Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54820 |
| ensemblid | ENSG00000072864.16 |
| hgncid | 17619 |
| symbol | NDE1 |
| name | nudE neurodevelopment protein 1 |
| refseq_nuc | NM_017668.3 |
| refseq_prot | NP_060138.1 |
| ensembl_nuc | ENST00000396354.6 |
| ensembl_prot | ENSP00000379642.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 15650245 |
| end | 15726353 |
| strand | + |
| ver | v1.2 |
| region | chr16:15650245-15726353 |
| region5000 | chr16:15645245-15731353 |
| regionname0 | NDE1_chr16_15650245_15726353 |
| regionname5000 | NDE1_chr16_15645245_15731353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 335 | 365 | 92 | 67 | 155 | 14 | 36 | 115 | NDE1_chr16_15645245_15731353 | NDE1 | MEDSG others(330): Show |
chr16 | 15645245 | 15731353 |
| a0002 | 0/0 | 335 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | MEDSG others(330): Show |
chr16 | 15645245 | 15731353 |
| a0003 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | MEDSG others(330): Show |
chr16 | 15645245 | 15731353 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1005 | 359 | 91 | 65 | 155 | 12 | 35 | NDE1_chr16_15645245_15731353 | NDE1 | ATGGA others(1000): Show |
chr16 | 15645245 | 15731353 | ||
| a0001c0002 | 0/0 | 1005 | 5 | 0 | 2 | 0 | 2 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | ATGGA others(1000): Show |
chr16 | 15645245 | 15731353 | ||
| a0001c0003 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | ATGGA others(1000): Show |
chr16 | 15645245 | 15731353 | ||
| a0002c0004 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | ATGGA others(1000): Show |
chr16 | 15645245 | 15731353 | ||
| a0003c0005 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | ATGGA others(1000): Show |
chr16 | 15645245 | 15731353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3203 | 102 | 27 | 20 | 32 | 3 | 20 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0002 | 0/1 | 3203 | 104 | 17 | 21 | 50 | 6 | 9 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0003 | 0/0 | 3203 | 52 | 0 | 3 | 46 | 0 | 3 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0004 | 0/0 | 3213 | 19 | 18 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3208): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0005 | 0/0 | 3213 | 12 | 0 | 2 | 8 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3208): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0006 | 0/0 | 3204 | 12 | 4 | 4 | 2 | 1 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3199): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0007 | 0/0 | 3203 | 10 | 9 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0008 | 0/0 | 3200 | 5 | 5 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3195): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0009 | 0/0 | 3203 | 5 | 0 | 4 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0010 | 0/0 | 3203 | 4 | 0 | 3 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0011 | 0/0 | 3203 | 3 | 2 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0012 | 0/0 | 3204 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3199): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0013 | 0/0 | 3203 | 3 | 0 | 0 | 3 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0014 | 0/0 | 3203 | 2 | 2 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0015 | 0/0 | 3203 | 2 | 0 | 0 | 1 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0016 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0017 | 0/0 | 3203 | 2 | 0 | 2 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0018 | 0/0 | 3203 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0019 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3199): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0020 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0021 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0022 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3209): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0023 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3208): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0024 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3195): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0025 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0026 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0027 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0028 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0029 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0030 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0031 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0032 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0001t0033 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0002t0001 | 0/0 | 3203 | 5 | 0 | 2 | 0 | 2 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0001c0003t0002 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0002c0004t0001 | 0/0 | 3203 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| a0003c0005t0001 | 0/0 | 3203 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | GCAGC others(3198): Show |
chr16 | 15645245 | 15731353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0007g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0008g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0010g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0011g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0013g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0015g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0016g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0017g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0018g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0019g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0021g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0022g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0024g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0025g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0027g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0028g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0029g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0030g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0031g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0032g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0001t0033g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| a0003c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0334 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0324 | EUR | GBR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0102 | EUR | FIN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00558 | hp1 | a0001 | c0001 | t0012 | g0064 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0100 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0101 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0325 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0206 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0152 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0317 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0361 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01167 | hp2 | a0001 | c0001 | t0017 | g0043 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0322 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01169 | hp1 | a0001 | c0001 | t0017 | g0044 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0323 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0335 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01243 | hp2 | a0001 | c0001 | t0031 | g0047 | AMR | PUR | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0327 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01257 | hp2 | a0001 | c0001 | t0010 | g0311 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0312 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0123 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01433 | hp2 | a0001 | c0001 | t0029 | g0078 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01496 | hp2 | a0001 | c0001 | t0011 | g0006 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0331 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0166 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0332 | EUR | IBS | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0352 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01952 | hp2 | a0001 | c0001 | t0030 | g0210 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0015 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0355 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02055 | hp2 | a0001 | c0001 | t0025 | g0310 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0354 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02155 | hp2 | a0001 | c0001 | t0018 | g0057 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CDX | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02280 | hp1 | a0001 | c0001 | t0026 | g0018 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0348 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0357 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0362 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0358 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0186 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0112 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02647 | hp2 | a0001 | c0001 | t0028 | g0295 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0356 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02818 | hp1 | a0001 | c0001 | t0027 | g0020 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0350 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0349 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0161 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0353 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0359 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03491 | hp2 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03516 | hp1 | a0001 | c0001 | t0024 | g0008 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0326 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | CHB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18944 | hp1 | a0001 | c0001 | t0016 | g0115 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18945 | hp1 | a0001 | c0001 | t0032 | g0089 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18948 | hp2 | a0003 | c0005 | t0001 | g0046 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18950 | hp2 | a0001 | c0001 | t0016 | g0238 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18952 | hp2 | a0001 | c0001 | t0013 | g0343 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18964 | hp1 | a0001 | c0001 | t0015 | g0017 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0279 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18970 | hp2 | a0001 | c0001 | t0033 | g0076 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0032 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18979 | hp1 | a0001 | c0001 | t0018 | g0094 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19003 | hp1 | a0001 | c0001 | t0020 | g0130 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19007 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19009 | hp1 | a0001 | c0001 | t0019 | g0012 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0007 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0160 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19066 | hp1 | a0001 | c0001 | t0013 | g0344 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0345 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ASW | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | TSI | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | GIH | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0351 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0360 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | USA | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0208 | REF | REF | NDE1_chr16_15645245_15731353 | NDE1 | chr16 | 15645245 | 15731353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15667357 | C | T | 1 | a0003 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.155C>T | p.Thr52Met | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/9 | 248/3203 | 155/1008 | 52/335 | chr16 | 15667357 | |||
| chr16:15696785 | C | T | 1 | a0002 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.872C>T | p.Ser291Phe | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/9 | 965/3203 | 872/1008 | 291/335 | chr16 | 15696785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15691259 | G | A | 1 | a0001c0003 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.639G>A | p.Pro213Pro | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/9 | 732/3203 | 639/1008 | 213/335 | chr16 | 15691259 | |||
| chr16:15696750 | C | T | 1 | a0001c0002 | 5 | HG00738.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
synonymous_variant | LOW | c.837C>T | p.Tyr279Tyr | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/9 | 930/3203 | 837/1008 | 279/335 | chr16 | 15696750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15650251 | G | A | 1 | a0001c0001t0014 | 2 | HG02970.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-87G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/9 | 14528 | chr16 | 15650251 | ||||||
| chr16:15650255 | C | T | 1 | a0001c0001t0033 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-83C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/9 | chr16 | 15650255 | |||||||
| chr16:15724284 | A | C | 14 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(11): Show |
125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*33A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 33 | chr16 | 15724284 | ||||||
| chr16:15724287 | G | A | 1 | a0001c0001t0011 | 3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*36G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 36 | chr16 | 15724287 | ||||||
| chr16:15724368 | G | A | 1 | a0001c0001t0017 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 117 | chr16 | 15724368 | ||||||
| chr16:15724437 | G | A | 1 | a0001c0001t0028 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 186 | chr16 | 15724437 | ||||||
| chr16:15724453 | G | A | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(16): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*202G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 202 | chr16 | 15724453 | ||||||
| chr16:15724489 | C | G | 1 | a0001c0001t0027 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 238 | chr16 | 15724489 | ||||||
| chr16:15724635 | C | T | 1 | a0001c0001t0026 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 384 | chr16 | 15724635 | ||||||
| chr16:15724796 | G | A | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 others(1): Show |
33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*545G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 545 | chr16 | 15724796 | ||||||
| chr16:15724902 | G | T | 1 | a0001c0001t0025 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*651G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 651 | chr16 | 15724902 | ||||||
| chr16:15724919 | G | A | 1 | a0001c0001t0029 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 668 | chr16 | 15724919 | ||||||
| chr16:15724985 | A | G | 1 | a0001c0001t0009 | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*734A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 734 | chr16 | 15724985 | ||||||
