Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 402665 |
| ensemblid | ENSG00000142549.10 |
| hgncid | 34550 |
| symbol | IGLON5 |
| name | IgLON family member 5 |
| refseq_nuc | NM_001101372.3 |
| refseq_prot | NP_001094842.1 |
| ensembl_nuc | ENST00000270642.9 |
| ensembl_prot | ENSP00000270642.8 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 51311644 |
| end | 51330891 |
| strand | + |
| ver | v1.2 |
| region | chr19:51311644-51330891 |
| region5000 | chr19:51306644-51335891 |
| regionname0 | IGLON5_chr19_51311644_51330891 |
| regionname5000 | IGLON5_chr19_51306644_51335891 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 336 | 408 | 94 | 73 | 177 | 16 | 46 | 135 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPPPA others(331): Show |
chr19 | 51306644 | 51335891 |
| a0002 | 0/0 | 336 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPPPA others(331): Show |
chr19 | 51306644 | 51335891 |
| a0003 | 0/0 | 336 | 3 | 0 | 0 | 1 | 0 | 2 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPPAA others(331): Show |
chr19 | 51306644 | 51335891 |
| a0004 | 0/0 | 336 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPAPA others(331): Show |
chr19 | 51306644 | 51335891 |
| a0005 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPPPA others(331): Show |
chr19 | 51306644 | 51335891 |
| a0006 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | MPPPA others(331): Show |
chr19 | 51306644 | 51335891 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1008 | 403 | 93 | 73 | 174 | 16 | 45 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0001c0003 | 0/0 | 1008 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0001c0006 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0001c0008 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0001c0009 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0002c0002 | 0/0 | 1008 | 4 | 0 | 0 | 4 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0003c0004 | 0/0 | 1008 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0003c0010 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0004c0011 | 0/0 | 1008 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0005c0007 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 | ||
| a0006c0005 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATGCC others(1003): Show |
chr19 | 51306644 | 51335891 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3347 | 203 | 22 | 50 | 95 | 7 | 28 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0002 | 0/0 | 3343 | 31 | 18 | 4 | 5 | 2 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0003 | 0/0 | 3348 | 28 | 1 | 2 | 18 | 2 | 5 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0004 | 0/0 | 3349 | 19 | 1 | 0 | 16 | 1 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3344): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0005 | 0/0 | 3345 | 11 | 9 | 2 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0006 | 0/0 | 3343 | 9 | 9 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0007 | 0/0 | 3348 | 10 | 0 | 4 | 4 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0008 | 0/0 | 3349 | 8 | 0 | 0 | 6 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3344): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0009 | 0/0 | 3348 | 5 | 0 | 1 | 3 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0010 | 0/0 | 3351 | 5 | 1 | 2 | 0 | 2 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3346): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0011 | 0/0 | 3350 | 4 | 0 | 1 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3345): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0012 | 0/0 | 3348 | 3 | 0 | 0 | 1 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0013 | 0/0 | 3349 | 3 | 0 | 1 | 1 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3344): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0014 | 0/0 | 3344 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3339): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0015 | 0/0 | 3344 | 3 | 2 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3339): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0016 | 0/0 | 3350 | 3 | 1 | 1 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3345): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0017 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0018 | 0/0 | 3337 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3332): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0019 | 0/0 | 3345 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0020 | 0/0 | 3348 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0021 | 0/0 | 3347 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0022 | 0/0 | 3347 | 2 | 1 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0023 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0024 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0025 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0026 | 0/0 | 3353 | 2 | 0 | 2 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3348): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0027 | 0/0 | 3344 | 2 | 1 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3339): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0028 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | ATCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0029 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0030 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3346): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0031 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0032 | 0/1 | 3348 | 1 | 0 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0033 | 0/0 | 3343 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0034 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0035 | 0/0 | 3346 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3341): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0036 | 0/0 | 3352 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3347): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0037 | 0/0 | 3346 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3341): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0038 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3318): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0039 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0040 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0041 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0042 | 0/0 | 3347 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0043 | 0/0 | 3347 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0044 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0045 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0046 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0047 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0048 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0049 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0050 | 0/0 | 3348 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3343): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0051 | 0/0 | 3352 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3347): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0052 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0053 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0054 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3340): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0055 | 0/0 | 3344 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3339): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0056 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3349): Show |
chr19 | 51306644 | 51335891 |
| a0001c0001t0057 | 0/0 | 3346 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3341): Show |
chr19 | 51306644 | 51335891 |
| a0001c0003t0001 | 0/0 | 3347 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0006t0001 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0008t0001 | 0/0 | 3347 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0001c0009t0006 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0002c0002t0001 | 0/0 | 3347 | 4 | 0 | 0 | 4 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0003c0004t0001 | 0/0 | 3347 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0003c0010t0001 | 0/0 | 3347 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0004c0011t0001 | 0/0 | 3347 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3342): Show |
chr19 | 51306644 | 51335891 |
| a0005c0007t0002 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| a0006c0005t0002 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | GTCAG others(3338): Show |
chr19 | 51306644 | 51335891 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 7 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 3 | 3 | 1 | 3 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0003 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 6 | 1 | 3 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0022 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0007 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0010g0001 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0010g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0011g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0011g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0013g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0013g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0014g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0015g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0015g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0016g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0017g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0017g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0018g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0019g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0019g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0020g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0021g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0022g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0022g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0023g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0024g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0025g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0025g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0026g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0027g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0027g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0029g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0030g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0031g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0032g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0033g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0034g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0035g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0037g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0038g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0039g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0040g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0041g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0042g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0043g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0044g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0045g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0046g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0047g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0048g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0049g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0050g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0051g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0052g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0053g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0054g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0055g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0056g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0001t0057g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0003t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0001c0009t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0003c0004t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0003c0010t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0004c0011t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0005c0007t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| a0006c0005t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00323 | hp1 | a0001 | c0001 | t0022 | g0197 | EUR | FIN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00323 | hp2 | a0001 | c0001 | t0010 | g0001 | EUR | FIN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00544 | hp1 | a0001 | c0001 | t0008 | g0039 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00558 | hp2 | a0003 | c0010 | t0001 | g0156 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00609 | hp1 | a0001 | c0001 | t0020 | g0003 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0010 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00639 | hp1 | a0001 | c0001 | t0054 | g0077 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00733 | hp1 | a0004 | c0011 | t0001 | g0224 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0188 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01106 | hp1 | a0001 | c0001 | t0015 | g0066 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0187 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0218 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01257 