 1 | a0001c0001t0031 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 15/15 | 9 | chr11 | 111786388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:111786568 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1734-48A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786568 | |||||||
| chr11:111786735 | A | C | 1 | a0001c0001t0015g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1734-215T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786735 | |||||||
| chr11:111786757 | A | C | 1 | a0001c0001t0003g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1734-237T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111786757 | |||||||
| chr11:111787042 | A | G | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1734-522T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787042 | |||||||
| chr11:111787126 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1734-606G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787126 | |||||||
| chr11:111787310 | G | A | 2 | a0001c0001t0003g0215 a0001c0001t0008g0216 |
2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1734-790C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787310 | |||||||
| chr11:111787419 | C | G | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-899G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787419 | |||||||
| chr11:111787419 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-899G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787419 | |||||||
| chr11:111787450 | T | A | 1 | a0002c0002t0001g0295 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1734-930A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787450 | |||||||
| chr11:111787451 | A | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-931T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787451 | |||||||
| chr11:111787488 | G | A | 1 | a0002c0002t0004g0086 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1734-968C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787488 | |||||||
| chr11:111787557 | C | T | 5 | a0001c0001t0011g0129 a0001c0001t0016g0127 a0001c0001t0016g0128 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-1037G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787557 | |||||||
| chr11:111787735 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-1215C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787735 | |||||||
| chr11:111787939 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1734-1419A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111787939 | |||||||
| chr11:111788159 | C | A | 1 | a0002c0002t0001g0038 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1734-1639G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788159 | |||||||
| chr11:111788188 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0195 |
3 | HG01255.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1734-1668C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788188 | |||||||
| chr11:111788264 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1734-1744G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788264 | |||||||
| chr11:111788358 | A | G | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734-1838T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788358 | |||||||
| chr11:111788387 | T | C | 76 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0210 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1734-1867A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111788387 | |||||||
| chr11:111789000 | C | T | 7 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1734-2480G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789000 | |||||||
| chr11:111789019 | TC | T | 97 | a0001c0001t0001g0212 a0001c0001t0004g0110 a0002c0002t0001g0001 others(94): Show |
101 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1734-2500delG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789019 | |||||||
| chr11:111789020 | C | T | 111 | a0001c0001t0001g0014 a0001c0001t0003g0010 a0001c0001t0003g0013 others(108): Show |
113 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1734-2500G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789020 | |||||||
| chr11:111789070 | T | C | 4 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0298 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-2550A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789070 | |||||||
| chr11:111789103 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1734-2583T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789103 | |||||||
| chr11:111789200 | A | G | 230 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(227): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-2680T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789200 | |||||||
| chr11:111789285 | T | C | 2 | a0001c0001t0003g0263 a0001c0001t0003g0277 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1734-2765A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789285 | |||||||
| chr11:111789286 | C | G | 1 | a0002c0002t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734-2766G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789286 | |||||||
| chr11:111789296 | T | A | 4 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 others(1): Show |
4 | HG00733.hp2 HG01099.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-2776A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789296 | |||||||
| chr11:111789515 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-2995G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789515 | |||||||
| chr11:111789653 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1734-3133A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789653 | |||||||
| chr11:111789718 | G | A | 3 | a0001c0001t0002g0159 a0001c0001t0002g0165 a0001c0001t0002g0192 |
3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1734-3198C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789718 | |||||||
| chr11:111789743 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1734-3223G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789743 | |||||||
| chr11:111789819 | C | CA | 6 | a0002c0002t0001g0003 a0002c0002t0001g0037 a0002c0002t0001g0038 others(3): Show |
7 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1734-3300dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789819 | |||||||
| chr11:111789988 | T | A | 1 | a0002c0002t0001g0048 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1734-3468A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111789988 | |||||||
| chr11:111790201 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-3681C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790201 | |||||||
| chr11:111790269 | G | A | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1734-3749C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790269 | |||||||
| chr11:111790626 | T | C | 1 | a0001c0001t0003g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1734-4106A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790626 | |||||||
| chr11:111790663 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-4143C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790663 | |||||||
| chr11:111790731 | C | G | 204 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0003g0010 others(201): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1734-4211G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790731 | |||||||
| chr11:111790962 | A | T | 230 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(227): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-4442T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111790962 | |||||||
| chr11:111791000 | C | G | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-4480G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791000 | |||||||
| chr11:111791385 | C | T | 92 | a0001c0001t0001g0212 a0001c0001t0004g0110 a0002c0002t0001g0001 others(89): Show |
96 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1734-4865G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791385 | |||||||
| chr11:111791429 | C | T | 6 | a0002c0002t0001g0055 a0002c0002t0001g0061 a0002c0002t0001g0078 others(3): Show |
6 | HG02056.hp2 HG02155.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734-4909G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791429 | |||||||
| chr11:111791600 | T | C | 1 | a0001c0001t0006g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1734-5080A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791600 | |||||||
| chr11:111791840 | C | A | 75 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0210 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1734-5320G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791840 | |||||||
| chr11:111791849 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1734-5329A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791849 | |||||||
| chr11:111791860 | G | A | 22 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(19): Show |
22 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1734-5340C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791860 | |||||||
| chr11:111791887 | T | C | 13 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(10): Show |
13 | HG02257.hp1 HG02258.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1734-5367A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791887 | |||||||
| chr11:111791980 | G | A | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-5460C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111791980 | |||||||
| chr11:111792190 | C | T | 1 | a0001c0001t0017g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1734-5670G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792190 | |||||||
| chr11:111792194 | A | G | 19 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(16): Show |
19 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1734-5674T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792194 | |||||||
| chr11:111792436 | C | T | 19 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(16): Show |
19 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1734-5916G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792436 | |||||||
| chr11:111792504 | C | T | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-5984G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792504 | |||||||
| chr11:111792979 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1734-6459A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111792979 | |||||||
| chr11:111793193 | A | G | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1734-6673T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793193 | |||||||
| chr11:111793322 | T | C | 2 | a0001c0001t0003g0281 a0001c0001t0003g0283 |
2 | NA18977.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1734-6802A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793322 | |||||||
| chr11:111793453 | A | C | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1734-6933T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793453 | |||||||
| chr11:111793479 | G | A | 2 | a0001c0001t0002g0135 a0001c0001t0002g0202 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1734-6959C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793479 | |||||||
| chr11:111793496 | T | C | 3 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0299 |
3 | HG02723.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1734-6976A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793496 | |||||||
| chr11:111793556 | G | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7036C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793556 | |||||||
| chr11:111793557 | C | G | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1734-7037G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793557 | |||||||
| chr11:111793558 | A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7038T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793558 | |||||||
| chr11:111793589 | T | G | 1 | a0002c0002t0004g0026 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1734-7069A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793589 | |||||||
| chr11:111793632 | G | A | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-7112C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793632 | |||||||
| chr11:111793633 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1734-7113A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793633 | |||||||
| chr11:111793677 | C | T | 75 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0210 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1734-7157G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793677 | |||||||
| chr11:111793693 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-7173C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793693 | |||||||
| chr11:111793757 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1734-7237C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793757 | |||||||
| chr11:111793760 | C | CA | 23 | a0001c0001t0002g0191 a0001c0001t0003g0259 a0001c0001t0005g0005 others(20): Show |
24 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1734-7241dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111793760 | |||||||
| chr11:111794085 | C | T | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-7565G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794085 | |||||||
| chr11:111794086 | G | A | 1 | a0001c0001t0003g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1734-7566C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794086 | |||||||
| chr11:111794181 | A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-7661T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794181 | |||||||
| chr11:111794681 | C | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1734-8161G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794681 | |||||||
| chr11:111794758 | G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1734-8238C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794758 | |||||||
| chr11:111794956 | G | A | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734-8436C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111794956 | |||||||
| chr11:111795007 | G | A | 21 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(18): Show |
21 | HG00733.hp2 HG01099.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1734-8487C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795007 | |||||||
| chr11:111795068 | AAG | A | 8 | a0001c0001t0009g0285 a0001c0001t0011g0129 a0001c0001t0016g0127 others(5): Show |
8 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1734-8550_1734-854 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795068 | |||||||
| chr11:111795350 | G | A | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-8830C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795350 | |||||||
| chr11:111795382 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0158 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1734-8862C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795382 | |||||||
| chr11:111795391 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0006g0142 a0001c0001t0006g0143 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734-8871C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795391 | |||||||
| chr11:111795404 | C | T | 230 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(227): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1734-8884G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795404 | |||||||
| chr11:111795510 | G | A | 2 | a0002c0002t0001g0018 a0002c0002t0001g0089 |
2 | HG00609.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1734-8990C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795510 | |||||||
| chr11:111795548 | A | C | 1 | a0001c0001t0002g0008 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1734-9028T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795548 | |||||||
| chr11:111795686 | C | T | 2 | a0002c0002t0001g0039 a0002c0002t0001g0074 |
2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1734-9166G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795686 | |||||||
| chr11:111795831 | A | G | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734-9311T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795831 | |||||||
| chr11:111795945 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1734-9425G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795945 | |||||||
| chr11:111795992 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1734-9472G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111795992 | |||||||
| chr11:111796617 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1734-10097C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796617 | |||||||
| chr11:111796790 | G | A | 1 | a0001c0001t0013g0151 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1734-10270C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796790 | |||||||
| chr11:111796940 | T | G | 1 | a0002c0002t0021g0068 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1734-10420A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796940 | |||||||
| chr11:111796951 | C | T | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | NA18977.hp1 NA19054.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734-10431G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796951 | |||||||
| chr11:111796965 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1734-10445C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111796965 | |||||||
| chr11:111797231 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1734-10711A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797231 | |||||||
| chr11:111797461 | T | C | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1734-10941A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797461 | |||||||
| chr11:111797463 | C | T | 1 | a0002c0002t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1734-10943G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797463 | |||||||
| chr11:111797498 | C | T | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1734-10978G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797498 | |||||||
| chr11:111797532 | A | C | 76 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0210 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1734-11012T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797532 | |||||||
| chr11:111797553 | G | A | 13 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(10): Show |
