Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57701 |
| ensemblid | ENSG00000167566.17 |
| hgncid | 29321 |
| symbol | NCKAP5L |
| name | NCK associated protein 5 like |
| refseq_nuc | NM_001037806.4 |
| refseq_prot | NP_001032895.2 |
| ensembl_nuc | ENST00000335999.7 |
| ensembl_prot | ENSP00000337998.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49791152 |
| end | 49828413 |
| strand | - |
| ver | v1.2 |
| region | chr12:49791152-49828413 |
| region5000 | chr12:49786152-49833413 |
| regionname0 | NCKAP5L_chr12_49791152_49828413 |
| regionname5000 | NCKAP5L_chr12_49786152_49833413 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1334 | 233 | 68 | 45 | 80 | 14 | 24 | 60 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0002 | 0/0 | 1334 | 97 | 1 | 15 | 74 | 0 | 7 | 54 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0003 | 0/0 | 1334 | 15 | 10 | 3 | 0 | 0 | 2 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0004 | 0/0 | 1334 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0005 | 0/0 | 1334 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0006 | 0/0 | 1334 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0007 | 0/0 | 1334 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0008 | 0/0 | 1334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0009 | 0/0 | 1334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0010 | 0/0 | 1334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0011 | 0/0 | 1334 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0012 | 0/0 | 1334 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0013 | 0/0 | 1334 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0014 | 0/0 | 1334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| a0015 | 0/0 | 1334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | MSEAM others(1329): Show |
chr12 | 49786152 | 49833413 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4002 | 104 | 35 | 19 | 30 | 9 | 11 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0003 | 1/1 | 4002 | 86 | 17 | 23 | 28 | 5 | 11 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0004 | 0/0 | 4002 | 35 | 12 | 1 | 21 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0012 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0022 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0023 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0024 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0027 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0028 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0029 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0001c0031 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0002c0002 | 0/0 | 4002 | 92 | 1 | 14 | 71 | 0 | 6 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0002c0007 | 0/0 | 4002 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0002c0009 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0002c0014 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0002c0015 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0003c0005 | 0/0 | 4002 | 12 | 8 | 2 | 0 | 0 | 2 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0003c0008 | 0/0 | 4002 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0003c0011 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0004c0006 | 0/0 | 4002 | 10 | 10 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0005c0017 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0006c0018 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0007c0019 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0008c0026 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0009c0021 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0010c0025 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0011c0020 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0012c0030 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0013c0013 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0014c0010 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 | ||
| a0015c0016 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | ATGTC others(3997): Show |
chr12 | 49786152 | 49833413 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4882 | 79 | 16 | 18 | 29 | 7 | 9 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0001t0002 | 0/0 | 4882 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0001t0003 | 0/0 | 4882 | 13 | 8 | 0 | 1 | 2 | 2 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0001t0004 | 0/0 | 4882 | 10 | 9 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0003t0002 | 1/1 | 4882 | 84 | 17 | 23 | 26 | 5 | 11 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0003t0005 | 0/0 | 4882 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0004t0001 | 0/0 | 4882 | 35 | 12 | 1 | 21 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0012t0002 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0022t0002 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0023t0001 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0024t0001 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0027t0003 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0028t0001 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0029t0001 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0001c0031t0002 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0002c0002t0001 | 0/0 | 4882 | 92 | 1 | 14 | 71 | 0 | 6 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0002c0007t0001 | 0/0 | 4882 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0002c0009t0001 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0002c0014t0001 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0002c0015t0001 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0003c0005t0001 | 0/0 | 4882 | 12 | 8 | 2 | 0 | 0 | 2 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0003c0008t0001 | 0/0 | 4882 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0003c0011t0001 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0004c0006t0001 | 0/0 | 4882 | 10 | 10 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0005c0017t0001 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0006c0018t0002 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0007c0019t0002 | 0/0 | 4882 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0008c0026t0001 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0009c0021t0002 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0010c0025t0006 | 0/0 | 4871 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4866): Show |
chr12 | 49786152 | 49833413 |
| a0011c0020t0002 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0012c0030t0002 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0013c0013t0002 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0014c0010t0002 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| a0015c0016t0001 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | GGCAC others(4877): Show |
chr12 | 49786152 | 49833413 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 1 | 2 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0001 | 1/0 | 10 | 1 | 2 | 5 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0002 | 0/1 | 9 | 0 | 5 | 1 | 1 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0003 | 0/0 | 8 | 1 | 3 | 1 | 1 | 2 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0003t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0012t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0022t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0023t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0024t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0027t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0028t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0029t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0001c0031t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0007t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0014t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0002c0015t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0008t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0003c0011t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0004c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0005c0017t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0006c0018t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0007c0019t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0008c0026t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0009c0021t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0010c0025t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0011c0020t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0012c0030t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0013c0013t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0014c0010t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| a0015c0016t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0003 | EUR | GBR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0158 | EUR | FIN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00438 | hp2 | a0001 | c0004 | t0001 | g0271 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0210 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00735 | hp1 | a0005 | c0017 | t0001 | g0059 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00738 | hp1 | a0002 | c0015 | t0001 | g0055 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00741 | hp1 | a0006 | c0018 | t0002 | g0160 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01070 | hp2 | a0007 | c0019 | t0002 | g0213 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0152 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0151 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0262 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01099 | hp2 | a0001 | c0031 | t0002 | g0156 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01109 | hp1 | a0003 | c0011 | t0001 | g0050 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01167 | hp1 | a0003 | c0005 | t0001 | g0025 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0079 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01169 | hp1 | a0003 | c0005 | t0001 | g0025 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0155 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0154 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01346 | hp2 | a0001 | c0029 | t0001 | g0066 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0208 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0159 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0147 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0001 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0229 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0234 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0261 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02055 | hp1 | a0004 | c0006 | t0001 | g0070 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0264 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0263 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0274 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02145 | hp2 | a0003 | c0005 | t0001 | g0114 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | CDX | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0040 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02258 | hp2 | a0008 | c0026 | t0001 | g0068 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02280 | hp2 | a0003 | c0005 | t0001 | g0086 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0214 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0162 | AMR | PEL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02451 | hp2 | a0003 | c0005 | t0001 | g0115 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0251 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0224 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02615 | hp1 | a0009 | c0021 | t0002 | g0146 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02647 | hp1 | a0004 | c0006 | t0001 | g0218 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02717 | hp1 | a0004 | c0006 | t0001 | g0072 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02723 | hp1 | a0003 | c0008 | t0001 | g0084 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0036 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02809 | hp2 | a0004 | c0006 | t0001 | g0140 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02886 | hp2 | a0004 | c0006 | t0001 | g0242 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0085 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02896 | hp1 | a0004 | c0006 | t0001 | g0022 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02897 | hp2 | a0004 | c0006 | t0001 | g0022 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02922 | hp1 | a0001 | c0024 | t0001 | g0204 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0260 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02965 | hp2 | a0003 | c0005 | t0001 | g0139 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0077 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0240 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0076 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0047 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03098 | hp2 | a0010 | c0025 | t0006 | g0074 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0048 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0035 