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01258 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0001 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01884 | hp1 | a0001 | c0001 | t0035 | g0065 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01934 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01975 | hp2 | a0001 | c0001 | t0042 | g0001 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02055 | hp1 | a0005 | c0007 | t0002 | g0049 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02055 | hp2 | a0001 | c0001 | t0034 | g0069 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02056 | hp1 | a0001 | c0001 | t0038 | g0009 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02071 | hp1 | a0001 | c0001 | t0021 | g0010 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0012 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02135 | hp2 | a0001 | c0001 | t0009 | g0048 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02145 | hp2 | a0001 | c0001 | t0027 | g0215 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02155 | hp1 | a0001 | c0006 | t0001 | g0126 | EAS | CDX | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0011 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0230 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02280 | hp1 | a0001 | c0001 | t0023 | g0075 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0240 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0038 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0113 | EAS | KHV | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0059 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0045 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02615 | hp1 | a0001 | c0001 | t0055 | g0212 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0016 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0095 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02809 | hp1 | a0001 | c0001 | t0040 | g0101 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02809 | hp2 | a0001 | c0001 | t0049 | g0076 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0235 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02895 | hp2 | a0001 | c0001 | t0024 | g0029 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02896 | hp1 | a0001 | c0001 | t0052 | g0030 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0029 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0052 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03098 | hp1 | a0006 | c0005 | t0002 | g0074 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03098 | hp2 | a0001 | c0001 | t0019 | g0144 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0054 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0205 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0016 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03486 | hp2 | a0001 | c0001 | t0041 | g0073 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03490 | hp2 | a0003 | c0004 | t0001 | g0035 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03492 | hp1 | a0003 | c0004 | t0001 | g0035 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03516 | hp1 | a0001 | c0009 | t0006 | g0241 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0211 | AFR | ESN | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0210 | AFR | GWD | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0209 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0048 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03834 | hp1 | a0001 | c0001 | t0043 | g0002 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03834 | hp2 | a0001 | c0001 | t0012 | g0002 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03942 | hp2 | a0001 | c0008 | t0001 | g0003 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0220 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0229 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04184 | hp2 | a0001 | c0001 | t0013 | g0172 | SAS | BEB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0002 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | CHB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18906 | hp1 | a0001 | c0001 | t0039 | g0085 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18943 | hp1 | a0001 | c0001 | t0011 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18946 | hp2 | a0001 | c0001 | t0047 | g0183 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18952 | hp2 | a0001 | c0001 | t0046 | g0160 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18957 | hp2 | a0001 | c0001 | t0037 | g0041 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18963 | hp1 | a0001 | c0001 | t0045 | g0159 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18987 | hp1 | a0001 | c0001 | t0048 | g0128 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18987 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0133 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18997 | hp1 | a0001 | c0001 | t0011 | g0044 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19000 | hp2 | a0001 | c0001 | t0053 | g0080 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0125 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19001 | hp2 | a0001 | c0001 | t0027 | g0083 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19005 | hp2 | a0001 | c0001 | t0016 | g0012 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19009 | hp1 | a0001 | c0001 | t0057 | g0041 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19060 | hp1 | a0001 | c0001 | t0008 | g0111 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19068 | hp1 | a0001 | c0001 | t0021 | g0021 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19068 | hp2 | a0001 | c0001 | t0031 | g0158 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19070 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19078 | hp2 | a0001 | c0001 | t0050 | g0141 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19082 | hp2 | a0001 | c0001 | t0030 | g0020 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19084 | hp1 | a0001 | c0001 | t0029 | g0123 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19088 | hp1 | a0001 | c0001 | t0044 | g0127 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19090 | hp2 | a0001 | c0001 | t0051 | g0008 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ASW | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20129 | hp2 | a0001 | c0001 | t0019 | g0038 | AFR | ASW | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0161 | EUR | TSI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20805 | hp2 | a0001 | c0001 | t0033 | g0067 | EUR | TSI | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | GIH | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | ACB | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | USA | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | USA | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18955 | hp1 | a0001 | c0001 | t0036 | g0046 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20300 | hp1 | a0001 | c0001 | t0056 | g0162 | AFR | USA | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0208 | AFR | USA | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0236 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0146 | REF | REF | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | IGLON5_chr19_51306644_51335891 | IGLON5 | chr19 | 51306644 | 51335891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:51311854 | C | G | 1 | a0004 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.7C>G | p.Pro3Ala | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 211/3347 | 7/1011 | 3/336 | chr19 | 51311854 | |||
| chr19:51311857 | C | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.10C>G | p.Pro4Ala | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 214/3347 | 10/1011 | 4/336 | chr19 | 51311857 | |||
| chr19:51311858 | C | G | 1 | a0003 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.11C>G | p.Pro4Arg | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 215/3347 | 11/1011 | 4/336 | chr19 | 51311858 | |||
| chr19:51327770 | C | T | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.806C>T | p.Thr269Met | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/8 | 1010/3347 | 806/1011 | 269/336 | chr19 | 51327770 | |||
| chr19:51328709 | G | A | 1 | a0002 | 4 | HG00621.hp2 NA18961.hp2 NA18975.hp1 others(1): Show |
missense_variant | MODERATE | c.961G>A | p.Gly321Arg | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1165/3347 | 961/1011 | 321/336 | chr19 | 51328709 | |||
| chr19:51328756 | G | A | 1 | a0006 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1008G>A | p.Met336Ile | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1212/3347 | 1008/1011 | 336/336 | chr19 | 51328756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:51322101 | C | T | 1 | a0001c0009 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.117C>T | p.Ala39Ala | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/8 | 321/3347 | 117/1011 | 39/336 | chr19 | 51322101 | |||
| chr19:51323779 | C | T | 1 | a0001c0008 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.276C>T | p.Pro92Pro | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/8 | 480/3347 | 276/1011 | 92/336 | chr19 | 51323779 | |||
| chr19:51327843 | C | A | 1 | a0001c0003 | 2 | HG00423.hp1 NA19010.hp2 |
synonymous_variant | LOW | c.879C>A | p.Ala293Ala | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/8 | 1083/3347 | 879/1011 | 293/336 | chr19 | 51327843 | |||
| chr19:51328696 | C | T | 1 | a0001c0006 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.948C>T | p.Ala316Ala | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1152/3347 | 948/1011 | 316/336 | chr19 | 51328696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:51311644 | G | A | 1 | a0001c0001t0028 | 1 | NA19070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-204G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 204 | chr19 | 51311644 | ||||||
| chr19:51311696 | G | GC | 11 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0027 others(8): Show |
28 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-145dupC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 144 | INFO_REALIGN_3_PRIME | chr19 | 51311696 | |||||
| chr19:51311700 | C | A | 2 | a0001c0001t0020 a0001c0001t0021 |
4 | HG00609.hp1 HG00621.hp1 HG02071.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-148C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 148 | chr19 | 51311700 | ||||||
| chr19:51311707 | C | A | 1 | a0001c0001t0029 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-141C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 141 | chr19 | 51311707 | ||||||
| chr19:51311710 | CT | C | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(12): Show |
52 | HG00099.hp2 HG00609.hp1 HG01081.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-137delT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 137 | chr19 | 51311710 | ||||||
| chr19:51311711 | T | C | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
102 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-137T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 137 | chr19 | 51311711 | ||||||
| chr19:51311711 | T | TC | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(6): Show |
12 | HG00609.hp2 HG01099.hp1 HG01175.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-131dupC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 130 | INFO_REALIGN_3_PRIME | chr19 | 51311711 | |||||
| chr19:51311718 | G | GC | 3 | a0001c0001t0012 a0001c0001t0030 a0001c0001t0031 |
5 | HG03831.hp1 HG03834.hp2 NA18987.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-125dupC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 124 | INFO_REALIGN_3_PRIME | chr19 | 51311718 | |||||
| chr19:51311755 | G | C | 1 | a0001c0001t0033 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-93G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 93 | chr19 | 51311755 | ||||||
| chr19:51311769 | T | TC | 16 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(13): Show |
60 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-73dupC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 72 | INFO_REALIGN_3_PRIME | chr19 | 51311769 | |||||
| chr19:51311776 | T | C | 1 | a0001c0001t0050 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 72 | chr19 | 51311776 | ||||||
| chr19:51311807 | G | GC | 6 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0016 others(3): Show |
14 | HG01175.hp1 HG01192.hp1 HG01934.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-34dupC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 33 | INFO_REALIGN_3_PRIME | chr19 | 51311807 | |||||
| chr19:51311827 | C | A | 1 | a0001c0001t0022 | 2 | HG00323.hp1 HG02257.hp1 |
5_prime_UTR_variant | MODIFIER | c.-21C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/8 | 21 | chr19 | 51311827 | ||||||
| chr19:51328785 | C | T | 1 | a0001c0001t0019 | 3 | HG02451.hp2 HG03098.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 26 | chr19 | 51328785 | ||||||
| chr19:51328869 | A | C | 1 | a0001c0001t0049 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 110 | chr19 | 51328869 | ||||||
| chr19:51328953 | A | T | 1 | a0001c0001t0048 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 194 | chr19 | 51328953 | ||||||
| chr19:51329008 | C | T | 1 | a0001c0001t0047 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 249 | chr19 | 51329008 | ||||||
| chr19:51329017 | G | A | 8 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0023 others(5): Show |
19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 258 | chr19 | 51329017 | ||||||
| chr19:51329131 | T | G | 1 | a0001c0001t0049 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 372 | chr19 | 51329131 | ||||||