14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1734-11033C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797553 | |||||||
| chr11:111797751 | C | T | 2 | a0001c0001t0003g0214 a0001c0001t0003g0261 |
2 | NA18968.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1734-11231G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797751 | |||||||
| chr11:111797861 | C | T | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1734-11341G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797861 | |||||||
| chr11:111797888 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1734-11368C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797888 | |||||||
| chr11:111797888 | G | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734-11368C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797888 | |||||||
| chr11:111797895 | A | T | 209 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0003g0010 others(206): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1734-11375T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111797895 | |||||||
| chr11:111798081 | C | T | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1734-11561G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798081 | |||||||
| chr11:111798152 | G | C | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+11491C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798152 | |||||||
| chr11:111798190 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+11453C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798190 | |||||||
| chr11:111798535 | T | A | 2 | a0001c0001t0001g0212 a0002c0002t0001g0031 |
2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1733+11108A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798535 | |||||||
| chr11:111798911 | C | T | 1 | a0002c0002t0004g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1733+10732G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111798911 | |||||||
| chr11:111799038 | A | G | 21 | a0001c0001t0001g0014 a0001c0001t0005g0005 a0001c0001t0005g0111 others(18): Show |
22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1733+10605T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799038 | |||||||
| chr11:111799335 | T | C | 209 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0003g0010 others(206): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1733+10308A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799335 | |||||||
| chr11:111799358 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0256 |
3 | HG02647.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1733+10285C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799358 | |||||||
| chr11:111799436 | C | T | 1 | a0001c0001t0005g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1733+10207G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799436 | |||||||
| chr11:111799446 | C | CT | 74 | a0001c0001t0001g0014 a0001c0001t0003g0010 a0001c0001t0003g0013 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1733+10196dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799446 | |||||||
| chr11:111799446 | CT | C | 29 | a0001c0001t0002g0131 a0001c0001t0002g0171 a0001c0001t0002g0184 others(26): Show |
30 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1733+10196delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799446 | |||||||
| chr11:111799551 | T | C | 1 | a0001c0001t0003g0259 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1733+10092A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799551 | |||||||
| chr11:111799590 | C | T | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+10053G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111799590 | |||||||
| chr11:111800134 | A | C | 97 | a0001c0001t0004g0110 a0002c0002t0001g0001 a0002c0002t0001g0003 others(94): Show |
101 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1733+9509T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800134 | |||||||
| chr11:111800256 | G | A | 99 | a0001c0001t0004g0110 a0002c0002t0001g0001 a0002c0002t0001g0003 others(96): Show |
103 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1733+9387C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800256 | |||||||
| chr11:111800296 | T | C | 79 | a0001c0001t0001g0212 a0001c0001t0002g0167 a0001c0001t0002g0175 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1733+9347A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800296 | |||||||
| chr11:111800307 | T | C | 1 | a0002c0002t0001g0053 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1733+9336A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800307 | |||||||
| chr11:111800467 | C | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(10): Show |
14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+9176G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800467 | |||||||
| chr11:111800667 | A | G | 1 | a0001c0001t0003g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1733+8976T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800667 | |||||||
| chr11:111800766 | G | T | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+8877C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800766 | |||||||
| chr11:111800819 | A | G | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+8824T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800819 | |||||||
| chr11:111800996 | T | C | 4 | a0001c0001t0004g0110 a0002c0002t0004g0021 a0002c0002t0004g0101 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+8647A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111800996 | |||||||
| chr11:111801001 | C | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(10): Show |
14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1733+8642G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801001 | |||||||
| chr11:111801093 | T | C | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+8550A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801093 | |||||||
| chr11:111801287 | T | G | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1733+8356A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801287 | |||||||
| chr11:111801579 | G | C | 1 | a0001c0001t0003g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1733+8064C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801579 | |||||||
| chr11:111801622 | G | C | 2 | a0002c0002t0021g0011 a0002c0002t0021g0068 |
2 | HG00621.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1733+8021C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801622 | |||||||
| chr11:111801758 | C | G | 2 | a0001c0001t0003g0230 a0001c0001t0003g0232 |
2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1733+7885G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111801758 | |||||||
| chr11:111802144 | C | T | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+7499G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802144 | |||||||
| chr11:111802151 | T | C | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+7492A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802151 | |||||||
| chr11:111802296 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1733+7347T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802296 | |||||||
| chr11:111802386 | C | G | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1733+7257G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802386 | |||||||
| chr11:111802476 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1733+7167G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802476 | |||||||
| chr11:111802815 | A | G | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1733+6828T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111802815 | |||||||
| chr11:111803004 | G | A | 1 | a0002c0002t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1733+6639C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803004 | |||||||
| chr11:111803099 | T | G | 4 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0298 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+6544A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803099 | |||||||
| chr11:111803110 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1733+6533A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803110 | |||||||
| chr11:111803198 | A | C | 7 | a0002c0002t0001g0043 a0002c0002t0001g0049 a0002c0002t0001g0066 others(4): Show |
7 | HG01192.hp1 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1733+6445T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803198 | |||||||
| chr11:111803334 | T | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+6309A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803334 | |||||||
| chr11:111803503 | GA | G | 297 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(294): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1733+6139delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803503 | |||||||
| chr11:111803562 | C | T | 1 | a0001c0010t0002g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1733+6081G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803562 | |||||||
| chr11:111803729 | A | G | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+5914T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111803729 | |||||||
| chr11:111804082 | AAG | A | 8 | a0001c0001t0009g0285 a0001c0001t0011g0129 a0001c0001t0016g0127 others(5): Show |
8 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1733+5559_1733+556 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804082 | |||||||
| chr11:111804132 | CA | C | 220 | a0001c0001t0001g0212 a0001c0001t0001g0287 a0001c0001t0001g0291 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1733+5510delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804132 | |||||||
| chr11:111804132 | CAA | C | 9 | a0001c0001t0001g0014 a0001c0001t0010g0289 a0001c0001t0015g0146 others(6): Show |
9 | HG02735.hp1 HG02886.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733+5509_1733+551 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804132 | |||||||
| chr11:111804159 | C | T | 20 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(17): Show |
20 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1733+5484G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804159 | |||||||
| chr11:111804174 | A | G | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+5469T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804174 | |||||||
| chr11:111804209 | A | T | 1 | a0001c0001t0003g0279 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1733+5434T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804209 | |||||||
| chr11:111804242 | T | G | 1 | a0001c0001t0003g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1733+5401A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804242 | |||||||
| chr11:111804368 | A | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1733+5275T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804368 | |||||||
| chr11:111804583 | C | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1733+5060G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804583 | |||||||
| chr11:111804901 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1733+4742C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804901 | |||||||
| chr11:111804911 | A | G | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+4732T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804911 | |||||||
| chr11:111804932 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1733+4711A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804932 | |||||||
| chr11:111804950 | C | T | 4 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+4693G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111804950 | |||||||
| chr11:111805145 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1733+4498T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805145 | |||||||
| chr11:111805274 | G | C | 3 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0074 |
3 | HG01109.hp1 HG03490.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1733+4369C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805274 | |||||||
| chr11:111805331 | G | A | 1 | a0007c0009t0002g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1733+4312C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805331 | |||||||
| chr11:111805602 | A | G | 2 | a0002c0002t0001g0053 a0006c0008t0001g0057 |
2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1733+4041T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805602 | |||||||
| chr11:111805846 | G | A | 2 | a0001c0006t0003g0258 a0001c0006t0003g0262 |
2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1733+3797C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805846 | |||||||
| chr11:111805905 | G | C | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1733+3738C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111805905 | |||||||
| chr11:111806150 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1733+3493C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806150 | |||||||
| chr11:111806328 | T | G | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1733+3315A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806328 | |||||||
| chr11:111806345 | C | T | 1 | a0001c0001t0003g0236 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1733+3298G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806345 | |||||||
| chr11:111806393 | T | A | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+3250A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806393 | |||||||
| chr11:111806401 | G | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+3242C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806401 | |||||||
| chr11:111806496 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1733+3147C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806496 | |||||||
| chr11:111806543 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+3100G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806543 | |||||||
| chr11:111806971 | A | T | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1733+2672T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806971 | |||||||
| chr11:111806973 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+2670T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111806973 | |||||||
| chr11:111807258 | T | A | 98 | a0001c0001t0004g0110 a0002c0002t0001g0001 a0002c0002t0001g0003 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1733+2385A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807258 | |||||||
| chr11:111807661 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1733+1982C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807661 | |||||||
| chr11:111807698 | A | AGGTG | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1733+1941_1733+194 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807698 | |||||||
| chr11:111807734 | G | A | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1733+1909C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807734 | |||||||
| chr11:111807777 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+1866G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807777 | |||||||
| chr11:111807800 | A | T | 131 | a0001c0001t0001g0014 a0001c0001t0002g0209 a0001c0001t0004g0110 others(128): Show |
136 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1733+1843T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111807800 | |||||||
| chr11:111808023 | T | C | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1733+1620A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808023 | |||||||
| chr11:111808047 | T | C | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1733+1596A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808047 | |||||||
| chr11:111808538 | C | T | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1733+1105G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808538 | |||||||
| chr11:111808634 | G | A | 1 | a0001c0001t0019g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1733+1009C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808634 | |||||||
| chr11:111808645 | T | C | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1733+998A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808645 | |||||||
| chr11:111808791 | C | G | 1 | a0004c0004t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1733+852G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808791 | |||||||
| chr11:111808845 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1733+798G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808845 | |||||||
| chr11:111808850 | A | T | 6 | a0002c0002t0001g0015 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
6 | HG00609.hp2 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.1733+793T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808850 | |||||||
| chr11:111808907 | C | G | 1 | a0001c0001t0003g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1733+736G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111808907 | |||||||
| chr11:111809050 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+593G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809050 | |||||||
| chr11:111809223 | G | T | 1 | a0001c0001t0002g0008 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1733+420C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809223 | |||||||
| chr11:111809229 | A | G | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1733+414T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809229 | |||||||
| chr11:111809251 | G | A | 9 | a0001c0001t0002g0178 a0001c0001t0009g0285 a0001c0001t0011g0129 others(6): Show |
9 | HG01952.hp1 HG02145.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733+392C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809251 | |||||||
| chr11:111809403 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1733+240C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809403 | |||||||
| chr11:111809407 | G | A | 1 | a0001c0001t0003g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1733+236C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809407 | |||||||
| chr11:111809517 | T | TAC | 14 | a0001c0001t0002g0157 a0001c0001t0003g0268 a0001c0001t0010g0288 others(11): Show |
14 | HG01515.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1733+124_1733+125d others(4): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | |||||||
| chr11:111809517 | T | TACAC | 113 | a0001c0001t0001g0014 a0001c0001t0004g0110 a0001c0001t0005g0005 others(110): Show |