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03195 | hp1 | a0004 | c0006 | t0001 | g0071 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0100 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0241 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0273 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0250 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0161 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0164 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0267 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0165 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03540 | hp1 | a0001 | c0012 | t0002 | g0255 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | GWD | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03579 | hp1 | a0003 | c0005 | t0001 | g0049 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03654 | hp2 | a0011 | c0020 | t0002 | g0230 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0228 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03688 | hp1 | a0012 | c0030 | t0002 | g0150 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0233 | SAS | PJL | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0232 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03831 | hp2 | a0002 | c0014 | t0001 | g0109 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03834 | hp1 | a0013 | c0013 | t0002 | g0157 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0002 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03927 | hp2 | a0001 | c0023 | t0001 | g0221 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04115 | hp1 | a0003 | c0005 | t0001 | g0090 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0167 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | STU | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18612 | hp2 | a0002 | c0009 | t0001 | g0166 | EAS | CHB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | CHB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0040 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18906 | hp2 | a0003 | c0008 | t0001 | g0247 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18940 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0174 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18941 | hp2 | a0002 | c0007 | t0001 | g0108 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18944 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18945 | hp2 | a0001 | c0003 | t0005 | g0082 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18963 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18978 | hp2 | a0014 | c0010 | t0002 | g0212 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18987 | hp1 | a0001 | c0003 | t0002 | g0148 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18988 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18990 | hp1 | a0001 | c0003 | t0005 | g0226 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0237 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19003 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19030 | hp1 | a0004 | c0006 | t0001 | g0067 | AFR | LWK | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | LWK | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19054 | hp1 | a0001 | c0003 | t0002 | g0220 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19062 | hp2 | a0002 | c0007 | t0001 | g0209 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19063 | hp1 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19063 | hp2 | a0015 | c0016 | t0001 | g0103 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19068 | hp1 | a0001 | c0003 | t0002 | g0207 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19070 | hp1 | a0001 | c0028 | t0001 | g0197 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0239 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19240 | hp1 | a0003 | c0005 | t0001 | g0177 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20129 | hp1 | a0004 | c0006 | t0001 | g0069 | AFR | ASW | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ASW | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0145 | EUR | TSI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | TSI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20905 | hp1 | a0003 | c0005 | t0001 | g0113 | SAS | GIH | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | GIH | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02559 | hp1 | a0001 | c0027 | t0003 | g0243 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0035 | AFR | ACB | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG06807 | hp1 | a0001 | c0022 | t0002 | g0254 | AFR | USA | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0081 | AFR | USA | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | USA | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0003 | AFR | USA | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | LWK | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0063 | AFR | LWK | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0002 | REF | REF | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0001 | REF | REF | NCKAP5L_chr12_49786152_49833413 | NCKAP5L | chr12 | 49786152 | 49833413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49791912 | G | A | 1 | a0011 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.3932C>T | p.Pro1311Leu | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 4122/4882 | 3932/4005 | 1311/1334 | chr12 | 49791912 | |||
| chr12:49792011 | C | T | 1 | a0008 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.3833G>A | p.Arg1278His | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 4023/4882 | 3833/4005 | 1278/1334 | chr12 | 49792011 | |||
| chr12:49792012 | G | C | 1 | a0009 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.3832C>G | p.Arg1278Gly | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 4022/4882 | 3832/4005 | 1278/1334 | chr12 | 49792012 | |||
| chr12:49793783 | C | T | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3209G>A | p.Arg1070Gln | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 9/13 | 3399/4882 | 3209/4005 | 1070/1334 | chr12 | 49793783 | |||
| chr12:49794911 | T | G | 1 | a0015 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.2949A>C | p.Glu983Asp | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 3139/4882 | 2949/4005 | 983/1334 | chr12 | 49794911 | |||
| chr12:49795692 | C | A | 1 | a0005 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.2168G>T | p.Gly723Val | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2358/4882 | 2168/4005 | 723/1334 | chr12 | 49795692 | |||
| chr12:49795692 | C | G | 1 | a0007 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.2168G>C | p.Gly723Ala | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2358/4882 | 2168/4005 | 723/1334 | chr12 | 49795692 | |||
| chr12:49795785 | G | A | 2 | a0004 a0008 |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
missense_variant | MODERATE | c.2075C>T | p.Thr692Ile | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2265/4882 | 2075/4005 | 692/1334 | chr12 | 49795785 | |||
| chr12:49795819 | A | G | 4 | a0002 a0003 a0005 others(1): Show |
114 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
missense_variant | MODERATE | c.2041T>C | p.Ser681Pro | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2231/4882 | 2041/4005 | 681/1334 | chr12 | 49795819 | |||
| chr12:49796377 | C | T | 1 | a0006 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1483G>A | p.Gly495Ser | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1673/4882 | 1483/4005 | 495/1334 | chr12 | 49796377 | |||
| chr12:49796884 | A | T | 3 | a0002 a0005 a0015 |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
missense_variant | MODERATE | c.976T>A | p.Leu326Met | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1166/4882 | 976/4005 | 326/1334 | chr12 | 49796884 | |||
| chr12:49796892 | C | T | 1 | a0013 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.968G>A | p.Arg323His | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1158/4882 | 968/4005 | 323/1334 | chr12 | 49796892 | |||
| chr12:49797342 | G | A | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.518C>T | p.Pro173Leu | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 708/4882 | 518/4005 | 173/1334 | chr12 | 49797342 | |||
| chr12:49803110 | C | T | 1 | a0014 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.179G>A | p.Arg60His | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 4/13 | 369/4882 | 179/4005 | 60/1334 | chr12 | 49803110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49792802 | T | C | 1 | a0001c0023 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.3525A>G | p.Thr1175Thr | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 11/13 | 3715/4882 | 3525/4005 | 1175/1334 | chr12 | 49792802 | |||
| chr12:49794863 | G | C | 1 | a0001c0022 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2997C>G | p.Gly999Gly | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 3187/4882 | 2997/4005 | 999/1334 | chr12 | 49794863 | |||
| chr12:49794995 | C | T | 1 | a0002c0015 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2865G>A | p.Lys955Lys | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 3055/4882 | 2865/4005 | 955/1334 | chr12 | 49794995 | |||
| chr12:49795433 | C | T | 1 | a0002c0014 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.2427G>A | p.Lys809Lys | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2617/4882 | 2427/4005 | 809/1334 | chr12 | 49795433 | |||
| chr12:49795616 | C | T | 1 | a0001c0024 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.2244G>A | p.Gly748Gly | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2434/4882 | 2244/4005 | 748/1334 | chr12 | 49795616 | |||
| chr12:49796024 | C | A | 18 | a0001c0001 a0001c0024 a0001c0027 others(15): Show |
234 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(231): Show |
synonymous_variant | LOW | c.1836G>T | p.Ser612Ser | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 2026/4882 | 1836/4005 | 612/1334 | chr12 | 49796024 | |||
| chr12:49796051 | T | G | 20 | a0001c0001 a0001c0004 a0001c0023 others(17): Show |
270 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(267): Show |
synonymous_variant | LOW | c.1809A>C | p.Val603Val | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1999/4882 | 1809/4005 | 603/1334 | chr12 | 49796051 | |||
| chr12:49796378 | G | A | 1 | a0001c0027 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1482C>T | p.Asp494Asp | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1672/4882 | 1482/4005 | 494/1334 | chr12 | 49796378 | |||
| chr12:49796420 | G | A | 1 | a0001c0028 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.1440C>T | p.Leu480Leu | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1630/4882 | 1440/4005 | 480/1334 | chr12 | 49796420 | |||
| chr12:49796828 | G | A | 1 | a0003c0008 | 2 | HG02723.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.1032C>T | p.Ala344Ala | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1222/4882 | 1032/4005 | 344/1334 | chr12 | 49796828 | |||
| chr12:49796870 | C | T | 10 | a0002c0002 a0002c0007 a0002c0009 others(7): Show |
114 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
synonymous_variant | LOW | c.990G>A | p.Gln330Gln | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1180/4882 | 990/4005 | 330/1334 | chr12 | 49796870 | |||
| chr12:49797005 | G | A | 1 | a0001c0029 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.855C>T | p.Gly285Gly | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 1045/4882 | 855/4005 | 285/1334 | chr12 | 49797005 | |||
| chr12:49797137 | C | T | 1 | a0002c0007 | 2 | NA18941.hp2 NA19062.hp2 |
synonymous_variant | LOW | c.723G>A | p.Ala241Ala | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 913/4882 | 723/4005 | 241/1334 | chr12 | 49797137 | |||
| chr12:49797305 | C | T | 1 | a0001c0012 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.555G>A | p.Arg185Arg | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 745/4882 | 555/4005 | 185/1334 | chr12 | 49797305 | |||
| chr12:49797347 | G | A | 1 | a0001c0031 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.513C>T | p.Ala171Ala | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/13 | 703/4882 | 513/4005 | 171/1334 | chr12 | 49797347 | |||
| chr12:49801866 | C | T | 1 | a0003c0011 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.333G>A | p.Thr111Thr | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/13 | 523/4882 | 333/4005 | 111/1334 | chr12 | 49801866 | |||
| chr12:49803154 | C | T | 1 | a0002c0009 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.135G>A | p.Ser45Ser | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 4/13 | 325/4882 | 135/4005 | 45/1334 | chr12 | 49803154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49791260 | G | A | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0027t0003 others(1): Show |
25 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 579 | chr12 | 49791260 | ||||||
| chr12:49791551 | A | G | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
268 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*288T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 288 | chr12 | 49791551 | ||||||
| chr12:49791734 | TGGTCCCT others(4): Show |
T | 1 | a0010c0025t0006 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94_*104delCTGAAGG others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 94 | chr12 | 49791734 | ||||||
