Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57122 |
| ensemblid | ENSG00000111581.10 |
| hgncid | 29914 |
| symbol | NUP107 |
| name | nucleoporin 107 |
| refseq_nuc | NM_020401.4 |
| refseq_prot | NP_065134.1 |
| ensembl_nuc | ENST00000229179.9 |
| ensembl_prot | ENSP00000229179.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 68686978 |
| end | 68745809 |
| strand | + |
| ver | v1.2 |
| region | chr12:68686978-68745809 |
| region5000 | chr12:68681978-68750809 |
| regionname0 | NUP107_chr12_68686978_68745809 |
| regionname5000 | NUP107_chr12_68681978_68750809 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 925 | 392 | 79 | 60 | 202 | 18 | 31 | 160 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0002 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0003 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0004 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0005 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0006 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| a0007 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | MDRSG others(920): Show |
chr12 | 68681978 | 68750809 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2775 | 286 | 67 | 37 | 147 | 10 | 24 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0002 | 0/1 | 2775 | 90 | 6 | 20 | 54 | 5 | 4 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0003 | 0/0 | 2775 | 8 | 5 | 1 | 0 | 0 | 2 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0004 | 0/0 | 2775 | 3 | 0 | 0 | 0 | 3 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0007 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0010 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0011 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0013 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0001c0015 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0002c0008 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0003c0006 | 0/0 | 2775 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0004c0014 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0005c0012 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0006c0005 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 | ||
| a0007c0009 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | ATGGA others(2770): Show |
chr12 | 68681978 | 68750809 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6213 | 91 | 14 | 20 | 45 | 5 | 7 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0003 | 0/0 | 6213 | 64 | 2 | 3 | 43 | 2 | 14 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0004 | 0/0 | 6213 | 66 | 4 | 8 | 49 | 2 | 3 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0005 | 0/0 | 6213 | 14 | 13 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0006 | 1/0 | 6213 | 13 | 11 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0007 | 0/0 | 6213 | 10 | 8 | 2 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0008 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0010 | 0/0 | 6213 | 4 | 4 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0011 | 0/0 | 6213 | 3 | 0 | 0 | 3 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0013 | 0/0 | 6213 | 3 | 0 | 0 | 3 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0014 | 0/0 | 6213 | 3 | 3 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0015 | 0/0 | 6213 | 2 | 2 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0016 | 0/0 | 6213 | 2 | 2 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0017 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0018 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0019 | 0/0 | 6213 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0020 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0021 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0023 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0025 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0026 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0027 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0001t0028 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0002t0002 | 0/1 | 6213 | 83 | 6 | 15 | 53 | 5 | 3 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0002t0009 | 0/0 | 6213 | 6 | 0 | 5 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0002t0024 | 0/0 | 6224 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6219): Show |
chr12 | 68681978 | 68750809 |
| a0001c0003t0008 | 0/0 | 6213 | 5 | 2 | 1 | 0 | 0 | 2 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0003t0012 | 0/0 | 6213 | 3 | 3 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0004t0005 | 0/0 | 6213 | 2 | 0 | 0 | 0 | 2 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0004t0022 | 0/0 | 6213 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0007t0003 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0010t0007 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0011t0002 | 0/0 | 6213 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0013t0003 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0001c0015t0008 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0002c0008t0002 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0003c0006t0002 | 0/0 | 6213 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0004c0014t0003 | 0/0 | 6213 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0005c0012t0005 | 0/0 | 6213 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0006c0005t0002 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| a0007c0009t0001 | 0/0 | 6213 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | GAAGG others(6208): Show |
chr12 | 68681978 | 68750809 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0010g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0015g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0016g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0018g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0019g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0020g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0021g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0023g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0026g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0027g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0001t0028g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0002t0024g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0008g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0003t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0004t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0004t0022g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0007t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0010t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0011t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0013t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0001c0015t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0002c0008t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0003c0006t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0004c0014t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0005c0012t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0006c0005t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| a0007c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0148 | EUR | GBR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0337 | EUR | GBR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0074 | EUR | GBR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0090 | EUR | GBR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00280 | hp2 | a0001 | c0001 | t0019 | g0197 | EUR | FIN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | FIN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0109 | EUR | FIN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0056 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00642 | hp2 | a0001 | c0001 | t0021 | g0005 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | CHS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01070 | hp2 | a0001 | c0002 | t0009 | g0091 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01071 | hp1 | a0001 | c0002 | t0009 | g0093 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01074 | hp1 | a0001 | c0002 | t0009 | g0122 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01081 | hp1 | a0001 | c0002 | t0009 | g0077 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01109 | hp1 | a0001 | c0001 | t0020 | g0200 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01175 | hp1 | a0001 | c0013 | t0003 | g0199 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01261 | hp2 | a0001 | c0003 | t0008 | g0038 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01433 | hp1 | a0002 | c0008 | t0002 | g0067 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01516 | hp1 | a0001 | c0004 | t0005 | g0060 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0021 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01517 | hp2 | a0001 | c0004 | t0005 | g0061 | EUR | IBS | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02004 | hp2 | a0003 | c0006 | t0002 | g0128 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02055 | hp2 | a0001 | c0003 | t0012 | g0031 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | CDX | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CDX | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CDX | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CDX | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02300 | hp2 | a0001 | c0015 | t0008 | g0033 | AMR | PEL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0228 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02602 | hp2 | a0004 | c0014 | t0003 | g0146 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02622 | hp2 | a0005 | c0012 | t0005 | g0213 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0351 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02647 | hp2 | a0001 | c0003 | t0012 | g0032 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02683 | hp1 | a0001 | c0011 | t0002 | g0350 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0058 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0045 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0043 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0211 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0281 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02922 | hp1 | a0001 | c0003 | t0008 | g0036 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02976 | hp1 | a0001 | c0001 | t0026 | g0282 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0355 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0231 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03490 | hp1 | a0001 | c0002 | t0009 | g0113 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0352 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0049 | AFR | ESN | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03579 | hp1 | a0001 | c0003 | t0008 | g0035 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0257 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03704 | hp1 | a0001 | c0003 | t0008 | g0037 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03834 | hp2 | a0001 | c0003 | t0008 | g0034 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0353 | SAS | BEB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | STU | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | YRI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | CHB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | CHB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18906 | hp1 | a0001 | c0003 | t0012 | g0030 | AFR | YRI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0193 | AFR | YRI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18941 | hp1 | a0006 | c0005 | t0002 | g0134 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18945 | hp2 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0165 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18962 | hp2 | a0001 | c0001 | t0013 | g0172 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0356 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18980 | hp2 | a0001 | c0001 | t0013 | g0170 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18984 | hp2 | a0001 | c0007 | t0003 | g0040 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18987 | hp1 | a0001 | c0002 | t0024 | g0073 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18993 | hp2 | a0001 | c0001 | t0018 | g0153 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18998 | hp1 | a0001 | c0001 | t0028 | g0334 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19005 | hp2 | a0007 | c0009 | t0001 | g0289 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19009 | hp1 | a0001 | c0001 | t0011 | g0164 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | LWK | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | LWK | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19043 | hp1 | a0001 | c0010 | t0007 | g0055 | AFR | LWK | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0354 | AFR | LWK | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19063 | hp2 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19083 | hp1 | a0001 | c0001 | t0027 | g0329 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | ASW | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ASW | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0129 | EUR | TSI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20805 | hp1 | a0001 | c0004 | t0022 | g0059 | EUR | TSI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | TSI | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01123 | hp1 | a0001 | c0002 | t0009 | g0094 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0239 | AFR | ACB | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0238 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | MSL | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | USA | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | USA | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0051 | AFR | USA | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0127 | REF | REF | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0233 | REF | REF | NUP107_chr12_68681978_68750809 | NUP107 | chr12 | 68681978 | 68750809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68692016 | C | T | 1 | a0002 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.352C>T | p.Arg118Cys | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/28 | 440/6213 | 352/2778 | 118/925 | chr12 | 68692016 | |||
| chr12:68692040 | G | C | 1 | a0007 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.376G>C | p.Glu126Gln | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/28 | 464/6213 | 376/2778 | 126/925 | chr12 | 68692040 | |||
| chr12:68709259 | A | T | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.751A>T | p.Thr251Ser | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/28 | 839/6213 | 751/2778 | 251/925 | chr12 | 68709259 | |||
| chr12:68735295 | A | G | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2453A>G | p.Tyr818Cys | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/28 | 2541/6213 | 2453/2778 | 818/925 | chr12 | 68735295 | |||
| chr12:68735330 | G | T | 1 | a0003 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.2488G>T | p.Val830Leu | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/28 | 2576/6213 | 2488/2778 | 830/925 | chr12 | 68735330 | |||
| chr12:68741837 | A | G | 1 | a0006 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.2527A>G | p.Thr843Ala | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 27/28 | 2615/6213 | 2527/2778 | 843/925 | chr12 | 68741837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68689025 | G | A | 5 | a0001c0002 a0001c0007 a0002c0008 others(2): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
synonymous_variant | LOW | c.72G>A | p.Arg24Arg | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 2/28 | 160/6213 | 72/2778 | 24/925 | chr12 | 68689025 | |||