118 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1733+122_1733+125d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | |||||||
| chr11:111809517 | T | TACACAC | 7 | a0001c0001t0005g0118 a0001c0001t0005g0121 a0002c0002t0001g0031 others(4): Show |
7 | HG00597.hp1 HG00738.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733+120_1733+125d others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | |||||||
| chr11:111809517 | T | TACACACA others(3): Show |
1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1733+116_1733+125d others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | |||||||
| chr11:111809517 | T | TACACACA others(5): Show |
2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1733+114_1733+125d others(14): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809517 | |||||||
| chr11:111809605 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1733+38G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 14/14 | chr11 | 111809605 | |||||||
| chr11:111809899 | T | C | 1 | a0002c0002t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1603-126A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809899 | |||||||
| chr11:111809909 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-136C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809909 | |||||||
| chr11:111809962 | C | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-189G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111809962 | |||||||
| chr11:111810181 | C | T | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-408G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810181 | |||||||
| chr11:111810282 | T | C | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1603-509A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810282 | |||||||
| chr11:111810320 | G | C | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1603-547C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810320 | |||||||
| chr11:111810370 | T | A | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-597A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810370 | |||||||
| chr11:111810376 | C | G | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-603G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810376 | |||||||
| chr11:111810544 | C | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-771G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111810544 | |||||||
| chr11:111811323 | A | G | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603-1550T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811323 | |||||||
| chr11:111811440 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0063 a0002c0002t0001g0070 others(1): Show |
4 | NA18939.hp1 NA18955.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-1667C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811440 | |||||||
| chr11:111811480 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1603-1707A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811480 | |||||||
| chr11:111811542 | C | CA | 11 | a0001c0001t0002g0131 a0001c0001t0002g0202 a0001c0001t0005g0119 others(8): Show |
11 | HG01109.hp1 HG01952.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603-1770dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811542 | |||||||
| chr11:111811542 | CA | C | 103 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0003g0010 others(100): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1603-1770delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811542 | |||||||
| chr11:111811597 | T | C | 2 | a0001c0001t0003g0263 a0001c0001t0003g0277 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1603-1824A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811597 | |||||||
| chr11:111811603 | CATGTGGT others(17): Show |
C | 1 | a0001c0001t0002g0172 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1603-1854_1603-183 others(28): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811603 | |||||||
| chr11:111811644 | C | T | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-1871G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811644 | |||||||
| chr11:111811747 | A | G | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-1974T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811747 | |||||||
| chr11:111811886 | A | G | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-2113T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111811886 | |||||||
| chr11:111812129 | T | A | 3 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0266 |
3 | HG01069.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1603-2356A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812129 | |||||||
| chr11:111812267 | T | C | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1603-2494A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812267 | |||||||
| chr11:111812418 | T | C | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603-2645A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812418 | |||||||
| chr11:111812670 | ACTTTGGG others(14): Show |
A | 1 | a0001c0001t0003g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1603-2918_1603-289 others(25): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812670 | |||||||
| chr11:111812842 | C | T | 1 | a0002c0002t0001g0019 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1603-3069G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812842 | |||||||
| chr11:111812852 | G | A | 3 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-3079C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812852 | |||||||
| chr11:111812867 | A | G | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-3094T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812867 | |||||||
| chr11:111812899 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-3126C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812899 | |||||||
| chr11:111812915 | C | CAAAAA | 7 | a0001c0001t0008g0265 a0001c0001t0012g0197 a0001c0001t0020g0108 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-3147_1603-314 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111812915 | C | CAAAAAA | 88 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0002g0176 others(85): Show |
90 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1603-3148_1603-314 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111812915 | C | CAAAAAAA | 68 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(65): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.1603-3149_1603-314 others(11): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111812915 | C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0294 a0001c0001t0002g0149 a0001c0001t0002g0150 others(10): Show |
13 | HG00733.hp2 HG01099.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603-3150_1603-314 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111812915 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(9): Show |
12 | HG02723.hp1 HG02895.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603-3151_1603-314 others(13): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111812915 | CAAAAAA | C | 99 | a0001c0001t0004g0110 a0002c0002t0001g0001 a0002c0002t0001g0003 others(96): Show |
103 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1603-3148_1603-314 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111812915 | |||||||
| chr11:111813179 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1603-3406G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813179 | |||||||
| chr11:111813184 | G | A | 3 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0299 |
3 | HG02723.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1603-3411C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813184 | |||||||
| chr11:111813251 | T | C | 3 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0002g0189 |
3 | HG01261.hp2 HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1603-3478A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813251 | |||||||
| chr11:111813289 | T | G | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-3516A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813289 | |||||||
| chr11:111813353 | G | A | 10 | a0002c0002t0001g0016 a0002c0002t0001g0028 a0002c0002t0001g0029 others(7): Show |
10 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-3580C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813353 | |||||||
| chr11:111813515 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1603-3742G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813515 | |||||||
| chr11:111813644 | T | C | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-3871A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813644 | |||||||
| chr11:111813675 | C | A | 1 | a0001c0001t0005g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1603-3902G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813675 | |||||||
| chr11:111813748 | C | G | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-3975G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111813748 | |||||||
| chr11:111814129 | A | G | 4 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0298 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-4356T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814129 | |||||||
| chr11:111814535 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1603-4762C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814535 | |||||||
| chr11:111814685 | A | G | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-4912T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814685 | |||||||
| chr11:111814693 | A | G | 1 | a0002c0002t0004g0036 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-4920T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814693 | |||||||
| chr11:111814746 | T | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-4973A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111814746 | |||||||
| chr11:111815096 | G | A | 2 | a0001c0001t0003g0263 a0001c0001t0003g0277 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1603-5323C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815096 | |||||||
| chr11:111815158 | G | A | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-5385C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815158 | |||||||
| chr11:111815267 | T | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-5494A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815267 | |||||||
| chr11:111815289 | T | C | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-5516A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815289 | |||||||
| chr11:111815303 | T | A | 1 | a0001c0001t0002g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1603-5530A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815303 | |||||||
| chr11:111815313 | G | A | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1603-5540C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815313 | |||||||
| chr11:111815367 | C | T | 3 | a0001c0001t0003g0238 a0001c0001t0003g0268 a0001c0001t0008g0265 |
3 | NA18939.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1603-5594G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815367 | |||||||
| chr11:111815667 | G | GT | 3 | a0001c0001t0007g0231 a0001c0001t0007g0245 a0001c0001t0007g0264 |
3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1603-5895_1603-589 others(5): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815667 | |||||||
| chr11:111815668 | A | T | 3 | a0001c0001t0007g0231 a0001c0001t0007g0245 a0001c0001t0007g0264 |
3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1603-5895T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815668 | |||||||
| chr11:111815686 | T | C | 3 | a0001c0001t0002g0159 a0001c0001t0002g0165 a0001c0001t0002g0192 |
3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1603-5913A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815686 | |||||||
| chr11:111815858 | G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1603-6085C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815858 | |||||||
| chr11:111815941 | T | C | 1 | a0001c0001t0003g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1603-6168A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111815941 | |||||||
| chr11:111816011 | A | T | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-6238T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816011 | |||||||
| chr11:111816076 | C | T | 230 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(227): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1603-6303G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816076 | |||||||
| chr11:111816139 | T | C | 1 | a0002c0002t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1603-6366A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816139 | |||||||
| chr11:111816318 | T | C | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1603-6545A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816318 | |||||||
| chr11:111816677 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1603-6904A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816677 | |||||||
| chr11:111816733 | T | G | 3 | a0001c0001t0002g0159 a0001c0001t0002g0165 a0001c0001t0002g0192 |
3 | HG01256.hp1 HG01258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1603-6960A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816733 | |||||||
| chr11:111816745 | A | G | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1603-6972T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111816745 | |||||||
| chr11:111817034 | A | G | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-7261T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817034 | |||||||
| chr11:111817268 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1603-7495C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817268 | |||||||
| chr11:111817411 | T | C | 5 | a0001c0001t0011g0129 a0001c0001t0016g0127 a0001c0001t0016g0128 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-7638A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817411 | |||||||
| chr11:111817563 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-7790G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817563 | |||||||
| chr11:111817603 | C | A | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-7830G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817603 | |||||||
| chr11:111817777 | C | CT | 9 | a0001c0001t0002g0162 a0001c0001t0003g0010 a0001c0001t0003g0256 others(6): Show |
10 | HG00733.hp2 HG01099.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-8005dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817777 | |||||||
| chr11:111817777 | CT | C | 8 | a0001c0001t0002g0156 a0001c0001t0002g0161 a0003c0003t0001g0123 others(5): Show |
8 | HG01884.hp1 HG01975.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-8005delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817777 | |||||||
| chr11:111817782 | T | C | 3 | a0002c0002t0001g0071 a0002c0002t0001g0080 a0002c0002t0029g0082 |
3 | HG02602.hp2 HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1603-8009A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817782 | |||||||
| chr11:111817784 | T | C | 1 | a0001c0001t0007g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1603-8011A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817784 | |||||||
| chr11:111817865 | C | T | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603-8092G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817865 | |||||||
| chr11:111817868 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1603-8095C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111817868 | |||||||
| chr11:111818022 | G | A | 1 | a0007c0009t0002g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1603-8249C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818022 | |||||||
| chr11:111818158 | G | A | 3 | a0001c0001t0010g0288 a0001c0001t0010g0289 a0001c0001t0010g0290 |
3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-8385C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818158 | |||||||
| chr11:111818273 | A | G | 2 | a0001c0001t0003g0250 a0001c0001t0003g0251 |
2 | HG02004.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1603-8500T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818273 | |||||||
| chr11:111818455 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1603-8682C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818455 | |||||||
| chr11:111818525 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0202 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-8752G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818525 | |||||||
| chr11:111818597 | A | C | 1 | a0001c0001t0003g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1603-8824T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818597 | |||||||
| chr11:111818623 | C | T | 3 | a0001c0001t0010g0288 a0001c0001t0010g0289 a0001c0001t0010g0290 |
3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-8850G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818623 | |||||||
| chr11:111818692 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-8919A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818692 | |||||||
| chr11:111818812 | C | G | 1 | a0001c0001t0003g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1603-9039G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818812 | |||||||
| chr11:111818871 | A | G | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-9098T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111818871 | |||||||
| chr11:111819118 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-9345C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819118 | |||||||
| chr11:111819293 | A | G | 12 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(9): Show |
12 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-9520T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819293 | |||||||
| chr11:111819298 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1603-9525A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819298 | |||||||
| chr11:111819348 | G | T | 3 | a0002c0002t0001g0028 a0002c0002t0001g0067 a0002c0002t0001g0088 |
3 | NA18941.hp1 NA18979.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1603-9575C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819348 | |||||||
| chr11:111819399 | C | T | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-9626G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819399 | |||||||