| chr12:49791746 | G | A | 1 | a0010c0025t0006 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 93 | chr12 | 49791746 | ||||||
| chr12:49791793 | G | C | 1 | a0001c0003t0005 | 2 | NA18945.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 13/13 | 46 | chr12 | 49791793 | ||||||
| chr12:49828396 | C | T | 1 | a0001c0001t0004 | 10 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-173G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/13 | 24352 | chr12 | 49828396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49792069 | G | C | 1 | a0002c0002t0001g0192 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3793-18C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 12/12 | chr12 | 49792069 | |||||||
| chr12:49792261 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3792+185G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 12/12 | chr12 | 49792261 | |||||||
| chr12:49792265 | A | G | 1 | a0010c0025t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3792+181T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 12/12 | chr12 | 49792265 | |||||||
| chr12:49792286 | G | T | 90 | a0002c0002t0001g0005 a0002c0002t0001g0010 a0002c0002t0001g0011 others(87): Show |
112 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.3792+160C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 12/12 | chr12 | 49792286 | |||||||
| chr12:49792605 | G | GGAAGGTG others(3): Show |
1 | a0001c0001t0003g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3650-27_3650-18dup others(10): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 11/12 | chr12 | 49792605 | |||||||
| chr12:49793174 | G | A | 8 | a0001c0001t0003g0061 a0001c0001t0004g0013 a0001c0001t0004g0018 others(5): Show |
11 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3340+178C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 10/12 | chr12 | 49793174 | |||||||
| chr12:49793199 | T | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3340+153A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 10/12 | chr12 | 49793199 | |||||||
| chr12:49793277 | C | T | 23 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3340+75G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 10/12 | chr12 | 49793277 | |||||||
| chr12:49793434 | C | T | 1 | a0002c0002t0001g0116 | 1 | NA18948.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.3259-1G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 9/12 | chr12 | 49793434 | |||||||
| chr12:49793466 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0193 others(1): Show |
5 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3259-33A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 9/12 | chr12 | 49793466 | |||||||
| chr12:49793577 | G | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3259-144C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 9/12 | chr12 | 49793577 | |||||||
| chr12:49793629 | A | G | 3 | a0002c0002t0001g0024 a0002c0002t0001g0088 a0002c0002t0001g0099 |
4 | NA18978.hp1 NA19057.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.3258+105T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 9/12 | chr12 | 49793629 | |||||||
| chr12:49793917 | A | T | 1 | a0015c0016t0001g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3096-21T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49793917 | |||||||
| chr12:49793962 | C | T | 1 | a0001c0022t0002g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3096-66G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49793962 | |||||||
| chr12:49794028 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3096-132G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794028 | |||||||
| chr12:49794215 | C | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3096-319G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794215 | |||||||
| chr12:49794223 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3096-327A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794223 | |||||||
| chr12:49794605 | A | ACCC | 43 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0016 others(40): Show |
56 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.3095+157_3095+159d others(5): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794605 | |||||||
| chr12:49794605 | A | ACCCC | 26 | a0002c0002t0001g0005 a0002c0002t0001g0014 a0002c0002t0001g0019 others(23): Show |
33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.3095+156_3095+159d others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794605 | |||||||
| chr12:49794605 | A | ACCT | 11 | a0002c0002t0001g0015 a0002c0002t0001g0092 a0002c0002t0001g0110 others(8): Show |
13 | HG00621.hp1 HG00621.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.3095+159_3095+160i others(5): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794605 | |||||||
| chr12:49794608 | C | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.3095+157G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794608 | |||||||
| chr12:49794612 | CA | C | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
154 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.3095+152delT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794612 | |||||||
| chr12:49794613 | A | C | 93 | a0001c0001t0003g0248 a0001c0023t0001g0221 a0002c0002t0001g0005 others(90): Show |
115 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3095+152T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794613 | |||||||
| chr12:49794613 | A | G | 1 | a0003c0005t0001g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3095+152T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794613 | |||||||
| chr12:49794651 | T | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.3095+114A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794651 | |||||||
| chr12:49794728 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3095+37G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 8/12 | chr12 | 49794728 | |||||||
| chr12:49797400 | G | A | 2 | a0003c0005t0001g0025 a0003c0005t0001g0115 |
3 | HG01167.hp1 HG01169.hp1 HG02451.hp2 |
splice_region_variant&intron_variant | LOW | c.466-6C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797400 | |||||||
| chr12:49797490 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.466-96C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797490 | |||||||
| chr12:49797606 | G | A | 1 | a0001c0003t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.466-212C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797606 | |||||||
| chr12:49797886 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0135 |
2 | HG02155.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.465+464C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797886 | |||||||
| chr12:49797929 | T | C | 10 | a0004c0006t0001g0022 a0004c0006t0001g0067 a0004c0006t0001g0069 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+421A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797929 | |||||||
| chr12:49797929 | T | G | 1 | a0002c0002t0001g0095 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.465+421A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49797929 | |||||||
| chr12:49798197 | C | A | 2 | a0001c0001t0001g0215 a0001c0028t0001g0197 |
2 | NA18959.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.465+153G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49798197 | |||||||
| chr12:49798226 | T | C | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
268 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.465+124A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49798226 | |||||||
| chr12:49798328 | C | T | 23 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.465+22G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 7/12 | chr12 | 49798328 | |||||||
| chr12:49799185 | C | T | 24 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(21): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.352-722G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799185 | |||||||
| chr12:49799188 | G | C | 24 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(21): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.352-725C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799188 | |||||||
| chr12:49799312 | A | AT | 25 | a0001c0003t0002g0175 a0001c0004t0001g0004 a0001c0004t0001g0009 others(22): Show |
36 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.352-850dupA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799312 | |||||||
| chr12:49799312 | AT | A | 88 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0004g0045 others(85): Show |
110 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.352-850delA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799312 | |||||||
| chr12:49799487 | A | T | 2 | a0001c0003t0002g0208 a0001c0003t0002g0210 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.352-1024T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799487 | |||||||
| chr12:49799507 | G | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.352-1044C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799507 | |||||||
| chr12:49799597 | G | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.352-1134C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799597 | |||||||
| chr12:49799711 | G | A | 3 | a0001c0003t0002g0033 a0001c0003t0002g0207 a0001c0003t0002g0214 |
4 | HG00597.hp2 HG02293.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1248C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799711 | |||||||
| chr12:49799743 | G | A | 1 | a0001c0001t0003g0245 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.352-1280C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799743 | |||||||
| chr12:49799781 | G | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.352-1318C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799781 | |||||||
| chr12:49799817 | C | T | 1 | a0003c0005t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.352-1354G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799817 | |||||||
| chr12:49799928 | G | A | 24 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(21): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.352-1465C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49799928 | |||||||
| chr12:49800143 | C | T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-1680G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800143 | |||||||
| chr12:49800239 | A | G | 1 | a0002c0002t0001g0057 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.351+1609T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800239 | |||||||
| chr12:49800429 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
13 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+1419C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800429 | |||||||
| chr12:49800493 | C | T | 1 | a0001c0004t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.351+1355G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800493 | |||||||
| chr12:49800647 | G | C | 1 | a0001c0003t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.351+1201C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800647 | |||||||
| chr12:49800709 | C | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0052 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.351+1139G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800709 | |||||||
| chr12:49800940 | A | G | 23 | a0001c0004t0001g0004 a0001c0004t0001g0009 a0001c0004t0001g0040 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.351+908T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49800940 | |||||||
| chr12:49801337 | T | C | 1 | a0002c0002t0001g0088 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.351+511A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801337 | |||||||
| chr12:49801366 | C | T | 10 | a0004c0006t0001g0022 a0004c0006t0001g0067 a0004c0006t0001g0069 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.351+482G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801366 | |||||||
| chr12:49801447 | G | A | 1 | a0010c0025t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.351+401C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801447 | |||||||
| chr12:49801494 | A | T | 182 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
233 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.351+354T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801494 | |||||||
| chr12:49801606 | C | A | 1 | a0003c0011t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.351+242G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801606 | |||||||
| chr12:49801607 | A | G | 182 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
233 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.351+241T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801607 | |||||||
| chr12:49801628 | C | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0060 a0001c0001t0003g0062 |
4 | HG02257.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+220G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801628 | |||||||
| chr12:49801656 | G | A | 1 | a0003c0005t0001g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.351+192C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801656 | |||||||
| chr12:49801685 | G | T | 22 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(19): Show |
27 | HG01167.hp2 HG01346.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.351+163C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801685 | |||||||