| chr12:68692021 | C | T | 1 | a0001c0015 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.357C>T | p.Ser119Ser | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/28 | 445/6213 | 357/2778 | 119/925 | chr12 | 68692021 | |||
| chr12:68696889 | T | C | 1 | a0001c0010 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.519T>C | p.Leu173Leu | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/28 | 607/6213 | 519/2778 | 173/925 | chr12 | 68696889 | |||
| chr12:68696904 | A | G | 2 | a0001c0003 a0001c0015 |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
synonymous_variant | LOW | c.534A>G | p.Glu178Glu | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/28 | 622/6213 | 534/2778 | 178/925 | chr12 | 68696904 | |||
| chr12:68700827 | A | G | 1 | a0001c0004 | 3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.654A>G | p.Thr218Thr | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/28 | 742/6213 | 654/2778 | 218/925 | chr12 | 68700827 | |||
| chr12:68719404 | C | T | 1 | a0001c0013 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.1147C>T | p.Leu383Leu | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 13/28 | 1235/6213 | 1147/2778 | 383/925 | chr12 | 68719404 | |||
| chr12:68721918 | G | A | 5 | a0001c0002 a0001c0011 a0002c0008 others(2): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
synonymous_variant | LOW | c.1389G>A | p.Gln463Gln | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 16/28 | 1477/6213 | 1389/2778 | 463/925 | chr12 | 68721918 | |||
| chr12:68733465 | C | T | 1 | a0001c0004 | 3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.2115C>T | p.His705His | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/28 | 2203/6213 | 2115/2778 | 705/925 | chr12 | 68733465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68687022 | T | C | 1 | a0001c0001t0017 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/28 | 44 | chr12 | 68687022 | ||||||
| chr12:68742472 | T | C | 1 | a0001c0002t0009 | 6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 10 | chr12 | 68742472 | ||||||
| chr12:68742707 | T | A | 31 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(28): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*245T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 245 | chr12 | 68742707 | ||||||
| chr12:68742725 | T | A | 1 | a0001c0001t0011 | 3 | NA18961.hp1 NA18968.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*263T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 263 | chr12 | 68742725 | ||||||
| chr12:68742746 | T | C | 1 | a0001c0001t0025 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 284 | chr12 | 68742746 | ||||||
| chr12:68742821 | C | T | 1 | a0001c0001t0028 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 359 | chr12 | 68742821 | ||||||
| chr12:68742838 | C | T | 1 | a0001c0001t0027 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 376 | chr12 | 68742838 | ||||||
| chr12:68742963 | A | AAACTTCC others(4): Show |
1 | a0001c0002t0024 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504_*514dupCTTCCT others(5): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 515 | INFO_REALIGN_3_PRIME | chr12 | 68742963 | |||||
| chr12:68743113 | A | T | 3 | a0001c0001t0007 a0001c0001t0014 a0001c0010t0007 |
14 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*651A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 651 | chr12 | 68743113 | ||||||
| chr12:68743144 | C | T | 7 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0024 others(4): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*682C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 682 | chr12 | 68743144 | ||||||
| chr12:68743261 | A | C | 1 | a0001c0001t0014 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*799A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 799 | chr12 | 68743261 | ||||||
| chr12:68743353 | G | A | 1 | a0001c0001t0018 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*891G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 891 | chr12 | 68743353 | ||||||
| chr12:68743354 | A | T | 1 | a0001c0001t0018 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 892 | chr12 | 68743354 | ||||||
| chr12:68743447 | C | T | 5 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0027 others(2): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 985 | chr12 | 68743447 | ||||||
| chr12:68743547 | A | G | 1 | a0001c0001t0023 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1085A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1085 | chr12 | 68743547 | ||||||
| chr12:68743671 | C | A | 1 | a0001c0001t0015 | 2 | HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1209C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1209 | chr12 | 68743671 | ||||||
| chr12:68743672 | T | C | 4 | a0001c0001t0008 a0001c0003t0008 a0001c0003t0012 others(1): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1210T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1210 | chr12 | 68743672 | ||||||
| chr12:68743728 | T | A | 1 | a0001c0001t0019 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1266 | chr12 | 68743728 | ||||||
| chr12:68744061 | T | G | 1 | a0001c0001t0020 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1599T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1599 | chr12 | 68744061 | ||||||
| chr12:68744175 | C | T | 7 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0024 others(4): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1713C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1713 | chr12 | 68744175 | ||||||
| chr12:68744198 | T | C | 10 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0013 others(7): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1736T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 1736 | chr12 | 68744198 | ||||||
| chr12:68744476 | T | C | 1 | a0001c0001t0021 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2014T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2014 | chr12 | 68744476 | ||||||
| chr12:68744643 | C | T | 1 | a0001c0001t0013 | 3 | NA18945.hp2 NA18962.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2181C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2181 | chr12 | 68744643 | ||||||
| chr12:68744751 | T | G | 5 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0027 others(2): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2289T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2289 | chr12 | 68744751 | ||||||
| chr12:68744764 | G | A | 4 | a0001c0001t0008 a0001c0003t0008 a0001c0003t0012 others(1): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2302G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2302 | chr12 | 68744764 | ||||||
| chr12:68744843 | C | T | 1 | a0001c0001t0010 | 4 | HG02486.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2381C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2381 | chr12 | 68744843 | ||||||
| chr12:68744922 | C | T | 2 | a0001c0001t0004 a0001c0001t0025 |
67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2460C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2460 | chr12 | 68744922 | ||||||
| chr12:68745213 | A | G | 1 | a0001c0001t0016 | 2 | HG02723.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2751A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2751 | chr12 | 68745213 | ||||||
| chr12:68745330 | T | C | 1 | a0001c0004t0022 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2868 | chr12 | 68745330 | ||||||
| chr12:68745378 | G | T | 1 | a0001c0003t0012 | 3 | HG02055.hp2 HG02647.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2916G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 2916 | chr12 | 68745378 | ||||||
| chr12:68745558 | C | T | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3096C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 28/28 | 3096 | chr12 | 68745558 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68687969 | A | C | 1 | a0001c0001t0004g0356 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.8+896A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68687969 | |||||||
| chr12:68688159 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | NA18956.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.9-803T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688159 | |||||||
| chr12:68688186 | G | T | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.9-776G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688186 | |||||||
| chr12:68688186 | GT | G | 105 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(102): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.9-765delT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 68688186 | ||||||
| chr12:68688186 | GTT | G | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.9-766_9-765delTT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 68688186 | ||||||
| chr12:68688238 | T | C | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.9-724T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688238 | |||||||
| chr12:68688758 | T | G | 1 | a0001c0007t0003g0040 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.9-204T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688758 | |||||||
| chr12:68688815 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.9-147C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688815 | |||||||
| chr12:68688816 | G | A | 70 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(67): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.9-146G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688816 | |||||||
| chr12:68688870 | CT | C | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.9-91delT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688870 | |||||||
| chr12:68688889 | A | G | 109 | a0001c0001t0003g0352 a0001c0001t0003g0353 a0001c0001t0005g0057 others(106): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.9-73A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 1/27 | chr12 | 68688889 | |||||||
| chr12:68689174 | T | G | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100+121T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 2/27 | chr12 | 68689174 | |||||||
| chr12:68689314 | A | G | 1 | a0001c0001t0010g0351 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.101-219A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 2/27 | chr12 | 68689314 | |||||||
| chr12:68689457 | A | G | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.101-76A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 2/27 | chr12 | 68689457 | |||||||
| chr12:68689655 | C | T | 2 | a0001c0001t0003g0198 a0001c0013t0003g0199 |
2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.187+36C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68689655 | |||||||
| chr12:68690002 | A | G | 180 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(177): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.187+383A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690002 | |||||||
| chr12:68690045 | T | G | 1 | a0001c0001t0003g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.187+426T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690045 | |||||||
| chr12:68690046 | G | T | 1 | a0001c0001t0003g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.187+427G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690046 | |||||||
| chr12:68690060 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0046 others(4): Show |
7 | HG01361.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+441A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690060 | |||||||
| chr12:68690134 | T | A | 1 | a0001c0001t0003g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.188-497T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690134 | |||||||
| chr12:68690166 | C | CA | 16 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0205 others(13): Show |
16 | HG00558.hp2 HG02056.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-451dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 68690166 | ||||||
| chr12:68690166 | CA | C | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.188-451delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 68690166 | ||||||
| chr12:68690346 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(74): Show |
87 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.188-285C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690346 | |||||||
| chr12:68690492 | A | G | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-139A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690492 | |||||||
| chr12:68690537 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.188-94G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 3/27 | chr12 | 68690537 | |||||||
| chr12:68690761 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(73): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.303+15A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68690761 | |||||||
| chr12:68690832 | A | G | 1 | a0006c0005t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.303+86A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68690832 | |||||||
| chr12:68690936 | T | C | 1 | a0001c0001t0004g0209 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.303+190T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68690936 | |||||||
| chr12:68690952 | T | C | 196 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(193): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.303+206T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68690952 | |||||||
| chr12:68690990 | G | A | 72 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(69): Show |
76 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.303+244G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68690990 | |||||||
| chr12:68691033 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.303+287T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68691033 | |||||||
| chr12:68691430 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(68): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.304-538G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68691430 | |||||||
| chr12:68691701 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0016g0043 a0001c0001t0016g0045 |
3 | HG02723.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.304-267G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68691701 | |||||||
| chr12:68691705 | G | A | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-263G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68691705 | |||||||
| chr12:68691838 | A | AG | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-127dupG | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 68691838 | ||||||
| chr12:68691862 | A | G | 1 | a0001c0002t0002g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-106A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | chr12 | 68691862 | |||||||
| chr12:68691885 | AC | A | 3 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 |
3 | HG02717.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.304-81delC | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 68691885 | ||||||
| chr12:68692195 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.448+83C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692195 | |||||||
| chr12:68692314 | C | T | 1 | a0001c0001t0019g0197 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.448+202C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692314 | |||||||
| chr12:68692362 | C | T | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448+250C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692362 | |||||||
| chr12:68692441 | T | A | 71 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(68): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.448+329T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692441 | |||||||
| chr12:68692443 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.448+331G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692443 | |||||||
| chr12:68692533 | C | T | 1 | a0001c0001t0006g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.448+421C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692533 | |||||||
| chr12:68692573 | C | T | 2 | a0001c0001t0006g0281 a0001c0001t0026g0282 |