| chr11:111819460 | T | C | 11 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1603-9687A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819460 | |||||||
| chr11:111819607 | A | G | 209 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(206): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1603-9834T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819607 | |||||||
| chr11:111819804 | G | C | 2 | a0002c0002t0001g0018 a0002c0002t0001g0089 |
2 | HG00609.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1603-10031C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819804 | |||||||
| chr11:111819806 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0025g0133 |
2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1603-10033T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819806 | |||||||
| chr11:111819858 | T | G | 1 | a0001c0001t0002g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1603-10085A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819858 | |||||||
| chr11:111819863 | G | A | 13 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(10): Show |
14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603-10090C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819863 | |||||||
| chr11:111819899 | G | C | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1603-10126C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819899 | |||||||
| chr11:111819952 | A | G | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1603-10179T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111819952 | |||||||
| chr11:111820088 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1603-10315C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820088 | |||||||
| chr11:111820407 | C | A | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-10634G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820407 | |||||||
| chr11:111820579 | G | C | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-10806C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820579 | |||||||
| chr11:111820736 | G | A | 3 | a0002c0002t0001g0052 a0002c0002t0001g0056 a0002c0002t0001g0091 |
3 | HG02698.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1603-10963C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820736 | |||||||
| chr11:111820755 | C | T | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-10982G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820755 | |||||||
| chr11:111820920 | G | GCA | 19 | a0001c0001t0001g0014 a0001c0001t0006g0142 a0001c0001t0006g0144 others(16): Show |
19 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1603-11149_1603-11 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | G | GCACA | 81 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-11151_1603-11 others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | G | GCACACA | 7 | a0001c0001t0003g0239 a0001c0001t0003g0282 a0001c0001t0005g0005 others(4): Show |
8 | HG00597.hp2 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603-11153_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | G | GCACACAC others(3): Show |
1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-11157_1603-11 others(16): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | G | GCGCACA | 7 | a0001c0001t0005g0111 a0001c0001t0005g0114 a0001c0001t0005g0116 others(4): Show |
7 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-11148_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | GCA | G | 93 | a0001c0001t0002g0156 a0001c0001t0002g0160 a0001c0001t0002g0186 others(90): Show |
97 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1603-11149_1603-11 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | GCACACA | G | 4 | a0004c0004t0001g0096 a0004c0004t0001g0097 a0004c0004t0001g0098 others(1): Show |
4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-11153_1603-11 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111820920 | GCACACAC others(5): Show |
G | 2 | a0002c0002t0004g0025 a0002c0002t0004g0026 |
2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1603-11159_1603-11 others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111820920 | |||||||
| chr11:111821036 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1603-11263G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821036 | |||||||
| chr11:111821143 | C | T | 3 | a0001c0001t0010g0288 a0001c0001t0010g0289 a0001c0001t0010g0290 |
3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1603-11370G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821143 | |||||||
| chr11:111821243 | C | T | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-11470G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821243 | |||||||
| chr11:111821249 | G | A | 1 | a0001c0001t0018g0301 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1603-11476C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821249 | |||||||
| chr11:111821295 | C | G | 6 | a0002c0002t0001g0015 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
6 | HG00609.hp2 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-11522G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821295 | |||||||
| chr11:111821458 | G | A | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603-11685C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821458 | |||||||
| chr11:111821781 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1603-12008C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821781 | |||||||
| chr11:111821893 | G | C | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603-12120C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821893 | |||||||
| chr11:111821925 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1603-12152G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821925 | |||||||
| chr11:111821940 | G | C | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-12167C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111821940 | |||||||
| chr11:111822099 | G | T | 2 | a0002c0002t0001g0058 a0002c0002t0001g0060 |
2 | HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1603-12326C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822099 | |||||||
| chr11:111822100 | A | T | 2 | a0002c0002t0001g0058 a0002c0002t0001g0060 |
2 | HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1603-12327T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822100 | |||||||
| chr11:111822146 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0009g0285 a0001c0001t0011g0129 others(6): Show |
9 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603-12373G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822146 | |||||||
| chr11:111822275 | G | A | 1 | a0001c0001t0008g0216 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1603-12502C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822275 | |||||||
| chr11:111822310 | G | C | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1603-12537C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822310 | |||||||
| chr11:111822408 | C | CA | 243 | a0001c0001t0001g0212 a0001c0001t0001g0293 a0001c0001t0002g0002 others(240): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1603-12636dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | |||||||
| chr11:111822408 | C | CAA | 32 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0294 others(29): Show |
32 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1603-12637_1603-12 others(8): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | |||||||
| chr11:111822408 | C | CAAA | 7 | a0001c0001t0003g0274 a0001c0001t0005g0296 a0001c0001t0005g0297 others(4): Show |
7 | HG02723.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-12638_1603-12 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822408 | |||||||
| chr11:111822493 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1603-12720G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822493 | |||||||
| chr11:111822538 | C | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1603-12765G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822538 | |||||||
| chr11:111822558 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1603-12785T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822558 | |||||||
| chr11:111822613 | C | A | 1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1603-12840G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822613 | |||||||
| chr11:111822677 | C | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1603-12904G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822677 | |||||||
| chr11:111822730 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-12957G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822730 | |||||||
| chr11:111822930 | G | A | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1603-13157C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822930 | |||||||
| chr11:111822949 | G | A | 1 | a0002c0002t0001g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1603-13176C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111822949 | |||||||
| chr11:111823074 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+13091C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823074 | |||||||
| chr11:111823139 | T | C | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1602+13026A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823139 | |||||||
| chr11:111823433 | C | G | 7 | a0002c0002t0002g0023 a0002c0002t0004g0021 a0002c0002t0004g0086 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+12732G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823433 | |||||||
| chr11:111823479 | A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+12686T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823479 | |||||||
| chr11:111823590 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1602+12575A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823590 | |||||||
| chr11:111823668 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1602+12497C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823668 | |||||||
| chr11:111823766 | T | C | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+12399A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823766 | |||||||
| chr11:111823788 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1602+12377A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111823788 | |||||||
| chr11:111824111 | G | A | 2 | a0001c0001t0020g0107 a0001c0001t0020g0108 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1602+12054C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824111 | |||||||
| chr11:111824164 | G | A | 2 | a0002c0002t0001g0053 a0006c0008t0001g0057 |
2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1602+12001C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824164 | |||||||
| chr11:111824243 | C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+11922G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824243 | |||||||
| chr11:111824306 | G | GA | 86 | a0001c0001t0003g0237 a0002c0002t0001g0001 a0002c0002t0001g0003 others(83): Show |
90 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1602+11858dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824306 | |||||||
| chr11:111824360 | T | C | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+11805A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824360 | |||||||
| chr11:111824693 | T | C | 13 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(10): Show |
14 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+11472A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824693 | |||||||
| chr11:111824985 | C | T | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+11180G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111824985 | |||||||
| chr11:111825011 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1602+11154C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825011 | |||||||
| chr11:111825120 | A | C | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+11045T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825120 | |||||||
| chr11:111825489 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+10676T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825489 | |||||||
| chr11:111825519 | T | C | 4 | a0004c0004t0001g0096 a0004c0004t0001g0097 a0004c0004t0001g0098 others(1): Show |
4 | HG00597.hp1 NA18968.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+10646A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825519 | |||||||
| chr11:111825570 | C | T | 1 | a0002c0002t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1602+10595G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825570 | |||||||
| chr11:111825692 | T | C | 15 | a0001c0001t0005g0005 a0001c0001t0005g0111 a0001c0001t0005g0114 others(12): Show |
16 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+10473A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825692 | |||||||
| chr11:111825716 | T | C | 204 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(201): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1602+10449A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825716 | |||||||
| chr11:111825775 | C | T | 1 | a0005c0007t0009g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1602+10390G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111825775 | |||||||
| chr11:111826021 | G | A | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1602+10144C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826021 | |||||||
| chr11:111826066 | C | CAAT | 3 | a0001c0001t0002g0135 a0001c0001t0002g0202 a0002c0002t0004g0054 |
3 | HG02055.hp2 HG03098.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1602+10096_1602+10 others(9): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826066 | C | CAATAAT | 129 | a0001c0001t0001g0212 a0001c0001t0002g0002 a0001c0001t0002g0006 others(126): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1602+10093_1602+10 others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826066 | C | CAATAATA others(2): Show |
25 | a0001c0001t0002g0155 a0001c0001t0002g0182 a0001c0001t0003g0222 others(22): Show |
26 | HG00408.hp2 HG00733.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1602+10090_1602+10 others(15): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826066 | C | CAATAATA others(5): Show |
93 | a0001c0001t0001g0014 a0001c0001t0001g0293 a0001c0001t0002g0131 others(90): Show |
96 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1602+10087_1602+10 others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826066 | C | CAATAATA others(8): Show |
43 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0294 others(40): Show |
43 | HG01884.hp1 HG01952.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1602+10084_1602+10 others(21): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826066 | C | CAATAATA others(11): Show |
4 | a0001c0001t0003g0240 a0001c0001t0005g0296 a0002c0002t0004g0026 others(1): Show |
4 | HG03098.hp2 HG04204.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+10081_1602+10 others(24): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826066 | |||||||
| chr11:111826391 | TA | T | 210 | a0001c0001t0001g0212 a0001c0001t0001g0287 a0001c0001t0001g0291 others(207): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1602+9773delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826391 | |||||||
| chr11:111826393 | A | T | 1 | a0001c0001t0003g0292 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1602+9772T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826393 | |||||||
| chr11:111826401 | A | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+9764T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826401 | |||||||
| chr11:111826407 | A | C | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1602+9758T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826407 | |||||||
| chr11:111826518 | G | A | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+9647C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826518 | |||||||
| chr11:111826549 | C | T | 1 | a0001c0001t0025g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1602+9616G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826549 | |||||||
| chr11:111826639 | A | G | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1602+9526T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826639 | |||||||
| chr11:111826849 | G | A | 3 | a0001c0001t0010g0288 a0001c0001t0010g0289 a0001c0001t0010g0290 |
3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1602+9316C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826849 | |||||||
| chr11:111826980 | T | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+9185A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111826980 | |||||||
| chr11:111827353 | G | C | 1 | a0001c0001t0002g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1602+8812C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827353 | |||||||
| chr11:111827435 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8730T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827435 | |||||||
| chr11:111827492 | CAT | C | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1602+8671_1602+867 others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827492 | |||||||
| chr11:111827604 | C | T | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1602+8561G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827604 | |||||||
| chr11:111827605 | G | A | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+8560C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827605 | |||||||
| chr11:111827673 | G | C | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1602+8492C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827673 | |||||||
| chr11:111827781 | C | A | 5 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+8384G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827781 | |||||||
| chr11:111827867 | C | CA | 7 | a0001c0001t0002g0154 a0001c0001t0002g0174 a0001c0001t0003g0253 others(4): Show |
7 | HG00544.hp1 HG02155.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+8297dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827867 | |||||||
| chr11:111827913 | C | T | 1 | a0001c0001t0002g0009 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1602+8252G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827913 | |||||||
| chr11:111827914 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8251C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827914 | |||||||
| chr11:111827974 | C | G | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+8191G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111827974 | |||||||