| chr12:49801779 | T | C | 1 | a0001c0003t0002g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.351+69A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801779 | |||||||
| chr12:49801789 | G | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.351+59C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 6/12 | chr12 | 49801789 | |||||||
| chr12:49802182 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.232-215G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802182 | |||||||
| chr12:49802300 | G | A | 1 | a0002c0009t0001g0166 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.232-333C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802300 | |||||||
| chr12:49802350 | G | A | 10 | a0004c0006t0001g0022 a0004c0006t0001g0067 a0004c0006t0001g0069 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.232-383C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802350 | |||||||
| chr12:49802372 | C | T | 1 | a0002c0002t0001g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.232-405G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802372 | |||||||
| chr12:49802498 | C | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.231+460G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802498 | |||||||
| chr12:49802539 | G | A | 2 | a0002c0002t0001g0117 a0002c0002t0001g0118 |
2 | HG01109.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.231+419C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802539 | |||||||
| chr12:49802595 | A | G | 1 | a0001c0004t0001g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.231+363T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802595 | |||||||
| chr12:49802611 | T | C | 182 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
233 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.231+347A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 5/12 | chr12 | 49802611 | |||||||
| chr12:49803006 | G | C | 1 | a0001c0027t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.193-10C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 4/12 | chr12 | 49803006 | |||||||
| chr12:49803026 | A | G | 1 | a0001c0004t0001g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.193-30T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 4/12 | chr12 | 49803026 | |||||||
| chr12:49803075 | G | T | 2 | a0002c0002t0001g0056 a0002c0002t0001g0057 |
2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.192+22C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 4/12 | chr12 | 49803075 | |||||||
| chr12:49803363 | G | T | 1 | a0003c0008t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.124-198C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803363 | |||||||
| chr12:49803480 | C | T | 2 | a0001c0023t0001g0221 a0002c0002t0001g0107 |
2 | HG00558.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.124-315G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803480 | |||||||
| chr12:49803518 | A | T | 1 | a0001c0003t0002g0211 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.124-353T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803518 | |||||||
| chr12:49803519 | G | C | 1 | a0001c0029t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.124-354C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803519 | |||||||
| chr12:49803578 | T | C | 1 | a0001c0022t0002g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.123+344A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803578 | |||||||
| chr12:49803602 | G | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
215 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.123+320C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803602 | |||||||
| chr12:49803713 | C | T | 2 | a0003c0005t0001g0139 a0004c0006t0001g0140 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.123+209G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803713 | |||||||
| chr12:49803725 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
57 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.123+197C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803725 | |||||||
| chr12:49803737 | G | A | 1 | a0004c0006t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.123+185C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 3/12 | chr12 | 49803737 | |||||||
| chr12:49804097 | G | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
66 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-36-17C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804097 | |||||||
| chr12:49804369 | C | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-36-289G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804369 | |||||||
| chr12:49804486 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-36-406C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804486 | |||||||
| chr12:49804601 | G | A | 1 | a0001c0003t0002g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-36-521C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804601 | |||||||
| chr12:49804629 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0073 others(2): Show |
7 | HG01884.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-549G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804629 | |||||||
| chr12:49804778 | T | A | 1 | a0001c0029t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-36-698A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804778 | |||||||
| chr12:49804825 | C | T | 2 | a0001c0003t0002g0163 a0013c0013t0002g0157 |
2 | HG03834.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-36-745G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49804825 | |||||||
| chr12:49805152 | T | A | 33 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(30): Show |
45 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-37+828A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805152 | |||||||
| chr12:49805160 | G | A | 33 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(30): Show |
45 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-37+820C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805160 | |||||||
| chr12:49805186 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+794G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805186 | |||||||
| chr12:49805304 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0045 a0001c0001t0004g0046 |
4 | HG01167.hp2 HG02572.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+676G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805304 | |||||||
| chr12:49805387 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-37+593G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805387 | |||||||
| chr12:49805533 | G | C | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
266 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.-37+447C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805533 | |||||||
| chr12:49805659 | C | T | 1 | a0002c0002t0001g0096 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-37+321G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805659 | |||||||
| chr12:49805660 | G | A | 3 | a0001c0004t0001g0063 a0001c0029t0001g0066 a0010c0025t0006g0074 |
3 | HG01346.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-37+320C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805660 | |||||||
| chr12:49805691 | T | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-37+289A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805691 | |||||||
| chr12:49805868 | T | A | 93 | a0001c0001t0001g0105 a0001c0004t0001g0085 a0002c0002t0001g0005 others(90): Show |
115 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37+112A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 2/12 | chr12 | 49805868 | |||||||
| chr12:49806049 | GA | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-98-9delT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806049 | |||||||
| chr12:49806063 | C | T | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
265 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.-98-22G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806063 | |||||||
| chr12:49806116 | G | A | 1 | a0007c0019t0002g0213 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-98-75C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806116 | |||||||
| chr12:49806122 | C | T | 8 | a0004c0006t0001g0022 a0004c0006t0001g0067 a0004c0006t0001g0069 others(5): Show |
9 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-98-81G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806122 | |||||||
| chr12:49806166 | A | G | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(99): Show |
139 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-98-125T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806166 | |||||||
| chr12:49806168 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-98-127C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806168 | |||||||
| chr12:49806386 | T | A | 1 | a0003c0008t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-98-345A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806386 | |||||||
| chr12:49806649 | C | A | 1 | a0002c0002t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-98-608G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806649 | |||||||
| chr12:49806741 | C | T | 19 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(16): Show |
24 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.-98-700G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806741 | |||||||
| chr12:49806742 | G | A | 1 | a0003c0005t0001g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-98-701C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806742 | |||||||
| chr12:49806807 | T | A | 3 | a0001c0004t0001g0063 a0001c0029t0001g0066 a0010c0025t0006g0074 |
3 | HG01346.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-98-766A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806807 | |||||||
| chr12:49806862 | T | C | 2 | a0001c0004t0001g0063 a0001c0029t0001g0066 |
2 | HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-98-821A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806862 | |||||||
| chr12:49806928 | A | G | 1 | a0001c0003t0002g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-98-887T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806928 | |||||||
| chr12:49806966 | T | C | 1 | a0001c0004t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-98-925A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49806966 | |||||||
| chr12:49807000 | G | A | 1 | a0001c0003t0002g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-959C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807000 | |||||||
| chr12:49807246 | C | CGT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0038 others(20): Show |
29 | HG00639.hp1 HG01109.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-98-1207_-98-1206d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807246 | |||||||
| chr12:49807246 | C | CGTGT | 74 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0001g0138 others(71): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-98-1209_-98-1206d others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807246 | |||||||
| chr12:49807246 | C | CGTGTGT | 15 | a0001c0001t0001g0189 a0002c0002t0001g0011 a0002c0002t0001g0016 others(12): Show |
20 | HG00609.hp2 HG00621.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.-98-1211_-98-1206d others(8): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807246 | |||||||
| chr12:49807246 | CGT | C | 11 | a0001c0001t0001g0181 a0001c0022t0002g0254 a0001c0027t0003g0243 others(8): Show |
12 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-98-1207_-98-1206d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807246 | |||||||
| chr12:49807665 | T | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(99): Show |
139 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-98-1624A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807665 | |||||||
| chr12:49807736 | C | A | 1 | a0010c0025t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-98-1695G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807736 | |||||||
| chr12:49807808 | C | T | 11 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(8): Show |
13 | HG01515.hp2 HG01517.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.-98-1767G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807808 | |||||||
| chr12:49807839 | G | A | 11 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(8): Show |
13 | HG01515.hp2 HG01517.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.-98-1798C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807839 | |||||||
| chr12:49807851 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-98-1810G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807851 | |||||||
| chr12:49807887 | A | T | 22 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(19): Show |
27 | HG01167.hp2 HG01346.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.-98-1846T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807887 | |||||||
| chr12:49807969 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-98-1928T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49807969 | |||||||
| chr12:49808007 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-98-1966A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808007 | |||||||
| chr12:49808345 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0198 |
