Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5819 |
| ensemblid | ENSG00000130202.10 |
| hgncid | 9707 |
| symbol | NECTIN2 |
| name | nectin cell adhesion molecule 2 |
| refseq_nuc | NM_001042724.2 |
| refseq_prot | NP_001036189.1 |
| ensembl_nuc | ENST00000252483.10 |
| ensembl_prot | ENSP00000252483.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 44846297 |
| end | 44889223 |
| strand | + |
| ver | v1.2 |
| region | chr19:44846297-44889223 |
| region5000 | chr19:44841297-44894223 |
| regionname0 | NECTIN2_chr19_44846297_44889223 |
| regionname5000 | NECTIN2_chr19_44841297_44894223 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 538 | 347 | 89 | 68 | 141 | 14 | 33 | 110 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0002 | 0/0 | 538 | 11 | 0 | 9 | 1 | 0 | 1 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0003 | 0/0 | 538 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0004 | 0/0 | 538 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0005 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MAQAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0006 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0007 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0008 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0009 | 0/0 | 538 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0010 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0011 | 0/0 | 538 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| a0012 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | MARAA others(533): Show |
chr19 | 44841297 | 44894223 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1614 | 328 | 78 | 63 | 140 | 12 | 33 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0001c0003 | 0/0 | 1614 | 8 | 8 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0001c0004 | 0/0 | 1614 | 5 | 3 | 2 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0001c0006 | 0/0 | 1614 | 3 | 0 | 1 | 0 | 2 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0001c0007 | 0/0 | 1614 | 2 | 0 | 2 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0001c0012 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0002c0002 | 0/0 | 1614 | 11 | 0 | 9 | 1 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0003c0005 | 0/0 | 1614 | 4 | 4 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0003c0016 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0004c0013 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0005c0008 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0006c0015 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0007c0011 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0008c0014 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0009c0010 | 0/0 | 1614 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0010c0018 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0011c0017 | 0/0 | 1614 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 | ||
| a0012c0009 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | ATGGC others(1609): Show |
chr19 | 44841297 | 44894223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2690 | 274 | 61 | 55 | 113 | 11 | 32 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0002 | 0/0 | 2690 | 28 | 5 | 8 | 14 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0003 | 0/0 | 2690 | 7 | 0 | 0 | 7 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0004 | 0/0 | 2690 | 5 | 5 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0006 | 0/0 | 2690 | 4 | 4 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0007 | 0/0 | 2690 | 2 | 0 | 0 | 2 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0008 | 0/0 | 2690 | 2 | 2 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0010 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0011 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0013 | 0/0 | 2690 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0014 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0015 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0001t0016 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0003t0001 | 0/0 | 2690 | 3 | 3 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0003t0002 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0003t0005 | 0/0 | 2690 | 4 | 4 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0004t0001 | 0/0 | 2690 | 2 | 1 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0004t0002 | 0/0 | 2690 | 2 | 1 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0004t0012 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0006t0001 | 0/0 | 2690 | 3 | 0 | 1 | 0 | 2 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0007t0001 | 0/0 | 2690 | 2 | 0 | 2 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0001c0012t0002 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0002c0002t0001 | 0/0 | 2690 | 10 | 0 | 8 | 1 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0002c0002t0009 | 0/0 | 2690 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0003c0005t0001 | 0/0 | 2690 | 4 | 4 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0003c0016t0001 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0004c0013t0001 | 0/0 | 2690 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0005c0008t0001 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0006c0015t0001 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0007c0011t0001 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0008c0014t0001 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0009c0010t0002 | 0/0 | 2690 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0010c0018t0004 | 0/0 | 2690 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0011c0017t0001 | 0/0 | 2690 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| a0012c0009t0001 | 0/0 | 2690 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | GTGAC others(2685): Show |
chr19 | 44841297 | 44894223 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0010g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0011g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0013g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0015g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0001t0016g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0003t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0004t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0004t0012g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0006t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0006t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0007t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0001c0012t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0002c0002t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0003c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0003c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0003c0016t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0004c0013t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0005c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0006c0015t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0007c0011t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0008c0014t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0009c0010t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0010c0018t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0011c0017t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| a0012c0009t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0296 | EUR | FIN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0035 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0336 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0229 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0081 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01169 | hp1 | a0001 | c0007 | t0001 | g0082 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0147 | AMR | PUR | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01496 | hp2 | a0002 | c0002 | t0009 | g0052 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01516 | hp1 | a0001 | c0006 | t0001 | g0068 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01517 | hp1 | a0001 | c0006 | t0001 | g0079 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01975 | hp1 | a0004 | c0013 | t0001 | g0073 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02080 | hp2 | a0005 | c0008 | t0001 | g0181 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02145 | hp1 | a0001 | c0003 | t0005 | g0344 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02145 | hp2 | a0006 | c0015 | t0001 | g0146 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02258 | hp2 | a0001 | c0004 | t0002 | g0080 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0348 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02451 | hp2 | a0007 | c0011 | t0001 | g0234 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02615 | hp1 | a0003 | c0005 | t0001 | g0012 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02630 | hp1 | a0003 | c0016 | t0001 | g0063 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0086 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02717 | hp2 | a0003 | c0005 | t0001 | g0264 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0350 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02735 | hp2 | a0009 | c0010 | t0002 | g0067 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0266 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0267 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0233 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03041 | hp1 | a0010 | c0018 | t0004 | g0261 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03139 | hp2 | a0001 | c0003 | t0005 | g0342 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0012 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0349 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03516 | hp2 | a0001 | c0003 | t0005 | g0328 | AFR | ESN | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03942 | hp2 | a0011 | c0017 | t0001 | g0287 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18522 | hp1 | a0001 | c0003 | t0005 | g0343 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18963 | hp2 | a0001 | c0001 | t0015 | g0299 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18974 | hp1 | a0001 | c0012 | t0002 | g0183 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0269 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18993 | hp2 | a0012 | c0009 | t0001 | g0215 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19043 | hp1 | a0001 | c0004 | t0012 | g0346 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0351 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19064 | hp1 | a0001 | c0001 | t0014 | g0298 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20129 | hp1 | a0003 | c0005 | t0001 | g0246 | AFR | ASW | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | GIH | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | GIH | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02486 | hp1 | a0008 | c0014 | t0001 | g0238 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | MSL | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | USA | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | USA | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0280 | REF | REF | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0128 | REF | REF | NECTIN2_chr19_44841297_44894223 | NECTIN2 | chr19 | 44841297 | 44894223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44846533 | G | A | 1 | a0005 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.8G>A | p.Arg3Gln | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/9 | 237/2690 | 8/1617 | 3/538 | chr19 | 44846533 | |||
| chr19:44846563 | C | T | 1 | a0010 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.38C>T | p.Pro13Leu | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/9 | 267/2690 | 38/1617 | 13/538 | chr19 | 44846563 | |||
| chr19:44865483 | G | A | 1 | a0012 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.301G>A | p.Glu101Lys | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/9 | 530/2690 | 301/1617 | 101/538 | chr19 | 44865483 | |||
| chr19:44865553 | C | T | 1 | a0011 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.371C>T | p.Thr124Met | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/9 | 600/2690 | 371/1617 | 124/538 | chr19 | 44865553 | |||
| chr19:44871900 | G | C | 1 | a0009 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.526G>C | p.Asp176His | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/9 | 755/2690 | 526/1617 | 176/538 | chr19 | 44871900 | |||
| chr19:44872038 | C | T | 1 | a0006 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.664C>T | p.Arg222Cys | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/9 | 893/2690 | 664/1617 | 222/538 | chr19 | 44872038 | |||
| chr19:44872078 | C | T | 1 | a0008 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.704C>T | p.Thr235Met | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/9 | 933/2690 | 704/1617 | 235/538 | chr19 | 44872078 | |||
| chr19:44873997 | G | A | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.857G>A | p.Arg286His | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/9 | 1086/2690 | 857/1617 | 286/538 | chr19 | 44873997 | |||
| chr19:44882231 | G | A | 1 | a0004 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1063G>A | p.Ala355Thr | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/9 | 1292/2690 | 1063/1617 | 355/538 | chr19 | 44882231 | |||
| chr19:44888197 | C | T | 1 | a0003 | 5 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.1435C>T | p.Pro479Ser | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 1664/2690 | 1435/1617 | 479/538 | chr19 | 44888197 | |||
| chr19:44888248 | G | A | 1 | a0002 | 11 | HG00642.hp2 HG01168.hp2 HG01496.hp2 others(8): Show |
missense_variant | MODERATE | c.1486G>A | p.Asp496Asn | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 1715/2690 | 1486/1617 | 496/538 | chr19 | 44888248 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44865344 | C | T | 1 | a0001c0007 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.162C>T | p.Cys54Cys | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/9 | 391/2690 | 162/1617 | 54/538 | chr19 | 44865344 | |||
| chr19:44865548 | C | T | 1 | a0001c0003 | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
synonymous_variant | LOW | c.366C>T | p.Asp122Asp | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/9 | 595/2690 | 366/1617 | 122/538 | chr19 | 44865548 | |||
| chr19:44865653 | A | G | 2 | a0001c0004 a0003c0016 |
6 | HG00738.hp2 HG01243.hp2 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.471A>G | p.Arg157Arg | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/9 | 700/2690 | 471/1617 | 157/538 | chr19 | 44865653 | |||
| chr19:44874348 | G | A | 1 | a0001c0012 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.912G>A | p.Pro304Pro | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/9 | 1141/2690 | 912/1617 | 304/538 | chr19 | 44874348 | |||
| chr19:44885967 | G | A | 1 | a0001c0006 | 3 | HG00741.hp2 HG01516.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.1227G>A | p.Pro409Pro | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 7/9 | 1456/2690 | 1227/1617 | 409/538 | chr19 | 44885967 | |||
| chr19:44888161 | T | C | 1 | a0009c0010 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1399T>C | p.Leu467Leu | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 1628/2690 | 1399/1617 | 467/538 | chr19 | 44888161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44846347 | C | T | 2 | a0001c0001t0008 a0001c0001t0016 |
3 | HG02451.hp1 HG02723.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-179C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/9 | 179 | chr19 | 44846347 | ||||||
| chr19:44846378 | A | C | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | NA18963.hp2 NA19064.hp1 |
5_prime_UTR_variant | MODIFIER | c.-148A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/9 | 148 | chr19 | 44846378 | ||||||
| chr19:44846470 | C | T | 1 | a0001c0001t0003 | 7 | NA18960.hp2 NA18962.hp1 NA18964.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-56C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/9 | 56 | chr19 | 44846470 | ||||||
| chr19:44888397 | G | A | 2 | a0001c0001t0004 a0010c0018t0004 |
6 | HG01884.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 18 | chr19 | 44888397 | ||||||
| chr19:44888418 | T | A | 1 | a0001c0001t0007 | 2 | NA18955.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*39T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 39 | chr19 | 44888418 | ||||||
| chr19:44888494 | C | A | 1 | a0001c0003t0005 | 4 | HG02145.hp1 HG03139.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*115C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 115 | chr19 | 44888494 | ||||||
| chr19:44888551 | G | A | 1 | a0002c0002t0009 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 172 | chr19 | 44888551 | ||||||
| chr19:44888683 | C | A | 1 | a0001c0001t0010 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 304 | chr19 | 44888683 | ||||||