| chr19:51329131 | T | TGG | 2 | a0001c0001t0023 a0001c0001t0034 |
3 | HG02055.hp2 HG02280.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*373_*374insGG | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 374 | INFO_REALIGN_3_PRIME | chr19 | 51329131 | |||||
| chr19:51329133 | T | G | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(20): Show |
79 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 374 | chr19 | 51329133 | ||||||
| chr19:51329141 | T | G | 1 | a0001c0001t0039 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 382 | chr19 | 51329141 | ||||||
| chr19:51329157 | A | C | 1 | a0001c0001t0046 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 398 | chr19 | 51329157 | ||||||
| chr19:51329164 | C | T | 1 | a0001c0001t0054 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 405 | chr19 | 51329164 | ||||||
| chr19:51329210 | T | C | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0015 others(12): Show |
61 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*451T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 451 | chr19 | 51329210 | ||||||
| chr19:51329233 | G | GTA | 1 | a0001c0001t0018 | 3 | HG02572.hp2 HG02895.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475_*476dupTA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 477 | INFO_REALIGN_3_PRIME | chr19 | 51329233 | |||||
| chr19:51329648 | G | T | 1 | a0001c0001t0048 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*889G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 889 | chr19 | 51329648 | ||||||
| chr19:51329827 | G | GAC | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0016 others(2): Show |
28 | HG00741.hp2 HG01175.hp1 HG02040.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1095_*1096dupAC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1097 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329827 | G | GACAC | 2 | a0001c0001t0010 a0001c0001t0036 |
6 | HG00323.hp2 HG01358.hp1 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1093_*1096dupACAC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1097 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329827 | G | GACACAC | 2 | a0001c0001t0026 a0001c0001t0056 |
3 | HG01257.hp2 HG01258.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1091_*1096dupACAC others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1097 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329827 | GAC | G | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0015 others(15): Show |
67 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1095_*1096delAC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1095 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329827 | GACAC | G | 4 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0055 others(1): Show |
14 | HG02258.hp1 HG02486.hp2 HG02615.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1093_*1096delACAC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1093 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329827 | GACACACA others(5): Show |
G | 1 | a0001c0001t0018 | 3 | HG02572.hp2 HG02895.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1085_*1096delACAC others(8): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1085 | INFO_REALIGN_3_PRIME | chr19 | 51329827 | |||||
| chr19:51329835 | C | A | 1 | a0001c0001t0048 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1076 | chr19 | 51329835 | ||||||
| chr19:51329836 | A | C | 1 | a0001c0001t0048 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1077 | chr19 | 51329836 | ||||||
| chr19:51329854 | A | C | 1 | a0001c0001t0049 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1095 | chr19 | 51329854 | ||||||
| chr19:51329860 | G | A | 8 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0023 others(5): Show |
19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1101G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1101 | chr19 | 51329860 | ||||||
| chr19:51329966 | C | T | 1 | a0001c0001t0024 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1207C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1207 | chr19 | 51329966 | ||||||
| chr19:51330046 | CAGACATC others(18): Show |
C | 1 | a0001c0001t0038 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1288_*1312delAGAC others(21): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1288 | chr19 | 51330046 | ||||||
| chr19:51330072 | G | T | 1 | a0001c0001t0038 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1313 | chr19 | 51330072 | ||||||
| chr19:51330127 | A | G | 5 | a0001c0001t0028 a0001c0001t0031 a0001c0001t0037 others(2): Show |
5 | NA18957.hp2 NA18963.hp1 NA19009.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1368 | chr19 | 51330127 | ||||||
| chr19:51330198 | T | C | 1 | a0001c0001t0040 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1439T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1439 | chr19 | 51330198 | ||||||
| chr19:51330304 | A | G | 4 | a0001c0001t0023 a0001c0001t0034 a0001c0001t0035 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1545A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1545 | chr19 | 51330304 | ||||||
| chr19:51330363 | G | A | 2 | a0001c0001t0005 a0001c0001t0024 |
13 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1604G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1604 | chr19 | 51330363 | ||||||
| chr19:51330373 | A | G | 6 | a0001c0001t0028 a0001c0001t0031 a0001c0001t0037 others(3): Show |
6 | NA18957.hp2 NA18963.hp1 NA19009.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1614A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1614 | chr19 | 51330373 | ||||||
| chr19:51330511 | C | T | 1 | a0001c0001t0043 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1752C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1752 | chr19 | 51330511 | ||||||
| chr19:51330633 | T | A | 1 | a0001c0001t0049 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874T>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1874 | chr19 | 51330633 | ||||||
| chr19:51330714 | A | G | 1 | a0001c0001t0042 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1955 | chr19 | 51330714 | ||||||
| chr19:51330750 | T | C | 12 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0017 others(9): Show |
47 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 1991 | chr19 | 51330750 | ||||||
| chr19:51330802 | TTA | T | 18 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0017 others(15): Show |
53 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2049_*2050delAT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 2049 | INFO_REALIGN_3_PRIME | chr19 | 51330802 | |||||
| chr19:51330879 | A | C | 1 | a0001c0001t0049 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2120A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 8/8 | 2120 | chr19 | 51330879 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:51311964 | G | T | 5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+38G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51311964 | |||||||
| chr19:51311968 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.79+42G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51311968 | |||||||
| chr19:51311989 | G | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(139): Show |
207 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.79+63G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51311989 | |||||||
| chr19:51311995 | A | C | 3 | a0001c0001t0018g0235 a0001c0001t0018g0236 a0001c0003t0001g0050 |
4 | HG00423.hp1 HG02895.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+69A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51311995 | |||||||
| chr19:51312061 | G | C | 4 | a0001c0001t0006g0051 a0001c0001t0006g0053 a0001c0001t0014g0054 others(1): Show |
4 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+135G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312061 | |||||||
| chr19:51312065 | G | A | 5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+139G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312065 | |||||||
| chr19:51312070 | T | C | 3 | a0001c0001t0018g0235 a0001c0001t0018g0236 a0001c0003t0001g0050 |
4 | HG00423.hp1 HG02895.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+144T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312070 | |||||||
| chr19:51312227 | G | A | 5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+301G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312227 | |||||||
| chr19:51312228 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18978.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.79+302G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312228 | |||||||
| chr19:51312230 | A | G | 3 | a0001c0001t0018g0235 a0001c0001t0018g0236 a0001c0003t0001g0050 |
4 | HG00423.hp1 HG02895.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+304A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312230 | |||||||
| chr19:51312240 | G | T | 5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+314G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312240 | |||||||
| chr19:51312271 | C | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
211 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.79+345C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312271 | |||||||
| chr19:51312320 | G | A | 2 | a0001c0001t0019g0038 a0001c0001t0019g0144 |
3 | HG02451.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+394G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312320 | |||||||
| chr19:51312321 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.79+395G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312321 | |||||||
| chr19:51312450 | G | A | 9 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(6): Show |
14 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+524G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312450 | |||||||
| chr19:51312459 | A | T | 1 | a0001c0001t0050g0141 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.79+533A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312459 | |||||||
| chr19:51312636 | C | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(182): Show |
255 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.79+710C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312636 | |||||||
| chr19:51312654 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
5 | NA18944.hp2 NA18960.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+728C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312654 | |||||||
| chr19:51312690 | G | T | 33 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(30): Show |
37 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.79+764G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312690 | |||||||
| chr19:51312751 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+825G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312751 | |||||||
| chr19:51312813 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(182): Show |
255 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.79+887A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312813 | |||||||
| chr19:51312842 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+916G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312842 | |||||||
| chr19:51312919 | AG | A | 6 | a0001c0001t0006g0016 a0001c0001t0006g0061 a0001c0001t0006g0062 others(3): Show |
7 | HG02258.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+995delG | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51312919 | ||||||
| chr19:51312985 | C | A | 1 | a0001c0001t0004g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.79+1059C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51312985 | |||||||
| chr19:51313065 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
138 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.79+1139C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313065 | |||||||
| chr19:51313095 | G | A | 2 | a0001c0001t0019g0038 a0001c0001t0019g0144 |
3 | HG02451.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+1169G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313095 | |||||||
| chr19:51313126 | A | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(7): Show |
15 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+1200A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313126 | |||||||
| chr19:51313158 | C | G | 1 | a0001c0001t0050g0141 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.79+1232C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313158 | |||||||
| chr19:51313159 | G | C | 1 | a0001c0001t0050g0141 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.79+1233G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313159 | |||||||
| chr19:51313202 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.79+1276T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313202 | |||||||
| chr19:51313214 | G | A | 1 | a0001c0001t0004g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.79+1288G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313214 | |||||||
| chr19:51313239 | G | A | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+1313G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313239 | |||||||
| chr19:51313319 | T | G | 1 | a0001c0001t0025g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+1393T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313319 | |||||||
| chr19:51313322 | C | T | 75 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0025 others(72): Show |
90 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.79+1396C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313322 | |||||||
| chr19:51313498 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79+1572T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313498 | |||||||