2 | HG01069.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-98-2304G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808345 | |||||||
| chr12:49808413 | G | A | 1 | a0001c0003t0002g0163 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-98-2372C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808413 | |||||||
| chr12:49808554 | C | G | 2 | a0001c0004t0001g0262 a0001c0004t0001g0267 |
2 | HG01099.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-98-2513G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808554 | |||||||
| chr12:49808637 | C | T | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-98-2596G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808637 | |||||||
| chr12:49808648 | T | C | 32 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(29): Show |
44 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-98-2607A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808648 | |||||||
| chr12:49808922 | C | G | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-98-2881G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808922 | |||||||
| chr12:49808928 | G | A | 96 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0001g0137 others(93): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-98-2887C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808928 | |||||||
| chr12:49808960 | G | C | 1 | a0002c0002t0001g0118 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-98-2919C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808960 | |||||||
| chr12:49808964 | G | A | 2 | a0001c0004t0001g0063 a0001c0029t0001g0066 |
2 | HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-98-2923C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808964 | |||||||
| chr12:49808997 | G | C | 1 | a0001c0022t0002g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-98-2956C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49808997 | |||||||
| chr12:49809009 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-98-2968G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809009 | |||||||
| chr12:49809027 | G | A | 2 | a0003c0005t0001g0086 a0003c0005t0001g0100 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-98-2986C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809027 | |||||||
| chr12:49809041 | G | T | 1 | a0002c0002t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-98-3000C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809041 | |||||||
| chr12:49809076 | G | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-98-3035C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809076 | |||||||
| chr12:49809126 | C | G | 1 | a0004c0006t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-98-3085G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809126 | |||||||
| chr12:49809349 | C | G | 30 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(27): Show |
44 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-98-3308G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809349 | |||||||
| chr12:49809383 | C | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
95 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.-98-3342G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809383 | |||||||
| chr12:49809410 | C | A | 1 | a0013c0013t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-98-3369G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809410 | |||||||
| chr12:49809481 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-98-3440C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809481 | |||||||
| chr12:49809544 | G | A | 1 | a0001c0003t0002g0214 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-98-3503C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809544 | |||||||
| chr12:49809565 | C | T | 2 | a0001c0003t0002g0208 a0001c0003t0002g0210 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-98-3524G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809565 | |||||||
| chr12:49809625 | C | T | 1 | a0001c0004t0001g0263 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-98-3584G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809625 | |||||||
| chr12:49809682 | A | G | 1 | a0001c0003t0002g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-98-3641T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809682 | |||||||
| chr12:49809706 | G | A | 1 | a0002c0002t0001g0095 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-98-3665C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809706 | |||||||
| chr12:49809758 | T | C | 8 | a0004c0006t0001g0022 a0004c0006t0001g0067 a0004c0006t0001g0069 others(5): Show |
9 | HG02055.hp1 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-98-3717A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49809758 | |||||||
| chr12:49810201 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
10 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-98-4160C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810201 | |||||||
| chr12:49810225 | T | C | 8 | a0004c0006t0001g0067 a0004c0006t0001g0069 a0004c0006t0001g0070 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98-4184A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810225 | |||||||
| chr12:49810306 | G | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
218 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-98-4265C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810306 | |||||||
| chr12:49810522 | G | A | 1 | a0001c0003t0002g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-98-4481C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810522 | |||||||
| chr12:49810554 | C | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
137 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-98-4513G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810554 | |||||||
| chr12:49810641 | C | T | 1 | a0001c0003t0002g0076 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-98-4600G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810641 | |||||||
| chr12:49810680 | C | G | 24 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(21): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-98-4639G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810680 | |||||||
| chr12:49810926 | A | G | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
267 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.-98-4885T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810926 | |||||||
| chr12:49810975 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-98-4934A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49810975 | |||||||
| chr12:49811000 | G | A | 1 | a0002c0002t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-98-4959C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811000 | |||||||
| chr12:49811190 | T | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0060 a0001c0001t0003g0062 others(5): Show |
9 | HG01346.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-98-5149A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811190 | |||||||
| chr12:49811328 | C | A | 1 | a0001c0027t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-98-5287G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811328 | |||||||
| chr12:49811333 | A | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
10 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-98-5292T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811333 | |||||||
| chr12:49811630 | TG | T | 22 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(19): Show |
33 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-98-5590delC | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811630 | |||||||
| chr12:49811680 | G | C | 96 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0136 others(93): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-98-5639C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811680 | |||||||
| chr12:49811719 | A | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
77 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-98-5678T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811719 | |||||||
| chr12:49811760 | G | C | 15 | a0001c0001t0003g0034 a0001c0001t0003g0061 a0001c0001t0003g0078 others(12): Show |
19 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.-98-5719C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811760 | |||||||
| chr12:49811822 | T | C | 9 | a0001c0001t0003g0061 a0001c0001t0004g0013 a0001c0001t0004g0018 others(6): Show |
12 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-98-5781A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811822 | |||||||
| chr12:49811911 | G | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
140 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-98-5870C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811911 | |||||||
| chr12:49811915 | C | T | 24 | a0001c0001t0001g0258 a0001c0001t0003g0021 a0001c0001t0003g0060 others(21): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-98-5874G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811915 | |||||||
| chr12:49811929 | G | A | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
141 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-98-5888C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49811929 | |||||||
| chr12:49812081 | G | A | 10 | a0001c0001t0001g0073 a0004c0006t0001g0022 a0004c0006t0001g0067 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-98-6040C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812081 | |||||||
| chr12:49812214 | C | T | 6 | a0002c0002t0001g0101 a0002c0002t0001g0117 a0002c0002t0001g0118 others(3): Show |
6 | HG00621.hp1 HG01109.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-6173G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812214 | |||||||
| chr12:49812387 | C | CT | 25 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(22): Show |
34 | HG01167.hp2 HG01361.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.-98-6347dupA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812387 | |||||||
| chr12:49812418 | A | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
267 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.-98-6377T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812418 | |||||||
| chr12:49812674 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-98-6633G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812674 | |||||||
| chr12:49812705 | T | C | 2 | a0001c0003t0002g0077 a0001c0003t0002g0081 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-98-6664A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812705 | |||||||
| chr12:49812761 | G | T | 1 | a0001c0003t0002g0250 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-98-6720C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812761 | |||||||
| chr12:49812838 | T | C | 1 | a0001c0001t0003g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98-6797A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812838 | |||||||
| chr12:49812882 | A | G | 6 | a0001c0001t0003g0034 a0001c0001t0003g0078 a0001c0001t0003g0244 others(3): Show |
7 | HG01515.hp2 HG01517.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-98-6841T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812882 | |||||||
| chr12:49812895 | AAAAATGG others(5): Show |
A | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-98-6866_-98-6855d others(14): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812895 | |||||||
| chr12:49812940 | G | A | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
267 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.-98-6899C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49812940 | |||||||
| chr12:49813136 | A | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
141 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-98-7095T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813136 | |||||||
| chr12:49813194 | T | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
142 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-98-7153A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813194 | |||||||
| chr12:49813255 | T | C | 1 | a0001c0003t0002g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-98-7214A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813255 | |||||||
| chr12:49813334 | C | T | 1 | a0010c0025t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-98-7293G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813334 | |||||||
| chr12:49813343 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
144 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-98-7302A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813343 | |||||||
| chr12:49813488 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0193 a0001c0001t0001g0194 |
4 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-98-7447A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813488 | |||||||
| chr12:49813554 | G | A | 1 | a0003c0005t0001g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-98-7513C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813554 | |||||||
| chr12:49813577 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
142 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-98-7536T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813577 | |||||||
| chr12:49813623 | G | A | 1 | a0002c0002t0001g0116 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98-7582C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813623 | |||||||