2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.448+461C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692573 | |||||||
| chr12:68692574 | G | A | 71 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(68): Show |
75 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.448+462G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692574 | |||||||
| chr12:68692577 | T | TA | 13 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0004g0222 others(10): Show |
13 | HG00673.hp2 HG00735.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.448+477dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68692577 | ||||||
| chr12:68692590 | C | A | 6 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+478C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692590 | |||||||
| chr12:68692590 | CA | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(67): Show |
80 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.448+489delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68692590 | ||||||
| chr12:68692591 | A | C | 6 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0001g0291 others(3): Show |
6 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+479A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692591 | |||||||
| chr12:68692734 | C | A | 1 | a0001c0002t0002g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.448+622C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692734 | |||||||
| chr12:68692749 | A | AT | 93 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0007g0062 others(90): Show |
104 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.448+655dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68692749 | ||||||
| chr12:68692749 | A | ATT | 6 | a0001c0001t0003g0353 a0001c0002t0002g0070 a0001c0002t0002g0071 others(3): Show |
6 | HG00621.hp2 HG01978.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+654_448+655dup others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68692749 | ||||||
| chr12:68692749 | AT | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(68): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.448+655delT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68692749 | ||||||
| chr12:68692835 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.448+723C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692835 | |||||||
| chr12:68692836 | G | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0020 a0001c0001t0004g0223 others(2): Show |
8 | HG01074.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+724G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68692836 | |||||||
| chr12:68693039 | T | C | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.448+927T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693039 | |||||||
| chr12:68693081 | A | AT | 12 | a0001c0001t0004g0010 a0001c0001t0004g0269 a0001c0001t0004g0270 others(9): Show |
13 | HG00597.hp2 HG02257.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.448+972dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68693081 | ||||||
| chr12:68693081 | A | T | 12 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0280 others(9): Show |
12 | HG00558.hp2 HG01106.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.448+969A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693081 | |||||||
| chr12:68693084 | T | A | 2 | a0001c0001t0001g0285 a0001c0001t0020g0200 |
2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.448+972T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693084 | |||||||
| chr12:68693084 | TA | T | 4 | a0001c0001t0004g0008 a0001c0001t0004g0020 a0001c0001t0004g0224 others(1): Show |
7 | HG01074.hp2 HG01255.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+973delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693084 | |||||||
| chr12:68693085 | A | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0268 others(168): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.448+973A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693085 | |||||||
| chr12:68693089 | T | A | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+977T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693089 | |||||||
| chr12:68693177 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.448+1065A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693177 | |||||||
| chr12:68693399 | G | A | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448+1287G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693399 | |||||||
| chr12:68693423 | A | C | 1 | a0001c0001t0004g0275 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.448+1311A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693423 | |||||||
| chr12:68693500 | A | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.448+1388A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693500 | |||||||
| chr12:68693570 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0339 |
2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.448+1458C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693570 | |||||||
| chr12:68693613 | G | A | 3 | a0001c0001t0003g0137 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02056.hp2 HG02083.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.448+1501G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693613 | |||||||
| chr12:68693725 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.448+1613G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693725 | |||||||
| chr12:68693796 | A | C | 1 | a0001c0001t0017g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.448+1684A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693796 | |||||||
| chr12:68693940 | C | A | 1 | a0001c0001t0004g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448+1828C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693940 | |||||||
| chr12:68693994 | C | G | 1 | a0001c0001t0003g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.448+1882C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68693994 | |||||||
| chr12:68694120 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.448+2008C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694120 | |||||||
| chr12:68694132 | A | C | 1 | a0001c0001t0001g0338 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.448+2020A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694132 | |||||||
| chr12:68694386 | C | A | 1 | a0001c0001t0010g0351 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.448+2274C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694386 | |||||||
| chr12:68694431 | A | C | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.448+2319A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694431 | |||||||
| chr12:68694550 | A | C | 1 | a0001c0001t0004g0222 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.449-2269A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694550 | |||||||
| chr12:68694583 | C | A | 1 | a0001c0001t0015g0354 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.449-2236C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694583 | |||||||
| chr12:68694718 | G | A | 195 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(192): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.449-2101G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694718 | |||||||
| chr12:68694873 | T | G | 110 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(107): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.449-1946T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68694873 | |||||||
| chr12:68695189 | G | A | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.449-1630G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68695189 | |||||||
| chr12:68695219 | C | T | 3 | a0001c0001t0003g0192 a0001c0001t0003g0194 a0001c0001t0023g0193 |
3 | HG02145.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.449-1600C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68695219 | |||||||
| chr12:68695323 | T | C | 1 | a0001c0001t0004g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.449-1496T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68695323 | |||||||
| chr12:68695440 | T | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.449-1379T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68695440 | |||||||
| chr12:68695841 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01361.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-978G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68695841 | |||||||
| chr12:68696009 | TA | T | 9 | a0001c0001t0001g0337 a0001c0001t0001g0349 a0001c0001t0003g0190 others(6): Show |
9 | HG00099.hp2 HG02896.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-796delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68696009 | ||||||
| chr12:68696235 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.449-584C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68696235 | |||||||
| chr12:68696425 | C | T | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.449-394C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68696425 | |||||||
| chr12:68696483 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.449-336C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68696483 | |||||||
| chr12:68696569 | T | C | 110 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(107): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.449-250T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68696569 | |||||||
| chr12:68696674 | T | C | 2 | a0001c0001t0005g0212 a0005c0012t0005g0213 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.449-145T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | chr12 | 68696674 | |||||||
| chr12:68696793 | C | CT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(155): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.449-13dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68696793 | ||||||
| chr12:68696793 | C | CTT | 5 | a0001c0001t0001g0027 a0001c0001t0001g0335 a0001c0001t0001g0344 others(2): Show |
6 | HG03491.hp1 HG03942.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-14_449-13dupTT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 68696793 | ||||||
| chr12:68696974 | A | G | 85 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(82): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.552+52A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68696974 | |||||||
| chr12:68697023 | G | C | 85 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(82): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.552+101G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697023 | |||||||
| chr12:68697347 | C | T | 1 | a0001c0001t0004g0356 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.552+425C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697347 | |||||||
| chr12:68697438 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.552+516T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697438 | |||||||
| chr12:68697543 | A | G | 110 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(107): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.552+621A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697543 | |||||||
| chr12:68697583 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0340 |
3 | HG01167.hp1 HG02258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.552+661G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697583 | |||||||
| chr12:68697597 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552+675C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697597 | |||||||
| chr12:68697635 | A | C | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.552+713A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697635 | |||||||
| chr12:68697735 | T | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0075 |
2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.552+813T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697735 | |||||||
| chr12:68697736 | A | G | 347 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(344): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.552+814A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697736 | |||||||
| chr12:68697804 | T | C | 347 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(344): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.552+882T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697804 | |||||||
| chr12:68697959 | C | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.552+1037C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68697959 | |||||||
| chr12:68698007 | G | C | 1 | a0004c0014t0003g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.552+1085G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698007 | |||||||
| chr12:68698285 | A | C | 1 | a0001c0001t0006g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.552+1363A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698285 | |||||||
| chr12:68698778 | T | G | 85 | a0001c0001t0003g0196 a0001c0001t0003g0352 a0001c0001t0003g0353 others(82): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.552+1856T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698778 | |||||||
| chr12:68698808 | C | T | 8 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0001g0332 others(5): Show |
8 | HG02027.hp1 HG02040.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+1886C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698808 | |||||||
| chr12:68698873 | T | G | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.553-1853T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698873 | |||||||
| chr12:68698893 | G | A | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-1833G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68698893 | |||||||
| chr12:68699265 | C | T | 2 | a0001c0001t0004g0266 a0001c0001t0004g0267 |
2 | NA18966.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.553-1461C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699265 | |||||||
| chr12:68699409 | T | C | 71 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(68): Show |
75 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.553-1317T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699409 | |||||||
| chr12:68699465 | A | G | 106 | a0001c0001t0003g0352 a0001c0001t0003g0353 a0001c0001t0005g0057 others(103): Show |
121 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.553-1261A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699465 | |||||||
| chr12:68699513 | A | T | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-1213A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699513 | |||||||
| chr12:68699651 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.553-1075A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699651 | |||||||
| chr12:68699734 | T | G | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-992T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699734 | |||||||
| chr12:68699760 | G | A | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.553-966G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699760 | |||||||
| chr12:68699769 | C | T | 1 | a0001c0002t0002g0123 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.553-957C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68699769 | |||||||
| chr12:68699842 | AC | A | 4 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0266 others(1): Show |
4 | HG02056.hp1 NA18966.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-882delC | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr12 | 68699842 | ||||||
| chr12:68700071 | T | G | 1 | a0001c0001t0005g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.553-655T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700071 | |||||||
| chr12:68700179 | C | T | 1 | a0001c0001t0004g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.553-547C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700179 | |||||||
| chr12:68700226 | A | G | 1 | a0001c0002t0009g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.553-500A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700226 | |||||||
| chr12:68700265 | G | A | 2 | a0001c0001t0004g0236 a0001c0001t0004g0237 |
