Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4833 |
| ensemblid | ENSG00000103202.13 |
| hgncid | 7852 |
| symbol | NME4 |
| name | NME/NM23 nucleoside diphosphate kinase 4 |
| refseq_nuc | NM_005009.3 |
| refseq_prot | NP_005000.1 |
| ensembl_nuc | ENST00000219479.7 |
| ensembl_prot | ENSP00000219479.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 397199 |
| end | 400754 |
| strand | + |
| ver | v1.2 |
| region | chr16:397199-400754 |
| region5000 | chr16:392199-405754 |
| regionname0 | NME4_chr16_397199_400754 |
| regionname5000 | NME4_chr16_392199_405754 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 187 | 350 | 85 | 65 | 140 | 14 | 44 | 101 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| a0002 | 0/0 | 187 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| a0003 | 0/0 | 187 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| a0004 | 0/0 | 187 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| a0005 | 0/0 | 187 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| a0006 | 0/0 | 187 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | MGGLF others(182): Show |
chr16 | 392199 | 405754 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 561 | 185 | 34 | 38 | 88 | 8 | 15 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0001c0002 | 0/0 | 561 | 119 | 26 | 25 | 39 | 6 | 23 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0001c0003 | 0/0 | 561 | 24 | 11 | 2 | 9 | 0 | 2 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0001c0004 | 0/0 | 561 | 20 | 12 | 0 | 4 | 0 | 4 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0001c0005 | 0/0 | 561 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0002c0006 | 0/0 | 561 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0003c0010 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0004c0008 | 0/0 | 561 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0005c0009 | 0/0 | 561 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 | ||
| a0006c0007 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ATGGG others(556): Show |
chr16 | 392199 | 405754 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1000 | 184 | 34 | 38 | 87 | 8 | 15 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0001t0006 | 0/0 | 1000 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0002t0001 | 0/0 | 1000 | 115 | 22 | 25 | 39 | 6 | 23 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0002t0002 | 0/0 | 1000 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0002t0003 | 0/0 | 1000 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0002t0005 | 0/0 | 1000 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0003t0001 | 0/0 | 1000 | 24 | 11 | 2 | 9 | 0 | 2 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0004t0001 | 0/0 | 1000 | 15 | 7 | 0 | 4 | 0 | 4 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0004t0002 | 0/0 | 1000 | 5 | 5 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0001c0005t0001 | 0/0 | 1000 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0002c0006t0001 | 0/0 | 1000 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0003c0010t0001 | 0/0 | 1000 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0004c0008t0001 | 0/0 | 1000 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0005c0009t0004 | 0/0 | 1000 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| a0006c0007t0001 | 0/0 | 1000 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | ACAGC others(995): Show |
chr16 | 392199 | 405754 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 62 | 8 | 22 | 19 | 5 | 7 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0010 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0002 | 0/0 | 24 | 2 | 5 | 16 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0003 | 0/0 | 10 | 2 | 3 | 2 | 0 | 3 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0001c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0002c0006t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0002c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0003c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0004c0008t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0005c0009t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| a0006c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0088 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00558 | hp2 | a0003 | c0010 | t0001 | g0001 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01175 | hp2 | a0004 | c0008 | t0001 | g0182 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | IBS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0111 | EUR | IBS | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01891 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | KHV | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0116 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0172 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02895 | hp2 | a0002 | c0006 | t0001 | g0086 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02897 | hp2 | a0002 | c0006 | t0001 | g0138 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02970 | hp1 | a0005 | c0009 | t0004 | g0194 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0075 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0165 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0114 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0009 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0009 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | STU | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18987 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0200 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0177 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19090 | hp1 | a0006 | c0007 | t0001 | g0201 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0207 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | YRI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0124 | EUR | TSI | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | GIH | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0098 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0156 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0166 | AFR | USA | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | USA | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | USA | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | USA | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0073 | REF | REF | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NME4_chr16_392199_405754 | NME4 | chr16 | 392199 | 405754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:397272 | C | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.50C>G | p.Pro17Arg | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/5 | 74/1000 | 50/564 | 17/187 | chr16 | 397272 | |||
| chr16:399008 | G | T | 1 | a0002 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.110G>T | p.Arg37Leu | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/5 | 134/1000 | 110/564 | 37/187 | chr16 | 399008 | |||
| chr16:399076 | C | T | 1 | a0005 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.178C>T | p.Arg60Cys | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/5 | 202/1000 | 178/564 | 60/187 | chr16 | 399076 | |||
| chr16:399449 | G | A | 1 | a0006 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.296G>A | p.Arg99His | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 3/5 | 320/1000 | 296/564 | 99/187 | chr16 | 399449 | |||
| chr16:400309 | C | G | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.531C>G | p.Asp177Glu | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 555/1000 | 531/564 | 177/187 | chr16 | 400309 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:399399 | C | T | 1 | a0001c0005 | 2 | HG03579.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.246C>T | p.Ala82Ala | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 3/5 | 270/1000 | 246/564 | 82/187 | chr16 | 399399 | |||
| chr16:399659 | G | A | 6 | a0001c0002 a0001c0003 a0001c0005 others(3): Show |
149 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
synonymous_variant | LOW | c.360G>A | p.Ser120Ser | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/5 | 384/1000 | 360/564 | 120/187 | chr16 | 399659 | |||
| chr16:400309 | C | T | 4 | a0001c0002 a0001c0004 a0001c0005 others(1): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
synonymous_variant | LOW | c.531C>T | p.Asp177Asp | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 555/1000 | 531/564 | 177/187 | chr16 | 400309 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:400343 | G | T | 1 | a0001c0001t0006 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 1 | chr16 | 400343 | ||||||
| chr16:400362 | A | C | 1 | a0001c0002t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20A>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 20 | chr16 | 400362 | ||||||
| chr16:400362 | A | G | 2 | a0001c0002t0002 a0001c0004t0002 |
6 | HG01891.hp2 HG03130.hp2 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*20A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 20 | chr16 | 400362 | ||||||
| chr16:400363 | C | A | 1 | a0001c0002t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 21 | chr16 | 400363 | ||||||
| chr16:400368 | T | C | 1 | a0001c0002t0003 | 2 | HG02109.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 26 | chr16 | 400368 | ||||||