| chr12:49813779 | C | T | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-98-7738G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813779 | |||||||
| chr12:49813807 | C | T | 2 | a0003c0005t0001g0086 a0003c0005t0001g0100 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-98-7766G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813807 | |||||||
| chr12:49813874 | G | A | 8 | a0001c0001t0004g0013 a0001c0001t0004g0018 a0001c0001t0004g0042 others(5): Show |
11 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-98-7833C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49813874 | |||||||
| chr12:49814158 | A | ATT | 5 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0003t0002g0036 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98-8119_-98-8118d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814158 | |||||||
| chr12:49814160 | T | TTA | 6 | a0001c0003t0002g0035 a0001c0003t0002g0076 a0001c0003t0002g0158 others(3): Show |
7 | HG00323.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-98-8121_-98-8120d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814160 | |||||||
| chr12:49814160 | TTA | T | 109 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(106): Show |
135 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-98-8121_-98-8120d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814160 | |||||||
| chr12:49814160 | TTATA | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-98-8123_-98-8120d others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814160 | |||||||
| chr12:49814162 | A | T | 2 | a0001c0004t0001g0241 a0002c0002t0001g0127 |
2 | HG03453.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-98-8121T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814162 | |||||||
| chr12:49814164 | A | T | 93 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0136 others(90): Show |
115 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-98-8123T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814164 | |||||||
| chr12:49814231 | C | T | 217 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
281 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.-98-8190G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814231 | |||||||
| chr12:49814358 | C | T | 1 | a0001c0004t0001g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-98-8317G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814358 | |||||||
| chr12:49814478 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
78 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-98-8437G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814478 | |||||||
| chr12:49814483 | C | CA | 6 | a0001c0003t0002g0028 a0001c0003t0002g0239 a0001c0004t0001g0265 others(3): Show |
7 | HG01109.hp2 HG01975.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.-98-8443dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814483 | |||||||
| chr12:49814485 | A | G | 1 | a0001c0004t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-98-8444T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814485 | |||||||
| chr12:49814560 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
115 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.-98-8519T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814560 | |||||||
| chr12:49814591 | T | A | 1 | a0003c0005t0001g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-98-8550A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814591 | |||||||
| chr12:49814665 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-98-8624T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814665 | |||||||
| chr12:49814820 | G | C | 10 | a0001c0001t0001g0073 a0004c0006t0001g0022 a0004c0006t0001g0067 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-98-8779C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814820 | |||||||
| chr12:49814875 | T | C | 1 | a0001c0022t0002g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-98-8834A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814875 | |||||||
| chr12:49814933 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-98-8892A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814933 | |||||||
| chr12:49814949 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0060 a0001c0001t0003g0061 others(3): Show |
7 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-98-8908A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49814949 | |||||||
| chr12:49815151 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-98-9110A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815151 | |||||||
| chr12:49815747 | C | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
78 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-98-9706G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815747 | |||||||
| chr12:49815774 | G | T | 3 | a0002c0002t0001g0091 a0002c0002t0001g0119 a0002c0002t0001g0272 |
3 | HG00597.hp1 HG02080.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-98-9733C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815774 | |||||||
| chr12:49815798 | CT | C | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-98-9758delA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815798 | |||||||
| chr12:49815835 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
266 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.-98-9794G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815835 | |||||||
| chr12:49815899 | T | C | 1 | a0001c0027t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-98-9858A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49815899 | |||||||
| chr12:49816407 | C | G | 14 | a0001c0001t0003g0034 a0001c0001t0003g0078 a0001c0001t0003g0244 others(11): Show |
18 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98-10366G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816407 | |||||||
| chr12:49816493 | C | T | 23 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(20): Show |
28 | HG01167.hp2 HG01346.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-98-10452G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816493 | |||||||
| chr12:49816495 | C | CA | 56 | a0001c0001t0002g0253 a0001c0003t0002g0003 a0001c0003t0002g0026 others(53): Show |
70 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-98-10455dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAA | 13 | a0001c0001t0003g0034 a0001c0001t0003g0245 a0001c0001t0003g0248 others(10): Show |
17 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-98-10456_-98-1045 others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAA | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
43 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-98-10459_-98-1045 others(9): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAA | 26 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0053 others(23): Show |
32 | HG00140.hp1 HG00673.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.-98-10460_-98-1045 others(10): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAAA | 14 | a0001c0001t0001g0037 a0001c0001t0001g0200 a0001c0001t0001g0203 others(11): Show |
20 | HG00558.hp2 HG01175.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-98-10461_-98-1045 others(11): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0246 others(7): Show |
17 | HG00423.hp1 HG00673.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-98-10462_-98-1045 others(12): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0258 a0001c0004t0001g0264 a0001c0004t0001g0265 others(3): Show |
7 | HG00438.hp2 HG02071.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-98-10463_-98-1045 others(13): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAAA others(3): Show |
5 | a0001c0023t0001g0221 a0004c0006t0001g0067 a0004c0006t0001g0069 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-10464_-98-1045 others(14): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816495 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0073 a0004c0006t0001g0071 a0004c0006t0001g0072 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-98-10465_-98-1045 others(15): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816495 | |||||||
| chr12:49816556 | T | C | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-98-10515A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816556 | |||||||
| chr12:49816567 | A | C | 1 | a0001c0004t0001g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-98-10526T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816567 | |||||||
| chr12:49816581 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-98-10540G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816581 | |||||||
| chr12:49816752 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
106 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.-98-10711C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816752 | |||||||
| chr12:49816798 | T | TA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
130 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-98-10758dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816798 | |||||||
| chr12:49816798 | T | TAA | 10 | a0001c0001t0001g0073 a0004c0006t0001g0022 a0004c0006t0001g0067 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-98-10759_-98-1075 others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816798 | |||||||
| chr12:49816902 | T | C | 1 | a0012c0030t0002g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-98-10861A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816902 | |||||||
| chr12:49816903 | T | C | 1 | a0012c0030t0002g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-98-10862A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49816903 | |||||||
| chr12:49817030 | T | C | 1 | a0001c0003t0002g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-98-10989A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817030 | |||||||
| chr12:49817411 | A | G | 1 | a0001c0003t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-99+10911T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817411 | |||||||
| chr12:49817532 | C | G | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10790G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817532 | |||||||
| chr12:49817535 | A | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10787T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817535 | |||||||
| chr12:49817546 | T | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10776A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817546 | |||||||
| chr12:49817547 | T | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10775A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817547 | |||||||
| chr12:49817548 | A | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10774T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817548 | |||||||
| chr12:49817623 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-99+10699G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817623 | |||||||
| chr12:49817791 | C | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
78 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-99+10531G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817791 | |||||||
| chr12:49817957 | C | T | 1 | a0001c0004t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-99+10365G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817957 | |||||||
| chr12:49817965 | C | T | 6 | a0001c0001t0003g0034 a0001c0001t0003g0078 a0001c0001t0003g0244 others(3): Show |
7 | HG01515.hp2 HG01517.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-99+10357G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817965 | |||||||
| chr12:49817988 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-99+10334C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49817988 | |||||||
| chr12:49818080 | C | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+10242G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818080 | |||||||
| chr12:49818092 | G | A | 23 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0060 others(20): Show |
28 | HG01167.hp2 HG01346.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-99+10230C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818092 | |||||||
| chr12:49818133 | G | A | 1 | a0001c0003t0002g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-99+10189C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818133 | |||||||
| chr12:49818133 | G | GA | 13 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0181 others(10): Show |
14 | HG01168.hp1 HG01169.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99+10188dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818133 | |||||||
| chr12:49818164 | T | C | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-99+10158A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818164 | |||||||
| chr12:49818202 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
9 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99+10120T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818202 | |||||||
| chr12:49818415 | GCAAT | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
141 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-99+9903_-99+9906d others(6): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818415 | |||||||
| chr12:49818509 | C | T | 3 | a0002c0002t0001g0024 a0002c0002t0001g0088 a0002c0002t0001g0099 |