| chr11:111828087 | A | G | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1602+8078T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828087 | |||||||
| chr11:111828116 | C | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1602+8049G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828116 | |||||||
| chr11:111828147 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+8018A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828147 | |||||||
| chr11:111828185 | C | A | 11 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1602+7980G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828185 | |||||||
| chr11:111828206 | T | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1602+7959A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828206 | |||||||
| chr11:111828216 | T | C | 1 | a0002c0002t0004g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1602+7949A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828216 | |||||||
| chr11:111828290 | G | T | 5 | a0001c0001t0002g0154 a0001c0001t0002g0161 a0001c0001t0002g0178 others(2): Show |
5 | HG01975.hp2 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+7875C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828290 | |||||||
| chr11:111828310 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG00639.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1602+7855G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828310 | |||||||
| chr11:111828448 | T | C | 1 | a0004c0004t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1602+7717A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828448 | |||||||
| chr11:111828500 | C | T | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1602+7665G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828500 | |||||||
| chr11:111828817 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1602+7348G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828817 | |||||||
| chr11:111828955 | T | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+7210A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111828955 | |||||||
| chr11:111829034 | A | G | 1 | a0001c0001t0019g0244 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1602+7131T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829034 | |||||||
| chr11:111829370 | G | C | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1602+6795C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829370 | |||||||
| chr11:111829493 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1602+6672C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829493 | |||||||
| chr11:111829497 | G | A | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+6668C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829497 | |||||||
| chr11:111829508 | A | C | 1 | a0001c0001t0002g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1602+6657T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829508 | |||||||
| chr11:111829575 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+6590A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829575 | |||||||
| chr11:111829586 | C | T | 1 | a0002c0002t0004g0075 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1602+6579G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829586 | |||||||
| chr11:111829651 | A | C | 5 | a0001c0001t0002g0154 a0001c0001t0002g0161 a0001c0001t0002g0178 others(2): Show |
5 | HG01975.hp2 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+6514T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829651 | |||||||
| chr11:111829742 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+6423C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829742 | |||||||
| chr11:111829902 | T | C | 4 | a0001c0001t0004g0110 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+6263A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829902 | |||||||
| chr11:111829913 | G | C | 1 | a0001c0001t0003g0240 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1602+6252C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111829913 | |||||||
| chr11:111830072 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+6093A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830072 | |||||||
| chr11:111830371 | T | C | 11 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1602+5794A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830371 | |||||||
| chr11:111830438 | C | G | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+5727G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830438 | |||||||
| chr11:111830546 | G | A | 204 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(201): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1602+5619C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830546 | |||||||
| chr11:111830560 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0011g0129 a0001c0001t0016g0127 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+5605T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830560 | |||||||
| chr11:111830996 | C | G | 1 | a0002c0002t0001g0004 | 2 | NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1602+5169G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111830996 | |||||||
| chr11:111831109 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1602+5056G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831109 | |||||||
| chr11:111831126 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+5039G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831126 | |||||||
| chr11:111831130 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+5035A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831130 | |||||||
| chr11:111831229 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(20): Show |
23 | HG00733.hp2 HG01099.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1602+4936G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831229 | |||||||
| chr11:111831233 | G | A | 2 | a0001c0001t0003g0254 a0001c0001t0008g0228 |
2 | NA18985.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1602+4932C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831233 | |||||||
| chr11:111831470 | C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+4695G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831470 | |||||||
| chr11:111831521 | A | G | 1 | a0001c0001t0023g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1602+4644T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831521 | |||||||
| chr11:111831652 | A | C | 14 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(11): Show |
15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1602+4513T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111831652 | |||||||
| chr11:111832446 | A | AT | 9 | a0001c0001t0001g0014 a0001c0001t0009g0285 a0001c0001t0011g0129 others(6): Show |
9 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+3718dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832446 | |||||||
| chr11:111832468 | T | A | 1 | a0001c0001t0002g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1602+3697A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832468 | |||||||
| chr11:111832468 | T | G | 294 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(291): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1602+3697A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832468 | |||||||
| chr11:111832636 | T | C | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1602+3529A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832636 | |||||||
| chr11:111832796 | A | G | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1602+3369T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832796 | |||||||
| chr11:111832822 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1602+3343C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832822 | |||||||
| chr11:111832889 | G | A | 1 | a0001c0005t0011g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1602+3276C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111832889 | |||||||
| chr11:111833181 | T | C | 1 | a0001c0001t0023g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1602+2984A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833181 | |||||||
| chr11:111833183 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+2982A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833183 | |||||||
| chr11:111833216 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1602+2949G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833216 | |||||||
| chr11:111833704 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1602+2461G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111833704 | |||||||
| chr11:111834086 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+2079G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834086 | |||||||
| chr11:111834303 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1602+1862C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834303 | |||||||
| chr11:111834350 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1602+1815T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834350 | |||||||
| chr11:111834404 | T | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0202 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+1761A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834404 | |||||||
| chr11:111834455 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1602+1710C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834455 | |||||||
| chr11:111834596 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+1569T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834596 | |||||||
| chr11:111834771 | G | A | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+1394C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111834771 | |||||||
| chr11:111835075 | AGATGTGG others(11): Show |
A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(18): Show |
21 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+1072_1602+108 others(22): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835075 | |||||||
| chr11:111835094 | C | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(18): Show |
21 | HG01952.hp1 HG02145.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+1071G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835094 | |||||||
| chr11:111835382 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1602+783C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835382 | |||||||
| chr11:111835388 | G | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
62 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1602+777C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835388 | |||||||
| chr11:111835442 | T | A | 6 | a0001c0001t0001g0014 a0001c0001t0011g0129 a0001c0001t0016g0127 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+723A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835442 | |||||||
| chr11:111835759 | G | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0158 |
2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1602+406C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835759 | |||||||
| chr11:111835812 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0256 |
3 | HG02647.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1602+353C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835812 | |||||||
| chr11:111835830 | A | G | 1 | a0001c0001t0003g0243 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1602+335T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111835830 | |||||||
| chr11:111836044 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+121G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 13/14 | chr11 | 111836044 | |||||||
| chr11:111836308 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1473-14T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836308 | |||||||
| chr11:111836493 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1473-199A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836493 | |||||||
| chr11:111836584 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1473-290A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836584 | |||||||
| chr11:111836663 | T | C | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1473-369A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836663 | |||||||
| chr11:111836731 | T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473-437A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836731 | |||||||
| chr11:111836888 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1472+580G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111836888 | |||||||
| chr11:111837074 | T | C | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1472+394A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 12/14 | chr11 | 111837074 | |||||||
| chr11:111837672 | T | A | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1325-57A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837672 | |||||||
| chr11:111837673 | A | T | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1325-58T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837673 | |||||||
| chr11:111837858 | T | G | 19 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(16): Show |
20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1325-243A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837858 | |||||||
| chr11:111837945 | T | A | 207 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(204): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1324+304A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 11/14 | chr11 | 111837945 | |||||||
| chr11:111838459 | C | A | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1174-60G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838459 | |||||||
| chr11:111838490 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0121 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1174-91C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838490 | |||||||
| chr11:111838524 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1174-125G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838524 | |||||||
| chr11:111838591 | G | A | 2 | a0001c0001t0020g0107 a0001c0001t0020g0108 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1174-192C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838591 | |||||||
| chr11:111838709 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0195 |
3 | HG01255.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1174-310T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111838709 | |||||||
| chr11:111839049 | AT | A | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-651delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839049 | |||||||
| chr11:111839066 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1174-667G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839066 | |||||||
| chr11:111839299 | A | G | 1 | a0001c0001t0003g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1174-900T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839299 | |||||||
| chr11:111839311 | T | C | 230 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(227): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1174-912A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839311 | |||||||
| chr11:111839340 | C | T | 1 | a0001c0001t0020g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1174-941G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839340 | |||||||
| chr11:111839356 | C | T | 11 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0020g0107 others(8): Show |
11 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-957G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839356 | |||||||
| chr11:111839376 | G | A | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1174-977C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839376 | |||||||
| chr11:111839414 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1174-1015C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839414 | |||||||
| chr11:111839584 | G | A | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1173+1071C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839584 | |||||||
| chr11:111839588 | CA | C | 20 | a0001c0001t0003g0241 a0001c0001t0004g0110 a0001c0001t0005g0005 others(17): Show |
21 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1173+1066delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839588 | |||||||
| chr11:111839601 | A | AG | 25 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(22): Show |
25 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1173+1053dupC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839601 | |||||||
| chr11:111839601 | AG | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(62): Show |
69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1173+1053delC | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839601 | |||||||
| chr11:111839603 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1173+1052C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839603 | |||||||
| chr11:111839605 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1173+1050C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839605 | |||||||
| chr11:111839826 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1173+829A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839826 | |||||||
| chr11:111839907 | C | A | 1 | a0001c0001t0003g0230 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1173+748G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111839907 | |||||||
| chr11:111840070 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1173+585C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840070 | |||||||
| chr11:111840202 | G | C | 3 | a0001c0001t0003g0259 a0001c0006t0003g0258 a0001c0006t0003g0262 |
3 | NA18943.hp1 NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1173+453C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840202 | |||||||
| chr11:111840489 | C | G | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1173+166G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 10/14 | chr11 | 111840489 | |||||||
| chr11:111840943 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-134G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111840943 | |||||||
| chr11:111840958 | G | A | 1 | a0002c0002t0004g0075 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1019-149C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111840958 | |||||||