| chr16:400564 | G | A | 1 | a0005c0009t0004 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 5/5 | 222 | chr16 | 400564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:397319 | T | TG | 12 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0205 others(9): Show |
12 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.91+10dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397319 | ||||||
| chr16:397345 | C | CG | 11 | a0001c0001t0001g0176 a0001c0002t0001g0017 a0001c0002t0001g0175 others(8): Show |
13 | HG00609.hp1 HG00733.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.91+34dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397345 | ||||||
| chr16:397348 | A | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.91+35A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397348 | |||||||
| chr16:397348 | A | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0184 a0001c0001t0001g0185 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+35A>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397348 | |||||||
| chr16:397353 | A | G | 2 | a0001c0001t0001g0183 a0001c0004t0001g0207 |
2 | NA19090.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+40A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397353 | |||||||
| chr16:397354 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+41G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397354 | |||||||
| chr16:397361 | G | A | 2 | a0001c0002t0002g0076 a0001c0004t0002g0075 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.91+48G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397361 | |||||||
| chr16:397366 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(21): Show |
36 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.91+53C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397366 | |||||||
| chr16:397407 | G | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(26): Show |
42 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.91+94G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397407 | |||||||
| chr16:397416 | A | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
216 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.91+103A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397416 | |||||||
| chr16:397457 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+144G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397457 | |||||||
| chr16:397473 | C | T | 2 | a0001c0002t0002g0076 a0001c0004t0002g0075 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.91+160C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397473 | |||||||
| chr16:397520 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.91+207G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397520 | |||||||
| chr16:397532 | C | A | 1 | a0001c0002t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91+219C>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397532 | |||||||
| chr16:397561 | A | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
212 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.91+248A>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397561 | |||||||
| chr16:397562 | G | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
212 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.91+249G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397562 | |||||||
| chr16:397568 | G | C | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+255G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397568 | |||||||
| chr16:397569 | C | G | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+256C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397569 | |||||||
| chr16:397596 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.91+283A>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397596 | |||||||
| chr16:397599 | G | T | 1 | a0001c0002t0001g0161 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+286G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397599 | |||||||
| chr16:397629 | G | C | 1 | a0001c0002t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.91+316G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397629 | |||||||
| chr16:397636 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.91+323G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397636 | |||||||
| chr16:397637 | A | G | 1 | a0001c0002t0001g0082 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.91+324A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397637 | |||||||
| chr16:397648 | C | G | 1 | a0001c0004t0001g0074 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.91+335C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397648 | |||||||
| chr16:397650 | G | C | 1 | a0001c0004t0001g0074 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.91+337G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397650 | |||||||
| chr16:397652 | C | CGGGGTGG others(427): Show |
1 | a0001c0001t0001g0188 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.91+357_91+358insGG others(432): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(426): Show |
1 | a0001c0001t0001g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.91+357_91+358insGG others(431): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(394): Show |
1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.91+357_91+358insGG others(399): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(435): Show |
1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.91+357_91+358insGG others(440): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(950): Show |
1 | a0001c0001t0001g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91+357_91+358insGG others(955): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(397): Show |
1 | a0001c0001t0001g0186 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+357_91+358insGG others(402): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | CGGGGTGG others(396): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0192 a0001c0001t0001g0193 |
4 | HG02257.hp2 HG02258.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+357_91+358insGG others(401): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397652 | ||||||
| chr16:397652 | C | G | 1 | a0001c0004t0001g0074 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.91+339C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397652 | |||||||
| chr16:397657 | T | TG | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG00609.hp2 HG02486.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+349dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397657 | ||||||
| chr16:397663 | T | TG | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
10 | HG01168.hp2 HG02135.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.91+355dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397663 | ||||||
| chr16:397665 | G | GGGGTGTG others(261): Show |
1 | a0001c0003t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+365_91+366insGT others(266): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397665 | ||||||
| chr16:397669 | T | TGTGGGGG others(607): Show |
1 | a0004c0008t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91+365_91+366insGG others(612): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397669 | ||||||
| chr16:397669 | T | TGTGGGGG others(285): Show |
1 | a0001c0002t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+365_91+366insGT others(290): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397669 | ||||||
| chr16:397669 | T | TGTGGGGG others(645): Show |
1 | a0001c0002t0001g0159 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.91+365_91+366insGT others(650): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397669 | ||||||
| chr16:397671 | T | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0089 a0001c0004t0001g0088 |
3 | HG00544.hp2 HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.91+358T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397671 | |||||||
| chr16:397671 | T | TG | 91 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(88): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.91+365dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397671 | ||||||
| chr16:397671 | T | TGG | 16 | a0001c0002t0001g0015 a0001c0002t0001g0081 a0001c0002t0001g0090 others(13): Show |
18 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.91+364_91+365dupGG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397671 | ||||||
| chr16:397695 | T | TGGGGGGT others(352): Show |
1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.91+387_91+388insGT others(357): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397695 | ||||||
| chr16:397695 | T | TGGGGGTG others(162): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0205 |
3 | HG01884.hp2 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.91+393_91+394insGG others(167): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397695 | ||||||
| chr16:397701 | T | G | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+388T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397701 | |||||||
| chr16:397702 | G | GGGGGGTG others(353): Show |
1 | a0001c0002t0003g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGT others(358): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397702 | ||||||
| chr16:397703 | G | GGGGGGGT others(455): Show |
1 | a0001c0003t0001g0154 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(460): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGGT others(451): Show |
1 | a0001c0003t0001g0155 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(456): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(15): Show |