| chr19:51313574 | T | TTTCTTTC others(7): Show |
5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1671_79+1684dup others(14): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313574 | ||||||
| chr19:51313574 | TTTCTTTC others(7): Show |
T | 23 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(20): Show |
27 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+1671_79+1684del others(14): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313574 | ||||||
| chr19:51313623 | T | C | 1 | a0001c0001t0006g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+1697T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313623 | |||||||
| chr19:51313633 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
137 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.79+1707C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313633 | |||||||
| chr19:51313635 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(41): Show |
66 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.79+1709C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313635 | |||||||
| chr19:51313637 | C | CTCTCTCT others(17): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG00544.hp1 HG01981.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1715_79+1738dup others(24): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313637 | ||||||
| chr19:51313637 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+1711C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313637 | |||||||
| chr19:51313639 | C | CTTT | 6 | a0001c0001t0001g0216 a0001c0001t0002g0234 a0001c0001t0004g0207 others(3): Show |
6 | HG01106.hp1 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1714_79+1715ins others(3): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313639 | ||||||
| chr19:51313639 | C | CTTTTT | 7 | a0001c0001t0001g0217 a0001c0001t0002g0030 a0001c0001t0002g0068 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1714_79+1715ins others(5): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313639 | ||||||
| chr19:51313639 | C | CTTTTTTC others(2): Show |
6 | a0001c0001t0002g0031 a0001c0001t0016g0209 a0001c0001t0017g0208 others(3): Show |
7 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1714_79+1715ins others(9): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313639 | ||||||
| chr19:51313639 | C | CTTTTTTC others(6): Show |
1 | a0001c0001t0017g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79+1714_79+1715ins others(13): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313639 | ||||||
| chr19:51313639 | C | CTTTTTTC others(18): Show |
1 | a0001c0001t0002g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.79+1714_79+1715ins others(25): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313639 | ||||||
| chr19:51313640 | TC | T | 11 | a0001c0001t0001g0232 a0001c0001t0002g0084 a0001c0001t0002g0086 others(8): Show |
11 | HG01081.hp2 HG02622.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+1715delC | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313640 | |||||||
| chr19:51313640 | TCTCTC | T | 47 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0025 others(44): Show |
62 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.79+1715_79+1719del others(5): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313640 | |||||||
| chr19:51313641 | C | T | 8 | a0001c0001t0001g0216 a0001c0001t0002g0234 a0001c0001t0004g0207 others(5): Show |
8 | HG01106.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+1715C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313641 | |||||||
| chr19:51313643 | C | T | 27 | a0001c0001t0001g0217 a0001c0001t0001g0232 a0001c0001t0002g0030 others(24): Show |
28 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+1717C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313643 | |||||||
| chr19:51313645 | C | CTCTTTCT others(5): Show |
1 | a0001c0001t0042g0001 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.79+1720_79+1721ins others(12): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313645 | ||||||
| chr19:51313645 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0232 others(16): Show |
19 | HG01081.hp2 HG01106.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+1719C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313645 | |||||||
| chr19:51313646 | TTTTTCTT others(6): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.79+1724_79+1736del others(13): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313646 | ||||||
| chr19:51313647 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0232 others(17): Show |
20 | HG01081.hp2 HG01106.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.79+1721T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313647 | |||||||
| chr19:51313647 | T | TTC | 15 | a0001c0001t0001g0217 a0001c0001t0002g0030 a0001c0001t0002g0031 others(12): Show |
16 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+1722_79+1723ins others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.79+1723_79+1724ins others(11): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
32 | HG00558.hp2 HG00673.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.79+1768_79+1771dup others(4): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTC others(3): Show |
1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+1727_79+1728ins others(10): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTT others(1): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.79+1764_79+1771dup others(8): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTT others(5): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(20): Show |
25 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+1760_79+1771dup others(12): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTT others(9): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(15): Show |
21 | HG00597.hp2 HG00741.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+1756_79+1771dup others(16): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTT others(21): Show |
1 | a0001c0001t0001g0009 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.79+1738_79+1739ins others(28): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | T | TTTTCTTT others(13): Show |
1 | a0001c0001t0001g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.79+1752_79+1771dup others(20): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313647 | TTTTC | T | 6 | a0001c0001t0001g0199 a0001c0001t0003g0012 a0001c0001t0005g0013 others(3): Show |
7 | HG00735.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1768_79+1771del others(4): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313647 | ||||||
| chr19:51313651 | C | CTTTCTTT others(13): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0145 a0001c0001t0001g0173 others(3): Show |
10 | HG01123.hp2 HG01934.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1738_79+1739ins others(20): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313651 | ||||||
| chr19:51313672 | TTTCTTTC others(16): Show |
T | 2 | a0001c0001t0001g0093 a0001c0001t0008g0111 |
2 | HG01496.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.79+1756_79+1778del others(23): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313672 | ||||||
| chr19:51313676 | TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0001g0003 a0001c0001t0003g0003 |
3 | HG01175.hp2 HG02015.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.79+1760_79+1778del others(19): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313676 | ||||||
| chr19:51313680 | TTTCTTTC others(8): Show |
T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(22): Show |
33 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.79+1764_79+1778del others(15): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313680 | ||||||
| chr19:51313684 | TTTCTTTC others(4): Show |
T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(31): Show |
41 | HG01106.hp2 HG01192.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+1768_79+1778del others(11): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313684 | ||||||
| chr19:51313688 | TTTCTTTC | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(31): Show |
42 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+1774_79+1780del others(7): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313688 | ||||||
| chr19:51313692 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0001g0005 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.79+1771_79+1772ins others(15): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313692 | ||||||
| chr19:51313692 | TTTC | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(35): Show |
48 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.79+1772_79+1774del others(3): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313692 | ||||||
| chr19:51313695 | C | CT | 48 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0098 others(45): Show |
52 | HG00423.hp1 HG00733.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.79+1771dupT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313695 | ||||||
| chr19:51313695 | C | CTTTCT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0107 others(2): Show |
5 | HG02080.hp2 HG03704.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1771_79+1772ins others(5): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313695 | ||||||
| chr19:51313695 | C | CTTTCTTT others(2): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0003g0008 others(1): Show |
5 | HG00597.hp1 HG00733.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1771_79+1772ins others(9): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313695 | ||||||
| chr19:51313695 | C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.79+1771_79+1772ins others(13): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313695 | ||||||
| chr19:51313695 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0003g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.79+1771_79+1772ins others(17): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51313695 | ||||||
| chr19:51313698 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.79+1772C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313698 | |||||||
| chr19:51313699 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.79+1773T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313699 | |||||||
| chr19:51313719 | C | A | 1 | a0001c0001t0055g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.79+1793C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313719 | |||||||
| chr19:51313802 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.79+1876G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313802 | |||||||
| chr19:51313907 | T | C | 1 | a0001c0001t0025g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+1981T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313907 | |||||||
| chr19:51313925 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.79+1999A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313925 | |||||||
| chr19:51313936 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+2010C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313936 | |||||||
| chr19:51313939 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.79+2013A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51313939 | |||||||
| chr19:51314053 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.79+2127C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314053 | |||||||
| chr19:51314162 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(175): Show |
247 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.79+2236C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314162 | |||||||
| chr19:51314177 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.79+2251C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314177 | |||||||
| chr19:51314179 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.79+2253C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314179 | |||||||
| chr19:51314187 | A | AT | 68 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0026 others(65): Show |
89 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.79+2275dupT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51314187 | ||||||
| chr19:51314187 | A | ATT | 28 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(25): Show |
32 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.79+2274_79+2275dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51314187 | ||||||
| chr19:51314403 | C | T | 34 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0055 others(31): Show |
43 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.79+2477C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314403 | |||||||
| chr19:51314482 | C | T | 1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+2556C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314482 | |||||||
| chr19:51314517 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
138 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.79+2591C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314517 | |||||||
| chr19:51314532 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.79+2606G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314532 | |||||||
| chr19:51314610 | T | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
158 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.79+2684T>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314610 | |||||||
| chr19:51314740 | T | G | 3 | a0001c0001t0018g0235 a0001c0001t0018g0236 a0001c0003t0001g0050 |
4 | HG00423.hp1 HG02895.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2814T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314740 | |||||||
| chr19:51314835 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.79+2909T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314835 | |||||||