| chr19:44888684 | C | T | 1 | a0001c0001t0013 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*305C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 305 | chr19 | 44888684 | ||||||
| chr19:44888778 | G | A | 1 | a0001c0001t0011 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 399 | chr19 | 44888778 | ||||||
| chr19:44888835 | C | T | 1 | a0001c0001t0006 | 4 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*456C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 456 | chr19 | 44888835 | ||||||
| chr19:44888997 | C | T | 7 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0015 others(4): Show |
35 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*618C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 618 | chr19 | 44888997 | ||||||
| chr19:44889026 | G | T | 1 | a0001c0001t0016 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 647 | chr19 | 44889026 | ||||||
| chr19:44889165 | T | C | 1 | a0001c0004t0012 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*786T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 9/9 | 786 | chr19 | 44889165 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44846706 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.88+93C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44846706 | |||||||
| chr19:44846930 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.88+317G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44846930 | |||||||
| chr19:44847131 | G | T | 1 | a0001c0001t0001g0358 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.88+518G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847131 | |||||||
| chr19:44847397 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.88+784G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847397 | |||||||
| chr19:44847465 | A | C | 3 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 |
3 | HG02258.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.88+852A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847465 | |||||||
| chr19:44847498 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG01123.hp2 HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.88+885A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847498 | |||||||
| chr19:44847511 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.88+898G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847511 | |||||||
| chr19:44847522 | C | G | 4 | a0001c0001t0002g0351 a0001c0001t0008g0349 a0001c0001t0008g0350 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+909C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847522 | |||||||
| chr19:44847544 | A | C | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88+931A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847544 | |||||||
| chr19:44847570 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.88+957G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847570 | |||||||
| chr19:44847604 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.88+991A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847604 | |||||||
| chr19:44847649 | C | T | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+1036C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847649 | |||||||
| chr19:44847678 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | NA18960.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.88+1065C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847678 | |||||||
| chr19:44847738 | C | G | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+1125C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847738 | |||||||
| chr19:44847806 | A | AGAGC | 4 | a0001c0001t0001g0345 a0001c0003t0005g0342 a0001c0003t0005g0343 others(1): Show |
4 | HG02145.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1194_88+1197dup others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44847806 | ||||||
| chr19:44847816 | C | T | 1 | a0001c0001t0002g0341 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.88+1203C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44847816 | |||||||
| chr19:44848174 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18952.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.88+1561T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44848174 | |||||||
| chr19:44848489 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.88+1876A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44848489 | |||||||
| chr19:44848607 | C | G | 1 | a0001c0004t0002g0336 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.88+1994C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44848607 | |||||||
| chr19:44848634 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.88+2021A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44848634 | |||||||
| chr19:44848680 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.88+2067T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44848680 | |||||||
| chr19:44849065 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.88+2452G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849065 | |||||||
| chr19:44849068 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.88+2455G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849068 | |||||||
| chr19:44849162 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.88+2549G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849162 | |||||||
| chr19:44849230 | A | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0091 others(119): Show |
125 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.88+2617A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849230 | |||||||
| chr19:44849325 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+2712A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849325 | |||||||
| chr19:44849504 | C | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18952.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.88+2891C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849504 | |||||||
| chr19:44849518 | G | T | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+2905G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849518 | |||||||
| chr19:44849547 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.88+2934C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849547 | |||||||
| chr19:44849612 | G | A | 3 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 |
3 | HG02258.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.88+2999G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849612 | |||||||
| chr19:44849772 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+3159C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849772 | |||||||
| chr19:44849877 | C | A | 1 | a0001c0001t0002g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.88+3264C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44849877 | |||||||
| chr19:44850004 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.88+3391C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850004 | |||||||
| chr19:44850506 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.88+3893G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850506 | |||||||
| chr19:44850617 | C | A | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+4004C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850617 | |||||||
| chr19:44850661 | A | G | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.88+4048A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850661 | |||||||
| chr19:44850770 | G | C | 3 | a0001c0003t0005g0342 a0001c0003t0005g0343 a0001c0003t0005g0344 |
3 | HG02145.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.88+4157G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850770 | |||||||
| chr19:44850787 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
106 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.88+4174T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850787 | |||||||
| chr19:44850862 | T | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG02717.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+4249T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850862 | |||||||
| chr19:44850864 | TGGCCTTC others(3): Show |
T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0003t0001g0085 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4259_88+4268del others(10): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44850864 | ||||||
| chr19:44850981 | G | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.88+4368G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44850981 | |||||||
| chr19:44851039 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
106 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.88+4426A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44851039 | |||||||
| chr19:44851068 | CTCCCTCA others(28): Show |
C | 2 | a0001c0007t0001g0081 a0001c0007t0001g0082 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.88+4483_88+4517del others(35): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44851068 | ||||||
| chr19:44852010 | T | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0345 a0001c0001t0001g0347 others(3): Show |
6 | HG02145.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+5397T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852010 | |||||||
| chr19:44852029 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.88+5416G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852029 | |||||||
| chr19:44852078 | G | A | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88+5465G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852078 | |||||||
| chr19:44852089 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.88+5476C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852089 | |||||||
| chr19:44852253 | A | G | 3 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 |
3 | HG02258.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.88+5640A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852253 | |||||||
| chr19:44852295 | A | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.88+5682A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852295 | |||||||
| chr19:44852334 | G | GAGACGGG others(16): Show |
1 | a0001c0001t0001g0016 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.88+5722_88+5744dup others(23): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44852334 | ||||||
| chr19:44852338 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(41): Show |
46 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.88+5725C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852338 | |||||||
| chr19:44852435 | G | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG02055.hp2 HG02148.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+5822G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852435 | |||||||
| chr19:44852435 | GT | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.88+5832delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44852435 | ||||||
| chr19:44852436 | T | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG02055.hp2 HG02148.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+5823T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852436 | |||||||
| chr19:44852437 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00438.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.88+5824T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852437 | |||||||
| chr19:44852451 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.88+5838A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852451 | |||||||
| chr19:44852464 | C | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(77): Show |
83 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.88+5851C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852464 | |||||||
| chr19:44852486 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
95 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.88+5873A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852486 | |||||||
| chr19:44852526 | C | CA | 23 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0104 others(20): Show |
23 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.88+5928dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44852526 | ||||||
| chr19:44852526 | CA | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0090 others(91): Show |
97 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.88+5928delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44852526 | ||||||
| chr19:44852568 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+5955A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852568 | |||||||
| chr19:44852603 | T | C | 3 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 |
3 | HG02258.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.88+5990T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852603 | |||||||
| chr19:44852637 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.88+6024A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852637 | |||||||
| chr19:44852663 | A | G | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+6050A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852663 | |||||||
| chr19:44852680 | G | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | NA18955.hp2 NA19058.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.88+6067G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852680 | |||||||
| chr19:44852884 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.88+6271C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852884 | |||||||
| chr19:44852953 | T | A | 20 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(17): Show |
20 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+6340T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44852953 | |||||||
| chr19:44853087 | C | T | 10 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(7): Show |
10 | HG00738.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+6474C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853087 | |||||||
| chr19:44853107 | G | GA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+6506dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44853107 | ||||||
| chr19:44853107 | GA | G | 17 | a0001c0001t0001g0089 a0001c0001t0001g0097 a0001c0001t0001g0317 others(14): Show |
17 | HG01517.hp1 HG02145.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+6506delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44853107 | ||||||
| chr19:44853186 | G | A | 15 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(12): Show |
16 | HG00733.hp2 HG02109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+6573G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853186 | |||||||
| chr19:44853207 | T | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.88+6594T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853207 | |||||||
| chr19:44853220 | G | A | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+6607G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853220 | |||||||
| chr19:44853282 | T | C | 1 | a0002c0002t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.88+6669T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853282 | |||||||
| chr19:44853417 | A | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(45): Show |
50 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.88+6804A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853417 | |||||||
| chr19:44853495 | C | CT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.88+6893dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44853495 | ||||||
| chr19:44853629 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.88+7016C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853629 | |||||||
| chr19:44853638 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(39): Show |
44 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.88+7025G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853638 | |||||||
| chr19:44853738 | C | T | 18 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(15): Show |
18 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.88+7125C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853738 | |||||||
| chr19:44853746 | C | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(75): Show |
81 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.88+7133C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853746 | |||||||
| chr19:44853877 | G | C | 1 | a0003c0016t0001g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+7264G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853877 | |||||||
| chr19:44853878 | A | T | 1 | a0003c0016t0001g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+7265A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44853878 | |||||||
| chr19:44854034 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(76): Show |
82 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.88+7421G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854034 | |||||||
| chr19:44854080 | G | A | 1 | a0001c0001t0010g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.88+7467G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854080 | |||||||
| chr19:44854120 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(60): Show |
65 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.88+7507T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854120 | |||||||