1 | a0001c0002t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(20): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(313): Show |
1 | a0001c0001t0001g0039 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(318): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(377): Show |
1 | a0001c0001t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(382): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(353): Show |
1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(358): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(345): Show |
1 | a0001c0004t0001g0074 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(350): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(348): Show |
1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(84): Show |
1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(89): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(443): Show |
1 | a0001c0001t0001g0042 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(448): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(349): Show |
1 | a0001c0001t0001g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(354): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(348): Show |
1 | a0001c0001t0001g0029 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(347): Show |
1 | a0001c0001t0001g0044 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(352): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(723): Show |
1 | a0001c0001t0001g0045 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(728): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(795): Show |
1 | a0001c0001t0001g0046 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(800): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(348): Show |
1 | a0001c0001t0001g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(347): Show |
1 | a0001c0001t0001g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(352): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(583): Show |
1 | a0001c0001t0001g0049 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(588): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(347): Show |
1 | a0001c0001t0001g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(352): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(347): Show |
1 | a0001c0001t0001g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(352): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(346): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0052 |
5 | HG01255.hp2 NA18944.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+393_91+394insGG others(351): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(315): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.91+393_91+394insGG others(320): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(346): Show |
1 | a0001c0001t0001g0055 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(351): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(345): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0057 |
5 | HG02040.hp2 NA18947.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+393_91+394insGG others(350): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(375): Show |
1 | a0001c0001t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(380): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(345): Show |
1 | a0001c0001t0001g0019 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.91+393_91+394insGG others(350): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(344): Show |
1 | a0001c0001t0001g0058 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGG others(349): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(204): Show |
2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.91+393_91+394insGG others(209): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGGTG others(342): Show |
1 | a0001c0001t0006g0059 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGG others(347): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGTGT others(290): Show |
1 | a0001c0004t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGT others(295): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGTGT others(385): Show |
1 | a0001c0001t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGTGT others(283): Show |
1 | a0001c0001t0001g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91+393_91+394insGT others(288): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397703 | G | GGGGGTGT others(336): Show |
1 | a0001c0002t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.91+393_91+394insGT others(341): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397703 | ||||||
| chr16:397705 | GGT | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0004t0001g0165 others(1): Show |
4 | HG02109.hp1 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+396_91+397delTG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397705 | ||||||
| chr16:397707 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
61 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.91+394T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397707 | |||||||
| chr16:397707 | T | TGCTGGGG others(336): Show |
1 | a0001c0002t0001g0082 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.91+395_91+396insCT others(341): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(334): Show |
1 | a0001c0002t0001g0002 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(339): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(288): Show |
1 | a0001c0001t0001g0026 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(293): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(440): Show |
1 | a0001c0002t0001g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(445): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(348): Show |
1 | a0001c0001t0001g0065 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(284): Show |
1 | a0001c0001t0001g0001 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(289): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(389): Show |
1 | a0001c0001t0001g0001 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(394): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(387): Show |
1 | a0001c0001t0001g0001 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(392): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(450): Show |
1 | a0001c0001t0001g0001 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(455): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(350): Show |
1 | a0001c0001t0001g0001 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.91+419_91+420insGT others(355): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(313): Show |
1 | a0001c0001t0001g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91+419_91+420insGT others(318): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(399): Show |
1 | a0001c0001t0001g0031 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.91+425_91+426insGT others(404): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(341): Show |
1 | a0001c0002t0001g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.91+425_91+426insGT others(346): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(222): Show |
1 | a0001c0001t0001g0001 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(227): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(418): Show |
1 | a0001c0001t0001g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(423): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(257): Show |
1 | a0001c0001t0001g0028 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(262): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(286): Show |
1 | a0001c0001t0001g0001 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGG others(291): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(387): Show |
1 | a0001c0001t0001g0001 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGG others(392): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(356): Show |
1 | a0001c0001t0001g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(361): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(429): Show |
1 | a0001c0001t0001g0001 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(434): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(354): Show |
1 | a0001c0001t0001g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(359): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(247): Show |
1 | a0001c0001t0001g0001 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(252): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(253): Show |
1 | a0001c0001t0001g0001 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(258): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(417): Show |
1 | a0001c0001t0001g0001 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(422): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(284): Show |
1 | a0001c0004t0001g0009 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(289): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(390): Show |
1 | a0001c0001t0001g0001 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(395): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(385): Show |
1 | a0001c0001t0001g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(385): Show |
1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(282): Show |
1 | a0001c0001t0001g0001 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(287): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(416): Show |