| chr19:51314897 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(168): Show |
239 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.79+2971T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314897 | |||||||
| chr19:51314940 | C | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(7): Show |
15 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+3014C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314940 | |||||||
| chr19:51314970 | T | C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(7): Show |
15 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+3044T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51314970 | |||||||
| chr19:51315008 | C | T | 11 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(8): Show |
12 | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+3082C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315008 | |||||||
| chr19:51315084 | ATCTTCAA others(13): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.79+3159_79+3178del others(20): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315084 | |||||||
| chr19:51315124 | G | A | 14 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(11): Show |
16 | HG00423.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+3198G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315124 | |||||||
| chr19:51315276 | G | GA | 37 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0002g0007 others(34): Show |
46 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.79+3351dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315276 | ||||||
| chr19:51315352 | A | G | 61 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0055 others(58): Show |
77 | HG00423.hp1 HG00639.hp1 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.79+3426A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315352 | |||||||
| chr19:51315369 | G | A | 1 | a0001c0001t0025g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+3443G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315369 | |||||||
| chr19:51315422 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.79+3496G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315422 | |||||||
| chr19:51315508 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.79+3582G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315508 | |||||||
| chr19:51315541 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(110): Show |
169 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.79+3615G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315541 | |||||||
| chr19:51315592 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
138 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.79+3666T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315592 | |||||||
| chr19:51315688 | C | CT | 25 | a0001c0001t0001g0012 a0001c0001t0001g0143 a0001c0001t0001g0150 others(22): Show |
26 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+3787dupT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | C | CTTTTTTT | 6 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0060 others(3): Show |
10 | HG02109.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+3781_79+3787dup others(7): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0237 a0001c0009t0006g0241 |
2 | HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79+3764_79+3787dup others(24): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0002g0238 a0001c0001t0002g0239 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.79+3787_79+3788ins others(29): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0025g0240 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79+3787_79+3788ins others(30): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | CT | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0155 a0001c0001t0007g0154 others(2): Show |
6 | HG01993.hp1 HG03516.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+3787delT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | CTTTTTTT | C | 34 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0002g0007 others(31): Show |
43 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.79+3781_79+3787del others(7): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315688 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0008g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.79+3776_79+3787del others(12): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51315688 | ||||||
| chr19:51315713 | T | G | 3 | a0001c0001t0001g0018 a0001c0001t0007g0018 a0001c0001t0008g0095 |
4 | HG02738.hp1 NA18977.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+3787T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315713 | |||||||
| chr19:51315713 | T | TTG | 7 | a0001c0001t0001g0021 a0001c0001t0001g0097 a0001c0001t0001g0114 others(4): Show |
7 | HG02083.hp1 HG02523.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+3787_79+3788ins others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315713 | |||||||
| chr19:51315713 | T | TTTG | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
106 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.79+3787_79+3788ins others(3): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315713 | |||||||
| chr19:51315713 | T | TTTTG | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0110 others(13): Show |
22 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+3787_79+3788ins others(4): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315713 | |||||||
| chr19:51315757 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
252 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.79+3831A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315757 | |||||||
| chr19:51315969 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+4043C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315969 | |||||||
| chr19:51315985 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0088 |
2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.79+4059C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315985 | |||||||
| chr19:51315991 | G | T | 5 | a0001c0001t0001g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+4065G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51315991 | |||||||
| chr19:51316012 | G | C | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4086G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316012 | |||||||
| chr19:51316014 | T | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4088T>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316014 | |||||||
| chr19:51316017 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4091C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316017 | |||||||
| chr19:51316018 | A | ATTTGCTC others(60): Show |
1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4092_79+4093ins others(67): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316018 | |||||||
| chr19:51316032 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4106C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316032 | |||||||
| chr19:51316033 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4107C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316033 | |||||||
| chr19:51316041 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4115G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316041 | |||||||
| chr19:51316043 | G | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4117G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316043 | |||||||
| chr19:51316046 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4120C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316046 | |||||||
| chr19:51316049 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4123C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316049 | |||||||
| chr19:51316051 | G | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4125G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316051 | |||||||
| chr19:51316052 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4126A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316052 | |||||||
| chr19:51316053 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4127A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316053 | |||||||
| chr19:51316066 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4140C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316066 | |||||||
| chr19:51316072 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4146G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316072 | |||||||
| chr19:51316073 | C | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4147C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316073 | |||||||
| chr19:51316078 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4152G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316078 | |||||||
| chr19:51316081 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4155C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316081 | |||||||
| chr19:51316085 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4159C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316085 | |||||||
| chr19:51316086 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4160C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316086 | |||||||
| chr19:51316087 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4161T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316087 | |||||||
| chr19:51316094 | C | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4168C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316094 | |||||||
| chr19:51316095 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4169C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316095 | |||||||
| chr19:51316095 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.79+4169C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316095 | |||||||
| chr19:51316097 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4171G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316097 | |||||||
| chr19:51316098 | C | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4172C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316098 | |||||||
| chr19:51316102 | T | C | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4176T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316102 | |||||||
| chr19:51316105 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4179G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316105 | |||||||
| chr19:51316109 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4183G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316109 | |||||||
| chr19:51316115 | G | T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4189G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316115 | |||||||
| chr19:51316116 | C | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4190C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316116 | |||||||
| chr19:51316118 | G | C | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4192G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316118 | |||||||
| chr19:51316120 | T | TTATTGTT others(5): Show |
1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4194_79+4195ins others(12): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316120 | |||||||
| chr19:51316123 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4197A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316123 | |||||||
| chr19:51316124 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4198T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316124 | |||||||
| chr19:51316127 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG00733.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.79+4201C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316127 | |||||||
| chr19:51316136 | A | C | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4210A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316136 | |||||||
| chr19:51316137 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4211G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316137 | |||||||
| chr19:51316138 | G | C | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4212G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316138 | |||||||
| chr19:51316140 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4214G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316140 | |||||||
| chr19:51316142 | TGAAGACT others(64): Show |
T | 1 | a0001c0001t0003g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79+4217_79+4287del others(71): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316142 | |||||||
| chr19:51316174 | C | T | 1 | a0001c0001t0017g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.79+4248C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316174 | |||||||
| chr19:51316182 | C | CA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
9 | HG00609.hp1 HG01175.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+4272dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316182 | ||||||
| chr19:51316182 | CA | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(27): Show |
32 | HG00544.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.79+4272delA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316182 | ||||||
| chr19:51316182 | CAA | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.79+4271_79+4272del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316182 | ||||||
| chr19:51316216 | G | A | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+4290G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316216 | |||||||
| chr19:51316277 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.79+4351G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316277 | |||||||
| chr19:51316278 | G | A | 6 | a0001c0001t0006g0016 a0001c0001t0006g0061 a0001c0001t0006g0062 others(3): Show |