| chr16:15725114 | C | G | 2 | a0001c0001t0015 a0001c0001t0021 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*863C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 863 | chr16 | 15725114 | ||||||
| chr16:15725134 | T | TA | 3 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0019 |
16 | HG00140.hp2 HG00558.hp1 HG01074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*898dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 899 | INFO_REALIGN_3_PRIME | chr16 | 15725134 | |||||
| chr16:15725134 | TA | T | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0023 |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*898delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | INFO_REALIGN_3_PRIME | chr16 | 15725134 | |||||
| chr16:15725147 | AAAC | A | 2 | a0001c0001t0008 a0001c0001t0024 |
6 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*898_*900delACA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | INFO_REALIGN_3_PRIME | chr16 | 15725147 | |||||
| chr16:15725148 | A | C | 1 | a0001c0001t0002 | 2 | NA18982.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*897A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 897 | chr16 | 15725148 | ||||||
| chr16:15725149 | A | G | 1 | a0001c0001t0025 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 898 | chr16 | 15725149 | ||||||
| chr16:15725150 | C | A | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(4): Show |
29 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*899C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 899 | chr16 | 15725150 | ||||||
| chr16:15725162 | C | A | 1 | a0001c0001t0016 | 2 | NA18944.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*911C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 911 | chr16 | 15725162 | ||||||
| chr16:15725164 | A | C | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0010 others(3): Show |
38 | HG01109.hp1 HG01255.hp1 HG01257.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*913A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 913 | chr16 | 15725164 | ||||||
| chr16:15725194 | C | T | 1 | a0001c0001t0018 | 2 | HG02155.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*943C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 943 | chr16 | 15725194 | ||||||
| chr16:15725198 | G | A | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 947 | chr16 | 15725198 | ||||||
| chr16:15725352 | G | A | 1 | a0001c0001t0027 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1101 | chr16 | 15725352 | ||||||
| chr16:15725459 | T | TTGTCCCT others(4): Show |
4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 others(1): Show |
33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insTCCC others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1211 | INFO_REALIGN_3_PRIME | chr16 | 15725459 | |||||
| chr16:15725471 | G | A | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 others(1): Show |
33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1220G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1220 | chr16 | 15725471 | ||||||
| chr16:15725550 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 others(1): Show |
33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1299A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1299 | chr16 | 15725550 | ||||||
| chr16:15725556 | C | A | 1 | a0001c0001t0020 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1305C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1305 | chr16 | 15725556 | ||||||
| chr16:15725588 | C | G | 1 | a0001c0001t0031 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1337C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1337 | chr16 | 15725588 | ||||||
| chr16:15725640 | G | A | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0022 |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1389G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1389 | chr16 | 15725640 | ||||||
| chr16:15725746 | T | C | 1 | a0001c0001t0021 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1495T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1495 | chr16 | 15725746 | ||||||
| chr16:15725974 | C | T | 2 | a0001c0001t0004 a0001c0001t0022 |
20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1723C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1723 | chr16 | 15725974 | ||||||
| chr16:15726013 | T | C | 1 | a0001c0001t0030 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1762T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1762 | chr16 | 15726013 | ||||||
| chr16:15726035 | A | G | 2 | a0001c0001t0007 a0001c0001t0014 |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1784A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1784 | chr16 | 15726035 | ||||||
| chr16:15726041 | T | C | 1 | a0001c0001t0033 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1790 | chr16 | 15726041 | ||||||
| chr16:15726101 | G | A | 1 | a0001c0001t0013 | 3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1850G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 1850 | chr16 | 15726101 | ||||||
| chr16:15726341 | T | C | 2 | a0001c0001t0011 a0001c0001t0024 |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2090T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 9/9 | 2090 | chr16 | 15726341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15650298 | A | G | 1 | a0001c0001t0003g0364 | 1 | NA18960.hp1 | splice_region_variant&intron_variant | LOW | c.-44+4A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650298 | |||||||
| chr16:15650317 | C | T | 2 | a0001c0001t0002g0362 a0001c0001t0002g0363 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-44+23C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650317 | |||||||
| chr16:15650392 | C | T | 15 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(12): Show |
15 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+98C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650392 | |||||||
| chr16:15650414 | G | C | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+120G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650414 | |||||||
| chr16:15650432 | T | C | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+138T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650432 | |||||||
| chr16:15650472 | T | C | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+178T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650472 | |||||||
| chr16:15650566 | G | A | 4 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(1): Show |
4 | NA18998.hp2 NA19009.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+272G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650566 | |||||||
| chr16:15650783 | G | C | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+489G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650783 | |||||||
| chr16:15650890 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+596C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15650890 | |||||||
| chr16:15651035 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(4): Show |
7 | NA18952.hp2 NA18998.hp2 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+741C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651035 | |||||||
| chr16:15651060 | C | A | 1 | a0001c0001t0002g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-44+766C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651060 | |||||||
| chr16:15651103 | C | T | 1 | a0001c0001t0002g0342 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-44+809C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651103 | |||||||
| chr16:15651334 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-44+1040G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651334 | |||||||