1 | a0001c0001t0001g0034 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(421): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(351): Show |
1 | a0001c0001t0001g0001 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(356): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(490): Show |
1 | a0001c0001t0001g0001 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(388): Show |
1 | a0001c0001t0001g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(393): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(277): Show |
1 | a0001c0001t0001g0009 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(282): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(389): Show |
1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(394): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(373): Show |
1 | a0001c0001t0001g0001 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(378): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(282): Show |
1 | a0001c0001t0001g0018 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(287): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(252): Show |
1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(257): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(544): Show |
1 | a0001c0001t0001g0001 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(549): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(275): Show |
1 | a0001c0001t0001g0001 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(280): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(386): Show |
1 | a0001c0001t0001g0001 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(391): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(386): Show |
1 | a0001c0001t0001g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(391): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(385): Show |
1 | a0001c0001t0001g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(349): Show |
1 | a0001c0001t0001g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(354): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(385): Show |
1 | a0001c0004t0001g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(384): Show |
2 | a0001c0001t0001g0001 a0001c0003t0001g0001 |
5 | HG00099.hp2 HG00639.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(389): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(383): Show |
1 | a0001c0001t0001g0001 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(388): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(414): Show |
1 | a0001c0001t0001g0195 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(419): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(348): Show |
1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(524): Show |
1 | a0001c0001t0001g0001 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(529): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(385): Show |
1 | a0001c0001t0001g0001 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(384): Show |
1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.91+432_91+433insGT others(389): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(885): Show |
1 | a0001c0001t0001g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(890): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(414): Show |
1 | a0001c0001t0001g0001 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(419): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(251): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0064 |
7 | HG02165.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(256): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(281): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 |
5 | HG00544.hp1 HG01943.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(286): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(418): Show |
1 | a0001c0001t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(423): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(413): Show |
1 | a0001c0001t0001g0001 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(418): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(313): Show |
1 | a0001c0001t0001g0001 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(318): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(444): Show |
1 | a0001c0001t0001g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(449): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(387): Show |
1 | a0001c0004t0001g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(392): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(188): Show |
1 | a0001c0001t0001g0001 | 3 | NA18955.hp1 NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.91+432_91+433insGT others(193): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(262): Show |
1 | a0001c0002t0001g0017 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(267): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(331): Show |
1 | a0001c0002t0001g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(336): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(348): Show |
1 | a0001c0002t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(353): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(422): Show |
1 | a0001c0001t0001g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(427): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(626): Show |
1 | a0003c0010t0001g0001 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(631): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(302): Show |
1 | a0001c0001t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(307): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(308): Show |
1 | a0001c0001t0001g0010 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(313): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(347): Show |
1 | a0001c0002t0001g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(352): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(350): Show |
1 | a0001c0002t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(355): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(345): Show |
2 | a0001c0002t0001g0016 a0001c0002t0001g0104 |
3 | HG02486.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.91+431_91+432insTG others(350): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(341): Show |
1 | a0001c0001t0001g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(346): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(340): Show |
1 | a0001c0001t0001g0004 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(345): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(342): Show |
1 | a0001c0001t0001g0004 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(347): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(260): Show |
1 | a0001c0002t0001g0002 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(265): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(332): Show |
1 | a0001c0002t0001g0015 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(337): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(364): Show |
1 | a0001c0002t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(369): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(301): Show |
1 | a0001c0001t0001g0010 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(306): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(300): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0080 |
2 | NA18962.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.91+431_91+432insTG others(305): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(330): Show |
1 | a0001c0002t0001g0002 | 4 | HG00738.hp2 NA18939.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+431_91+432insTG others(335): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(471): Show |
1 | a0001c0002t0001g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(476): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(258): Show |
1 | a0001c0002t0001g0015 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(263): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(257): Show |
3 | a0001c0002t0001g0002 a0001c0002t0001g0102 a0001c0003t0001g0004 |
6 | HG01952.hp2 HG01975.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+431_91+432insTG others(262): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(329): Show |
1 | a0001c0002t0001g0002 | 5 | NA18612.hp2 NA18747.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+431_91+432insTG others(334): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(332): Show |
1 | a0001c0002t0001g0002 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(337): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(302): Show |
1 | a0001c0002t0001g0017 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(307): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(339): Show |
1 | a0001c0001t0001g0004 | 2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.91+431_91+432insTG others(344): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(354): Show |
1 | a0001c0004t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(359): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(262): Show |
1 | a0001c0003t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(267): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(331): Show |
1 | a0001c0002t0001g0002 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(336): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(329): Show |
1 | a0001c0002t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(334): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(22): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0164 others(1): Show |