| chr19:44854167 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA19058.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.88+7554G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854167 | |||||||
| chr19:44854287 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.88+7674C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854287 | |||||||
| chr19:44854390 | G | GT | 4 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0250 others(1): Show |
4 | NA18998.hp1 NA18999.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+7784dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44854390 | ||||||
| chr19:44854682 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.88+8069A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854682 | |||||||
| chr19:44854769 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0097 a0001c0001t0001g0347 |
3 | HG02622.hp2 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.88+8156C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854769 | |||||||
| chr19:44854770 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+8157G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854770 | |||||||
| chr19:44854812 | C | CA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+8207dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44854812 | ||||||
| chr19:44854820 | A | T | 1 | a0007c0011t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.88+8207A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854820 | |||||||
| chr19:44854827 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.88+8214T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854827 | |||||||
| chr19:44854851 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.88+8238C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854851 | |||||||
| chr19:44854884 | G | A | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.88+8271G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854884 | |||||||
| chr19:44854924 | G | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
47 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.88+8311G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854924 | |||||||
| chr19:44854978 | C | T | 43 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(40): Show |
43 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.88+8365C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44854978 | |||||||
| chr19:44855093 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.88+8480G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855093 | |||||||
| chr19:44855096 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.88+8483T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855096 | |||||||
| chr19:44855117 | CA | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
182 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.88+8518delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44855117 | ||||||
| chr19:44855191 | C | T | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0055 others(8): Show |
12 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+8578C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855191 | |||||||
| chr19:44855219 | A | G | 4 | a0001c0001t0001g0345 a0001c0003t0005g0342 a0001c0003t0005g0343 others(1): Show |
4 | HG02145.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+8606A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855219 | |||||||
| chr19:44855243 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
43 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.88+8630G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855243 | |||||||
| chr19:44855374 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.88+8761G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855374 | |||||||
| chr19:44855680 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.88+9067T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855680 | |||||||
| chr19:44855699 | ACCTGATT others(3): Show |
A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0002g0140 others(1): Show |
4 | NA18951.hp1 NA18980.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9091_88+9100del others(10): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44855699 | ||||||
| chr19:44855791 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.88+9178C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855791 | |||||||
| chr19:44855891 | C | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
49 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.88+9278C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44855891 | |||||||
| chr19:44856120 | G | T | 4 | a0001c0001t0001g0345 a0001c0003t0005g0342 a0001c0003t0005g0343 others(1): Show |
4 | HG02145.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-9151G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856120 | |||||||
| chr19:44856313 | A | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(58): Show |
63 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.89-8958A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856313 | |||||||
| chr19:44856329 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(79): Show |
84 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.89-8942C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856329 | |||||||
| chr19:44856410 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89-8861A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856410 | |||||||
| chr19:44856449 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0219 others(79): Show |
84 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.89-8822G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856449 | |||||||
| chr19:44856602 | C | A | 6 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
6 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-8669C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856602 | |||||||
| chr19:44856688 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.89-8583G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856688 | |||||||
| chr19:44856743 | G | C | 16 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0257 others(13): Show |
17 | HG00733.hp2 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-8528G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856743 | |||||||
| chr19:44856847 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0104 a0001c0001t0002g0237 |
3 | HG02257.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.89-8424G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856847 | |||||||
| chr19:44856890 | A | C | 1 | a0002c0002t0001g0173 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.89-8381A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856890 | |||||||
| chr19:44856926 | C | T | 8 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
8 | HG01099.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-8345C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44856926 | |||||||
| chr19:44857231 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0109 a0001c0001t0002g0237 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-8040T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857231 | |||||||
| chr19:44857235 | C | CT | 23 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
23 | HG00099.hp1 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-8019dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857235 | ||||||
| chr19:44857235 | C | CTT | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.89-8020_89-8019dup others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857235 | ||||||
| chr19:44857235 | C | CTTT | 16 | a0001c0001t0001g0048 a0001c0001t0001g0078 a0001c0001t0001g0102 others(13): Show |
16 | HG01433.hp2 HG02056.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-8021_89-8019dup others(3): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857235 | ||||||
| chr19:44857265 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0002g0171 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.89-8006C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857265 | |||||||
| chr19:44857316 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.89-7955G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857316 | |||||||
| chr19:44857326 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-7945C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857326 | |||||||
| chr19:44857327 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.89-7944G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857327 | |||||||
| chr19:44857362 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.89-7909C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857362 | |||||||
| chr19:44857497 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0090 others(48): Show |
53 | HG00323.hp2 HG00621.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.89-7774G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857497 | |||||||
| chr19:44857505 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.89-7766A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857505 | |||||||
| chr19:44857526 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.89-7744delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857526 | |||||||
| chr19:44857692 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.89-7579G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857692 | |||||||
| chr19:44857697 | G | GGGTTTT | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7573_89-7568dup others(6): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857697 | ||||||
| chr19:44857705 | G | GT | 13 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0209 others(10): Show |
13 | HG01123.hp2 HG01928.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.89-7561dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857705 | ||||||
| chr19:44857705 | G | GTT | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(50): Show |
54 | HG00438.hp1 HG00738.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.89-7562_89-7561dup others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857705 | ||||||
| chr19:44857705 | G | GTTT | 6 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0227 others(3): Show |
6 | HG00621.hp1 HG00733.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7563_89-7561dup others(3): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44857705 | ||||||
| chr19:44857705 | G | T | 2 | a0001c0001t0004g0251 a0001c0001t0004g0253 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.89-7566G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857705 | |||||||
| chr19:44857709 | T | G | 1 | a0001c0001t0001g0016 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.89-7562T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857709 | |||||||
| chr19:44857709 | T | TG | 7 | a0001c0001t0001g0047 a0001c0001t0001g0274 a0001c0001t0002g0341 others(4): Show |
7 | HG02723.hp1 NA18960.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7562_89-7561ins others(1): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857709 | |||||||
| chr19:44857710 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.89-7561T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857710 | |||||||
| chr19:44857710 | TG | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0139 others(1): Show |
4 | HG01167.hp2 NA18951.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7560delG | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857710 | |||||||
| chr19:44857711 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.89-7560G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857711 | |||||||
| chr19:44857717 | T | G | 1 | a0001c0001t0004g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.89-7554T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857717 | |||||||
| chr19:44857967 | G | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
57 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-7304G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44857967 | |||||||
| chr19:44858024 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.89-7247A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858024 | |||||||
| chr19:44858086 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0354 a0001c0001t0006g0099 |
3 | HG01123.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.89-7185C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858086 | |||||||
| chr19:44858157 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.89-7114T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858157 | |||||||
| chr19:44858290 | A | T | 2 | a0001c0001t0014g0298 a0001c0001t0015g0299 |
2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.89-6981A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858290 | |||||||
| chr19:44858317 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0050 others(63): Show |
69 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.89-6954G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858317 | |||||||
| chr19:44858325 | C | CT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.89-6936dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44858325 | ||||||
| chr19:44858375 | T | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-6896T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858375 | |||||||
| chr19:44858385 | G | A | 9 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(6): Show |
9 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-6886G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858385 | |||||||
| chr19:44858389 | A | G | 68 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0074 others(65): Show |
70 | HG00140.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.89-6882A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858389 | |||||||
| chr19:44858438 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.89-6833T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858438 | |||||||
| chr19:44858512 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0252 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-6759G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858512 | |||||||
| chr19:44858568 | T | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(64): Show |
68 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.89-6703T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858568 | |||||||
| chr19:44858570 | C | G | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.89-6701C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858570 | |||||||
| chr19:44858689 | C | T | 9 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(6): Show |
9 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-6582C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858689 | |||||||
| chr19:44858703 | T | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-6568T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858703 | |||||||
| chr19:44858776 | G | A | 10 | a0001c0001t0001g0225 a0001c0001t0002g0222 a0002c0002t0001g0005 others(7): Show |
11 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-6495G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858776 | |||||||
| chr19:44858822 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-6449T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858822 | |||||||
| chr19:44858895 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.89-6376G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44858895 | |||||||
| chr19:44859012 | G | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(51): Show |
55 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.89-6259G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859012 | |||||||
| chr19:44859024 | C | G | 9 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(6): Show |
9 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-6247C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859024 | |||||||
| chr19:44859045 | C | T | 4 | a0001c0001t0001g0268 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-6226C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859045 | |||||||
| chr19:44859129 | C | G | 1 | a0001c0004t0001g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.89-6142C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859129 | |||||||
| chr19:44859410 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-5861G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859410 | |||||||
| chr19:44859452 | A | G | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-5819A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859452 | |||||||
| chr19:44859483 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.89-5788G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859483 | |||||||
| chr19:44859495 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.89-5776G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859495 | |||||||
| chr19:44859552 | C | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(64): Show |
68 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.89-5719C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859552 | |||||||
| chr19:44859681 | G | A | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-5590G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859681 | |||||||