7 | HG02258.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4352G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316278 | |||||||
| chr19:51316344 | C | CA | 31 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0237 others(28): Show |
38 | HG01109.hp2 HG01175.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.79+4433dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316344 | ||||||
| chr19:51316344 | CA | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0185 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+4433delA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316344 | ||||||
| chr19:51316360 | G | A | 23 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0237 others(20): Show |
30 | HG00423.hp1 HG01109.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+4434G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316360 | |||||||
| chr19:51316463 | C | CT | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(17): Show |
24 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+4546dupT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316463 | ||||||
| chr19:51316463 | CT | C | 24 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0237 others(21): Show |
31 | HG00423.hp1 HG01109.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.79+4546delT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316463 | ||||||
| chr19:51316498 | C | CT | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(38): Show |
57 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.79+4585dupT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316498 | ||||||
| chr19:51316498 | C | CTT | 12 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0145 others(9): Show |
17 | HG00544.hp1 HG01123.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+4584_79+4585dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316498 | ||||||
| chr19:51316498 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79+4585_79+4586ins others(25): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51316498 | ||||||
| chr19:51316503 | T | C | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.79+4577T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316503 | |||||||
| chr19:51316512 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.79+4586A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316512 | |||||||
| chr19:51316516 | C | T | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(7): Show |
15 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+4590C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316516 | |||||||
| chr19:51316519 | A | G | 1 | a0001c0001t0025g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+4593A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316519 | |||||||
| chr19:51316847 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.79+4921T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316847 | |||||||
| chr19:51316937 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.79+5011G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316937 | |||||||
| chr19:51316949 | C | G | 45 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0002g0007 others(42): Show |
55 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+5023C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51316949 | |||||||
| chr19:51317030 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0007g0045 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.80-5034A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317030 | |||||||
| chr19:51317071 | A | G | 1 | a0001c0001t0048g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.80-4993A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317071 | |||||||
| chr19:51317072 | G | A | 1 | a0001c0001t0048g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.80-4992G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317072 | |||||||
| chr19:51317141 | G | C | 1 | a0001c0001t0009g0220 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.80-4923G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317141 | |||||||
| chr19:51317209 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-4855C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317209 | |||||||
| chr19:51317269 | G | A | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(7): Show |
15 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.80-4795G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317269 | |||||||
| chr19:51317270 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.80-4794G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317270 | |||||||
| chr19:51317306 | G | A | 1 | a0001c0001t0041g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4758G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317306 | |||||||
| chr19:51317583 | A | AGGAGTCA others(21): Show |
1 | a0001c0001t0001g0171 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.80-4480_80-4453dup others(28): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51317583 | ||||||
| chr19:51317613 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0008g0130 |
2 | NA18980.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.80-4451C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317613 | |||||||
| chr19:51317755 | C | T | 1 | a0001c0001t0013g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.80-4309C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317755 | |||||||
| chr19:51317812 | C | G | 1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-4252C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317812 | |||||||
| chr19:51317834 | T | C | 6 | a0001c0001t0001g0217 a0001c0001t0001g0237 a0001c0001t0018g0235 others(3): Show |
7 | HG00423.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4230T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317834 | |||||||
| chr19:51317861 | G | A | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-4203G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317861 | |||||||
| chr19:51317937 | C | T | 1 | a0001c0001t0054g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.80-4127C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51317937 | |||||||
| chr19:51318008 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG01081.hp1 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.80-4056G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318008 | |||||||
| chr19:51318016 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-4048C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318016 | |||||||
| chr19:51318053 | C | T | 17 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(14): Show |
23 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-4011C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318053 | |||||||
| chr19:51318162 | T | C | 6 | a0001c0001t0006g0016 a0001c0001t0006g0061 a0001c0001t0006g0062 others(3): Show |
7 | HG02258.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3902T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318162 | |||||||
| chr19:51318325 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80-3739C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318325 | |||||||
| chr19:51318380 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.80-3684A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318380 | |||||||
| chr19:51318437 | C | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(15): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-3627C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318437 | |||||||
| chr19:51318535 | C | T | 17 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(14): Show |
23 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-3529C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318535 | |||||||
| chr19:51318573 | T | TA | 10 | a0001c0001t0001g0173 a0001c0001t0004g0174 a0001c0001t0005g0227 others(7): Show |
11 | HG02258.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-3479dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51318573 | ||||||
| chr19:51318725 | ACT | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.80-3336_80-3335del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51318725 | ||||||
| chr19:51318895 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.80-3169C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318895 | |||||||
| chr19:51318913 | G | A | 1 | a0003c0010t0001g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80-3151G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51318913 | |||||||
| chr19:51319045 | C | A | 2 | a0001c0001t0019g0038 a0001c0001t0019g0144 |
3 | HG02451.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-3019C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319045 | |||||||
| chr19:51319074 | A | T | 1 | a0001c0001t0048g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.80-2990A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319074 | |||||||
| chr19:51319092 | G | A | 17 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0005g0013 others(14): Show |
23 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-2972G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319092 | |||||||
| chr19:51319252 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.80-2812C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319252 | |||||||
| chr19:51319298 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.80-2766T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319298 | |||||||
| chr19:51319304 | C | CGT | 2 | a0001c0001t0019g0038 a0001c0001t0019g0144 |
3 | HG02451.hp2 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-2738_80-2737dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51319304 | ||||||
| chr19:51319304 | C | CGTGT | 7 | a0001c0001t0005g0013 a0001c0001t0005g0056 a0001c0001t0005g0058 others(4): Show |
11 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-2740_80-2737dup others(4): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51319304 | ||||||
| chr19:51319304 | C | T | 3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0044g0127 |
3 | HG02257.hp2 HG02818.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.80-2760C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319304 | |||||||
| chr19:51319304 | CGT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.80-2738_80-2737del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51319304 | ||||||
| chr19:51319306 | T | C | 3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0044g0127 |
3 | HG02257.hp2 HG02818.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.80-2758T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319306 | |||||||
| chr19:51319326 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0002g0233 |
2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.80-2738T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319326 | |||||||
| chr19:51319379 | G | A | 2 | a0001c0001t0034g0069 a0001c0001t0035g0065 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.80-2685G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319379 | |||||||
| chr19:51319506 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.80-2558A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319506 | |||||||
| chr19:51319627 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.80-2437G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319627 | |||||||
| chr19:51319721 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0007g0033 |
2 | HG01346.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.80-2343G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319721 | |||||||
| chr19:51319730 | T | C | 1 | a0001c0001t0039g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.80-2334T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319730 | |||||||
| chr19:51319761 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
163 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.80-2303A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319761 | |||||||
| chr19:51319849 | G | A | 1 | a0006c0005t0002g0074 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-2215G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319849 | |||||||
| chr19:51319940 | C | T | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0216 others(29): Show |
36 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.80-2124C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51319940 | |||||||
| chr19:51320033 | A | ATG | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.80-2018_80-2017dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51320033 | ||||||
| chr19:51320033 | ATG | A | 4 | a0001c0001t0018g0235 a0001c0001t0018g0236 a0001c0001t0031g0158 others(1): Show |
5 | HG00423.hp1 HG02895.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-2018_80-2017del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51320033 | ||||||
| chr19:51320066 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.80-1998C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320066 | |||||||
| chr19:51320067 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.80-1997A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320067 | |||||||
| chr19:51320250 | G | A | 11 | a0001c0001t0005g0227 a0001c0001t0006g0016 a0001c0001t0006g0061 others(8): Show |
13 | HG00423.hp1 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-1814G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320250 | |||||||
| chr19:51320251 | C | T | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-1813C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320251 | |||||||
| chr19:51320269 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0003g0015 |
3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.80-1795C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320269 | |||||||