4 | NA18978.hp1 NA19057.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+9813G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818509 | |||||||
| chr12:49818560 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0183 a0001c0001t0001g0202 |
6 | HG00639.hp1 HG01192.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+9762G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818560 | |||||||
| chr12:49818613 | T | A | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
141 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-99+9709A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818613 | |||||||
| chr12:49818652 | G | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+9670C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818652 | |||||||
| chr12:49818656 | A | G | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+9666T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818656 | |||||||
| chr12:49818700 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-99+9622A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818700 | |||||||
| chr12:49818714 | C | T | 1 | a0001c0003t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-99+9608G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818714 | |||||||
| chr12:49818813 | G | C | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-99+9509C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818813 | |||||||
| chr12:49818832 | C | A | 1 | a0001c0003t0002g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+9490G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818832 | |||||||
| chr12:49818845 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
266 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.-99+9477G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818845 | |||||||
| chr12:49818857 | T | G | 10 | a0001c0001t0001g0073 a0004c0006t0001g0022 a0004c0006t0001g0067 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+9465A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818857 | |||||||
| chr12:49818867 | T | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+9455A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818867 | |||||||
| chr12:49818949 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-99+9373G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818949 | |||||||
| chr12:49818999 | C | T | 1 | a0001c0001t0003g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-99+9323G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49818999 | |||||||
| chr12:49819031 | T | TA | 43 | a0001c0001t0001g0073 a0001c0001t0001g0258 a0001c0001t0003g0034 others(40): Show |
56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-99+9290dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819031 | |||||||
| chr12:49819031 | TA | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(29): Show |
41 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-99+9290delT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819031 | |||||||
| chr12:49819032 | A | T | 1 | a0001c0003t0002g0208 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-99+9290T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819032 | |||||||
| chr12:49819137 | T | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
141 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-99+9185A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819137 | |||||||
| chr12:49819168 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-99+9154G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819168 | |||||||
| chr12:49819169 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-99+9153C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819169 | |||||||
| chr12:49819170 | G | A | 1 | a0001c0004t0001g0267 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-99+9152C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819170 | |||||||
| chr12:49819208 | A | G | 23 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(20): Show |
34 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-99+9114T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819208 | |||||||
| chr12:49819218 | G | A | 1 | a0002c0002t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-99+9104C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819218 | |||||||
| chr12:49819293 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
67 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-99+9029G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819293 | |||||||
| chr12:49819311 | CA | C | 49 | a0001c0001t0001g0258 a0001c0001t0003g0021 a0001c0001t0003g0034 others(46): Show |
65 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-99+9010delT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819311 | |||||||
| chr12:49819311 | CAAA | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
77 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-99+9008_-99+9010d others(5): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819311 | |||||||
| chr12:49819328 | T | A | 2 | a0001c0003t0002g0227 a0001c0003t0002g0231 |
2 | NA18940.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-99+8994A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819328 | |||||||
| chr12:49819349 | T | G | 1 | a0001c0003t0002g0233 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-99+8973A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819349 | |||||||
| chr12:49819471 | C | T | 249 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(246): Show |
323 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.-99+8851G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819471 | |||||||
| chr12:49819474 | A | G | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+8848T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819474 | |||||||
| chr12:49819516 | T | C | 1 | a0001c0027t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+8806A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819516 | |||||||
| chr12:49819548 | C | T | 1 | a0001c0004t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-99+8774G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819548 | |||||||
| chr12:49819652 | G | A | 9 | a0001c0001t0001g0246 a0001c0001t0003g0021 a0001c0001t0003g0060 others(6): Show |
10 | HG01346.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+8670C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819652 | |||||||
| chr12:49819751 | C | T | 1 | a0001c0027t0003g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-99+8571G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819751 | |||||||
| chr12:49819870 | A | C | 1 | a0003c0008t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-99+8452T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819870 | |||||||
| chr12:49819966 | A | C | 1 | a0002c0002t0001g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-99+8356T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819966 | |||||||
| chr12:49819982 | G | T | 1 | a0001c0003t0002g0224 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-99+8340C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49819982 | |||||||
| chr12:49820030 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
78 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.-99+8292C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820030 | |||||||
| chr12:49820050 | C | T | 10 | a0001c0001t0001g0073 a0004c0006t0001g0022 a0004c0006t0001g0067 others(7): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-99+8272G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820050 | |||||||
| chr12:49820091 | T | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+8231A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820091 | |||||||
| chr12:49820221 | A | T | 1 | a0009c0021t0002g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-99+8101T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820221 | |||||||
| chr12:49820245 | C | A | 14 | a0001c0001t0003g0034 a0001c0001t0003g0078 a0001c0001t0003g0244 others(11): Show |
18 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-99+8077G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820245 | |||||||
| chr12:49820273 | C | A | 1 | a0002c0002t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-99+8049G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820273 | |||||||
| chr12:49820274 | C | A | 1 | a0002c0002t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-99+8048G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820274 | |||||||
| chr12:49820313 | C | CT | 33 | a0001c0001t0001g0169 a0001c0001t0001g0180 a0001c0001t0001g0181 others(30): Show |
36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.-99+8008dupA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820313 | |||||||
| chr12:49820313 | C | CTT | 16 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(13): Show |
26 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-99+8007_-99+8008d others(4): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820313 | |||||||
| chr12:49820313 | CT | C | 28 | a0001c0001t0001g0073 a0001c0001t0001g0138 a0001c0001t0001g0205 others(25): Show |
33 | HG01069.hp1 HG01167.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-99+8008delA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820313 | |||||||
| chr12:49820356 | G | A | 1 | a0003c0005t0001g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-99+7966C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820356 | |||||||
| chr12:49820380 | G | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
8 | HG01884.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+7942C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820380 | |||||||
| chr12:49820408 | C | T | 24 | a0001c0001t0001g0246 a0001c0001t0003g0021 a0001c0001t0003g0034 others(21): Show |
29 | HG01167.hp2 HG01346.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.-99+7914G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820408 | |||||||
| chr12:49820517 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0060 a0001c0001t0003g0061 others(3): Show |
7 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+7805C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820517 | |||||||
| chr12:49820594 | C | T | 19 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(16): Show |
29 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-99+7728G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820594 | |||||||
| chr12:49820595 | G | A | 2 | a0001c0003t0002g0164 a0001c0003t0002g0165 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-99+7727C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820595 | |||||||
| chr12:49820670 | C | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0060 a0001c0001t0003g0061 others(3): Show |
7 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-99+7652G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820670 | |||||||
| chr12:49820756 | C | T | 2 | a0001c0004t0001g0040 a0001c0004t0001g0260 |
3 | HG02258.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-99+7566G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820756 | |||||||
| chr12:49820854 | C | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
74 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-99+7468G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820854 | |||||||
| chr12:49820954 | T | A | 1 | a0004c0006t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-99+7368A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49820954 | |||||||
| chr12:49821035 | T | C | 1 | a0001c0003t0002g0239 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-99+7287A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821035 | |||||||
| chr12:49821065 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+7257C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821065 | |||||||
| chr12:49821068 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-99+7254T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821068 | |||||||
| chr12:49821241 | A | C | 157 | a0001c0001t0001g0073 a0001c0001t0001g0104 a0001c0001t0001g0105 others(154): Show |
198 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.-99+7081T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821241 | |||||||
| chr12:49821273 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-99+7049G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821273 | |||||||
| chr12:49821354 | C | T | 4 | a0001c0003t0002g0035 a0001c0003t0002g0076 a0001c0003t0002g0249 others(1): Show |
5 | HG02486.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+6968G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821354 | |||||||
| chr12:49821368 | G | T | 3 | a0001c0001t0003g0034 a0001c0001t0003g0244 a0001c0001t0003g0245 |
4 | HG01515.hp2 HG01517.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+6954C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821368 | |||||||
| chr12:49821418 | A | G | 29 | a0001c0001t0001g0258 a0001c0001t0004g0013 a0001c0001t0004g0018 others(26): Show |
43 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-99+6904T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821418 | |||||||
| chr12:49821536 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-99+6786G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821536 | |||||||
| chr12:49821538 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-99+6784A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821538 | |||||||