| chr19:44859825 | C | CA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0117 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-5430dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44859825 | ||||||
| chr19:44859825 | CA | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-5430delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44859825 | ||||||
| chr19:44859896 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.89-5375C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859896 | |||||||
| chr19:44859973 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | NA18986.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.89-5298G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859973 | |||||||
| chr19:44859997 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-5274G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44859997 | |||||||
| chr19:44860042 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(46): Show |
50 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.89-5229C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860042 | |||||||
| chr19:44860135 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.89-5136C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860135 | |||||||
| chr19:44860220 | T | C | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-5051T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860220 | |||||||
| chr19:44860443 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.89-4828A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860443 | |||||||
| chr19:44860534 | T | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-4737T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860534 | |||||||
| chr19:44860608 | A | T | 10 | a0001c0001t0001g0225 a0001c0001t0002g0222 a0002c0002t0001g0005 others(7): Show |
11 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-4663A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860608 | |||||||
| chr19:44860706 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.89-4565G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860706 | |||||||
| chr19:44860722 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.89-4549C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860722 | |||||||
| chr19:44860750 | G | A | 1 | a0001c0012t0002g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.89-4521G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44860750 | |||||||
| chr19:44860955 | TA | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-4302delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44860955 | ||||||
| chr19:44861236 | A | C | 1 | a0001c0001t0004g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.89-4035A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861236 | |||||||
| chr19:44861282 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.89-3989G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861282 | |||||||
| chr19:44861366 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3905C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861366 | |||||||
| chr19:44861525 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3746A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861525 | |||||||
| chr19:44861558 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3713A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861558 | |||||||
| chr19:44861815 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3456A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861815 | |||||||
| chr19:44861852 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.89-3419C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861852 | |||||||
| chr19:44861991 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3280T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44861991 | |||||||
| chr19:44862011 | A | G | 11 | a0001c0001t0001g0352 a0001c0003t0001g0085 a0001c0003t0001g0249 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-3260A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862011 | |||||||
| chr19:44862044 | G | A | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.89-3227G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862044 | |||||||
| chr19:44862050 | T | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0318 a0001c0001t0001g0320 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3221T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862050 | |||||||
| chr19:44862137 | C | G | 1 | a0001c0001t0003g0180 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.89-3134C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862137 | |||||||
| chr19:44862138 | G | C | 1 | a0001c0001t0003g0180 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.89-3133G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862138 | |||||||
| chr19:44862153 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-3118C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862153 | |||||||
| chr19:44862219 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-3052T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862219 | |||||||
| chr19:44862267 | TCACTGTG others(16): Show |
T | 2 | a0001c0001t0001g0089 a0001c0001t0002g0171 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.89-3003_89-2981del others(23): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862267 | |||||||
| chr19:44862268 | CACTGTGT others(17): Show |
C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
57 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-3002_89-2979del others(24): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862268 | |||||||
| chr19:44862268 | CACTGTGT others(764): Show |
C | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-3002_89-2232del | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862268 | |||||||
| chr19:44862293 | T | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
57 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-2978T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862293 | |||||||
| chr19:44862347 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-2924A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862347 | |||||||
| chr19:44862365 | A | C | 1 | a0001c0001t0002g0297 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.89-2906A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862365 | |||||||
| chr19:44862366 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-2905G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862366 | |||||||
| chr19:44862384 | A | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-2887A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862384 | |||||||
| chr19:44862415 | AAAAAAAA others(5): Show |
A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0074 others(65): Show |
70 | HG00140.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.89-2851_89-2840del others(12): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862415 | ||||||
| chr19:44862466 | TA | T | 60 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0075 others(57): Show |
61 | HG00140.hp1 HG00544.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.89-2793delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862466 | ||||||
| chr19:44862475 | A | AAAG | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-2794_89-2793ins others(3): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862475 | ||||||
| chr19:44862560 | G | A | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-2711G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862560 | |||||||
| chr19:44862704 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-2567A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862704 | |||||||
| chr19:44862754 | C | T | 1 | a0001c0001t0004g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.89-2517C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862754 | |||||||
| chr19:44862773 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0002g0093 |
2 | HG00423.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.89-2498G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862773 | |||||||
| chr19:44862917 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.89-2354A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862917 | |||||||
| chr19:44862921 | G | A | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-2350G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44862921 | |||||||
| chr19:44862992 | C | CA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.89-2259dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862992 | ||||||
| chr19:44862992 | C | CAA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0182 a0001c0001t0001g0243 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2260_89-2259dup others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862992 | ||||||
| chr19:44862992 | CA | C | 91 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0060 others(88): Show |
94 | HG00140.hp1 HG00544.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.89-2259delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862992 | ||||||
| chr19:44862992 | CAAAA | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0069 others(48): Show |
52 | HG00323.hp2 HG00733.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.89-2262_89-2259del others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44862992 | ||||||
| chr19:44863018 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-2253C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863018 | |||||||
| chr19:44863040 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-2231T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863040 | |||||||
| chr19:44863042 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-2229A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863042 | |||||||
| chr19:44863088 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-2183G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863088 | |||||||
| chr19:44863153 | G | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-2118G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863153 | |||||||
| chr19:44863240 | C | T | 1 | a0001c0001t0008g0349 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.89-2031C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863240 | |||||||
| chr19:44863346 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-1925G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863346 | |||||||
| chr19:44863399 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-1872G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863399 | |||||||
| chr19:44863460 | C | T | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-1811C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863460 | |||||||
| chr19:44863522 | T | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-1749T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863522 | |||||||
| chr19:44863566 | T | A | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.89-1705T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863566 | |||||||
| chr19:44863573 | A | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
58 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-1698A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863573 | |||||||
| chr19:44863660 | CGTG | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0006g0266 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-1607_89-1605del others(3): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44863660 | ||||||
| chr19:44863664 | G | A | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-1607G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863664 | |||||||
| chr19:44863682 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.89-1589T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863682 | |||||||
| chr19:44863828 | C | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0322 others(3): Show |
6 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1443C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44863828 | |||||||
| chr19:44863841 | C | CAA | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.89-1419_89-1418dup others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44863841 | ||||||
| chr19:44864012 | T | C | 1 | a0001c0001t0001g0358 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.89-1259T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TC | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0060 others(116): Show |
123 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.89-1249dupC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44864012 | ||||||
| chr19:44864012 | T | TTC | 46 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(43): Show |
47 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TTCC | 5 | a0001c0001t0001g0223 a0001c0001t0001g0240 a0001c0001t0001g0354 others(2): Show |
5 | HG01123.hp2 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(3): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TTCCC | 7 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0027 others(4): Show |
7 | HG01516.hp2 HG02735.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TTCCCC | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(28): Show |
34 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(5): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TTCCCCC | 37 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0024 others(34): Show |
38 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(6): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864012 | T | TTCCCCCC | 10 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0044 others(7): Show |
11 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-1259_89-1258ins others(7): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864012 | |||||||
| chr19:44864021 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-1250C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864021 | |||||||
| chr19:44864023 | A | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0255 a0001c0001t0001g0291 others(1): Show |
4 | HG01943.hp1 HG02004.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-1248A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864023 | |||||||
| chr19:44864073 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.89-1198G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864073 | |||||||
| chr19:44864164 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.89-1107G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864164 | |||||||
| chr19:44864173 | AAAAC | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.89-1086_89-1083del others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44864173 | ||||||
| chr19:44864216 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.89-1055A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864216 | |||||||
| chr19:44864245 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.89-1026G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864245 | |||||||
| chr19:44864249 | T | TC | 4 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG02135.hp1 NA18969.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-1021dupC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44864249 | ||||||
| chr19:44864315 | G | GA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.89-948dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 44864315 | ||||||
| chr19:44864434 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.89-837C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864434 | |||||||
| chr19:44864520 | C | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.89-751C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864520 | |||||||
| chr19:44864558 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.89-713C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864558 | |||||||
| chr19:44864648 | A | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0104 others(31): Show |
35 | HG00738.hp2 HG01099.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.89-623A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864648 | |||||||
| chr19:44864715 | G | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.89-556G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864715 | |||||||
| chr19:44864752 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-519C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864752 | |||||||
| chr19:44864753 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.89-518A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864753 | |||||||
| chr19:44864768 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-503C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864768 | |||||||
| chr19:44864784 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.89-487C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864784 | |||||||
| chr19:44864825 | C | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
57 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-446C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864825 | |||||||
| chr19:44864911 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.89-360T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864911 | |||||||
| chr19:44864920 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.89-351C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864920 | |||||||