| chr19:51320315 | C | T | 8 | a0001c0001t0005g0227 a0001c0001t0006g0016 a0001c0001t0006g0061 others(5): Show |
9 | HG02258.hp1 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-1749C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320315 | |||||||
| chr19:51320453 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80-1611C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320453 | |||||||
| chr19:51320546 | C | T | 1 | a0001c0001t0003g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.80-1518C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320546 | |||||||
| chr19:51320586 | G | A | 1 | a0001c0001t0005g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-1478G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320586 | |||||||
| chr19:51320608 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-1456G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320608 | |||||||
| chr19:51320609 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-1455C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320609 | |||||||
| chr19:51320637 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.80-1427C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320637 | |||||||
| chr19:51320649 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.80-1415G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320649 | |||||||
| chr19:51320828 | C | G | 1 | a0001c0001t0003g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.80-1236C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320828 | |||||||
| chr19:51320923 | C | T | 2 | a0001c0001t0018g0235 a0001c0001t0018g0236 |
2 | HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80-1141C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320923 | |||||||
| chr19:51320940 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.80-1124T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320940 | |||||||
| chr19:51320947 | C | T | 7 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(4): Show |
12 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-1117C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320947 | |||||||
| chr19:51320956 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.80-1108T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320956 | |||||||
| chr19:51320966 | A | G | 1 | a0001c0001t0009g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.80-1098A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320966 | |||||||
| chr19:51320968 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.80-1096A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51320968 | |||||||
| chr19:51321023 | TTG | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0008g0130 |
3 | NA18973.hp1 NA18980.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.80-1031_80-1030del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51321023 | ||||||
| chr19:51321034 | T | TATGTGTG others(951): Show |
1 | a0001c0001t0006g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-778_80-777insTC others(956): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51321034 | ||||||
| chr19:51321039 | G | A | 1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-1025G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321039 | |||||||
| chr19:51321086 | G | T | 1 | a0001c0006t0001g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.80-978G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321086 | |||||||
| chr19:51321118 | G | A | 1 | a0001c0001t0006g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.80-946G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321118 | |||||||
| chr19:51321189 | C | T | 11 | a0001c0001t0005g0227 a0001c0001t0006g0016 a0001c0001t0006g0061 others(8): Show |
13 | HG00423.hp1 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-875C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321189 | |||||||
| chr19:51321287 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.80-777C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321287 | |||||||
| chr19:51321513 | ATG | A | 7 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(4): Show |
12 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-545_80-544delGT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51321513 | ||||||
| chr19:51321567 | ATC | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(34): Show |
53 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.80-495_80-494delCT | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | 51321567 | ||||||
| chr19:51321708 | G | A | 4 | a0001c0001t0031g0158 a0001c0001t0037g0041 a0001c0001t0045g0159 others(1): Show |
4 | NA18957.hp2 NA18963.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-356G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321708 | |||||||
| chr19:51321712 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80-352C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321712 | |||||||
| chr19:51321791 | G | A | 3 | a0001c0001t0004g0207 a0001c0001t0016g0209 a0001c0001t0025g0205 |
3 | HG02559.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80-273G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321791 | |||||||
| chr19:51321791 | G | T | 1 | a0001c0001t0048g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.80-273G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321791 | |||||||
| chr19:51321930 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.80-134T>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321930 | |||||||
| chr19:51321931 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.80-133G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321931 | |||||||
| chr19:51321984 | C | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(52): Show |
76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.80-80C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 1/7 | chr19 | 51321984 | |||||||
| chr19:51322214 | G | T | 1 | a0001c0001t0048g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.158+72G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322214 | |||||||
| chr19:51322306 | C | T | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+164C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322306 | |||||||
| chr19:51322361 | C | CAGAGAGA others(17): Show |
1 | a0001c0001t0001g0036 | 2 | HG00438.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.158+247_158+270dup others(24): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322361 | ||||||
| chr19:51322392 | A | AGGGACAG others(15): Show |
1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.158+261_158+282dup others(22): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322392 | ||||||
| chr19:51322394 | G | A | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+252G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322394 | |||||||
| chr19:51322397 | C | A | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+255C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322397 | |||||||
| chr19:51322403 | C | CCCAGAGA others(15): Show |
7 | a0001c0001t0002g0214 a0001c0001t0003g0011 a0001c0001t0005g0227 others(4): Show |
7 | HG02723.hp2 HG02886.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.158+332_158+353dup others(22): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322403 | ||||||
| chr19:51322403 | C | CCCAGAGA others(37): Show |
2 | a0001c0001t0001g0004 a0001c0001t0017g0211 |
2 | HG02083.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.158+310_158+353dup others(44): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322403 | ||||||
| chr19:51322403 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.158+261C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322403 | |||||||
| chr19:51322403 | CCCAGAGA others(15): Show |
C | 9 | a0001c0001t0003g0002 a0001c0001t0003g0108 a0001c0001t0019g0038 others(6): Show |
10 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+332_158+353del others(22): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322403 | ||||||
| chr19:51322403 | CCCAGAGA others(37): Show |
C | 1 | a0001c0001t0006g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.158+310_158+353del others(44): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322403 | ||||||
| chr19:51322405 | C | CAGAGAGA others(13): Show |
1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.158+270_158+271ins others(20): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322405 | ||||||
| chr19:51322409 | GAGAAGGG others(47): Show |
G | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+271_158+324del others(54): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322409 | ||||||
| chr19:51322425 | T | C | 1 | a0001c0001t0019g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.158+283T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322425 | |||||||
| chr19:51322447 | T | C | 1 | a0001c0001t0019g0038 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.158+305T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322447 | |||||||
| chr19:51322469 | T | C | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+327T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322469 | |||||||
| chr19:51322470 | C | T | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+328C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322470 | |||||||
| chr19:51322561 | C | G | 11 | a0001c0001t0001g0017 a0001c0001t0005g0071 a0001c0001t0005g0227 others(8): Show |
14 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158+419C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322561 | |||||||
| chr19:51322573 | C | CCT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
135 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.158+451_158+452dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322573 | ||||||
| chr19:51322595 | G | T | 1 | a0001c0001t0001g0047 | 2 | NA18950.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.158+453G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322595 | |||||||
| chr19:51322598 | T | C | 1 | a0001c0001t0001g0047 | 2 | NA18950.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.158+456T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322598 | |||||||
| chr19:51322599 | GCT | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.158+474_158+475del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322599 | ||||||
| chr19:51322709 | G | A | 4 | a0001c0001t0018g0059 a0001c0001t0018g0235 a0001c0001t0018g0236 others(1): Show |
5 | HG00423.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+567G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322709 | |||||||
| chr19:51322795 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
137 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.158+653C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322795 | |||||||
| chr19:51322820 | A | G | 8 | a0001c0001t0005g0227 a0001c0001t0006g0016 a0001c0001t0006g0061 others(5): Show |
9 | HG02258.hp1 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+678A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322820 | |||||||
| chr19:51322855 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.158+713T>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322855 | |||||||
| chr19:51322855 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0232 |
2 | HG00642.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.158+713T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322855 | |||||||
| chr19:51322858 | G | A | 1 | a0001c0001t0054g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.158+716G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322858 | |||||||
| chr19:51322878 | TTCTCTGG others(17): Show |
T | 1 | a0001c0001t0006g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.158+746_159-751del others(24): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51322878 | ||||||
| chr19:51322888 | A | G | 1 | a0001c0001t0013g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.158+746A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51322888 | |||||||
| chr19:51323030 | T | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0070 others(3): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-632T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323030 | |||||||
| chr19:51323114 | G | C | 1 | a0001c0001t0016g0209 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.159-548G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323114 | |||||||
| chr19:51323242 | GTGTC | G | 51 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(48): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.159-418_159-415del others(4): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51323242 | ||||||
| chr19:51323244 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
163 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.159-418G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323244 | |||||||
| chr19:51323246 | C | G | 1 | a0001c0001t0003g0008 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.159-416C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323246 | |||||||
| chr19:51323280 | G | C | 17 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(14): Show |
24 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.159-382G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323280 | |||||||
| chr19:51323299 | TCTCTCTC others(13): Show |
T | 4 | a0001c0001t0004g0161 a0001c0001t0004g0207 a0001c0001t0011g0188 others(1): Show |
4 | HG00741.hp2 HG02559.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-334_159-315del others(20): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr19 | 51323299 | ||||||
| chr19:51323539 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0118 others(15): Show |
22 | NA18939.hp2 NA18940.hp2 NA18943.hp1 others(19): Show |