| chr12:49821560 | A | G | 1 | a0001c0004t0001g0040 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-99+6762T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821560 | |||||||
| chr12:49821567 | C | G | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+6755G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821567 | |||||||
| chr12:49821585 | C | T | 1 | a0001c0003t0002g0224 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-99+6737G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821585 | |||||||
| chr12:49821636 | T | G | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+6686A>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821636 | |||||||
| chr12:49821834 | G | A | 1 | a0001c0012t0002g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-99+6488C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49821834 | |||||||
| chr12:49822026 | G | A | 20 | a0001c0001t0001g0073 a0001c0001t0003g0021 a0001c0001t0003g0060 others(17): Show |
22 | HG01346.hp2 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-99+6296C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822026 | |||||||
| chr12:49822030 | C | T | 1 | a0001c0003t0002g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-99+6292G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822030 | |||||||
| chr12:49822122 | C | T | 124 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
171 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.-99+6200G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822122 | |||||||
| chr12:49822154 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-99+6168T>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822154 | |||||||
| chr12:49822322 | C | T | 4 | a0001c0003t0002g0028 a0001c0003t0002g0175 a0001c0003t0002g0176 others(1): Show |
5 | NA18941.hp1 NA18951.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99+6000G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822322 | |||||||
| chr12:49822409 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-99+5913T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822409 | |||||||
| chr12:49822419 | G | C | 1 | a0010c0025t0006g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-99+5903C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822419 | |||||||
| chr12:49822449 | T | C | 1 | a0001c0003t0002g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-99+5873A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822449 | |||||||
| chr12:49822528 | G | A | 1 | a0001c0003t0002g0233 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-99+5794C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822528 | |||||||
| chr12:49822548 | A | AT | 19 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0169 others(16): Show |
22 | HG01433.hp1 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-99+5773dupA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822548 | |||||||
| chr12:49822548 | AT | A | 10 | a0001c0001t0001g0215 a0001c0001t0004g0013 a0001c0001t0004g0018 others(7): Show |
13 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99+5773delA | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822548 | |||||||
| chr12:49822554 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-99+5768A>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822554 | |||||||
| chr12:49822790 | C | T | 1 | a0001c0003t0002g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-99+5532G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822790 | |||||||
| chr12:49822965 | C | G | 7 | a0001c0001t0004g0013 a0001c0001t0004g0018 a0001c0001t0004g0042 others(4): Show |
10 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+5357G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49822965 | |||||||
| chr12:49823018 | T | C | 217 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
288 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.-99+5304A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823018 | |||||||
| chr12:49823020 | TG | T | 20 | a0001c0001t0001g0073 a0001c0001t0003g0021 a0001c0001t0003g0060 others(17): Show |
22 | HG01346.hp2 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-99+5301delC | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823020 | |||||||
| chr12:49823144 | C | G | 1 | a0002c0002t0001g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-99+5178G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823144 | |||||||
| chr12:49823380 | G | A | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+4942C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823380 | |||||||
| chr12:49823448 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
115 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.-99+4874G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823448 | |||||||
| chr12:49823647 | T | TA | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
121 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.-99+4674dupT | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823647 | |||||||
| chr12:49823667 | G | A | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-99+4655C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823667 | |||||||
| chr12:49823788 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-99+4534T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49823788 | |||||||
| chr12:49824341 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-99+3981C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824341 | |||||||
| chr12:49824411 | G | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+3911C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824411 | |||||||
| chr12:49824421 | C | A | 1 | a0001c0001t0001g0027 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-99+3901G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824421 | |||||||
| chr12:49824424 | A | T | 1 | a0001c0001t0001g0027 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-99+3898T>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824424 | |||||||
| chr12:49824650 | A | G | 250 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(247): Show |
324 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(321): Show |
intron_variant | MODIFIER | c.-99+3672T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824650 | |||||||
| chr12:49824722 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-99+3600C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824722 | |||||||
| chr12:49824724 | C | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+3598G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824724 | |||||||
| chr12:49824861 | C | T | 124 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
171 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.-99+3461G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824861 | |||||||
| chr12:49824869 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-99+3453G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824869 | |||||||
| chr12:49824903 | G | A | 1 | a0002c0009t0001g0166 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-99+3419C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49824903 | |||||||
| chr12:49825453 | C | G | 1 | a0001c0003t0002g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-99+2869G>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825453 | |||||||
| chr12:49825500 | C | T | 1 | a0002c0002t0001g0219 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-99+2822G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825500 | |||||||
| chr12:49825706 | T | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
97 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-99+2616A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825706 | |||||||
| chr12:49825725 | T | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-99+2597A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825725 | |||||||
| chr12:49825816 | C | A | 1 | a0004c0006t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-99+2506G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825816 | |||||||
| chr12:49825866 | C | T | 9 | a0002c0002t0001g0010 a0002c0002t0001g0014 a0002c0002t0001g0020 others(6): Show |
15 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-99+2456G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49825866 | |||||||
| chr12:49826004 | G | A | 2 | a0001c0003t0002g0220 a0002c0002t0001g0219 |
2 | NA19011.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-99+2318C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826004 | |||||||
| chr12:49826072 | G | C | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+2250C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826072 | |||||||
| chr12:49826266 | GAGACGTA others(1059): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-99+990_-99+2055de others(1): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826266 | |||||||
| chr12:49826302 | G | T | 1 | a0001c0023t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-99+2020C>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826302 | |||||||
| chr12:49826368 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-99+1954G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826368 | |||||||
| chr12:49826369 | G | A | 1 | a0001c0003t0002g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-99+1953C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826369 | |||||||
| chr12:49826903 | G | A | 1 | a0001c0029t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-99+1419C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826903 | |||||||
| chr12:49826967 | C | T | 14 | a0001c0001t0001g0246 a0001c0001t0003g0034 a0001c0001t0003g0244 others(11): Show |
18 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-99+1355G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826967 | |||||||
| chr12:49826969 | C | T | 1 | a0001c0003t0002g0079 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-99+1353G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49826969 | |||||||
| chr12:49827015 | C | T | 1 | a0001c0004t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-99+1307G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827015 | |||||||
| chr12:49827220 | T | C | 7 | a0001c0001t0004g0013 a0001c0001t0004g0018 a0001c0001t0004g0042 others(4): Show |
10 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+1102A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827220 | |||||||
| chr12:49827279 | G | A | 11 | a0001c0001t0001g0073 a0001c0004t0001g0075 a0004c0006t0001g0022 others(8): Show |
12 | HG02055.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99+1043C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827279 | |||||||
| chr12:49827322 | T | C | 2 | a0001c0003t0002g0035 a0001c0003t0002g0249 |
3 | HG02486.hp1 HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-99+1000A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827322 | |||||||
| chr12:49827477 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-99+845C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827477 | |||||||
| chr12:49827669 | C | T | 3 | a0002c0002t0001g0019 a0002c0002t0001g0051 a0002c0002t0001g0052 |
4 | HG00423.hp2 HG02132.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+653G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827669 | |||||||
| chr12:49827903 | C | A | 14 | a0001c0003t0002g0224 a0001c0003t0002g0225 a0001c0003t0002g0227 others(11): Show |
14 | HG00408.hp1 HG01928.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.-99+419G>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827903 | |||||||
| chr12:49827910 | A | G | 3 | a0003c0005t0001g0048 a0003c0005t0001g0049 a0003c0011t0001g0050 |
3 | HG01109.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-99+412T>C | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827910 | |||||||
| chr12:49827928 | G | A | 2 | a0002c0002t0001g0235 a0002c0002t0001g0236 |
2 | HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-99+394C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49827928 | |||||||
| chr12:49828077 | G | A | 22 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(19): Show |
33 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-99+245C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828077 | |||||||
| chr12:49828142 | G | A | 7 | a0001c0001t0004g0013 a0001c0001t0004g0018 a0001c0001t0004g0042 others(4): Show |
10 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-99+180C>T | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828142 | |||||||
| chr12:49828145 | T | TGGAGGGA | 22 | a0001c0001t0001g0258 a0001c0004t0001g0004 a0001c0004t0001g0009 others(19): Show |
33 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-99+170_-99+176dup others(7): Show |
NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828145 | |||||||
| chr12:49828163 | G | C | 3 | a0001c0003t0002g0237 a0001c0003t0002g0238 a0001c0003t0002g0239 |
3 | NA19001.hp2 NA19063.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-99+159C>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828163 | |||||||
| chr12:49828209 | T | C | 53 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(50): Show |
73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-99+113A>G | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828209 | |||||||
| chr12:49828248 | C | T | 1 | a0001c0004t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-99+74G>A | NCKAP5L | ENSG00000167566.17 | transcript | ENST00000335999.7 | protein_coding | 1/12 | chr12 | 49828248 |