2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.553-461G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700265 | |||||||
| chr12:68700327 | T | C | 10 | a0001c0001t0007g0001 a0001c0001t0007g0050 a0001c0001t0007g0053 others(7): Show |
14 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-399T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700327 | |||||||
| chr12:68700341 | C | T | 109 | a0001c0001t0003g0352 a0001c0001t0003g0353 a0001c0001t0005g0057 others(106): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.553-385C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700341 | |||||||
| chr12:68700664 | A | G | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.553-62A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 6/27 | chr12 | 68700664 | |||||||
| chr12:68701322 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.680+469T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68701322 | |||||||
| chr12:68701333 | C | T | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.680+480C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68701333 | |||||||
| chr12:68701353 | C | T | 10 | a0001c0001t0007g0001 a0001c0001t0007g0050 a0001c0001t0007g0053 others(7): Show |
14 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.680+500C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68701353 | |||||||
| chr12:68701358 | A | C | 1 | a0001c0001t0007g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.680+505A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68701358 | |||||||
| chr12:68701883 | C | T | 6 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(3): Show |
6 | HG01261.hp2 HG02300.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-853C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68701883 | |||||||
| chr12:68702074 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.681-662C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702074 | |||||||
| chr12:68702145 | C | T | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.681-591C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702145 | |||||||
| chr12:68702163 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.681-573A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702163 | |||||||
| chr12:68702217 | G | C | 1 | a0001c0001t0006g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681-519G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702217 | |||||||
| chr12:68702274 | C | G | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.681-462C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702274 | |||||||
| chr12:68702326 | T | C | 2 | a0001c0001t0006g0229 a0001c0001t0006g0230 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.681-410T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702326 | |||||||
| chr12:68702368 | A | G | 2 | a0001c0001t0005g0057 a0001c0001t0017g0058 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.681-368A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702368 | |||||||
| chr12:68702404 | C | T | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.681-332C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702404 | |||||||
| chr12:68702532 | T | C | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.681-204T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 7/27 | chr12 | 68702532 | |||||||
| chr12:68702795 | TATTA | T | 2 | a0001c0002t0002g0018 a0001c0002t0002g0135 |
3 | HG01256.hp1 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.729+15_729+18delAA others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68702795 | ||||||
| chr12:68702846 | A | AT | 61 | a0001c0001t0001g0268 a0001c0001t0004g0008 a0001c0001t0004g0009 others(58): Show |
70 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.729+76dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68702846 | ||||||
| chr12:68703000 | C | T | 7 | a0001c0002t0002g0004 a0001c0002t0002g0068 a0001c0002t0002g0119 others(4): Show |
9 | HG00558.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.729+216C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703000 | |||||||
| chr12:68703034 | C | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.729+250C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703034 | |||||||
| chr12:68703302 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.729+518A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703302 | |||||||
| chr12:68703359 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.729+575A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703359 | |||||||
| chr12:68703399 | A | G | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+615A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703399 | |||||||
| chr12:68703448 | G | GT | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.729+667dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68703448 | ||||||
| chr12:68703452 | G | T | 22 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(19): Show |
26 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.729+668G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703452 | |||||||
| chr12:68703460 | T | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.729+676T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703460 | |||||||
| chr12:68703513 | C | T | 3 | a0001c0002t0002g0069 a0001c0002t0002g0117 a0001c0002t0002g0118 |
3 | HG02071.hp2 NA18939.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.729+729C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703513 | |||||||
| chr12:68703737 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.729+953C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703737 | |||||||
| chr12:68703771 | T | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(277): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.729+987T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703771 | |||||||
| chr12:68703788 | T | A | 1 | a0001c0015t0008g0033 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.729+1004T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703788 | |||||||
| chr12:68703798 | G | A | 1 | a0003c0006t0002g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.729+1014G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703798 | |||||||
| chr12:68703944 | C | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG01361.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+1160C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68703944 | |||||||
| chr12:68704014 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(73): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.729+1230C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704014 | |||||||
| chr12:68704419 | G | A | 74 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(71): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.729+1635G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704419 | |||||||
| chr12:68704614 | C | T | 1 | a0001c0003t0012g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+1830C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704614 | |||||||
| chr12:68704644 | G | A | 2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | HG00099.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.729+1860G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704644 | |||||||
| chr12:68704709 | C | T | 10 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0214 others(7): Show |
12 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.729+1925C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704709 | |||||||
| chr12:68704859 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(13): Show |
18 | HG00597.hp1 HG00621.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+2075C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704859 | |||||||
| chr12:68704860 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.729+2076T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68704860 | |||||||
| chr12:68705185 | C | G | 1 | a0001c0010t0007g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.729+2401C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705185 | |||||||
| chr12:68705313 | C | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.729+2529C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705313 | |||||||
| chr12:68705532 | T | TA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(72): Show |
85 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.729+2768dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68705532 | ||||||
| chr12:68705532 | TA | T | 16 | a0001c0001t0003g0148 a0001c0001t0003g0191 a0001c0001t0004g0225 others(13): Show |
16 | HG00099.hp1 HG00639.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.729+2768delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68705532 | ||||||
| chr12:68705586 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.729+2802C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705586 | |||||||
| chr12:68705640 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.729+2856A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705640 | |||||||
| chr12:68705773 | G | A | 2 | a0001c0001t0003g0139 a0001c0001t0003g0150 |
2 | NA19064.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.729+2989G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705773 | |||||||
| chr12:68705959 | T | C | 1 | a0001c0001t0004g0240 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.729+3175T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68705959 | |||||||
| chr12:68706020 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.730-3218G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706020 | |||||||
| chr12:68706149 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01361.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.730-3089T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706149 | |||||||
| chr12:68706170 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01361.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.730-3068A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706170 | |||||||
| chr12:68706414 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730-2824C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706414 | |||||||
| chr12:68706415 | G | A | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.730-2823G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706415 | |||||||
| chr12:68706460 | G | A | 2 | a0001c0001t0004g0021 a0001c0001t0004g0222 |
3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.730-2778G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706460 | |||||||
| chr12:68706628 | C | T | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.730-2610C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706628 | |||||||
| chr12:68706643 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.730-2595T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706643 | |||||||
| chr12:68706918 | C | G | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.730-2320C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68706918 | |||||||
| chr12:68707108 | C | T | 1 | a0001c0001t0004g0263 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.730-2130C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707108 | |||||||
| chr12:68707150 | C | T | 1 | a0002c0008t0002g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.730-2088C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707150 | |||||||
| chr12:68707307 | GA | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(76): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.730-1921delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 68707307 | ||||||
| chr12:68707308 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.730-1930A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707308 | |||||||
| chr12:68707337 | C | T | 1 | a0001c0001t0004g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.730-1901C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707337 | |||||||
| chr12:68707362 | G | C | 1 | a0001c0001t0003g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.730-1876G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707362 | |||||||
| chr12:68707490 | A | G | 2 | a0001c0002t0002g0017 a0001c0002t0002g0110 |
3 | HG02451.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.730-1748A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707490 | |||||||
| chr12:68707698 | T | G | 1 | a0001c0013t0003g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.730-1540T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68707698 | |||||||
| chr12:68708228 | T | C | 1 | a0001c0002t0009g0077 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.730-1010T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708228 | |||||||
| chr12:68708249 | C | T | 195 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(192): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.730-989C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708249 | |||||||
| chr12:68708253 | T | C | 1 | a0001c0001t0006g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.730-985T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708253 | |||||||
| chr12:68708289 | G | T | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.730-949G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708289 | |||||||
| chr12:68708439 | C | T | 104 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(101): Show |
119 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.730-799C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708439 | |||||||
| chr12:68708449 | T | G | 1 | a0001c0001t0001g0327 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.730-789T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708449 | |||||||
| chr12:68708628 | T | A | 1 | a0001c0001t0005g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.730-610T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708628 | |||||||
| chr12:68708766 | G | A | 1 | a0001c0003t0008g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.730-472G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708766 | |||||||
| chr12:68708813 | T | G | 1 | a0001c0001t0003g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.730-425T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708813 | |||||||
| chr12:68708839 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0003g0145 a0001c0001t0016g0043 others(1): Show |
4 | HG02083.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-399G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708839 | |||||||
| chr12:68708946 | T | C | 84 | a0001c0001t0003g0352 a0001c0001t0003g0353 a0001c0002t0002g0003 others(81): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.730-292T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 8/27 | chr12 | 68708946 | |||||||
| chr12:68709374 | A | G | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.801+65A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709374 | |||||||
| chr12:68709418 | C | G | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.801+109C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709418 | |||||||
| chr12:68709458 | C | A | 1 | a0001c0001t0005g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.801+149C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709458 | |||||||
| chr12:68709586 | TGGAAAAA others(26): Show |
T | 1 | a0007c0009t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.801+278_801+310del others(33): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709586 | |||||||
| chr12:68709658 | G | A | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.802-347G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709658 | |||||||
| chr12:68709743 | G | T | 1 | a0001c0001t0001g0323 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.802-262G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709743 | |||||||
| chr12:68709762 | G | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.802-243G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709762 | |||||||
| chr12:68709837 | C | T | 1 | a0001c0001t0003g0185 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.802-168C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709837 | |||||||