| chr19:44864933 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
10 | HG02135.hp1 NA18948.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-338C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44864933 | |||||||
| chr19:44865063 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.89-208C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44865063 | |||||||
| chr19:44865166 | G | T | 4 | a0001c0001t0006g0266 a0001c0001t0006g0267 a0001c0001t0008g0349 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-105G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44865166 | |||||||
| chr19:44865167 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.89-104C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44865167 | |||||||
| chr19:44865197 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-74C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44865197 | |||||||
| chr19:44865261 | C | T | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.89-10C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 1/8 | chr19 | 44865261 | |||||||
| chr19:44865677 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02080.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.478+17C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865677 | |||||||
| chr19:44865678 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.478+18G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865678 | |||||||
| chr19:44865704 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0294 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.478+44G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865704 | |||||||
| chr19:44865876 | A | G | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.478+216A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865876 | |||||||
| chr19:44865946 | G | A | 2 | a0001c0007t0001g0081 a0001c0007t0001g0082 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.478+286G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865946 | |||||||
| chr19:44865960 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.478+300G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44865960 | |||||||
| chr19:44866009 | C | A | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.478+349C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866009 | |||||||
| chr19:44866009 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0223 |
2 | HG01496.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.478+349C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866009 | |||||||
| chr19:44866036 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.478+376G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866036 | |||||||
| chr19:44866173 | TA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.478+526delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44866173 | ||||||
| chr19:44866345 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.478+685C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866345 | |||||||
| chr19:44866392 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.478+732G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866392 | |||||||
| chr19:44866446 | C | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0006g0266 others(3): Show |
7 | HG02451.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+786C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866446 | |||||||
| chr19:44866745 | A | G | 4 | a0001c0001t0006g0266 a0001c0001t0006g0267 a0001c0001t0008g0349 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1085A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44866745 | |||||||
| chr19:44867020 | A | T | 1 | a0001c0001t0003g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.478+1360A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867020 | |||||||
| chr19:44867021 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.478+1361A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867021 | |||||||
| chr19:44867021 | AT | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0101 others(5): Show |
8 | HG01515.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1375delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44867021 | ||||||
| chr19:44867078 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
224 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.478+1418G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867078 | |||||||
| chr19:44867088 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.478+1428G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867088 | |||||||
| chr19:44867133 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0006g0266 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+1473C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867133 | |||||||
| chr19:44867138 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0006g0266 others(2): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+1478C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867138 | |||||||
| chr19:44867194 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.478+1534G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867194 | |||||||
| chr19:44867215 | T | A | 1 | a0001c0001t0003g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.478+1555T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867215 | |||||||
| chr19:44867297 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.478+1637T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867297 | |||||||
| chr19:44867313 | A | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.478+1653A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867313 | |||||||
| chr19:44867314 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.478+1654G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867314 | |||||||
| chr19:44867392 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.478+1732A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867392 | |||||||
| chr19:44867416 | C | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.478+1756C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867416 | |||||||
| chr19:44867446 | A | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0255 a0001c0001t0001g0291 others(1): Show |
4 | HG01943.hp1 HG02004.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1786A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867446 | |||||||
| chr19:44867481 | G | A | 2 | a0001c0001t0014g0298 a0001c0001t0015g0299 |
2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.478+1821G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867481 | |||||||
| chr19:44867544 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0006g0266 others(3): Show |
7 | HG02451.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+1884A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867544 | |||||||
| chr19:44867556 | T | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0320 |
2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.478+1896T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867556 | |||||||
| chr19:44867581 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.478+1921G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867581 | |||||||
| chr19:44867597 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.478+1937G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867597 | |||||||
| chr19:44867684 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0038 others(1): Show |
4 | HG00140.hp2 HG00639.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+2024C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867684 | |||||||
| chr19:44867836 | G | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG00099.hp2 HG01256.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+2176G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867836 | |||||||
| chr19:44867911 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
186 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.478+2251G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867911 | |||||||
| chr19:44867931 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+2271C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867931 | |||||||
| chr19:44867936 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.478+2276G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867936 | |||||||
| chr19:44867943 | A | C | 1 | a0001c0001t0002g0093 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.478+2283A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44867943 | |||||||
| chr19:44868202 | G | GA | 11 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.478+2553dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868202 | ||||||
| chr19:44868202 | GA | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.478+2553delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868202 | ||||||
| chr19:44868257 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.478+2597A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868257 | |||||||
| chr19:44868337 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.478+2677A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868337 | |||||||
| chr19:44868351 | C | CA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0090 others(15): Show |
18 | HG00438.hp2 HG01175.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.478+2710dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868351 | ||||||
| chr19:44868351 | CA | C | 65 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0088 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.478+2710delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868351 | ||||||
| chr19:44868428 | A | AT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.478+2776dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868428 | ||||||
| chr19:44868448 | T | TTTTTTC | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.478+2793_478+2798d others(8): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868448 | ||||||
| chr19:44868449 | T | C | 17 | a0001c0001t0001g0015 a0001c0001t0001g0225 a0001c0001t0001g0274 others(14): Show |
18 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.478+2789T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868449 | |||||||
| chr19:44868466 | C | CT | 129 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0049 others(126): Show |
133 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.478+2821dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868466 | ||||||
| chr19:44868466 | C | CTT | 8 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0208 others(5): Show |
8 | HG00735.hp1 HG01433.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+2820_478+2821d others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868466 | ||||||
| chr19:44868526 | G | A | 2 | a0001c0001t0001g0352 a0001c0001t0002g0334 |
2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.478+2866G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868526 | |||||||
| chr19:44868773 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0225 a0001c0001t0001g0274 others(14): Show |
18 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.479-3080C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868773 | |||||||
| chr19:44868866 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0290 |
2 | NA18998.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.479-2987C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868866 | |||||||
| chr19:44868872 | A | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.479-2981A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868872 | |||||||
| chr19:44868912 | G | GA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.479-2928dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868912 | ||||||
| chr19:44868912 | G | GAA | 11 | a0001c0001t0001g0098 a0001c0001t0001g0243 a0001c0001t0001g0278 others(8): Show |
11 | HG00621.hp2 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.479-2929_479-2928d others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44868912 | ||||||
| chr19:44868927 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(91): Show |
99 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.479-2926A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44868927 | |||||||
| chr19:44869023 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.479-2830G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869023 | |||||||
| chr19:44869072 | A | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.479-2781A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869072 | |||||||
| chr19:44869097 | T | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.479-2756T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869097 | |||||||
| chr19:44869121 | TCTC | T | 9 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0244 others(6): Show |
9 | HG01099.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.479-2727_479-2725d others(5): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44869121 | ||||||
| chr19:44869269 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0002g0237 a0001c0001t0002g0351 |
3 | HG02257.hp1 HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.479-2584A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869269 | |||||||
| chr19:44869450 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.479-2403G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869450 | |||||||
| chr19:44869537 | G | A | 62 | a0001c0001t0001g0049 a0001c0001t0001g0088 a0001c0001t0001g0090 others(59): Show |
63 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.479-2316G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869537 | |||||||
| chr19:44869541 | C | T | 21 | a0001c0001t0001g0108 a0001c0001t0001g0122 a0001c0001t0001g0123 others(18): Show |
22 | HG00639.hp2 HG00642.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.479-2312C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869541 | |||||||
| chr19:44869592 | C | CA | 54 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(51): Show |
56 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.479-2244dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44869592 | ||||||
| chr19:44869592 | C | CAA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0050 others(75): Show |
82 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.479-2245_479-2244d others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44869592 | ||||||
| chr19:44869599 | AAAAAAAA others(4): Show |
A | 10 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG02145.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-2249_479-2239d others(13): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44869599 | ||||||
| chr19:44869609 | AG | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0139 others(3): Show |
6 | HG03195.hp2 NA18951.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-2243delG | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869609 | |||||||
| chr19:44869610 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.479-2243G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869610 | |||||||
| chr19:44869641 | A | T | 4 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0178 others(1): Show |
4 | NA18960.hp2 NA18962.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-2212A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869641 | |||||||
| chr19:44869702 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(91): Show |
99 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.479-2151C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869702 | |||||||
| chr19:44869820 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.479-2033A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869820 | |||||||
| chr19:44869939 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.479-1914C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44869939 | |||||||
| chr19:44870019 | G | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0074 others(54): Show |
60 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.479-1834G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870019 | |||||||
| chr19:44870055 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.479-1798G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870055 | |||||||
| chr19:44870071 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.479-1782T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870071 | |||||||
| chr19:44870078 | C | T | 5 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-1775C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870078 | |||||||
| chr19:44870118 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0002g0059 a0001c0001t0002g0094 others(2): Show |
5 | HG01069.hp2 HG01257.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-1735G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870118 | |||||||
| chr19:44870141 | G | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0231 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.479-1712G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870141 | |||||||
| chr19:44870210 | A | C | 1 | a0007c0011t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.479-1643A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870210 | |||||||