| chr16:15651430 | G | GT | 21 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0340 others(18): Show |
21 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+1155dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15651430 | ||||||
| chr16:15651430 | GT | G | 60 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(57): Show |
61 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-44+1155delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15651430 | ||||||
| chr16:15651441 | T | G | 10 | a0001c0001t0002g0019 a0001c0001t0011g0004 a0001c0001t0011g0005 others(7): Show |
10 | HG01496.hp2 HG02040.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+1147T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651441 | |||||||
| chr16:15651441 | T | TG | 15 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(12): Show |
15 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+1147_-44+1148i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651441 | |||||||
| chr16:15651442 | T | G | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(15): Show |
18 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-44+1148T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651442 | |||||||
| chr16:15651443 | T | TG | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1149_-44+1150i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651443 | |||||||
| chr16:15651444 | T | G | 1 | a0001c0001t0001g0039 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-44+1150T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651444 | |||||||
| chr16:15651446 | T | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(73): Show |
77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-44+1152T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651446 | |||||||
| chr16:15651498 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0009g0102 others(1): Show |
4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1204G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651498 | |||||||
| chr16:15651663 | G | A | 7 | a0001c0001t0002g0153 a0001c0001t0007g0347 a0001c0001t0007g0348 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+1369G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651663 | |||||||
| chr16:15651673 | C | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+1379C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651673 | |||||||
| chr16:15651719 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-44+1425C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651719 | |||||||
| chr16:15651729 | C | T | 11 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0315 others(8): Show |
11 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+1435C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651729 | |||||||
| chr16:15651734 | C | T | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-44+1440C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651734 | |||||||
| chr16:15651735 | G | A | 4 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(1): Show |
4 | HG02040.hp1 HG02280.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1441G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15651735 | |||||||
| chr16:15652376 | C | T | 1 | a0001c0001t0003g0151 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-44+2082C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652376 | |||||||
| chr16:15652618 | A | C | 37 | a0001c0001t0001g0308 a0001c0001t0003g0002 a0001c0001t0003g0125 others(34): Show |
38 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44+2324A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652618 | |||||||
| chr16:15652716 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+2422C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652716 | |||||||
| chr16:15652776 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+2482G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652776 | |||||||
| chr16:15652800 | A | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+2506A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652800 | |||||||
| chr16:15652829 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0027g0020 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+2535A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652829 | |||||||
| chr16:15652856 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+2562G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652856 | |||||||
| chr16:15652912 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0287 others(21): Show |
24 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-44+2618C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652912 | |||||||
| chr16:15652934 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-44+2640G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652934 | |||||||
| chr16:15652944 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-44+2650A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15652944 | |||||||
| chr16:15653042 | G | A | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-44+2748G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653042 | |||||||
| chr16:15653182 | T | A | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+2888T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653182 | |||||||
| chr16:15653255 | C | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(200): Show |
204 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-44+2961C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653255 | |||||||
| chr16:15653577 | G | A | 3 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-44+3283G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653577 | |||||||
| chr16:15653781 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-44+3487G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653781 | |||||||
| chr16:15653797 | G | A | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-44+3503G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653797 | |||||||
| chr16:15653812 | C | G | 1 | a0001c0002t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-44+3518C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15653812 | |||||||
| chr16:15654026 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-44+3732C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654026 | |||||||
| chr16:15654085 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0340 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-44+3791T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654085 | |||||||
| chr16:15654193 | A | G | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+3899A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654193 | |||||||
| chr16:15654296 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-44+4002G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654296 | |||||||
| chr16:15654467 | G | A | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+4173G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654467 | |||||||
| chr16:15654497 | A | G | 64 | a0001c0001t0001g0308 a0001c0001t0002g0103 a0001c0001t0002g0105 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-44+4203A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654497 | |||||||
| chr16:15654523 | G | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-44+4229G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654523 | |||||||
| chr16:15654602 | CA | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(236): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-44+4322delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15654602 | ||||||
| chr16:15654615 | AAC | A | 6 | a0001c0001t0002g0019 a0001c0001t0011g0004 a0001c0001t0011g0006 others(3): Show |