| chr12:68709852 | G | A | 1 | a0001c0002t0002g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.802-153G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709852 | |||||||
| chr12:68709888 | C | CA | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.802-106dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 68709888 | ||||||
| chr12:68709959 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.802-46T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 9/27 | chr12 | 68709959 | |||||||
| chr12:68710156 | A | G | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.890+63A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710156 | |||||||
| chr12:68710183 | T | C | 1 | a0001c0002t0002g0117 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.890+90T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710183 | |||||||
| chr12:68710235 | A | G | 1 | a0001c0001t0006g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.890+142A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710235 | |||||||
| chr12:68710256 | T | G | 1 | a0001c0015t0008g0033 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.890+163T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710256 | |||||||
| chr12:68710336 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.890+243A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710336 | |||||||
| chr12:68710601 | G | A | 1 | a0001c0002t0002g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.890+508G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710601 | |||||||
| chr12:68710651 | T | TA | 97 | a0001c0001t0003g0188 a0001c0001t0004g0226 a0001c0001t0004g0242 others(94): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.890+576dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68710651 | ||||||
| chr12:68710651 | T | TAA | 71 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(68): Show |
75 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.890+575_890+576dup others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68710651 | ||||||
| chr12:68710651 | TA | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(74): Show |
87 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.890+576delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68710651 | ||||||
| chr12:68710684 | T | A | 74 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(71): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.890+591T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710684 | |||||||
| chr12:68710716 | A | G | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.890+623A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710716 | |||||||
| chr12:68710725 | A | G | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.890+632A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710725 | |||||||
| chr12:68710781 | T | C | 1 | a0001c0003t0012g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890+688T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710781 | |||||||
| chr12:68710847 | C | T | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.890+754C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710847 | |||||||
| chr12:68710896 | T | C | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.890+803T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710896 | |||||||
| chr12:68710915 | C | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.890+822C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710915 | |||||||
| chr12:68710951 | C | T | 1 | a0002c0008t0002g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.890+858C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710951 | |||||||
| chr12:68710982 | C | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.890+889C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710982 | |||||||
| chr12:68710998 | T | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.890+905T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68710998 | |||||||
| chr12:68711030 | G | T | 1 | a0001c0001t0001g0327 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.890+937G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711030 | |||||||
| chr12:68711031 | T | G | 1 | a0001c0001t0001g0327 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.890+938T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711031 | |||||||
| chr12:68711053 | A | T | 13 | a0001c0001t0003g0139 a0001c0001t0003g0143 a0001c0001t0003g0149 others(10): Show |
13 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.890+960A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711053 | |||||||
| chr12:68711076 | A | G | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.890+983A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711076 | |||||||
| chr12:68711123 | C | T | 2 | a0001c0001t0005g0057 a0001c0001t0017g0058 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.890+1030C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711123 | |||||||
| chr12:68711129 | G | A | 2 | a0001c0001t0003g0152 a0001c0001t0003g0190 |
2 | HG02074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.890+1036G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711129 | |||||||
| chr12:68711134 | C | T | 1 | a0001c0001t0004g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.890+1041C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711134 | |||||||
| chr12:68711184 | T | G | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.890+1091T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711184 | |||||||
| chr12:68711223 | C | T | 1 | a0001c0001t0023g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.890+1130C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711223 | |||||||
| chr12:68711265 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.890+1172C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711265 | |||||||
| chr12:68711280 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.890+1187G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711280 | |||||||
| chr12:68711459 | C | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0322 |
2 | HG00597.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.890+1366C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711459 | |||||||
| chr12:68711535 | C | CA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(74): Show |
87 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.890+1456dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68711535 | ||||||
| chr12:68711535 | CA | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0003g0139 others(6): Show |
9 | HG01361.hp1 HG02886.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.890+1456delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68711535 | ||||||
| chr12:68711879 | C | T | 1 | a0007c0009t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.890+1786C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711879 | |||||||
| chr12:68711880 | A | G | 1 | a0007c0009t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.890+1787A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711880 | |||||||
| chr12:68711888 | A | ATGTGTTT others(30): Show |
1 | a0007c0009t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.890+1796_890+1797i others(39): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68711888 | ||||||
| chr12:68711890 | T | G | 1 | a0007c0009t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.890+1797T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68711890 | |||||||
| chr12:68712097 | TAAAGGGA others(3): Show |
T | 1 | a0001c0001t0004g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.891-1632_891-1623d others(12): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712097 | |||||||
| chr12:68712266 | T | C | 84 | a0001c0001t0003g0352 a0001c0001t0003g0353 a0001c0002t0002g0003 others(81): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.891-1464T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712266 | |||||||
| chr12:68712309 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.891-1421C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712309 | |||||||
| chr12:68712418 | CA | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(293): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.891-1287delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68712418 | ||||||
| chr12:68712418 | CAA | C | 20 | a0001c0001t0001g0284 a0001c0001t0001g0326 a0001c0001t0001g0327 others(17): Show |
20 | HG00323.hp1 HG01099.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.891-1288_891-1287d others(4): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68712418 | ||||||
| chr12:68712418 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.891-1298_891-1287d others(14): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68712418 | ||||||
| chr12:68712438 | A | G | 75 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(72): Show |
79 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.891-1292A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712438 | |||||||
| chr12:68712441 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
5 | NA18977.hp1 NA18989.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-1289A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712441 | |||||||
| chr12:68712651 | T | G | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.891-1079T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712651 | |||||||
| chr12:68712696 | G | T | 2 | a0001c0001t0006g0229 a0001c0001t0006g0230 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.891-1034G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712696 | |||||||
| chr12:68712980 | A | G | 22 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(19): Show |
26 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.891-750A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712980 | |||||||
| chr12:68712985 | CTT | C | 3 | a0001c0001t0001g0044 a0001c0001t0016g0043 a0001c0001t0016g0045 |
3 | HG02723.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.891-744_891-743del others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68712985 | |||||||
| chr12:68713197 | A | AC | 8 | a0001c0001t0007g0001 a0001c0001t0007g0053 a0001c0001t0007g0054 others(5): Show |
12 | HG01167.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.891-528dupC | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68713197 | ||||||
| chr12:68713244 | G | A | 3 | a0001c0001t0006g0281 a0001c0001t0018g0153 a0001c0001t0026g0282 |
3 | HG02895.hp2 HG02976.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.891-486G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68713244 | |||||||
| chr12:68713375 | C | CA | 37 | a0001c0001t0001g0048 a0001c0001t0001g0293 a0001c0001t0001g0298 others(34): Show |
38 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.891-337dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68713375 | ||||||
| chr12:68713375 | CA | C | 94 | a0001c0001t0003g0175 a0001c0001t0005g0057 a0001c0001t0006g0281 others(91): Show |
109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.891-337delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr12 | 68713375 | ||||||
| chr12:68713491 | A | C | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.891-239A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68713491 | |||||||
| chr12:68713493 | G | A | 10 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0064 others(7): Show |
12 | HG00673.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.891-237G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 10/27 | chr12 | 68713493 | |||||||
| chr12:68714234 | G | T | 1 | a0001c0002t0002g0107 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.969+426G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714234 | |||||||
| chr12:68714252 | A | T | 3 | a0001c0001t0013g0170 a0001c0001t0013g0171 a0001c0001t0013g0172 |
3 | NA18945.hp2 NA18962.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.969+444A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714252 | |||||||
| chr12:68714471 | G | A | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.969+663G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714471 | |||||||
| chr12:68714536 | A | G | 1 | a0001c0001t0004g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.969+728A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714536 | |||||||
| chr12:68714668 | A | G | 86 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(83): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.969+860A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714668 | |||||||
| chr12:68714724 | C | T | 1 | a0001c0002t0002g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.970-903C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714724 | |||||||
| chr12:68714765 | T | G | 1 | a0001c0001t0006g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.970-862T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714765 | |||||||
| chr12:68714917 | T | C | 2 | a0001c0003t0008g0034 a0001c0003t0008g0037 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.970-710T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68714917 | |||||||
| chr12:68715129 | T | C | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.970-498T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715129 | |||||||
| chr12:68715292 | G | A | 5 | a0001c0001t0003g0139 a0001c0001t0003g0150 a0001c0001t0003g0181 others(2): Show |
5 | NA18955.hp2 NA18986.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.970-335G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715292 | |||||||
| chr12:68715305 | T | C | 347 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(344): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.970-322T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715305 | |||||||
| chr12:68715375 | T | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02040.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.970-252T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715375 | |||||||
| chr12:68715451 | G | A | 1 | a0001c0001t0010g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.970-176G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715451 | |||||||
| chr12:68715472 | C | T | 1 | a0001c0001t0004g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.970-155C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715472 | |||||||
| chr12:68715564 | G | T | 4 | a0001c0001t0004g0023 a0001c0001t0004g0257 a0001c0001t0004g0258 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-63G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 11/27 | chr12 | 68715564 | |||||||
| chr12:68715749 | T | C | 1 | a0001c0002t0002g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1083+9T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68715749 | |||||||
| chr12:68715781 | A | G | 2 | a0001c0001t0004g0255 a0001c0001t0004g0256 |
2 | NA18982.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1083+41A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68715781 | |||||||
| chr12:68715837 | T | C | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1083+97T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68715837 | |||||||
| chr12:68715879 | C | T | 1 | a0001c0001t0004g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1083+139C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68715879 | |||||||
| chr12:68715934 | T | A | 1 | a0001c0001t0006g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1083+194T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68715934 | |||||||
| chr12:68716039 | C | G | 1 | a0001c0001t0003g0169 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1083+299C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716039 | |||||||
| chr12:68716040 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1083+300G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716040 | |||||||
| chr12:68716122 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1083+382C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716122 | |||||||