intron_variant | MODIFIER | c.159-123G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323539 | |||||||
| chr19:51323600 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0193 others(1): Show |
5 | HG00738.hp1 HG01981.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-62C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323600 | |||||||
| chr19:51323604 | G | T | 1 | a0001c0001t0022g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.159-58G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 2/7 | chr19 | 51323604 | |||||||
| chr19:51323982 | A | T | 1 | a0001c0001t0005g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+88A>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51323982 | |||||||
| chr19:51324140 | G | A | 17 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(14): Show |
24 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.391+246G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324140 | |||||||
| chr19:51324204 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0145 a0001c0001t0001g0148 others(3): Show |
14 | HG01109.hp1 HG01167.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+310G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324204 | |||||||
| chr19:51324299 | C | A | 2 | a0001c0001t0005g0227 a0001c0001t0006g0078 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.391+405C>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324299 | |||||||
| chr19:51324340 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.391+446A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324340 | |||||||
| chr19:51324373 | G | A | 1 | a0001c0003t0001g0050 | 2 | HG00423.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.391+479G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324373 | |||||||
| chr19:51324441 | G | A | 1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.391+547G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324441 | |||||||
| chr19:51324485 | G | A | 1 | a0001c0009t0006g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.391+591G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324485 | |||||||
| chr19:51324673 | G | A | 2 | a0001c0001t0004g0020 a0001c0001t0030g0020 |
3 | NA18995.hp1 NA19077.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.392-673G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324673 | |||||||
| chr19:51324846 | T | A | 1 | a0001c0001t0045g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.392-500T>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324846 | |||||||
| chr19:51324881 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
137 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.392-465T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51324881 | |||||||
| chr19:51325018 | A | C | 1 | a0001c0001t0047g0183 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.392-328A>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51325018 | |||||||
| chr19:51325157 | C | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(38): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.392-189C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51325157 | |||||||
| chr19:51325205 | GGGAGGAG others(33): Show |
G | 1 | a0001c0001t0056g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.392-119_392-80delA others(39): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr19 | 51325205 | ||||||
| chr19:51325233 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.392-113T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51325233 | |||||||
| chr19:51325299 | G | T | 1 | a0001c0001t0045g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.392-47G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51325299 | |||||||
| chr19:51325341 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(55): Show |
86 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
splice_region_variant&intron_variant | LOW | c.392-5C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 3/7 | chr19 | 51325341 | |||||||
| chr19:51325483 | G | A | 2 | a0001c0001t0023g0052 a0001c0001t0023g0075 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.511+18G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325483 | |||||||
| chr19:51325594 | G | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(39): Show |
59 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.511+129G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325594 | |||||||
| chr19:51325717 | G | A | 1 | a0001c0001t0029g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.511+252G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325717 | |||||||
| chr19:51325763 | C | G | 6 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(3): Show |
11 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+298C>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325763 | |||||||
| chr19:51325780 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.511+315G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325780 | |||||||
| chr19:51325796 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
138 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.511+331A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325796 | |||||||
| chr19:51325842 | CCT | C | 68 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(65): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.511+384_511+385del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 51325842 | ||||||
| chr19:51325844 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
138 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.511+379T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325844 | |||||||
| chr19:51325860 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG01081.hp1 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.511+395C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325860 | |||||||
| chr19:51325906 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.511+441A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325906 | |||||||
| chr19:51325919 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.511+454G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51325919 | |||||||
| chr19:51326033 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.511+568G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51326033 | |||||||
| chr19:51326057 | C | T | 25 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(22): Show |
31 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.511+592C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51326057 | |||||||
| chr19:51326090 | T | C | 8 | a0001c0001t0006g0051 a0001c0001t0006g0053 a0001c0001t0014g0054 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.511+625T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51326090 | |||||||
| chr19:51326145 | GA | G | 15 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0070 others(12): Show |
16 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.512-617delA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 51326145 | ||||||
| chr19:51326294 | G | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(40): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.512-470G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51326294 | |||||||
| chr19:51326720 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18978.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.512-44T>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | chr19 | 51326720 | |||||||
| chr19:51326740 | CCCT | C | 4 | a0001c0001t0001g0046 a0001c0001t0004g0174 a0001c0001t0004g0177 others(1): Show |
4 | NA18954.hp2 NA18955.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-14_512-12delCC others(1): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr19 | 51326740 | ||||||
| chr19:51326967 | G | T | 1 | a0001c0001t0045g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.646+69G>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 5/7 | chr19 | 51326967 | |||||||
| chr19:51326986 | G | A | 1 | a0001c0003t0001g0050 | 2 | HG00423.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.646+88G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 5/7 | chr19 | 51326986 | |||||||
| chr19:51327043 | C | T | 1 | a0004c0011t0001g0224 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.647-37C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 5/7 | chr19 | 51327043 | |||||||
| chr19:51327345 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.767+145G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 6/7 | chr19 | 51327345 | |||||||
| chr19:51327361 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.767+161G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 6/7 | chr19 | 51327361 | |||||||
| chr19:51327608 | G | A | 3 | a0001c0001t0017g0208 a0001c0001t0017g0210 a0001c0001t0017g0211 |
3 | HG03516.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.768-124G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 6/7 | chr19 | 51327608 | |||||||
| chr19:51328267 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0007g0033 |
5 | HG01346.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+381C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328267 | |||||||
| chr19:51328307 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.923-364G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328307 | |||||||
| chr19:51328339 | C | CA | 10 | a0001c0001t0001g0045 a0001c0001t0001g0196 a0001c0001t0001g0201 others(7): Show |
10 | HG01169.hp2 HG01358.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.923-317dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAA | 12 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0070 others(9): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.923-318_923-317dup others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0041g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.923-326_923-317dup others(10): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0024g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.923-327_923-317dup others(11): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0017g0210 a0001c0001t0017g0211 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.923-328_923-317dup others(12): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(6): Show |
13 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.923-329_923-317dup others(13): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(7): Show |
9 | a0001c0001t0005g0071 a0001c0001t0006g0051 a0001c0001t0006g0053 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.923-330_923-317dup others(14): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0006g0016 a0001c0001t0006g0061 a0001c0001t0006g0064 others(3): Show |
7 | HG02258.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.923-331_923-317dup others(15): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.923-317_923-316ins others(16): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0006g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.923-317_923-316ins others(17): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0019g0038 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.923-317_923-316ins others(21): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328339 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0019g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.923-317_923-316ins others(22): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328339 | ||||||
| chr19:51328504 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.923-167A>G | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328504 | |||||||
| chr19:51328505 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.923-166G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328505 | |||||||
| chr19:51328505 | G | GA | 75 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0024 others(72): Show |
99 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.923-149dupA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328505 | ||||||
| chr19:51328505 | GA | G | 36 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0155 others(33): Show |
38 | HG01169.hp1 HG01884.hp2 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.923-149delA | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328505 | ||||||
| chr19:51328505 | GAA | G | 9 | a0001c0001t0005g0013 a0001c0001t0005g0028 a0001c0001t0005g0056 others(6): Show |
14 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.923-150_923-149del others(2): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr19 | 51328505 | ||||||
| chr19:51328519 | A | AG | 10 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0150 others(7): Show |
15 | HG00544.hp1 HG01123.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.923-152_923-151ins others(1): Show |
IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328519 | |||||||
| chr19:51328523 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0232 |
3 | HG00642.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.923-148G>A | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328523 | |||||||
| chr19:51328573 | G | C | 43 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0070 others(40): Show |
51 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.923-98G>C | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328573 | |||||||
| chr19:51328636 | C | T | 1 | a0001c0001t0013g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.923-35C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328636 | |||||||
| chr19:51328666 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0003g0015 |
3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
splice_region_variant&intron_variant | LOW | c.923-5C>T | IGLON5 | ENSG00000142549.10 | transcript | ENST00000270642.9 | protein_coding | 7/7 | chr19 | 51328666 |