9 | HG02132.hp2 HG02735.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+418_91+419insTG others(27): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(53): Show |
1 | a0001c0001t0001g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.91+418_91+419insTG others(58): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(329): Show |
1 | a0001c0002t0001g0002 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.91+418_91+419insTG others(334): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397707 | T | TGTGGGGG others(258): Show |
1 | a0001c0002t0001g0203 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.91+402_91+403insTG others(263): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397707 | ||||||
| chr16:397708 | G | GGTGAGGG others(356): Show |
1 | a0001c0004t0001g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.91+395_91+396insGT others(361): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397708 | |||||||
| chr16:397708 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.91+395G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397708 | |||||||
| chr16:397709 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0205 others(1): Show |
5 | HG01884.hp2 HG02027.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+396T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397709 | |||||||
| chr16:397709 | T | TGAGGGAG others(584): Show |
1 | a0001c0001t0001g0001 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91+397_91+398insAG others(589): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(252): Show |
1 | a0001c0004t0002g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+397_91+398insAG others(257): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(259): Show |
1 | a0001c0004t0001g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91+397_91+398insAG others(264): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(258): Show |
2 | a0001c0004t0001g0024 a0001c0004t0002g0013 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.91+397_91+398insAG others(263): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(197): Show |
1 | a0001c0004t0002g0013 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.91+397_91+398insAG others(202): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(668): Show |
1 | a0001c0001t0001g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.91+397_91+398insAG others(673): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(784): Show |
1 | a0001c0001t0001g0184 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+397_91+398insAG others(789): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(747): Show |
1 | a0005c0009t0004g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91+397_91+398insAG others(752): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(161): Show |
1 | a0001c0004t0002g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.91+397_91+398insAG others(166): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(450): Show |
1 | a0001c0003t0001g0012 | 3 | HG02451.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.91+397_91+398insAG others(455): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGAGGGAG others(450): Show |
1 | a0001c0003t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.91+397_91+398insAG others(455): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(342): Show |
1 | a0001c0002t0001g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(347): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(399): Show |
1 | a0001c0001t0001g0001 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(404): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(391): Show |
1 | a0001c0001t0001g0001 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(396): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(341): Show |
1 | a0001c0002t0001g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(346): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(497): Show |
1 | a0001c0003t0001g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(502): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(86): Show |
1 | a0001c0001t0001g0006 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.91+403_91+404insGT others(91): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(279): Show |
1 | a0001c0001t0001g0001 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.91+425_91+426insGT others(284): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(290): Show |
1 | a0001c0004t0001g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(295): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(419): Show |
1 | a0001c0001t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(424): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(358): Show |
1 | a0001c0001t0001g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(363): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(397): Show |
1 | a0001c0001t0001g0022 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(402): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(352): Show |
1 | a0001c0001t0001g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(357): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(350): Show |
1 | a0001c0001t0001g0001 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(355): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(385): Show |
1 | a0001c0001t0001g0001 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(390): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(350): Show |
1 | a0001c0001t0001g0021 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(355): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(291): Show |
1 | a0001c0001t0001g0001 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(296): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(391): Show |
1 | a0001c0001t0001g0018 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(396): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(310): Show |
1 | a0001c0002t0001g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(315): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(260): Show |
1 | a0001c0002t0001g0002 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(265): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(332): Show |
1 | a0001c0002t0001g0015 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(337): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(377): Show |
1 | a0001c0002t0001g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(382): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(258): Show |
2 | a0001c0002t0001g0002 a0001c0002t0001g0092 |
2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.91+431_91+432insTG others(263): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(342): Show |
1 | a0001c0001t0001g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(347): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(316): Show |
1 | a0001c0002t0001g0002 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.91+423_91+424insTG others(321): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(449): Show |
1 | a0001c0001t0001g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91+423_91+424insTG others(454): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(86): Show |
1 | a0001c0001t0001g0169 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91+418_91+419insTG others(91): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(83): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0014 |
4 | HG02071.hp1 NA18941.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+418_91+419insTG others(88): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397709 | T | TGGGGGGG others(84): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0014 |
3 | HG00408.hp2 NA18952.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.91+418_91+419insTG others(89): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397709 | ||||||
| chr16:397716 | G | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0205 a0001c0002t0001g0159 others(4): Show |
15 | HG01175.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+403G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397716 | |||||||
| chr16:397716 | G | GGTGAGGG others(565): Show |
1 | a0001c0002t0001g0161 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(570): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397716 | |||||||
| chr16:397716 | G | GGTGAGGG others(484): Show |
1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+403_91+404insGT others(489): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397716 | |||||||
| chr16:397716 | G | GTGAGGGA others(483): Show |
1 | a0001c0002t0001g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.91+419_91+420insGT others(488): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(496): Show |
1 | a0001c0002t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(501): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(609): Show |
1 | a0001c0003t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(614): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(569): Show |
1 | a0001c0002t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(574): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(493): Show |
1 | a0001c0002t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(498): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(482): Show |