| chr19:44870282 | G | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0074 others(54): Show |
60 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.479-1571G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870282 | |||||||
| chr19:44870307 | C | T | 4 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-1546C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870307 | |||||||
| chr19:44870308 | G | A | 63 | a0001c0001t0001g0049 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
64 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.479-1545G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870308 | |||||||
| chr19:44870356 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.479-1497G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870356 | |||||||
| chr19:44870370 | G | T | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.479-1483G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870370 | |||||||
| chr19:44870482 | A | G | 57 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0074 others(54): Show |
60 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.479-1371A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870482 | |||||||
| chr19:44870516 | T | C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0003t0005g0328 others(3): Show |
6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-1337T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870516 | |||||||
| chr19:44870566 | T | TA | 17 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(14): Show |
17 | HG00733.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-1279dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44870566 | ||||||
| chr19:44870580 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.479-1273G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44870580 | |||||||
| chr19:44870729 | CT | C | 7 | a0001c0001t0001g0060 a0001c0001t0001g0216 a0001c0003t0001g0085 others(4): Show |
7 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-1110delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 44870729 | ||||||
| chr19:44871093 | T | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0074 others(54): Show |
60 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.479-760T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44871093 | |||||||
| chr19:44871157 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.479-696C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44871157 | |||||||
| chr19:44871158 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.479-695G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44871158 | |||||||
| chr19:44871430 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.479-423A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44871430 | |||||||
| chr19:44871436 | G | A | 1 | a0001c0001t0002g0351 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.479-417G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 2/8 | chr19 | 44871436 | |||||||
| chr19:44872156 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp2 | splice_region_variant&intron_variant | LOW | c.775+7G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872156 | |||||||
| chr19:44872161 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.775+12G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872161 | |||||||
| chr19:44872265 | T | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0252 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.775+116T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872265 | |||||||
| chr19:44872328 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0289 a0001c0001t0001g0324 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.775+179A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872328 | |||||||
| chr19:44872507 | G | C | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0319 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+358G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872507 | |||||||
| chr19:44872688 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0131 a0005c0008t0001g0181 |
3 | HG02071.hp2 HG02080.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.775+539C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872688 | |||||||
| chr19:44872763 | CT | C | 8 | a0002c0002t0001g0005 a0002c0002t0001g0018 a0002c0002t0001g0053 others(5): Show |
9 | HG00642.hp2 HG01168.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+615delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872763 | |||||||
| chr19:44872787 | GTATTTAT | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.775+657_775+663del others(7): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 44872787 | ||||||
| chr19:44872793 | ATTAT | A | 5 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+650_775+653del others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 44872793 | ||||||
| chr19:44872818 | T | TTTATATA others(25): Show |
5 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+687_775+718dup others(32): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 44872818 | ||||||
| chr19:44872842 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.775+693A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44872842 | |||||||
| chr19:44873008 | A | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0240 others(15): Show |
19 | HG01099.hp1 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.775+859A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873008 | |||||||
| chr19:44873027 | C | G | 98 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0074 others(95): Show |
101 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.775+878C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873027 | |||||||
| chr19:44873060 | C | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.776-856C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873060 | |||||||
| chr19:44873230 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0042 |
2 | NA18969.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.776-686G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873230 | |||||||
| chr19:44873285 | G | A | 4 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-631G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873285 | |||||||
| chr19:44873383 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.776-533A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873383 | |||||||
| chr19:44873387 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.776-529C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873387 | |||||||
| chr19:44873427 | G | C | 1 | a0001c0004t0001g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.776-489G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873427 | |||||||
| chr19:44873504 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.776-412A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873504 | |||||||
| chr19:44873636 | A | AAC | 23 | a0001c0001t0001g0077 a0001c0001t0001g0104 a0001c0001t0001g0110 others(20): Show |
24 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.776-258_776-257dup others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 44873636 | ||||||
| chr19:44873636 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.776-280A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873636 | |||||||
| chr19:44873636 | AAC | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
144 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.776-258_776-257del others(2): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 44873636 | ||||||
| chr19:44873816 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.776-100C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873816 | |||||||
| chr19:44873822 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.776-94G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873822 | |||||||
| chr19:44873824 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0162 |
2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.776-92C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873824 | |||||||
| chr19:44873841 | C | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0075 others(25): Show |
30 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.776-75C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 3/8 | chr19 | 44873841 | |||||||
| chr19:44874073 | CGGGGCTG others(30): Show |
C | 1 | a0001c0001t0008g0349 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893+69_893+105delA others(36): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 44874073 | ||||||
| chr19:44874077 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.893+44G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/8 | chr19 | 44874077 | |||||||
| chr19:44874102 | AAGGGAGG others(30): Show |
A | 5 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+87_893+123delG others(36): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 44874102 | ||||||
| chr19:44874210 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0050 others(71): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.894-120G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/8 | chr19 | 44874210 | |||||||
| chr19:44874289 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.894-41C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 4/8 | chr19 | 44874289 | |||||||
| chr19:44874585 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+107G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874585 | |||||||
| chr19:44874599 | T | C | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+121T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874599 | |||||||
| chr19:44874632 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1042+154C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874632 | |||||||
| chr19:44874696 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1042+218G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874696 | |||||||
| chr19:44874698 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1042+220G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874698 | |||||||
| chr19:44874887 | C | T | 41 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0107 others(38): Show |
42 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1042+409C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44874887 | |||||||
| chr19:44875100 | C | T | 4 | a0001c0003t0001g0085 a0001c0003t0001g0249 a0001c0003t0001g0262 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+622C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875100 | |||||||
| chr19:44875237 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+759C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875237 | |||||||
| chr19:44875268 | C | CT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1042+805dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44875268 | ||||||
| chr19:44875320 | T | C | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+842T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875320 | |||||||
| chr19:44875323 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1042+845T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875323 | |||||||
| chr19:44875352 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+874G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875352 | |||||||
| chr19:44875462 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
12 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042+984C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875462 | |||||||
| chr19:44875502 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1024G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875502 | |||||||
| chr19:44875513 | G | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0225 a0001c0001t0001g0274 others(15): Show |
19 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1042+1035G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875513 | |||||||
| chr19:44875553 | A | G | 1 | a0001c0001t0003g0172 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1042+1075A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875553 | |||||||
| chr19:44875803 | A | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1042+1325A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875803 | |||||||
| chr19:44875850 | G | A | 1 | a0002c0002t0001g0173 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1042+1372G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875850 | |||||||
| chr19:44875850 | G | C | 1 | a0003c0016t0001g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1042+1372G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875850 | |||||||
| chr19:44875906 | G | A | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1428G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875906 | |||||||
| chr19:44875912 | C | T | 1 | a0001c0001t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1042+1434C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875912 | |||||||
| chr19:44875933 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1455C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875933 | |||||||
| chr19:44875960 | G | A | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1042+1482G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44875960 | |||||||
| chr19:44876015 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1042+1537C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876015 | |||||||
| chr19:44876052 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0049 others(67): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1042+1574T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876052 | |||||||
| chr19:44876079 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1042+1601C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876079 | |||||||
| chr19:44876081 | TCCCGAAA others(3): Show |
T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0289 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1042+1615_1042+162 others(14): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44876081 | ||||||
| chr19:44876094 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1616C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876094 | |||||||
| chr19:44876105 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1042+1627C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876105 | |||||||
| chr19:44876107 | AAATTATC others(3): Show |
A | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1042+1632_1042+164 others(14): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44876107 | ||||||
| chr19:44876174 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1042+1696C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876174 | |||||||
| chr19:44876259 | G | A | 56 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(53): Show |
57 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1042+1781G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876259 | |||||||
| chr19:44876273 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1795C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876273 | |||||||
| chr19:44876309 | AC | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1042+1832delC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876309 | |||||||
| chr19:44876381 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1042+1903C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876381 | |||||||
| chr19:44876425 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1042+1947A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876425 | |||||||
| chr19:44876426 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1948C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876426 | |||||||
| chr19:44876473 | A | G | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+1995A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876473 | |||||||
| chr19:44876489 | A | G | 10 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0223 others(7): Show |
10 | HG00733.hp1 HG00741.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1042+2011A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876489 | |||||||
| chr19:44876534 | C | T | 28 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0075 others(25): Show |
30 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042+2056C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876534 | |||||||
| chr19:44876869 | G | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1042+2391G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876869 | |||||||
| chr19:44876879 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1042+2401C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44876879 | |||||||
| chr19:44877078 | T | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0226 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+2600T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877078 | |||||||
| chr19:44877241 | G | C | 1 | a0001c0001t0001g0305 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1042+2763G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877241 | |||||||
| chr19:44877263 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1042+2785C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877263 | |||||||