6 | HG01496.hp2 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+4323_-44+4324d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15654615 | ||||||
| chr16:15654616 | A | C | 20 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+4322A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654616 | |||||||
| chr16:15654617 | C | A | 20 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+4323C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654617 | |||||||
| chr16:15654618 | A | C | 7 | a0001c0001t0002g0019 a0001c0001t0011g0004 a0001c0001t0011g0005 others(4): Show |
7 | HG01496.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+4324A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654618 | |||||||
| chr16:15654622 | A | C | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4328A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654622 | |||||||
| chr16:15654632 | C | A | 2 | a0001c0001t0015g0016 a0001c0001t0021g0015 |
2 | HG02040.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-44+4338C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654632 | |||||||
| chr16:15654763 | A | G | 2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-44+4469A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15654763 | |||||||
| chr16:15655006 | C | T | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+4712C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655006 | |||||||
| chr16:15655042 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44+4748A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655042 | |||||||
| chr16:15655160 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-44+4866G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655160 | |||||||
| chr16:15655342 | G | A | 2 | a0001c0001t0010g0311 a0001c0001t0010g0312 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-44+5048G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655342 | |||||||
| chr16:15655425 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-44+5131G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655425 | |||||||
| chr16:15655429 | G | C | 1 | a0001c0001t0002g0216 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-44+5135G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655429 | |||||||
| chr16:15655442 | G | T | 1 | a0001c0001t0006g0327 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5148G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655442 | |||||||
| chr16:15655444 | C | A | 1 | a0001c0001t0006g0327 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5150C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655444 | |||||||
| chr16:15655450 | C | A | 1 | a0001c0001t0006g0327 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44+5156C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655450 | |||||||
| chr16:15655571 | T | C | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+5277T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655571 | |||||||
| chr16:15655631 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-44+5337A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655631 | |||||||
| chr16:15655662 | A | G | 3 | a0001c0001t0003g0148 a0001c0001t0003g0309 a0001c0001t0003g0364 |
3 | NA18960.hp1 NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-44+5368A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655662 | |||||||
| chr16:15655791 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-44+5497A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655791 | |||||||
| chr16:15655946 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5652A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655946 | |||||||
| chr16:15655948 | G | C | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5654G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655948 | |||||||
| chr16:15655977 | T | G | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5683T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655977 | |||||||
| chr16:15655978 | G | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5684G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15655978 | |||||||
| chr16:15656064 | G | T | 1 | a0001c0001t0002g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-44+5770G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656064 | |||||||
| chr16:15656109 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5815C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656109 | |||||||
| chr16:15656146 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5852A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656146 | |||||||
| chr16:15656162 | G | A | 32 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(29): Show |
32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44+5868G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656162 | |||||||
| chr16:15656175 | G | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+5881G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656175 | |||||||
| chr16:15656297 | G | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6003G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656297 | |||||||
| chr16:15656298 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6004A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656298 | |||||||
| chr16:15656299 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6005G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656299 | |||||||
| chr16:15656368 | A | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6074A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656368 | |||||||
| chr16:15656370 | A | C | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6076A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656370 | |||||||
| chr16:15656411 | C | T | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-44+6117C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656411 | |||||||
| chr16:15656501 | T | A | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6207T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656501 | |||||||
| chr16:15656519 | T | TTTA | 39 | a0001c0001t0001g0213 a0001c0001t0001g0308 a0001c0001t0003g0002 others(36): Show |
40 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-44+6247_-44+6249d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15656519 | ||||||
| chr16:15656633 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-44+6339C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656633 | |||||||
| chr16:15656636 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-44+6342G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656636 | |||||||
| chr16:15656645 | T | A | 61 | a0001c0001t0001g0308 a0001c0001t0002g0019 a0001c0001t0003g0002 others(58): Show |
62 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.-44+6351T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656645 | |||||||
| chr16:15656697 | T | A | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6403T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656697 | |||||||
| chr16:15656733 | G | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6439G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656733 | |||||||
| chr16:15656734 | T | G | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+6440T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656734 | |||||||
| chr16:15656786 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-44+6492C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656786 | |||||||
| chr16:15656847 | G | T | 1 | a0001c0002t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-44+6553G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656847 | |||||||
| chr16:15656857 | G | A | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-44+6563G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15656857 | |||||||