1 | a0001c0002t0001g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(487): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(222): Show |
1 | a0001c0001t0001g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(227): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(558): Show |
1 | a0001c0002t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(563): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(759): Show |
1 | a0001c0002t0001g0110 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(764): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(420): Show |
1 | a0001c0002t0001g0111 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(425): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(544): Show |
1 | a0001c0002t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(549): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(490): Show |
1 | a0001c0003t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(488): Show |
1 | a0001c0002t0001g0113 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(493): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(451): Show |
1 | a0001c0005t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(456): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(490): Show |
1 | a0001c0002t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(733): Show |
1 | a0001c0002t0001g0115 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(738): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(450): Show |
1 | a0001c0005t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(455): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(490): Show |
1 | a0001c0003t0001g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(1154): Show |
1 | a0001c0002t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(1159): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(482): Show |
1 | a0001c0003t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(487): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(458): Show |
1 | a0001c0002t0001g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(463): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(527): Show |
1 | a0001c0002t0001g0119 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(532): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(524): Show |
1 | a0001c0003t0001g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(529): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(483): Show |
1 | a0001c0003t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(488): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(446): Show |
1 | a0001c0002t0001g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(451): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(1170): Show |
1 | a0001c0002t0001g0123 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(1175): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(1172): Show |
1 | a0001c0002t0001g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(1177): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(414): Show |
1 | a0001c0002t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(419): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(557): Show |
1 | a0001c0002t0001g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(562): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(490): Show |
1 | a0001c0002t0001g0204 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(563): Show |
1 | a0001c0002t0001g0178 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(568): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(564): Show |
1 | a0001c0002t0001g0127 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(569): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(487): Show |
1 | a0001c0003t0001g0128 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(492): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(488): Show |
4 | a0001c0002t0001g0003 a0001c0003t0001g0129 a0001c0003t0001g0130 others(1): Show |
13 | HG00408.hp1 HG00423.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(493): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(524): Show |
1 | a0001c0002t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(529): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(487): Show |
1 | a0001c0002t0001g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(492): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(465): Show |
1 | a0001c0002t0001g0096 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(470): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(464): Show |
1 | a0001c0002t0001g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(469): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(564): Show |
1 | a0001c0002t0001g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(569): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(564): Show |
1 | a0001c0002t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(569): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(927): Show |
1 | a0001c0002t0001g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(932): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(562): Show |
2 | a0001c0002t0001g0011 a0001c0002t0001g0180 |
5 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(567): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(594): Show |
1 | a0001c0002t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(599): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(538): Show |
1 | a0001c0002t0001g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(543): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(1166): Show |
1 | a0001c0002t0001g0137 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(1171): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(487): Show |
1 | a0002c0006t0001g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(492): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(635): Show |
1 | a0001c0002t0001g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(640): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(597): Show |
1 | a0001c0002t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(602): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(632): Show |
1 | a0001c0002t0001g0181 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(637): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(494): Show |
1 | a0001c0003t0001g0142 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(499): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(523): Show |
1 | a0001c0002t0001g0097 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(528): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(494): Show |
1 | a0001c0002t0001g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(499): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(506): Show |
1 | a0001c0003t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(511): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(630): Show |
1 | a0001c0002t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(635): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(1234): Show |
1 | a0001c0002t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(1239): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(487): Show |
1 | a0001c0002t0001g0160 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(492): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(528): Show |
1 | a0001c0002t0001g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(533): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397716 | G | GTGAGGGA others(526): Show |
1 | a0001c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(531): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397716 | ||||||
| chr16:397726 | C | CGGGGGGG others(3): Show |
1 | a0005c0009t0004g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91+419_91+420insGT others(8): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGG others(419): Show |
1 | a0001c0001t0001g0063 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.91+419_91+420insGT others(424): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGG others(428): Show |
1 | a0001c0001t0001g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.91+419_91+420insGT others(433): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(2): Show |
1 | a0001c0001t0001g0006 | 5 | HG00438.hp2 NA18941.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+417_91+425dupGG others(7): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(3): Show |
1 | a0001c0001t0001g0014 | 4 | HG00408.hp2 HG02071.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+416_91+425dupGG others(8): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(4): Show |
1 | a0001c0001t0001g0169 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91+415_91+425dupGG others(9): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(398): Show |
1 | a0001c0001t0001g0035 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(403): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(256): Show |
1 | a0001c0001t0001g0036 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(261): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(387): Show |
1 | a0001c0001t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(392): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(567): Show |
1 | a0001c0003t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(572): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(556): Show |
1 | a0001c0002t0005g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(561): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(551): Show |