| chr19:44877264 | G | A | 1 | a0001c0001t0013g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1042+2786G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877264 | |||||||
| chr19:44877288 | G | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1042+2810G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877288 | |||||||
| chr19:44877680 | G | A | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1042+3202G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877680 | |||||||
| chr19:44877680 | G | C | 10 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
10 | HG02145.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042+3202G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877680 | |||||||
| chr19:44877704 | C | A | 39 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0107 others(36): Show |
40 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1042+3226C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877704 | |||||||
| chr19:44877712 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1042+3234G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877712 | |||||||
| chr19:44877713 | G | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1042+3235G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877713 | |||||||
| chr19:44877824 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1042+3346C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44877824 | |||||||
| chr19:44877942 | TTGCAAAA others(10): Show |
T | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1042+3467_1042+348 others(21): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44877942 | ||||||
| chr19:44878015 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0241 a0001c0001t0001g0243 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042+3537C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878015 | |||||||
| chr19:44878035 | G | T | 14 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
14 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1042+3557G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878035 | |||||||
| chr19:44878048 | CCTCCTCC others(1): Show |
C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(12): Show |
15 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1042+3572_1042+357 others(12): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44878048 | ||||||
| chr19:44878102 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1042+3624T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878102 | |||||||
| chr19:44878163 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1042+3685T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878163 | |||||||
| chr19:44878178 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1042+3700G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878178 | |||||||
| chr19:44878464 | T | C | 12 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(9): Show |
12 | HG02145.hp1 HG02258.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1043-3747T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878464 | |||||||
| chr19:44878579 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0195 |
2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1043-3632C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878579 | |||||||
| chr19:44878654 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1043-3557C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878654 | |||||||
| chr19:44878660 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0034 others(66): Show |
72 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1043-3551C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878660 | |||||||
| chr19:44878718 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-3493G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878718 | |||||||
| chr19:44878719 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-3492A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878719 | |||||||
| chr19:44878742 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1043-3469C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878742 | |||||||
| chr19:44878777 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(225): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1043-3434A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878777 | |||||||
| chr19:44878818 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1043-3393C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878818 | |||||||
| chr19:44878835 | T | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0354 a0006c0015t0001g0146 |
3 | HG01123.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1043-3376T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878835 | |||||||
| chr19:44878905 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1043-3306A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44878905 | |||||||
| chr19:44879048 | G | A | 3 | a0001c0004t0001g0147 a0001c0004t0002g0336 a0003c0016t0001g0063 |
3 | HG00738.hp2 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1043-3163G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879048 | |||||||
| chr19:44879141 | G | A | 3 | a0001c0004t0001g0147 a0001c0004t0002g0336 a0003c0016t0001g0063 |
3 | HG00738.hp2 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1043-3070G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879141 | |||||||
| chr19:44879176 | T | C | 5 | a0001c0001t0002g0334 a0001c0003t0002g0086 a0001c0004t0001g0147 others(2): Show |
5 | HG00738.hp2 HG01243.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043-3035T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879176 | |||||||
| chr19:44879290 | T | C | 1 | a0001c0001t0003g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1043-2921T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879290 | |||||||
| chr19:44879394 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-2817C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879394 | |||||||
| chr19:44879395 | T | A | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1043-2816T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879395 | |||||||
| chr19:44879395 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-2816T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879395 | |||||||
| chr19:44879396 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-2815C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879396 | |||||||
| chr19:44879397 | C | T | 1 | a0006c0015t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1043-2814C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879397 | |||||||
| chr19:44879418 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01361.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1043-2793G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879418 | |||||||
| chr19:44879460 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1043-2751G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879460 | |||||||
| chr19:44879513 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1043-2698G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879513 | |||||||
| chr19:44879694 | C | T | 3 | a0001c0004t0001g0147 a0001c0004t0002g0336 a0003c0016t0001g0063 |
3 | HG00738.hp2 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1043-2517C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879694 | |||||||
| chr19:44879697 | G | A | 3 | a0001c0004t0001g0147 a0001c0004t0002g0336 a0003c0016t0001g0063 |
3 | HG00738.hp2 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1043-2514G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879697 | |||||||
| chr19:44879709 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
207 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1043-2502C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879709 | |||||||
| chr19:44879727 | T | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1043-2484T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879727 | |||||||
| chr19:44879739 | C | G | 1 | a0001c0001t0001g0310 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1043-2472C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879739 | |||||||
| chr19:44879774 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1043-2437C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879774 | |||||||
| chr19:44879780 | A | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1043-2431A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879780 | |||||||
| chr19:44879804 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
207 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1043-2407G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879804 | |||||||
| chr19:44879822 | T | C | 52 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(49): Show |
53 | HG00099.hp2 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1043-2389T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879822 | |||||||
| chr19:44879834 | A | AC | 55 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1043-2373dupC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44879834 | ||||||
| chr19:44879858 | A | G | 55 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1043-2353A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879858 | |||||||
| chr19:44879882 | T | A | 55 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(52): Show |
56 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1043-2329T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879882 | |||||||
| chr19:44879899 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1043-2312G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879899 | |||||||
| chr19:44879935 | T | C | 1 | a0001c0001t0004g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1043-2276T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44879935 | |||||||
| chr19:44880119 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1043-2092G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880119 | |||||||
| chr19:44880129 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1043-2082C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880129 | |||||||
| chr19:44880231 | G | A | 3 | a0001c0004t0001g0147 a0001c0004t0002g0336 a0003c0016t0001g0063 |
3 | HG00738.hp2 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1043-1980G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880231 | |||||||
| chr19:44880305 | G | A | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1043-1906G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880305 | |||||||
| chr19:44880326 | G | A | 17 | a0001c0001t0001g0225 a0001c0001t0001g0274 a0001c0001t0001g0304 others(14): Show |
18 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1043-1885G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880326 | |||||||
| chr19:44880475 | C | CT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(63): Show |
68 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1043-1706dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | C | CTT | 8 | a0001c0001t0001g0092 a0001c0001t0001g0124 a0001c0001t0001g0148 others(5): Show |
8 | HG00597.hp2 HG01167.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043-1707_1043-170 others(6): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | C | CTTT | 8 | a0001c0001t0001g0227 a0001c0001t0001g0274 a0001c0001t0001g0304 others(5): Show |
9 | HG01168.hp2 HG01243.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043-1708_1043-170 others(7): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CT | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0201 a0001c0001t0001g0204 others(11): Show |
14 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1043-1706delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CTT | C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0090 a0001c0001t0001g0101 others(28): Show |
31 | HG00733.hp2 HG01123.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1043-1707_1043-170 others(6): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CTTT | C | 34 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0107 others(31): Show |
35 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1043-1708_1043-170 others(7): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CTTTT | C | 27 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(24): Show |
28 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1043-1709_1043-170 others(8): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1043-1717_1043-170 others(16): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880475 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0188 |
3 | HG02080.hp1 NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1043-1718_1043-170 others(17): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880475 | ||||||
| chr19:44880551 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1043-1660G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880551 | |||||||
| chr19:44880573 | C | T | 28 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(25): Show |
29 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1043-1638C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880573 | |||||||
| chr19:44880774 | AT | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0104 others(17): Show |
20 | HG01257.hp2 HG01516.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1043-1419delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44880774 | ||||||
| chr19:44880820 | T | G | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1043-1391T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880820 | |||||||
| chr19:44880848 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1043-1363C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880848 | |||||||
| chr19:44880859 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1043-1352G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880859 | |||||||
| chr19:44880919 | C | T | 4 | a0001c0001t0001g0098 a0001c0004t0001g0147 a0001c0004t0002g0336 others(1): Show |
4 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043-1292C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880919 | |||||||
| chr19:44880922 | G | A | 4 | a0001c0001t0001g0098 a0001c0004t0001g0147 a0001c0004t0002g0336 others(1): Show |
4 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043-1289G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44880922 | |||||||
| chr19:44881025 | C | T | 1 | a0001c0004t0002g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1043-1186C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881025 | |||||||
| chr19:44881037 | G | C | 6 | a0001c0001t0001g0098 a0001c0001t0001g0353 a0001c0004t0001g0147 others(3): Show |
6 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043-1174G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881037 | |||||||
| chr19:44881075 | GC | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1043-1131delC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44881075 | ||||||
| chr19:44881081 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1043-1130G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881081 | |||||||
| chr19:44881148 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1043-1063T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881148 | |||||||
| chr19:44881497 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1043-714C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881497 | |||||||
| chr19:44881522 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-689T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881522 | |||||||
| chr19:44881522 | TC | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0041 others(60): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1043-688delC | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881522 | |||||||
| chr19:44881523 | C | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0211 others(1): Show |
4 | HG02071.hp2 HG02523.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043-688C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881523 | |||||||
| chr19:44881523 | C | CA | 12 | a0001c0001t0001g0075 a0001c0001t0001g0098 a0001c0001t0001g0168 others(9): Show |
12 | HG00438.hp1 HG00738.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1043-671dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44881523 | ||||||
| chr19:44881523 | CA | C | 52 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1043-671delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 44881523 | ||||||
| chr19:44881674 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0289 a0001c0001t0002g0065 |
3 | HG01167.hp1 HG01169.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1043-537G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881674 | |||||||
| chr19:44881696 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1043-515T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881696 | |||||||
| chr19:44881793 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043-418C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881793 | |||||||
| chr19:44881818 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-393T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881818 | |||||||
| chr19:44881844 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1043-367C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881844 | |||||||