| chr12:68716217 | TTTTC | T | 3 | a0001c0001t0006g0281 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG02895.hp2 NA18950.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1083+505_1083+508d others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68716217 | ||||||
| chr12:68716237 | C | CT | 14 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(11): Show |
18 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1083+500dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68716237 | ||||||
| chr12:68716240 | TC | T | 4 | a0001c0002t0002g0069 a0001c0002t0002g0075 a0001c0002t0002g0105 others(1): Show |
4 | HG03704.hp1 NA18939.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+501delC | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716240 | |||||||
| chr12:68716241 | C | CT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0046 others(13): Show |
16 | HG01975.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1083+504dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68716241 | ||||||
| chr12:68716241 | C | CTT | 64 | a0001c0001t0001g0340 a0001c0001t0003g0005 a0001c0001t0003g0006 others(61): Show |
68 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1083+503_1083+504d others(4): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68716241 | ||||||
| chr12:68716241 | C | T | 103 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(100): Show |
118 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1083+501C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716241 | |||||||
| chr12:68716245 | C | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(278): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1083+505C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716245 | |||||||
| chr12:68716320 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1083+580C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716320 | |||||||
| chr12:68716418 | A | G | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1083+678A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716418 | |||||||
| chr12:68716448 | C | T | 1 | a0001c0001t0004g0259 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1083+708C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716448 | |||||||
| chr12:68716450 | T | G | 2 | a0001c0001t0001g0268 a0001c0001t0004g0245 |
2 | HG02083.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1083+710T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716450 | |||||||
| chr12:68716582 | C | G | 2 | a0001c0001t0005g0212 a0005c0012t0005g0213 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1083+842C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716582 | |||||||
| chr12:68716731 | C | G | 355 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(352): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1083+991C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716731 | |||||||
| chr12:68716925 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1083+1185T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68716925 | |||||||
| chr12:68717108 | GGCTGGTC others(25): Show |
G | 1 | a0001c0001t0001g0327 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1083+1371_1083+140 others(36): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68717108 | ||||||
| chr12:68717289 | A | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1083+1549A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68717289 | |||||||
| chr12:68717293 | A | G | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+1553A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68717293 | |||||||
| chr12:68717399 | C | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1083+1659C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68717399 | |||||||
| chr12:68717503 | ATAT | A | 66 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(63): Show |
75 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1083+1770_1083+177 others(7): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68717503 | ||||||
| chr12:68717722 | T | C | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1084-1619T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68717722 | |||||||
| chr12:68718070 | A | G | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1084-1271A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68718070 | |||||||
| chr12:68718494 | A | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1084-847A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68718494 | |||||||
| chr12:68718545 | A | G | 1 | a0001c0001t0004g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1084-796A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68718545 | |||||||
| chr12:68718701 | A | AG | 77 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(74): Show |
87 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1084-634dupG | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718701 | ||||||
| chr12:68718749 | A | G | 1 | a0001c0001t0004g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1084-592A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68718749 | |||||||
| chr12:68718846 | T | TTATG | 79 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(76): Show |
88 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1084-451_1084-448d others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718846 | ||||||
| chr12:68718846 | T | TTATGTAT others(1): Show |
8 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0001g0305 others(5): Show |
8 | HG01123.hp2 HG02040.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-455_1084-448d others(10): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718846 | ||||||
| chr12:68718846 | TTATG | T | 160 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0048 others(157): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1084-451_1084-448d others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718846 | ||||||
| chr12:68718846 | TTATGTAT others(5): Show |
T | 2 | a0001c0002t0002g0103 a0001c0002t0002g0104 |
2 | NA18950.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1084-459_1084-448d others(14): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718846 | ||||||
| chr12:68718846 | TTATGTAT others(17): Show |
T | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1084-471_1084-448d others(26): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718846 | ||||||
| chr12:68718890 | G | GTATT | 6 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0046 others(3): Show |
6 | HG01361.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-444_1084-441d others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 68718890 | ||||||
| chr12:68718894 | T | G | 1 | a0001c0001t0001g0321 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1084-447T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68718894 | |||||||
| chr12:68719013 | C | A | 3 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0003g0169 |
3 | NA18973.hp2 NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1084-328C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68719013 | |||||||
| chr12:68719014 | G | A | 4 | a0001c0001t0010g0211 a0001c0001t0010g0238 a0001c0001t0010g0239 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-327G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68719014 | |||||||
| chr12:68719046 | G | C | 1 | a0001c0001t0001g0346 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1084-295G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68719046 | |||||||
| chr12:68719163 | A | G | 2 | a0001c0001t0003g0352 a0001c0001t0003g0353 |
2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1084-178A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68719163 | |||||||
| chr12:68719252 | A | G | 59 | a0001c0001t0001g0268 a0001c0001t0004g0008 a0001c0001t0004g0009 others(56): Show |
68 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1084-89A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 12/27 | chr12 | 68719252 | |||||||
| chr12:68719444 | AT | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1174+17delT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr12 | 68719444 | ||||||
| chr12:68719888 | G | A | 2 | a0001c0002t0002g0090 a0001c0002t0002g0112 |
2 | HG00140.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1251+234G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68719888 | |||||||
| chr12:68720286 | A | C | 1 | a0001c0001t0007g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1251+632A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68720286 | |||||||
| chr12:68720410 | A | C | 1 | a0001c0001t0004g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1252-708A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68720410 | |||||||
| chr12:68720554 | G | A | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1252-564G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68720554 | |||||||
| chr12:68720974 | C | T | 1 | a0001c0001t0004g0242 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1252-144C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68720974 | |||||||
| chr12:68721041 | A | G | 3 | a0001c0001t0004g0236 a0001c0001t0004g0237 a0001c0001t0004g0244 |
3 | NA18978.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1252-77A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68721041 | |||||||
| chr12:68721091 | A | G | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1252-27A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 14/27 | chr12 | 68721091 | |||||||
| chr12:68721273 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1311+96G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 15/27 | chr12 | 68721273 | |||||||
| chr12:68721475 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
6 | HG00280.hp1 HG00323.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+298A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 15/27 | chr12 | 68721475 | |||||||
| chr12:68721489 | C | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1311+312C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 15/27 | chr12 | 68721489 | |||||||
| chr12:68721716 | T | A | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1312-125T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 15/27 | chr12 | 68721716 | |||||||
| chr12:68721726 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1312-115C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 15/27 | chr12 | 68721726 | |||||||
| chr12:68722275 | T | C | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1506+123T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68722275 | |||||||
| chr12:68722403 | A | G | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1506+251A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68722403 | |||||||
| chr12:68722552 | C | G | 1 | a0001c0001t0004g0224 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1506+400C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68722552 | |||||||
| chr12:68722703 | C | T | 1 | a0001c0001t0003g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1506+551C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68722703 | |||||||
| chr12:68722986 | A | G | 1 | a0001c0001t0026g0282 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1506+834A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68722986 | |||||||
| chr12:68723143 | A | C | 1 | a0001c0001t0003g0176 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1506+991A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723143 | |||||||
| chr12:68723199 | T | A | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1506+1047T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723199 | |||||||
| chr12:68723221 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1506+1069A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723221 | |||||||
| chr12:68723303 | G | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1506+1151G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723303 | |||||||
| chr12:68723487 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1506+1335T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723487 | |||||||
| chr12:68723522 | G | C | 1 | a0001c0001t0003g0191 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1506+1370G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723522 | |||||||
| chr12:68723638 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1506+1486C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723638 | |||||||
| chr12:68723662 | T | G | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1506+1510T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723662 | |||||||
| chr12:68723821 | T | C | 2 | a0001c0001t0005g0057 a0001c0001t0017g0058 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1506+1669T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723821 | |||||||
| chr12:68723933 | T | C | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1506+1781T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68723933 | |||||||
| chr12:68724082 | A | G | 10 | a0001c0001t0007g0001 a0001c0001t0007g0050 a0001c0001t0007g0053 others(7): Show |
14 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1507-1645A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724082 | |||||||
| chr12:68724145 | A | T | 1 | a0001c0001t0004g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1507-1582A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724145 | |||||||
| chr12:68724174 | A | G | 2 | a0001c0001t0004g0020 a0001c0001t0004g0224 |
3 | HG01074.hp2 HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1507-1553A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724174 | |||||||
| chr12:68724224 | G | A | 1 | a0001c0001t0004g0020 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1507-1503G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724224 | |||||||
| chr12:68724420 | G | T | 1 | a0001c0001t0004g0267 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1507-1307G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724420 | |||||||
| chr12:68724798 | C | A | 2 | a0001c0001t0005g0212 a0005c0012t0005g0213 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1507-929C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724798 | |||||||
| chr12:68724936 | A | G | 1 | a0001c0001t0004g0023 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1507-791A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724936 | |||||||
| chr12:68724978 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1507-749G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68724978 | |||||||
| chr12:68725346 | C | T | 1 | a0001c0002t0002g0074 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1507-381C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68725346 | |||||||
| chr12:68725473 | A | C | 50 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0028 others(47): Show |
53 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1507-254A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 17/27 | chr12 | 68725473 | |||||||
| chr12:68725829 | T | TTG | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576+41_1576+42dup others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 68725829 | ||||||
| chr12:68725837 | G | GGTT | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(71): Show |
85 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1576+41_1576+42ins others(3): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | chr12 | 68725837 | |||||||
| chr12:68725837 | G | GGTTT | 7 | a0001c0002t0002g0076 a0001c0002t0002g0081 a0001c0002t0002g0090 others(4): Show |
7 | HG00140.hp2 HG01109.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576+41_1576+42ins others(4): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | chr12 | 68725837 | |||||||
| chr12:68725837 | G | GT | 58 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(55): Show |
66 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1576+58dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 68725837 | ||||||
| chr12:68725837 | G | GTT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1576+57_1576+58dup others(2): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 68725837 | ||||||