1 | a0001c0002t0001g0109 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(556): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(490): Show |
1 | a0001c0002t0001g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(553): Show |
1 | a0001c0002t0001g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(558): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(522): Show |
1 | a0001c0002t0001g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(527): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(622): Show |
1 | a0001c0002t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(627): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(550): Show |
1 | a0001c0002t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(555): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(586): Show |
1 | a0001c0002t0001g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(591): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(588): Show |
1 | a0001c0002t0001g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(593): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(512): Show |
1 | a0001c0003t0001g0172 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(517): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(478): Show |
1 | a0001c0004t0002g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(483): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(453): Show |
1 | a0001c0002t0002g0076 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(458): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(994): Show |
1 | a0001c0004t0001g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(999): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(890): Show |
1 | a0001c0004t0001g0166 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(895): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(835): Show |
1 | a0001c0001t0001g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(840): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(835): Show |
1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.91+431_91+432insTG others(840): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(302): Show |
1 | a0001c0001t0001g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(307): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGGT others(194): Show |
1 | a0001c0003t0001g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+423_91+424insTG others(199): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397726 | C | CGGGGGTG others(96): Show |
1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.91+418_91+419insTG others(101): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397726 | ||||||
| chr16:397733 | T | G | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+420T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397733 | |||||||
| chr16:397733 | T | TG | 5 | a0001c0001t0001g0020 a0001c0002t0001g0093 a0001c0002t0001g0101 others(2): Show |
6 | HG00558.hp1 HG03669.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+425dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397733 | ||||||
| chr16:397733 | T | TGGGGGTG others(288): Show |
1 | a0001c0001t0001g0037 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(293): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397733 | ||||||
| chr16:397733 | T | TGGGGGTG others(285): Show |
1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(290): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397733 | ||||||
| chr16:397733 | T | TGGGGGTG others(490): Show |
1 | a0006c0007t0001g0201 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGT others(495): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397733 | ||||||
| chr16:397738 | G | GGTGGGGG others(292): Show |
1 | a0001c0001t0001g0196 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.91+425_91+426insGT others(297): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397738 | |||||||
| chr16:397739 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0196 |
2 | HG03041.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.91+426T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397739 | |||||||
| chr16:397740 | G | GGGGGGGG others(271): Show |
1 | a0001c0001t0001g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(276): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(262): Show |
1 | a0001c0001t0001g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(267): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(273): Show |
1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(278): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(273): Show |
1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.91+432_91+433insGG others(278): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(270): Show |
1 | a0001c0001t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(275): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(270): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0186 a0001c0001t0001g0188 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+432_91+433insGG others(275): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGG others(99): Show |
1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGG others(104): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGT others(33): Show |
1 | a0001c0001t0001g0170 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(38): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGT others(64): Show |
1 | a0001c0001t0001g0164 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.91+432_91+433insGT others(69): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGGGT others(63): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0078 |
7 | HG02132.hp2 HG02735.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+432_91+433insGT others(68): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | GGGGGTGT others(311): Show |
1 | a0001c0001t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.91+431_91+432insTG others(316): Show |
NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397740 | ||||||
| chr16:397740 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0169 others(1): Show |
11 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+427G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397740 | |||||||
| chr16:397754 | C | T | 1 | a0005c0009t0004g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91+441C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397754 | |||||||
| chr16:397767 | G | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0185 a0001c0001t0001g0186 others(7): Show |
11 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+454G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397767 | |||||||
| chr16:397793 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+480T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397793 | |||||||
| chr16:397819 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.91+506C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397819 | |||||||
| chr16:397821 | G | A | 2 | a0001c0002t0002g0076 a0001c0004t0002g0075 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.91+508G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397821 | |||||||
| chr16:397826 | C | G | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+513C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397826 | |||||||
| chr16:397827 | G | C | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+514G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397827 | |||||||
| chr16:397828 | C | G | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+515C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397828 | |||||||
| chr16:397838 | G | GC | 10 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0032 others(7): Show |
11 | HG00597.hp2 HG01168.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+532dupC | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397838 | ||||||
| chr16:397910 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(7): Show |
22 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.91+597G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397910 | |||||||
| chr16:397925 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
13 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+612C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397925 | |||||||
| chr16:397948 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(8): Show |
14 | HG02109.hp1 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+635A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397948 | |||||||
| chr16:397963 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0205 a0001c0004t0001g0156 others(3): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+650C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397963 | |||||||
| chr16:397976 | G | GT | 3 | a0001c0001t0001g0100 a0001c0001t0001g0196 a0001c0002t0001g0158 |
3 | HG01891.hp1 NA18955.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.91+667dupT | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 397976 | ||||||
| chr16:397976 | G | T | 1 | a0001c0002t0001g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.91+663G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397976 | |||||||
| chr16:397980 | T | G | 2 | a0001c0002t0001g0103 a0001c0002t0005g0200 |
2 | NA19030.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.91+667T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 397980 | |||||||