| chr11:111841216 | A | G | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1019-407T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841216 | |||||||
| chr11:111841434 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1019-625G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841434 | |||||||
| chr11:111841529 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1019-720C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841529 | |||||||
| chr11:111841677 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-868G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841677 | |||||||
| chr11:111841758 | T | TAGAAATT others(332): Show |
1 | a0001c0001t0006g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1019-950_1019-949i others(341): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841758 | |||||||
| chr11:111841967 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1019-1158C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111841967 | |||||||
| chr11:111842014 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0180 |
2 | NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1019-1205T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842014 | |||||||
| chr11:111842034 | T | C | 3 | a0001c0001t0003g0238 a0001c0001t0003g0268 a0001c0001t0008g0265 |
3 | NA18939.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1019-1225A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842034 | |||||||
| chr11:111842073 | T | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-1264A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842073 | |||||||
| chr11:111842219 | A | C | 5 | a0002c0002t0001g0003 a0002c0002t0001g0037 a0002c0002t0001g0038 others(2): Show |
6 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019-1410T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842219 | |||||||
| chr11:111842452 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1019-1643G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842452 | |||||||
| chr11:111842595 | A | G | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-1786T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842595 | |||||||
| chr11:111842729 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018+1872A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842729 | |||||||
| chr11:111842865 | A | G | 7 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0232 others(4): Show |
7 | HG01123.hp2 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018+1736T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842865 | |||||||
| chr11:111842905 | C | T | 3 | a0001c0001t0018g0301 a0001c0001t0018g0302 a0001c0001t0028g0012 |
3 | HG00733.hp2 HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1018+1696G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842905 | |||||||
| chr11:111842906 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1018+1695C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111842906 | |||||||
| chr11:111843005 | G | A | 11 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1018+1596C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843005 | |||||||
| chr11:111843536 | T | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1018+1065A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843536 | |||||||
| chr11:111843979 | T | C | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018+622A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111843979 | |||||||
| chr11:111844293 | C | T | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+308G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844293 | |||||||
| chr11:111844360 | T | C | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1018+241A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844360 | |||||||
| chr11:111844464 | C | T | 1 | a0004c0004t0001g0097 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1018+137G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844464 | |||||||
| chr11:111844575 | C | T | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1018+26G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 9/14 | chr11 | 111844575 | |||||||
| chr11:111844755 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896-32C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844755 | |||||||
| chr11:111844847 | G | C | 79 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.896-124C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844847 | |||||||
| chr11:111844876 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896-153G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844876 | |||||||
| chr11:111844992 | C | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.896-269G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111844992 | |||||||
| chr11:111845313 | T | A | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.896-590A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845313 | |||||||
| chr11:111845347 | A | C | 209 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(206): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.896-624T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845347 | |||||||
| chr11:111845427 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-704C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845427 | |||||||
| chr11:111845639 | G | C | 1 | a0001c0001t0002g0157 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896-916C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845639 | |||||||
| chr11:111845975 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(13): Show |
16 | HG01952.hp1 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.896-1252T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111845975 | |||||||
| chr11:111846052 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-1329G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846052 | |||||||
| chr11:111846071 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.896-1348A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846071 | |||||||
| chr11:111846312 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.896-1589C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846312 | |||||||
| chr11:111846590 | A | C | 1 | a0001c0001t0003g0237 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.896-1867T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846590 | |||||||
| chr11:111846599 | G | A | 3 | a0001c0001t0009g0285 a0005c0007t0009g0284 a0005c0007t0009g0286 |
3 | HG01952.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.896-1876C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846599 | |||||||
| chr11:111846722 | G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.896-1999C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846722 | |||||||
| chr11:111846733 | A | G | 1 | a0004c0004t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.896-2010T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846733 | |||||||
| chr11:111846737 | G | C | 1 | a0002c0002t0004g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.896-2014C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846737 | |||||||
| chr11:111846935 | G | T | 3 | a0001c0001t0002g0156 a0001c0001t0002g0186 a0001c0001t0002g0194 |
3 | NA18969.hp1 NA18983.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.896-2212C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111846935 | |||||||
| chr11:111847076 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2353T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847076 | |||||||
| chr11:111847130 | A | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2407T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847130 | |||||||
| chr11:111847360 | T | C | 3 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0004g0059 |
3 | HG00544.hp1 HG02129.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.896-2637A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847360 | |||||||
| chr11:111847490 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-2767G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847490 | |||||||
| chr11:111847671 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-2948T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111847671 | |||||||
| chr11:111848045 | C | T | 3 | a0002c0002t0001g0063 a0002c0002t0001g0070 a0002c0002t0001g0084 |
3 | NA18955.hp2 NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.896-3322G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848045 | |||||||
| chr11:111848203 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-3480C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848203 | |||||||
| chr11:111848405 | T | C | 79 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.896-3682A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848405 | |||||||
| chr11:111848450 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.896-3727A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848450 | |||||||
| chr11:111848483 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-3760T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848483 | |||||||
| chr11:111848540 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.896-3817T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848540 | |||||||
| chr11:111848590 | C | CA | 21 | a0001c0001t0002g0208 a0001c0001t0003g0013 a0001c0001t0003g0260 others(18): Show |
22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.896-3868dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848590 | |||||||
| chr11:111848590 | CA | C | 10 | a0001c0001t0002g0160 a0002c0002t0001g0030 a0002c0002t0004g0021 others(7): Show |
10 | HG00621.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.896-3868delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848590 | |||||||
| chr11:111848694 | T | A | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.896-3971A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848694 | |||||||
| chr11:111848697 | T | A | 2 | a0001c0001t0003g0213 a0001c0001t0003g0276 |
2 | HG00558.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.896-3974A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848697 | |||||||
| chr11:111848812 | C | T | 5 | a0001c0001t0011g0129 a0001c0001t0016g0127 a0001c0001t0016g0128 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.896-4089G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848812 | |||||||
| chr11:111848830 | G | A | 5 | a0002c0002t0001g0016 a0002c0002t0001g0029 a0002c0002t0001g0033 others(2): Show |
5 | HG00408.hp1 HG00609.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.896-4107C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848830 | |||||||
| chr11:111848870 | G | A | 226 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.896-4147C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848870 | |||||||
| chr11:111848982 | A | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.896-4259T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848982 | |||||||
| chr11:111848999 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.896-4276T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111848999 | |||||||
| chr11:111849037 | GTTTC | G | 59 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(56): Show |
63 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.896-4318_896-4315d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849037 | |||||||
| chr11:111849061 | T | C | 13 | a0001c0001t0002g0131 a0001c0001t0011g0129 a0001c0001t0016g0127 others(10): Show |
13 | HG00733.hp2 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.895+4319A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849061 | |||||||
| chr11:111849090 | G | A | 1 | a0002c0002t0004g0026 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.895+4290C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849090 | |||||||
| chr11:111849201 | C | T | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+4179G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849201 | |||||||
| chr11:111849255 | C | G | 1 | a0001c0001t0023g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.895+4125G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849255 | |||||||
| chr11:111849349 | C | A | 128 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(125): Show |
133 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.895+4031G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849349 | |||||||
| chr11:111849504 | T | G | 4 | a0002c0002t0001g0028 a0002c0002t0001g0062 a0002c0002t0001g0067 others(1): Show |
4 | NA18941.hp1 NA18979.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+3876A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849504 | |||||||
| chr11:111849547 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.895+3833A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849547 | |||||||
| chr11:111849638 | C | G | 1 | a0001c0001t0003g0236 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.895+3742G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849638 | |||||||
| chr11:111849960 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.895+3420G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849960 | |||||||
| chr11:111849970 | A | C | 1 | a0001c0001t0003g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+3410T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111849970 | |||||||
| chr11:111850162 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+3218A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850162 | |||||||
| chr11:111850170 | T | C | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+3210A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850170 | |||||||
| chr11:111850222 | G | C | 2 | a0002c0002t0004g0025 a0002c0002t0004g0026 |
2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.895+3158C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850222 | |||||||
| chr11:111850585 | T | C | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.895+2795A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850585 | |||||||
| chr11:111850678 | G | T | 1 | a0001c0001t0002g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.895+2702C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850678 | |||||||
| chr11:111850706 | C | CAAAA | 65 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0210 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.895+2670_895+2673d others(6): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAA | 8 | a0001c0001t0001g0212 a0001c0001t0003g0232 a0001c0001t0003g0261 others(5): Show |
8 | HG00140.hp2 HG01358.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.895+2669_895+2673d others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(1): Show |
82 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0002c0002t0001g0001 others(79): Show |
86 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.895+2666_895+2673d others(10): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(2): Show |
18 | a0001c0001t0003g0219 a0002c0002t0001g0028 a0002c0002t0001g0032 others(15): Show |
18 | HG01192.hp1 HG01255.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.895+2665_895+2673d others(11): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0021g0068 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.895+2664_895+2673d others(12): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0006g0143 a0001c0001t0006g0144 a0001c0001t0006g0145 others(3): Show |
6 | HG02258.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+2660_895+2673d others(16): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0006g0142 a0003c0003t0001g0123 a0003c0003t0001g0124 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+2659_895+2673d others(17): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(9): Show |
1 | a0003c0003t0001g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.895+2658_895+2673d others(18): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(10): Show |
11 | a0001c0001t0004g0110 a0001c0001t0005g0111 a0001c0001t0005g0114 others(8): Show |
11 | HG00738.hp1 HG01099.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.895+2657_895+2673d others(19): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(11): Show |
5 | a0001c0001t0001g0014 a0001c0001t0005g0005 a0001c0001t0005g0119 others(2): Show |
6 | HG01123.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+2656_895+2673d others(20): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(12): Show |
5 | a0001c0001t0012g0196 a0001c0001t0012g0197 a0001c0001t0012g0199 others(2): Show |
5 | HG02572.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(21): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0291 a0001c0001t0005g0296 a0001c0001t0005g0298 others(3): Show |
6 | HG02809.hp1 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(22): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(14): Show |
9 | a0001c0001t0001g0287 a0001c0001t0001g0293 a0001c0001t0002g0139 others(6): Show |
9 | HG00741.hp1 HG01952.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(23): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(15): Show |
23 | a0001c0001t0001g0294 a0001c0001t0002g0002 a0001c0001t0002g0008 others(20): Show |
26 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(24): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(16): Show |
15 | a0001c0001t0002g0009 a0001c0001t0002g0135 a0001c0001t0002g0154 others(12): Show |
16 | HG00621.hp1 HG01255.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(25): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.895+2673_895+2674i others(26): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(18): Show |
3 | a0001c0001t0002g0193 a0001c0001t0002g0205 a0001c0001t0016g0127 |
3 | HG02922.hp2 HG03669.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(27): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(19): Show |
7 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0002g0176 others(4): Show |
7 | HG02273.hp2 HG02630.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(28): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(20): Show |
10 | a0001c0001t0002g0153 a0001c0001t0002g0180 a0001c0001t0002g0181 others(7): Show |
10 | HG00408.hp2 HG02135.hp1 HG04199.hp2 others(7): Show |
intron_variant | MODIFIER | c.895+2673_895+2674i others(29): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.895+2673_895+2674i others(30): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG02293.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(31): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0002g0156 a0001c0001t0002g0194 |