| chr12:68725837 | G | GTTT | 15 | a0001c0001t0001g0268 a0001c0001t0001g0287 a0001c0001t0001g0320 others(12): Show |
15 | HG00597.hp1 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1576+56_1576+58dup others(3): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 68725837 | ||||||
| chr12:68725843 | T | TTTG | 8 | a0001c0001t0007g0001 a0001c0001t0007g0053 a0001c0001t0007g0054 others(5): Show |
12 | HG01167.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1576+49_1576+50ins others(3): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 68725843 | ||||||
| chr12:68726850 | A | G | 1 | a0001c0003t0008g0036 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1695+233A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 19/27 | chr12 | 68726850 | |||||||
| chr12:68726861 | G | A | 104 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(101): Show |
119 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1695+244G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 19/27 | chr12 | 68726861 | |||||||
| chr12:68727062 | C | T | 9 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(6): Show |
9 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1696-289C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 19/27 | chr12 | 68727062 | |||||||
| chr12:68727266 | T | G | 1 | a0001c0001t0001g0317 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1696-85T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 19/27 | chr12 | 68727266 | |||||||
| chr12:68727566 | C | T | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1734+177C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727566 | |||||||
| chr12:68727567 | G | C | 8 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0083 others(5): Show |
10 | HG02074.hp1 HG02165.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734+178G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727567 | |||||||
| chr12:68727612 | A | C | 69 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(66): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1734+223A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727612 | |||||||
| chr12:68727719 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1734+330A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727719 | |||||||
| chr12:68727887 | A | T | 1 | a0001c0001t0003g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1734+498A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727887 | |||||||
| chr12:68727917 | C | T | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1734+528C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68727917 | |||||||
| chr12:68728009 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01361.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+620G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728009 | |||||||
| chr12:68728145 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(278): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1734+756A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728145 | |||||||
| chr12:68728285 | C | CA | 30 | a0001c0001t0001g0205 a0001c0001t0001g0290 a0001c0001t0001g0306 others(27): Show |
30 | HG00438.hp2 HG00642.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1734+914dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68728285 | ||||||
| chr12:68728285 | CA | C | 97 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(94): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1734+914delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68728285 | ||||||
| chr12:68728421 | C | CT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(168): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1734+1052dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68728421 | ||||||
| chr12:68728421 | C | CTT | 17 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0285 others(14): Show |
17 | HG00438.hp1 HG01978.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1734+1051_1734+105 others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68728421 | ||||||
| chr12:68728424 | T | TA | 15 | a0001c0001t0004g0010 a0001c0001t0004g0242 a0001c0001t0004g0249 others(12): Show |
16 | NA18747.hp2 NA18946.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.1734+1035_1734+103 others(5): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728424 | |||||||
| chr12:68728548 | C | T | 6 | a0001c0003t0008g0034 a0001c0003t0008g0035 a0001c0003t0008g0036 others(3): Show |
6 | HG01261.hp2 HG02300.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734+1159C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728548 | |||||||
| chr12:68728612 | A | G | 1 | a0001c0001t0007g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1734+1223A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728612 | |||||||
| chr12:68728664 | T | C | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1734+1275T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728664 | |||||||
| chr12:68728719 | C | CT | 14 | a0001c0001t0003g0147 a0001c0002t0002g0129 a0001c0002t0002g0130 others(11): Show |
14 | HG01106.hp2 HG01109.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1734+1345dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68728719 | ||||||
| chr12:68728771 | A | G | 1 | a0005c0012t0005g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1734+1382A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728771 | |||||||
| chr12:68728785 | A | G | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1734+1396A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728785 | |||||||
| chr12:68728812 | G | A | 1 | a0001c0002t0002g0095 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1734+1423G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728812 | |||||||
| chr12:68728837 | T | C | 1 | a0001c0002t0002g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1734+1448T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728837 | |||||||
| chr12:68728909 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1734+1520C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68728909 | |||||||
| chr12:68729078 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0016g0043 a0001c0001t0016g0045 |
3 | HG02723.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1734+1689C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729078 | |||||||
| chr12:68729351 | A | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1735-1759A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729351 | |||||||
| chr12:68729449 | T | C | 1 | a0001c0013t0003g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1735-1661T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729449 | |||||||
| chr12:68729496 | G | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1735-1614G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729496 | |||||||
| chr12:68729537 | G | C | 2 | a0001c0001t0007g0050 a0001c0001t0007g0056 |
2 | HG00639.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1735-1573G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729537 | |||||||
| chr12:68729540 | G | T | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1735-1570G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729540 | |||||||
| chr12:68729604 | T | A | 4 | a0001c0002t0002g0063 a0001c0002t0002g0089 a0001c0002t0002g0097 others(1): Show |
4 | HG02135.hp1 NA18983.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1506T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729604 | |||||||
| chr12:68729808 | T | G | 3 | a0001c0001t0006g0276 a0001c0001t0006g0277 a0001c0001t0006g0278 |
3 | HG02145.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1735-1302T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729808 | |||||||
| chr12:68729852 | G | A | 12 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(9): Show |
16 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1735-1258G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68729852 | |||||||
| chr12:68730157 | G | T | 1 | a0001c0001t0004g0255 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1735-953G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730157 | |||||||
| chr12:68730214 | C | CT | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(13): Show |
16 | HG00673.hp1 HG00735.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1735-875dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730214 | C | CTTTTTTT others(1): Show |
68 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(65): Show |
77 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1735-882_1735-875d others(10): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730214 | C | CTTTTTTT others(2): Show |
29 | a0001c0001t0001g0025 a0001c0001t0001g0290 a0001c0001t0001g0292 others(26): Show |
35 | HG00639.hp2 HG01070.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1735-883_1735-875d others(11): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730214 | C | CTTTTTTT others(3): Show |
53 | a0001c0001t0001g0346 a0001c0001t0005g0057 a0001c0001t0007g0050 others(50): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1735-884_1735-875d others(12): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730214 | C | CTTTTTTT others(4): Show |
22 | a0001c0001t0008g0039 a0001c0002t0002g0015 a0001c0002t0002g0016 others(19): Show |
25 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1735-885_1735-875d others(13): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730214 | C | CTTTTTTT others(5): Show |
5 | a0001c0002t0002g0063 a0001c0002t0002g0070 a0001c0002t0002g0086 others(2): Show |
5 | HG01978.hp2 HG02135.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-886_1735-875d others(14): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 68730214 | ||||||
| chr12:68730314 | G | A | 2 | a0001c0001t0003g0139 a0001c0001t0003g0150 |
2 | NA19064.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1735-796G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730314 | |||||||
| chr12:68730453 | A | T | 74 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(71): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1735-657A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730453 | |||||||
| chr12:68730461 | C | T | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1735-649C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730461 | |||||||
| chr12:68730607 | G | A | 1 | a0001c0003t0012g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1735-503G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730607 | |||||||
| chr12:68730733 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0348 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1735-377G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68730733 | |||||||
| chr12:68731087 | T | G | 1 | a0001c0001t0001g0318 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1735-23T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 20/27 | chr12 | 68731087 | |||||||
| chr12:68731296 | C | T | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1885+36C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 21/27 | chr12 | 68731296 | |||||||
| chr12:68731500 | T | G | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1886-107T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 21/27 | chr12 | 68731500 | |||||||
| chr12:68731505 | A | C | 2 | a0001c0002t0002g0018 a0001c0002t0002g0135 |
3 | HG01256.hp1 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1886-102A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 21/27 | chr12 | 68731505 | |||||||
| chr12:68731733 | G | T | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1998+14G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731733 | |||||||
| chr12:68731734 | G | T | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1998+15G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731734 | |||||||
| chr12:68731739 | C | T | 1 | a0001c0001t0005g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1998+20C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731739 | |||||||
| chr12:68731757 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1998+38C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731757 | |||||||
| chr12:68731798 | C | T | 82 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0012 others(79): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1998+79C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731798 | |||||||
| chr12:68731897 | G | A | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1998+178G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68731897 | |||||||
| chr12:68732058 | A | G | 181 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(178): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1998+339A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68732058 | |||||||
| chr12:68732208 | G | C | 8 | a0001c0001t0007g0001 a0001c0001t0007g0053 a0001c0001t0007g0054 others(5): Show |
12 | HG01167.hp2 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1999-429G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68732208 | |||||||
| chr12:68732244 | C | T | 1 | a0001c0001t0006g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1999-393C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68732244 | |||||||
| chr12:68732499 | T | G | 1 | a0001c0002t0002g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1999-138T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 22/27 | chr12 | 68732499 | |||||||
| chr12:68732852 | A | T | 1 | a0001c0002t0002g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2101+113A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68732852 | |||||||
| chr12:68732857 | A | T | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2101+118A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68732857 | |||||||
| chr12:68732875 | G | T | 4 | a0001c0001t0010g0211 a0001c0001t0010g0238 a0001c0001t0010g0239 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2101+136G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68732875 | |||||||
| chr12:68733096 | TTATC | T | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.2102-351_2102-348d others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 68733096 | ||||||
| chr12:68733102 | A | G | 1 | a0001c0001t0004g0250 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2102-350A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68733102 | |||||||
| chr12:68733189 | C | T | 1 | a0001c0001t0003g0174 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2102-263C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68733189 | |||||||
| chr12:68733296 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2102-156A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 23/27 | chr12 | 68733296 | |||||||
| chr12:68733717 | C | T | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2262+105C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68733717 | |||||||
| chr12:68733720 | C | T | 10 | a0001c0001t0008g0039 a0001c0003t0008g0034 a0001c0003t0008g0035 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.2262+108C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68733720 | |||||||
| chr12:68733764 | C | T | 2 | a0001c0001t0003g0194 a0001c0001t0023g0193 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2262+152C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68733764 | |||||||
| chr12:68733770 | C | G | 1 | a0001c0001t0004g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2262+158C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68733770 | |||||||
| chr12:68734188 | G | A | 1 | a0001c0001t0023g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2263-520G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68734188 | |||||||
| chr12:68734357 | C | T | 74 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(71): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2263-351C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68734357 | |||||||
| chr12:68734398 | A | G | 1 | a0001c0001t0026g0282 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2263-310A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68734398 | |||||||