| chr16:398026 | C | G | 1 | a0001c0002t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91+713C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398026 | |||||||
| chr16:398027 | G | C | 1 | a0001c0002t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91+714G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398027 | |||||||
| chr16:398131 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+818C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398131 | |||||||
| chr16:398132 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.91+819G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398132 | |||||||
| chr16:398164 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.92-826C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398164 | |||||||
| chr16:398172 | A | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(37): Show |
61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.92-818A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398172 | |||||||
| chr16:398307 | C | G | 1 | a0001c0002t0001g0092 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.92-683C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398307 | |||||||
| chr16:398399 | G | T | 9 | a0001c0002t0001g0109 a0001c0002t0001g0126 a0001c0002t0001g0139 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-591G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398399 | |||||||
| chr16:398401 | T | C | 9 | a0001c0002t0001g0109 a0001c0002t0001g0126 a0001c0002t0001g0139 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-589T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398401 | |||||||
| chr16:398435 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.92-555A>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398435 | |||||||
| chr16:398479 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
13 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-511C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398479 | |||||||
| chr16:398497 | G | A | 2 | a0001c0002t0002g0076 a0001c0004t0002g0075 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.92-493G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398497 | |||||||
| chr16:398561 | A | T | 79 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0081 others(76): Show |
94 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.92-429A>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398561 | |||||||
| chr16:398670 | C | A | 1 | a0001c0004t0001g0156 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.92-320C>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398670 | |||||||
| chr16:398696 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.92-294C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398696 | |||||||
| chr16:398715 | G | A | 2 | a0001c0002t0002g0076 a0001c0004t0002g0075 |
2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.92-275G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398715 | |||||||
| chr16:398751 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92-239G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398751 | |||||||
| chr16:398769 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92-221G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398769 | |||||||
| chr16:398916 | C | G | 1 | a0001c0002t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.92-74C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398916 | |||||||
| chr16:398931 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0100 others(7): Show |
13 | HG02109.hp1 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-59G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 1/4 | chr16 | 398931 | |||||||
| chr16:399162 | T | C | 103 | a0001c0001t0001g0004 a0001c0002t0001g0002 a0001c0002t0001g0003 others(100): Show |
151 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.225+39T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/4 | chr16 | 399162 | |||||||
| chr16:399162 | T | G | 1 | a0001c0002t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.225+39T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/4 | chr16 | 399162 | |||||||
| chr16:399163 | G | C | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225+40G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/4 | chr16 | 399163 | |||||||
| chr16:399178 | T | G | 105 | a0001c0001t0001g0004 a0001c0002t0001g0002 a0001c0002t0001g0003 others(102): Show |
153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.225+55T>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/4 | chr16 | 399178 | |||||||
| chr16:399345 | G | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0077 others(117): Show |
171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.226-34G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 2/4 | chr16 | 399345 | |||||||
| chr16:399554 | G | C | 18 | a0001c0001t0001g0004 a0001c0002t0001g0002 a0001c0002t0001g0015 others(15): Show |
50 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.328-73G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 3/4 | chr16 | 399554 | |||||||
| chr16:399574 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.328-53C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 3/4 | chr16 | 399574 | |||||||
| chr16:399582 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0031 |
4 | HG02698.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-45C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 3/4 | chr16 | 399582 | |||||||
| chr16:399743 | C | CG | 5 | a0001c0001t0001g0065 a0001c0002t0001g0081 a0001c0002t0001g0103 others(2): Show |
5 | HG00609.hp2 HG04184.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.440+9dupG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 399743 | ||||||
| chr16:399817 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.440+78A>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399817 | |||||||
| chr16:399906 | C | A | 1 | a0001c0004t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.440+167C>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399906 | |||||||
| chr16:399917 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.440+178T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399917 | |||||||
| chr16:399918 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.440+179C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399918 | |||||||
| chr16:399934 | T | C | 108 | a0001c0001t0001g0023 a0001c0001t0001g0079 a0001c0001t0001g0205 others(105): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.440+195T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399934 | |||||||
| chr16:399938 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.440+199G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399938 | |||||||
| chr16:399945 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.440+206C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399945 | |||||||
| chr16:399977 | G | C | 72 | a0001c0001t0001g0079 a0001c0002t0001g0003 a0001c0002t0001g0011 others(69): Show |
87 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.440+238G>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399977 | |||||||
| chr16:399979 | A | G | 66 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0081 others(63): Show |
81 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.440+240A>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399979 | |||||||
| chr16:399979 | A | T | 1 | a0001c0002t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.440+240A>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399979 | |||||||
| chr16:399980 | C | G | 1 | a0001c0002t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.441-239C>G | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399980 | |||||||
| chr16:399980 | C | T | 100 | a0001c0001t0001g0079 a0001c0002t0001g0002 a0001c0002t0001g0003 others(97): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.441-239C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399980 | |||||||
| chr16:399981 | G | T | 1 | a0001c0002t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.441-238G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 399981 | |||||||
| chr16:400017 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.441-202G>A | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400017 | |||||||
| chr16:400064 | G | T | 14 | a0001c0001t0001g0079 a0001c0002t0001g0109 a0001c0002t0001g0126 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.441-155G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400064 | |||||||
| chr16:400091 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.441-128C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400091 | |||||||
| chr16:400115 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0066 |
2 | HG00423.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.441-104G>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400115 | |||||||
| chr16:400140 | C | CAG | 84 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0079 others(81): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.441-79_441-78insAG | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400140 | |||||||
| chr16:400140 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.441-79C>T | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400140 | |||||||
| chr16:400165 | T | C | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(133): Show |
200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.441-54T>C | NME4 | ENSG00000103202.13 | transcript | ENST00000219479.7 | protein_coding | 4/4 | chr16 | 400165 |