| chr19:44881845 | G | A | 18 | a0001c0001t0001g0098 a0001c0001t0001g0278 a0001c0001t0001g0288 others(15): Show |
19 | HG00642.hp2 HG00738.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1043-366G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881845 | |||||||
| chr19:44881933 | G | A | 1 | a0001c0001t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1043-278G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44881933 | |||||||
| chr19:44882046 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
18 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.1043-165C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44882046 | |||||||
| chr19:44882099 | C | A | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1043-112C>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 5/8 | chr19 | 44882099 | |||||||
| chr19:44882502 | G | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0041 others(95): Show |
101 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1196+138G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882502 | |||||||
| chr19:44882661 | G | A | 1 | a0012c0009t0001g0215 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1196+297G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882661 | |||||||
| chr19:44882690 | C | CA | 136 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(133): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1196+351dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882690 | ||||||
| chr19:44882690 | C | CAA | 22 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0106 others(19): Show |
22 | HG00323.hp2 HG01257.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1196+350_1196+351d others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882690 | ||||||
| chr19:44882690 | C | CAAA | 16 | a0001c0001t0001g0142 a0001c0001t0001g0211 a0001c0001t0001g0270 others(13): Show |
17 | HG01069.hp2 HG01123.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.1196+349_1196+351d others(5): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882690 | ||||||
| chr19:44882690 | CA | C | 27 | a0001c0001t0001g0015 a0001c0001t0001g0069 a0001c0001t0001g0083 others(24): Show |
27 | HG00438.hp1 HG00733.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1196+351delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882690 | ||||||
| chr19:44882760 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1196+396C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882760 | |||||||
| chr19:44882772 | G | A | 23 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0221 others(20): Show |
24 | HG00642.hp2 HG01168.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1196+408G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882772 | |||||||
| chr19:44882782 | CA | C | 7 | a0001c0001t0001g0236 a0001c0001t0001g0273 a0001c0001t0001g0284 others(4): Show |
7 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+419delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882782 | |||||||
| chr19:44882783 | AT | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1196+435delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882783 | ||||||
| chr19:44882783 | ATT | A | 62 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0103 others(59): Show |
64 | HG00323.hp2 HG00642.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1196+434_1196+435d others(4): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44882783 | ||||||
| chr19:44882786 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1196+422T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882786 | |||||||
| chr19:44882789 | T | C | 3 | a0001c0001t0002g0237 a0001c0001t0002g0351 a0001c0004t0002g0080 |
3 | HG02257.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1196+425T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882789 | |||||||
| chr19:44882791 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1196+427T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882791 | |||||||
| chr19:44882842 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1196+478T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882842 | |||||||
| chr19:44882972 | A | G | 2 | a0001c0001t0002g0237 a0001c0001t0002g0351 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1196+608A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44882972 | |||||||
| chr19:44883024 | C | T | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1196+660C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883024 | |||||||
| chr19:44883065 | GCCA | G | 4 | a0001c0001t0001g0115 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+705_1196+707d others(5): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44883065 | ||||||
| chr19:44883203 | A | G | 10 | a0002c0002t0001g0005 a0002c0002t0001g0018 a0002c0002t0001g0053 others(7): Show |
11 | HG00642.hp2 HG01168.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1196+839A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883203 | |||||||
| chr19:44883210 | G | GTAA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0270 others(24): Show |
28 | HG00323.hp2 HG01069.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.1196+847_1196+849d others(5): Show |
NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44883210 | ||||||
| chr19:44883377 | C | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0222 a0001c0001t0002g0237 others(2): Show |
5 | HG01167.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1013C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883377 | |||||||
| chr19:44883423 | C | G | 1 | a0001c0001t0010g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1196+1059C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883423 | |||||||
| chr19:44883431 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1196+1067C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883431 | |||||||
| chr19:44883569 | C | G | 1 | a0001c0001t0002g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1196+1205C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883569 | |||||||
| chr19:44883598 | A | G | 14 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0231 others(11): Show |
14 | HG01099.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1196+1234A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883598 | |||||||
| chr19:44883620 | G | A | 1 | a0001c0001t0006g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1196+1256G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883620 | |||||||
| chr19:44883777 | A | C | 70 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(67): Show |
72 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.1196+1413A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883777 | |||||||
| chr19:44883800 | A | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(67): Show |
72 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.1196+1436A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883800 | |||||||
| chr19:44883880 | G | A | 1 | a0003c0005t0001g0012 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1196+1516G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44883880 | |||||||
| chr19:44884106 | T | TA | 12 | a0001c0001t0001g0290 a0001c0001t0001g0309 a0002c0002t0001g0005 others(9): Show |
13 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1196+1755dupA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44884106 | ||||||
| chr19:44884107 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1196+1743A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884107 | |||||||
| chr19:44884125 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1196+1761G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884125 | |||||||
| chr19:44884202 | C | G | 25 | a0001c0001t0001g0195 a0001c0001t0002g0009 a0001c0001t0002g0051 others(22): Show |
26 | HG00323.hp2 HG01069.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1197-1735C>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884202 | |||||||
| chr19:44884339 | G | A | 25 | a0001c0001t0001g0195 a0001c0001t0002g0009 a0001c0001t0002g0051 others(22): Show |
26 | HG00323.hp2 HG01069.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1197-1598G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884339 | |||||||
| chr19:44884604 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1197-1333C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884604 | |||||||
| chr19:44884632 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1197-1305G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884632 | |||||||
| chr19:44884873 | G | A | 25 | a0001c0001t0001g0195 a0001c0001t0002g0009 a0001c0001t0002g0051 others(22): Show |
26 | HG00323.hp2 HG01069.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1197-1064G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884873 | |||||||
| chr19:44884953 | T | C | 1 | a0001c0001t0002g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1197-984T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884953 | |||||||
| chr19:44884984 | T | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(66): Show |
71 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.1197-953T>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44884984 | |||||||
| chr19:44885027 | G | A | 1 | a0001c0004t0012g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1197-910G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885027 | |||||||
| chr19:44885140 | G | T | 1 | a0001c0001t0001g0283 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1197-797G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885140 | |||||||
| chr19:44885145 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1197-792C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885145 | |||||||
| chr19:44885187 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1197-750G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885187 | |||||||
| chr19:44885243 | A | G | 100 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(97): Show |
103 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1197-694A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885243 | |||||||
| chr19:44885278 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1197-659G>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885278 | |||||||
| chr19:44885292 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1197-645G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885292 | |||||||
| chr19:44885307 | C | CT | 6 | a0001c0001t0001g0092 a0001c0001t0001g0132 a0001c0001t0001g0307 others(3): Show |
6 | HG00423.hp2 HG00597.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197-608dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44885307 | ||||||
| chr19:44885307 | CT | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0034 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1197-608delT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44885307 | ||||||
| chr19:44885311 | T | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(97): Show |
104 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.1197-626T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885311 | |||||||
| chr19:44885315 | T | C | 1 | a0002c0002t0001g0174 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1197-622T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885315 | |||||||
| chr19:44885324 | T | A | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1197-613T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885324 | |||||||
| chr19:44885325 | T | A | 1 | a0001c0001t0002g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1197-612T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885325 | |||||||
| chr19:44885327 | T | A | 2 | a0001c0004t0001g0233 a0001c0007t0001g0082 |
2 | HG01169.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1197-610T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885327 | |||||||
| chr19:44885328 | T | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(109): Show |
116 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.1197-609T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885328 | |||||||
| chr19:44885329 | T | A | 111 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(108): Show |
115 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(112): Show |
intron_variant | MODIFIER | c.1197-608T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885329 | |||||||
| chr19:44885329 | TA | T | 3 | a0001c0001t0001g0272 a0001c0004t0001g0233 a0001c0007t0001g0082 |
3 | HG01169.hp1 HG02976.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1197-606delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44885329 | ||||||
| chr19:44885330 | A | T | 110 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(107): Show |
114 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.1197-607A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885330 | |||||||
| chr19:44885331 | A | T | 113 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(110): Show |
117 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(114): Show |
intron_variant | MODIFIER | c.1197-606A>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885331 | |||||||
| chr19:44885414 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1197-523C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885414 | |||||||
| chr19:44885622 | C | CT | 6 | a0001c0001t0004g0064 a0001c0001t0004g0251 a0001c0001t0004g0253 others(3): Show |
6 | HG01884.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197-309dupT | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 44885622 | ||||||
| chr19:44885917 | T | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(66): Show |
71 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.1197-20T>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 6/8 | chr19 | 44885917 | |||||||
| chr19:44886312 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1347+93A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886312 | |||||||
| chr19:44886339 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(31): Show |
35 | HG00738.hp1 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.1347+120G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886339 | |||||||
| chr19:44886470 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0275 |
2 | HG02683.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1347+251C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886470 | |||||||
| chr19:44886519 | G | A | 10 | a0002c0002t0001g0005 a0002c0002t0001g0018 a0002c0002t0001g0053 others(7): Show |
11 | HG00642.hp2 HG01168.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1347+300G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886519 | |||||||
| chr19:44886654 | C | T | 4 | a0001c0001t0006g0099 a0001c0001t0006g0263 a0001c0001t0006g0266 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+435C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886654 | |||||||
| chr19:44886770 | G | C | 3 | a0001c0001t0002g0171 a0001c0001t0002g0334 a0001c0004t0002g0080 |
3 | HG02258.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1347+551G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886770 | |||||||
| chr19:44886881 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1347+662G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886881 | |||||||
| chr19:44886884 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1347+665T>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44886884 | |||||||
| chr19:44887015 | CA | C | 11 | a0001c0001t0001g0075 a0001c0001t0001g0103 a0001c0001t0001g0221 others(8): Show |
11 | HG00738.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1347+811delA | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 44887015 | ||||||
| chr19:44887076 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0015 others(115): Show |
122 | HG00323.hp2 HG00642.hp2 HG00733.hp2 others(119): Show |
intron_variant | MODIFIER | c.1347+857A>G | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887076 | |||||||
| chr19:44887197 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1348-913A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887197 | |||||||
| chr19:44887312 | G | C | 1 | a0001c0001t0001g0352 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1348-798G>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887312 | |||||||
| chr19:44887313 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1348-797C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887313 | |||||||
| chr19:44887506 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0164 |
2 | NA18973.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1348-604G>A | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887506 | |||||||
| chr19:44887654 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0354 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1348-456A>C | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887654 | |||||||
| chr19:44887875 | C | T | 4 | a0001c0001t0002g0059 a0001c0001t0002g0094 a0001c0001t0002g0114 others(1): Show |
4 | HG01069.hp2 HG01257.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-235C>T | NECTIN2 | ENSG00000130202.10 | transcript | ENST00000252483.10 | protein_coding | 8/8 | chr19 | 44887875 |