| chr12:68734684 | TG | T | 17 | a0001c0001t0004g0010 a0001c0001t0004g0242 a0001c0001t0004g0249 others(14): Show |
18 | HG00597.hp2 NA18747.hp2 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.2263-22delG | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr12 | 68734684 | ||||||
| chr12:68734687 | T | C | 17 | a0001c0001t0004g0010 a0001c0001t0004g0242 a0001c0001t0004g0249 others(14): Show |
18 | HG00597.hp2 NA18747.hp2 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.2263-21T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 24/27 | chr12 | 68734687 | |||||||
| chr12:68734904 | G | A | 5 | a0001c0001t0001g0286 a0001c0001t0001g0291 a0001c0001t0001g0307 others(2): Show |
5 | HG01106.hp1 HG01168.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.2388+71G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 25/27 | chr12 | 68734904 | |||||||
| chr12:68734983 | G | A | 10 | a0001c0001t0007g0001 a0001c0001t0007g0050 a0001c0001t0007g0053 others(7): Show |
14 | HG00639.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2388+150G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 25/27 | chr12 | 68734983 | |||||||
| chr12:68735190 | G | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0347 a0001c0001t0001g0349 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2389-41G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 25/27 | chr12 | 68735190 | |||||||
| chr12:68735559 | A | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2502+215A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68735559 | |||||||
| chr12:68735741 | G | C | 1 | a0001c0001t0004g0237 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2502+397G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68735741 | |||||||
| chr12:68735946 | A | G | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2502+602A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68735946 | |||||||
| chr12:68735986 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2502+642T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68735986 | |||||||
| chr12:68736364 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2502+1020C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736364 | |||||||
| chr12:68736379 | A | G | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2502+1035A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736379 | |||||||
| chr12:68736642 | T | C | 1 | a0001c0002t0002g0101 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2502+1298T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736642 | |||||||
| chr12:68736686 | C | G | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2502+1342C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736686 | |||||||
| chr12:68736697 | A | G | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2502+1353A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736697 | |||||||
| chr12:68736717 | C | CT | 19 | a0001c0001t0001g0268 a0001c0001t0001g0314 a0001c0001t0001g0327 others(16): Show |
20 | HG00544.hp1 HG00597.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2502+1395dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736717 | C | CTT | 75 | a0001c0001t0015g0354 a0001c0001t0015g0355 a0001c0002t0002g0003 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.2502+1394_2502+139 others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736717 | C | CTTT | 8 | a0001c0002t0002g0070 a0001c0002t0002g0082 a0001c0002t0002g0085 others(5): Show |
8 | HG00438.hp1 HG00544.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2502+1393_2502+139 others(7): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736717 | C | CTTTTTTT others(3): Show |
3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2502+1386_2502+139 others(14): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736717 | CT | C | 24 | a0001c0001t0001g0310 a0001c0001t0003g0177 a0001c0001t0004g0226 others(21): Show |
30 | HG00639.hp1 HG01069.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2502+1395delT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736717 | CTT | C | 9 | a0001c0001t0005g0217 a0001c0001t0007g0050 a0001c0001t0007g0056 others(6): Show |
9 | HG00639.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2502+1394_2502+139 others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68736717 | ||||||
| chr12:68736861 | C | G | 4 | a0001c0001t0010g0211 a0001c0001t0010g0238 a0001c0001t0010g0239 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2502+1517C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68736861 | |||||||
| chr12:68737198 | A | T | 4 | a0001c0003t0008g0034 a0001c0003t0008g0037 a0001c0003t0008g0038 others(1): Show |
4 | HG01261.hp2 HG02300.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2502+1854A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737198 | |||||||
| chr12:68737312 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2502+1968C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737312 | |||||||
| chr12:68737379 | A | G | 2 | a0001c0001t0006g0281 a0001c0001t0026g0282 |
2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2502+2035A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737379 | |||||||
| chr12:68737560 | C | CA | 112 | a0001c0001t0001g0046 a0001c0001t0001g0207 a0001c0001t0001g0290 others(109): Show |
118 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.2502+2238dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737560 | ||||||
| chr12:68737560 | C | CAA | 13 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0152 others(10): Show |
13 | HG00423.hp2 HG02074.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2502+2237_2502+223 others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737560 | ||||||
| chr12:68737560 | C | CAAA | 56 | a0001c0001t0001g0268 a0001c0001t0004g0008 a0001c0001t0004g0009 others(53): Show |
65 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2502+2236_2502+223 others(7): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737560 | ||||||
| chr12:68737560 | C | CAAAA | 8 | a0001c0001t0004g0209 a0001c0001t0004g0223 a0001c0001t0004g0226 others(5): Show |
8 | HG00423.hp1 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2502+2235_2502+223 others(8): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737560 | ||||||
| chr12:68737560 | CA | C | 7 | a0001c0001t0001g0284 a0001c0001t0001g0294 a0001c0001t0001g0300 others(4): Show |
7 | HG00099.hp2 HG01099.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2502+2238delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737560 | ||||||
| chr12:68737648 | ATTCAGTC others(19): Show |
A | 9 | a0001c0001t0003g0137 a0001c0001t0003g0141 a0001c0001t0003g0144 others(6): Show |
9 | HG02056.hp2 HG02083.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2502+2332_2502+235 others(30): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68737648 | ||||||
| chr12:68737826 | T | A | 1 | a0001c0001t0020g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2502+2482T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737826 | |||||||
| chr12:68737908 | G | A | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2502+2564G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737908 | |||||||
| chr12:68737934 | G | A | 3 | a0001c0002t0002g0069 a0001c0002t0002g0117 a0001c0002t0002g0118 |
3 | HG02071.hp2 NA18939.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2502+2590G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737934 | |||||||
| chr12:68737940 | G | A | 1 | a0001c0001t0011g0164 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2502+2596G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68737940 | |||||||
| chr12:68738000 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(73): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2502+2656G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738000 | |||||||
| chr12:68738135 | G | A | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(70): Show |
77 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2502+2791G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738135 | |||||||
| chr12:68738160 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2502+2816C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738160 | |||||||
| chr12:68738198 | C | A | 13 | a0001c0001t0004g0010 a0001c0001t0004g0242 a0001c0001t0004g0250 others(10): Show |
14 | HG00597.hp2 NA18747.hp2 NA18946.hp1 others(11): Show |
intron_variant | MODIFIER | c.2502+2854C>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738198 | |||||||
| chr12:68738307 | G | A | 3 | a0001c0001t0003g0160 a0001c0001t0003g0173 a0001c0001t0018g0153 |
3 | NA18972.hp2 NA18993.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2502+2963G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738307 | |||||||
| chr12:68738450 | C | CA | 66 | a0001c0001t0001g0286 a0001c0001t0001g0311 a0001c0001t0003g0157 others(63): Show |
75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2502+3124dupA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68738450 | ||||||
| chr12:68738450 | C | CAA | 18 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0065 others(15): Show |
20 | HG00438.hp1 HG00735.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2502+3123_2502+312 others(6): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68738450 | ||||||
| chr12:68738450 | CA | C | 9 | a0001c0001t0001g0284 a0001c0001t0001g0294 a0001c0001t0001g0309 others(6): Show |
9 | HG01099.hp2 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.2502+3124delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68738450 | ||||||
| chr12:68738554 | A | G | 107 | a0001c0001t0005g0057 a0001c0001t0007g0001 a0001c0001t0007g0050 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2502+3210A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738554 | |||||||
| chr12:68738606 | C | G | 2 | a0001c0001t0005g0212 a0005c0012t0005g0213 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2503-3207C>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738606 | |||||||
| chr12:68738766 | T | C | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2503-3047T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738766 | |||||||
| chr12:68738785 | T | C | 1 | a0001c0001t0003g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2503-3028T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738785 | |||||||
| chr12:68738901 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0016g0043 a0001c0001t0016g0045 |
3 | HG02723.hp2 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2503-2912T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738901 | |||||||
| chr12:68738945 | G | C | 67 | a0001c0001t0001g0268 a0001c0001t0004g0008 a0001c0001t0004g0009 others(64): Show |
76 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2503-2868G>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68738945 | |||||||
| chr12:68738954 | CTTTTG | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0284 others(19): Show |
27 | HG01099.hp2 HG01975.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.2503-2851_2503-284 others(9): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68738954 | ||||||
| chr12:68738967 | C | CT | 76 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(73): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2503-2836dupT | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68738967 | ||||||
| chr12:68739021 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2503-2792A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739021 | |||||||
| chr12:68739076 | CGCCAAGA | C | 4 | a0001c0002t0002g0013 a0001c0002t0002g0084 a0001c0002t0002g0085 others(1): Show |
5 | HG02165.hp1 NA18948.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503-2736_2503-273 others(11): Show |
NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739076 | |||||||
| chr12:68739258 | T | G | 47 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0028 others(44): Show |
50 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.2503-2555T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739258 | |||||||
| chr12:68739266 | A | C | 1 | a0001c0002t0002g0124 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2503-2547A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739266 | |||||||
| chr12:68739294 | G | T | 2 | a0001c0001t0013g0170 a0001c0001t0013g0171 |
2 | NA18945.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2503-2519G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739294 | |||||||
| chr12:68739455 | A | C | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2503-2358A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739455 | |||||||
| chr12:68739749 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2503-2064A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739749 | |||||||
| chr12:68739836 | CA | C | 84 | a0001c0001t0001g0327 a0001c0001t0003g0178 a0001c0001t0004g0260 others(81): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2503-1961delA | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 68739836 | ||||||
| chr12:68739916 | T | G | 12 | a0001c0001t0005g0007 a0001c0001t0005g0210 a0001c0001t0005g0212 others(9): Show |
14 | HG01069.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2503-1897T>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68739916 | |||||||
| chr12:68740170 | G | A | 195 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(192): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2503-1643G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740170 | |||||||
| chr12:68740290 | A | G | 2 | a0001c0001t0005g0057 a0001c0001t0017g0058 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2503-1523A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740290 | |||||||
| chr12:68740417 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2503-1396T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740417 | |||||||
| chr12:68740474 | T | C | 2 | a0001c0001t0015g0354 a0001c0001t0015g0355 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2503-1339T>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740474 | |||||||
| chr12:68740705 | A | C | 1 | a0001c0001t0026g0282 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2503-1108A>C | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740705 | |||||||
| chr12:68740874 | A | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0048 others(5): Show |
8 | HG01361.hp1 HG02080.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2503-939A>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740874 | |||||||
| chr12:68740877 | T | A | 3 | a0001c0004t0005g0060 a0001c0004t0005g0061 a0001c0004t0022g0059 |
3 | HG01516.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2503-936T>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740877 | |||||||
| chr12:68740972 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2503-841G>A | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68740972 | |||||||
| chr12:68741055 | G | T | 1 | a0001c0001t0008g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2503-758G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68741055 | |||||||
| chr12:68741095 | G | T | 2 | a0001c0001t0004g0266 a0001c0001t0004g0267 |
2 | NA18966.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2503-718G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68741095 | |||||||
| chr12:68741110 | C | T | 180 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0019 others(177): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.2503-703C>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68741110 | |||||||
| chr12:68741366 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2503-447G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68741366 | |||||||
| chr12:68741719 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2503-94A>G | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 26/27 | chr12 | 68741719 | |||||||
| chr12:68742058 | G | T | 1 | a0001c0001t0005g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2670+78G>T | NUP107 | ENSG00000111581.10 | transcript | ENST00000229179.9 | protein_coding | 27/27 | chr12 | 68742058 |