2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.895+2673_895+2674i others(32): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850706 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.895+2673_895+2674i others(38): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850706 | |||||||
| chr11:111850893 | C | T | 5 | a0002c0002t0001g0016 a0002c0002t0001g0029 a0002c0002t0001g0033 others(2): Show |
5 | HG00408.hp1 HG00609.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+2487G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850893 | |||||||
| chr11:111850940 | T | G | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.895+2440A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850940 | |||||||
| chr11:111850950 | T | C | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.895+2430A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850950 | |||||||
| chr11:111850957 | C | T | 19 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(16): Show |
20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.895+2423G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111850957 | |||||||
| chr11:111851062 | C | G | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+2318G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851062 | |||||||
| chr11:111851083 | A | G | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.895+2297T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851083 | |||||||
| chr11:111851116 | A | G | 1 | a0002c0002t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.895+2264T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851116 | |||||||
| chr11:111851180 | A | G | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.895+2200T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851180 | |||||||
| chr11:111851347 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.895+2033G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851347 | |||||||
| chr11:111851477 | C | CA | 21 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(18): Show |
22 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.895+1902dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851477 | |||||||
| chr11:111851477 | CA | C | 179 | a0001c0001t0001g0212 a0001c0001t0001g0294 a0001c0001t0002g0150 others(176): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.895+1902delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851477 | |||||||
| chr11:111851711 | T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.895+1669A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111851711 | |||||||
| chr11:111852108 | G | C | 1 | a0001c0001t0002g0188 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.895+1272C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852108 | |||||||
| chr11:111852144 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.895+1236A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852144 | |||||||
| chr11:111852359 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.895+1021C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852359 | |||||||
| chr11:111852482 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0003g0211 a0001c0001t0003g0221 others(5): Show |
8 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+898G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852482 | |||||||
| chr11:111852897 | G | A | 2 | a0002c0002t0001g0071 a0002c0002t0029g0082 |
2 | HG02602.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.895+483C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852897 | |||||||
| chr11:111852939 | C | A | 2 | a0001c0001t0003g0263 a0001c0001t0003g0277 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.895+441G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852939 | |||||||
| chr11:111852942 | C | CA | 40 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(37): Show |
41 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.895+437dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | |||||||
| chr11:111852942 | C | CAA | 71 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.895+436_895+437dup others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | |||||||
| chr11:111852942 | C | CAAA | 6 | a0001c0001t0001g0294 a0001c0001t0003g0267 a0001c0001t0003g0268 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+435_895+437dup others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852942 | |||||||
| chr11:111852960 | T | A | 5 | a0001c0001t0011g0129 a0001c0001t0016g0127 a0001c0001t0016g0128 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+420A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852960 | |||||||
| chr11:111852961 | G | A | 1 | a0005c0007t0009g0286 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.895+419C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111852961 | |||||||
| chr11:111853058 | A | G | 30 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(27): Show |
31 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.895+322T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853058 | |||||||
| chr11:111853080 | TA | T | 128 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(125): Show |
133 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.895+299delT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853080 | |||||||
| chr11:111853261 | A | G | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+119T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 8/14 | chr11 | 111853261 | |||||||
| chr11:111853540 | G | A | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.790-55C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853540 | |||||||
| chr11:111853605 | T | C | 1 | a0002c0002t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.789+44A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853605 | |||||||
| chr11:111853609 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.789+40A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 7/14 | chr11 | 111853609 | |||||||
| chr11:111853974 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.702-238A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111853974 | |||||||
| chr11:111854023 | C | G | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.702-287G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854023 | |||||||
| chr11:111854095 | C | CT | 90 | a0001c0001t0001g0212 a0001c0001t0002g0135 a0001c0001t0002g0147 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.702-360dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854095 | |||||||
| chr11:111854095 | CT | C | 19 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(16): Show |
19 | HG01952.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.702-360delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854095 | |||||||
| chr11:111854263 | A | AT | 9 | a0001c0001t0001g0294 a0001c0001t0002g0134 a0001c0001t0002g0150 others(6): Show |
9 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-528dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | |||||||
| chr11:111854263 | AT | A | 135 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(132): Show |
140 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.702-528delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | |||||||
| chr11:111854263 | ATT | A | 10 | a0001c0001t0003g0229 a0001c0001t0003g0230 a0001c0001t0003g0232 others(7): Show |
10 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.702-529_702-528del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | |||||||
| chr11:111854263 | ATTT | A | 69 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.702-530_702-528del others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854263 | |||||||
| chr11:111854430 | C | T | 1 | a0002c0002t0001g0015 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.702-694G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854430 | |||||||
| chr11:111854454 | A | T | 1 | a0002c0002t0001g0027 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.702-718T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854454 | |||||||
| chr11:111854562 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702-826G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854562 | |||||||
| chr11:111854564 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702-828G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854564 | |||||||
| chr11:111854871 | C | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.702-1135G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854871 | |||||||
| chr11:111854884 | G | A | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702-1148C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854884 | |||||||
| chr11:111854958 | C | T | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702-1222G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111854958 | |||||||
| chr11:111855252 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.702-1516G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855252 | |||||||
| chr11:111855475 | C | G | 1 | a0002c0002t0001g0028 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.702-1739G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855475 | |||||||
| chr11:111855478 | G | A | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.702-1742C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855478 | |||||||
| chr11:111855530 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.702-1794T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855530 | |||||||
| chr11:111855541 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702-1805T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855541 | |||||||
| chr11:111855544 | G | A | 1 | a0003c0003t0026g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.702-1808C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855544 | |||||||
| chr11:111855699 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.701+1903A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855699 | |||||||
| chr11:111855924 | C | T | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.701+1678G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855924 | |||||||
| chr11:111855956 | C | T | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.701+1646G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111855956 | |||||||
| chr11:111856075 | G | A | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.701+1527C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856075 | |||||||
| chr11:111856084 | C | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.701+1518G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856084 | |||||||
| chr11:111856220 | T | C | 1 | a0001c0001t0015g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.701+1382A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856220 | |||||||
| chr11:111856276 | C | CA | 46 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(43): Show |
47 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.701+1325dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856276 | |||||||
| chr11:111856276 | C | CAA | 8 | a0001c0001t0003g0271 a0001c0001t0006g0142 a0001c0001t0006g0143 others(5): Show |
8 | HG00733.hp2 HG01099.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+1324_701+1325d others(4): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856276 | |||||||
| chr11:111856289 | A | AG | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.701+1312_701+1313i others(3): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856289 | |||||||
| chr11:111856292 | A | G | 1 | a0002c0002t0001g0027 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.701+1310T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856292 | |||||||
| chr11:111856460 | ATTTGT | A | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.701+1137_701+1141d others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856460 | |||||||
| chr11:111856504 | C | T | 231 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(228): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.701+1098G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856504 | |||||||
| chr11:111856625 | C | A | 13 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(10): Show |
14 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.701+977G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | |||||||
| chr11:111856625 | C | CT | 9 | a0001c0001t0002g0185 a0001c0001t0002g0193 a0001c0001t0005g0296 others(6): Show |
9 | HG00609.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.701+976dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | |||||||
| chr11:111856625 | CT | C | 8 | a0001c0001t0003g0223 a0001c0001t0003g0243 a0001c0001t0011g0129 others(5): Show |
8 | HG01516.hp2 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+976delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856625 | |||||||
| chr11:111856626 | T | A | 1 | a0001c0001t0005g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.701+976A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856626 | |||||||
| chr11:111856718 | G | T | 1 | a0002c0002t0001g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.701+884C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856718 | |||||||
| chr11:111856759 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.701+843C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856759 | |||||||
| chr11:111856781 | T | C | 19 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(16): Show |
20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.701+821A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856781 | |||||||
| chr11:111856824 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.701+778C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856824 | |||||||
| chr11:111856843 | A | C | 2 | a0002c0002t0004g0025 a0002c0002t0004g0026 |
2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.701+759T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111856843 | |||||||
| chr11:111857035 | A | C | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.701+567T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857035 | |||||||
| chr11:111857150 | G | A | 12 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(9): Show |
12 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.701+452C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857150 | |||||||
| chr11:111857153 | G | A | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.701+449C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 6/14 | chr11 | 111857153 | |||||||
| chr11:111857829 | T | C | 5 | a0001c0001t0003g0013 a0001c0001t0003g0210 a0001c0001t0003g0223 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-92A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111857829 | |||||||
| chr11:111858084 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.566-347C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858084 | |||||||
| chr11:111858121 | G | C | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-384C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858121 | |||||||
| chr11:111858188 | A | G | 207 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(204): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.566-451T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858188 | |||||||
| chr11:111858596 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0025g0133 |
2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.566-859T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858596 | |||||||
| chr11:111858714 | G | A | 1 | a0002c0002t0004g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-977C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858714 | |||||||
| chr11:111858727 | A | C | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-990T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858727 | |||||||
| chr11:111858832 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.566-1095G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111858832 | |||||||
| chr11:111859042 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.566-1305G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859042 | |||||||
| chr11:111859068 | T | C | 6 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-1331A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859068 | |||||||
| chr11:111859091 | A | T | 2 | a0001c0001t0002g0205 a0001c0010t0002g0206 |
2 | HG03669.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.566-1354T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859091 | |||||||
| chr11:111859227 | C | T | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.565+1320G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859227 | |||||||
| chr11:111859267 | A | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.565+1280T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859267 | |||||||
| chr11:111859282 | T | C | 1 | a0002c0002t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+1265A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859282 | |||||||
| chr11:111859497 | CT | C | 207 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(204): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.565+1049delA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859497 | |||||||
| chr11:111859650 | G | C | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.565+897C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859650 | |||||||
| chr11:111859850 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.565+697T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111859850 | |||||||
| chr11:111860063 | T | C | 1 | a0001c0001t0012g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.565+484A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111860063 | |||||||
| chr11:111860283 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.565+264G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 5/14 | chr11 | 111860283 | |||||||
| chr11:111860817 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.477-182C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860817 | |||||||
| chr11:111860852 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.477-217A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860852 | |||||||
| chr11:111860887 | T | C | 2 | a0001c0001t0015g0146 a0001c0001t0015g0203 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.477-252A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860887 | |||||||
| chr11:111860983 | G | A | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.477-348C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111860983 | |||||||
| chr11:111861250 | T | G | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.477-615A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861250 | |||||||
| chr11:111861492 | T | C | 76 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.477-857A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861492 | |||||||
| chr11:111861549 | G | A | 1 | a0001c0001t0011g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.477-914C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861549 | |||||||
| chr11:111861566 | T | C | 6 | a0002c0002t0004g0101 a0002c0002t0004g0102 a0002c0002t0004g0103 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.477-931A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861566 | |||||||
| chr11:111861579 | C | G | 1 | a0001c0001t0024g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.477-944G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861579 | |||||||
| chr11:111861886 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.477-1251C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861886 | |||||||
| chr11:111861912 | T | C | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477-1277A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111861912 | |||||||
| chr11:111862137 | A | G | 1 | a0002c0002t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.477-1502T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862137 | |||||||
| chr11:111862239 | C | CT | 9 | a0001c0001t0002g0147 a0001c0001t0010g0288 a0001c0001t0010g0289 others(6): Show |
9 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.477-1605dupA | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862239 | |||||||
| chr11:111862352 | A | G | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.477-1717T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862352 | |||||||
| chr11:111862523 | C | T | 5 | a0001c0001t0003g0013 a0001c0001t0003g0210 a0001c0001t0003g0223 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.477-1888G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862523 | |||||||
| chr11:111862584 | T | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.477-1949A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862584 | |||||||
| chr11:111862814 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.477-2179C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862814 | |||||||
| chr11:111862863 | T | C | 5 | a0001c0001t0001g0293 a0001c0001t0006g0142 a0001c0001t0006g0143 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.477-2228A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862863 | |||||||
| chr11:111862894 | G | A | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477-2259C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111862894 | |||||||
| chr11:111863090 | G | A | 1 | a0002c0002t0029g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.476+2091C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863090 | |||||||
| chr11:111863190 | C | T | 5 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 others(2): Show |
5 | HG01255.hp1 HG01884.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+1991G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863190 | |||||||
| chr11:111863374 | T | A | 79 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.476+1807A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863374 | |||||||
| chr11:111863420 | C | T | 290 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(287): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.476+1761G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863420 | |||||||
| chr11:111863441 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.476+1740A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863441 | |||||||
| chr11:111863467 | G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.476+1714C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863467 | |||||||
| chr11:111863568 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+1613C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863568 | |||||||
| chr11:111863686 | G | C | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.476+1495C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863686 | |||||||
| chr11:111863713 | T | C | 1 | a0002c0002t0001g0084 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.476+1468A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863713 | |||||||
| chr11:111863855 | G | A | 1 | a0001c0001t0017g0272 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.476+1326C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863855 | |||||||
| chr11:111863893 | A | G | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.476+1288T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863893 | |||||||
| chr11:111863980 | C | A | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.476+1201G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111863980 | |||||||
| chr11:111864121 | C | T | 80 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(77): Show |
84 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.476+1060G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864121 | |||||||
| chr11:111864149 | A | G | 1 | a0002c0002t0002g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.476+1032T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864149 | |||||||
| chr11:111864272 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+909C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864272 | |||||||
| chr11:111864589 | G | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.476+592C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864589 | |||||||
| chr11:111864673 | A | T | 1 | a0001c0001t0022g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476+508T>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864673 | |||||||
| chr11:111864692 | T | C | 1 | a0001c0001t0003g0278 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.476+489A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864692 | |||||||
| chr11:111864771 | T | A | 1 | a0001c0001t0030g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.476+410A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111864771 | |||||||
| chr11:111865072 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.476+109G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 4/14 | chr11 | 111865072 | |||||||
| chr11:111865258 | G | A | 1 | a0001c0001t0003g0273 | 1 | NA20805.hp1 | splice_region_variant&intron_variant | LOW | c.406-7C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865258 | |||||||
| chr11:111865297 | T | A | 1 | a0001c0001t0018g0302 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.406-46A>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865297 | |||||||
| chr11:111865859 | ATGTGGCT | A | 11 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0001g0293 others(8): Show |
11 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.406-615_406-609del others(7): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111865859 | |||||||
| chr11:111866093 | G | A | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.406-842C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866093 | |||||||
| chr11:111866161 | G | A | 1 | a0002c0002t0004g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406-910C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866161 | |||||||
| chr11:111866206 | G | A | 226 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0287 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.406-955C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866206 | |||||||
| chr11:111866241 | G | C | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-990C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866241 | |||||||
| chr11:111866289 | C | T | 19 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(16): Show |
20 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.406-1038G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866289 | |||||||
| chr11:111866365 | C | T | 1 | a0001c0001t0019g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.406-1114G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866365 | |||||||
| chr11:111866588 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.406-1337T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866588 | |||||||
| chr11:111866721 | C | G | 15 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(12): Show |
16 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.406-1470G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866721 | |||||||
| chr11:111866733 | A | C | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.406-1482T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866733 | |||||||
| chr11:111866764 | C | T | 3 | a0001c0001t0003g0217 a0001c0001t0003g0218 a0001c0001t0003g0219 |
3 | HG01255.hp1 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.406-1513G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866764 | |||||||
| chr11:111866858 | C | G | 1 | a0002c0002t0001g0088 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.406-1607G>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866858 | |||||||
| chr11:111866956 | G | A | 4 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0144 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+1646C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111866956 | |||||||
| chr11:111867044 | G | A | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.405+1558C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867044 | |||||||
| chr11:111867079 | A | G | 2 | a0001c0001t0003g0215 a0001c0001t0008g0216 |
2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.405+1523T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867079 | |||||||
| chr11:111867090 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.405+1512C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867090 | |||||||
| chr11:111867108 | A | C | 5 | a0003c0003t0001g0123 a0003c0003t0001g0124 a0003c0003t0001g0125 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+1494T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867108 | |||||||
| chr11:111867189 | C | T | 79 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.405+1413G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867189 | |||||||
| chr11:111867218 | G | A | 1 | a0001c0001t0015g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.405+1384C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867218 | |||||||
| chr11:111867263 | A | C | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405+1339T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867263 | |||||||
| chr11:111867445 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.405+1157G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867445 | |||||||
| chr11:111867508 | A | G | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.405+1094T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867508 | |||||||
| chr11:111867543 | A | G | 1 | a0002c0002t0004g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.405+1059T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867543 | |||||||
| chr11:111867742 | T | C | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.405+860A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867742 | |||||||
| chr11:111867920 | C | T | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405+682G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111867920 | |||||||
| chr11:111868200 | T | C | 1 | a0001c0001t0003g0274 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.405+402A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868200 | |||||||
| chr11:111868465 | T | C | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+137A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868465 | |||||||
| chr11:111868485 | T | C | 14 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(11): Show |
15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.405+117A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868485 | |||||||
| chr11:111868594 | G | T | 1 | a0002c0002t0001g0003 | 2 | HG01257.hp1 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.405+8C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 3/14 | chr11 | 111868594 | |||||||
| chr11:111868816 | C | T | 14 | a0001c0001t0004g0110 a0001c0001t0005g0005 a0001c0001t0005g0111 others(11): Show |
15 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-80G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868816 | |||||||
| chr11:111868831 | C | T | 1 | a0002c0002t0004g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-95G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868831 | |||||||
| chr11:111868930 | G | T | 1 | a0001c0001t0003g0214 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.271-194C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111868930 | |||||||
| chr11:111869074 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.271-338T>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869074 | |||||||
| chr11:111869411 | TAC | T | 3 | a0001c0001t0020g0107 a0001c0001t0020g0108 a0001c0001t0030g0109 |
3 | HG02572.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.271-677_271-676del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869411 | |||||||
| chr11:111869766 | T | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(54): Show |
61 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.270+466A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869766 | |||||||
| chr11:111869870 | GGT | G | 10 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0003g0292 others(7): Show |
10 | HG02723.hp1 HG02809.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+360_270+361del others(2): Show |
ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869870 | |||||||
| chr11:111869880 | C | T | 1 | a0002c0002t0004g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.270+352G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111869880 | |||||||
| chr11:111870001 | G | A | 2 | a0001c0001t0012g0196 a0001c0001t0012g0197 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.270+231C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870001 | |||||||
| chr11:111870103 | T | G | 1 | a0001c0001t0005g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270+129A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870103 | |||||||
| chr11:111870137 | G | A | 1 | a0001c0001t0003g0275 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.270+95C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 2/14 | chr11 | 111870137 | |||||||
| chr11:111870381 | G | GC | 72 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.132-12dupG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870381 | |||||||
| chr11:111870382 | C | CA | 32 | a0001c0001t0001g0014 a0001c0001t0001g0294 a0001c0001t0002g0201 others(29): Show |
32 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.132-13dupT | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870382 | |||||||
| chr11:111870382 | C | CCA | 4 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 others(1): Show |
4 | HG01109.hp2 NA18951.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-13_132-12insTG | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870382 | |||||||
| chr11:111870387 | A | C | 3 | a0001c0001t0001g0212 a0001c0001t0003g0210 a0001c0001t0003g0211 |
3 | HG00140.hp1 HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132-17T>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870387 | |||||||
| chr11:111870420 | C | T | 6 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0017 others(3): Show |
6 | HG00609.hp1 NA18946.hp2 NA19058.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-50G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870420 | |||||||
| chr11:111870607 | T | G | 6 | a0002c0002t0004g0101 a0002c0002t0004g0102 a0002c0002t0004g0103 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-237A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870607 | |||||||
| chr11:111870740 | T | C | 79 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0013 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.132-370A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870740 | |||||||
| chr11:111870746 | C | T | 98 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0004 others(95): Show |
102 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.132-376G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870746 | |||||||
| chr11:111870909 | T | C | 5 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(2): Show |
5 | HG00597.hp2 NA18977.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+443A>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870909 | |||||||
| chr11:111870973 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0291 others(13): Show |
16 | HG01952.hp1 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.131+379C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111870973 | |||||||
| chr11:111871040 | C | A | 1 | a0002c0002t0001g0295 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.131+312G>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871040 | |||||||
| chr11:111871087 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.131+265C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871087 | |||||||
| chr11:111871167 | G | C | 4 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0298 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.131+185C>G | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871167 | |||||||
| chr11:111871244 | G | A | 1 | a0002c0002t0004g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131+108C>T | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871244 | |||||||
| chr11:111871245 | T | G | 2 | a0001c0001t0018g0301 a0001c0001t0018g0302 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.131+107A>C | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871245 | |||||||
| chr11:111871310 | G | T | 1 | a0001c0001t0003g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.131+42C>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871310 | |||||||
| chr11:111871317 | C | T | 1 | a0001c0001t0028g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131+35G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871317 | |||||||
| chr11:111871347 | C | T | 1 | a0002c0002t0021g0011 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.131+5G>A | ALG9 | ENSG00000086848.15 | transcript | ENST00000616540.5 | protein_coding | 1/14 | chr11 | 111871347 |