| chr16:15657103 | T | G | 1 | a0001c0001t0006g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6809T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657103 | |||||||
| chr16:15657165 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+6871T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657165 | |||||||
| chr16:15657176 | C | T | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+6882C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657176 | |||||||
| chr16:15657222 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+6928C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657222 | |||||||
| chr16:15657388 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-44+7094C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657388 | |||||||
| chr16:15657500 | T | A | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-44+7206T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657500 | |||||||
| chr16:15657597 | T | C | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7139T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657597 | |||||||
| chr16:15657602 | A | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7134A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657602 | |||||||
| chr16:15657603 | T | A | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-7133T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657603 | |||||||
| chr16:15657632 | C | T | 1 | a0001c0001t0015g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-43-7104C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657632 | |||||||
| chr16:15657677 | C | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG01934.hp2 HG02129.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-7059C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657677 | |||||||
| chr16:15657680 | C | T | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-7056C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657680 | |||||||
| chr16:15657736 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(129): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-43-7000C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657736 | |||||||
| chr16:15657791 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-6945G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657791 | |||||||
| chr16:15657803 | T | C | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-6933T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657803 | |||||||
| chr16:15657815 | T | C | 1 | a0001c0001t0018g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-43-6921T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657815 | |||||||
| chr16:15657931 | A | T | 1 | a0001c0001t0018g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-43-6805A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15657931 | |||||||
| chr16:15658055 | G | T | 1 | a0001c0001t0002g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43-6681G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658055 | |||||||
| chr16:15658117 | G | T | 5 | a0001c0001t0002g0106 a0001c0001t0002g0280 a0001c0001t0002g0281 others(2): Show |
5 | HG00438.hp2 NA18747.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6619G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658117 | |||||||
| chr16:15658121 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-43-6615C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658121 | |||||||
| chr16:15658225 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-43-6511C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658225 | |||||||
| chr16:15658603 | T | G | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-6133T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658603 | |||||||
| chr16:15658758 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0217 a0001c0001t0002g0218 others(4): Show |
8 | HG00280.hp1 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-5978G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658758 | |||||||
| chr16:15658759 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-43-5977C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658759 | |||||||
| chr16:15658803 | C | T | 1 | a0001c0001t0006g0326 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-43-5933C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15658803 | |||||||
| chr16:15659066 | G | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-5670G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659066 | |||||||
| chr16:15659307 | CTA | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-43-5424_-43-5423d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659307 | ||||||
| chr16:15659425 | C | CT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0027 others(175): Show |
180 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.-43-5282dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | ||||||
| chr16:15659425 | C | CTT | 36 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0036 others(33): Show |
36 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43-5283_-43-5282d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | ||||||
| chr16:15659425 | CT | C | 11 | a0001c0001t0001g0049 a0001c0001t0002g0223 a0001c0001t0002g0225 others(8): Show |
11 | HG01517.hp1 HG02040.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-5282delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | ||||||
| chr16:15659425 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0007g0347 a0001c0001t0007g0348 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-43-5292_-43-5282d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | ||||||
| chr16:15659425 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0331 a0001c0001t0002g0332 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-43-5293_-43-5282d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659425 | ||||||
| chr16:15659598 | G | A | 30 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(27): Show |
30 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-43-5138G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659598 | |||||||
| chr16:15659609 | A | C | 1 | a0001c0001t0002g0270 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-43-5127A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659609 | |||||||
| chr16:15659693 | T | C | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(1): Show |
4 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-5043T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659693 | |||||||
| chr16:15659729 | G | A | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-5007G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659729 | |||||||
| chr16:15659748 | CT | C | 34 | a0001c0001t0001g0058 a0001c0001t0002g0013 a0001c0001t0002g0019 others(31): Show |
34 | HG01109.hp2 HG01168.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.-43-4970delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15659748 | ||||||
| chr16:15659926 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-43-4810T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659926 | |||||||
| chr16:15659993 | C | G | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-43-4743C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659993 | |||||||
| chr16:15659998 | C | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-4738C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15659998 | |||||||
| chr16:15660136 | C | G | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-4600C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660136 | |||||||
| chr16:15660262 | G | C | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-4474G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660262 | |||||||
| chr16:15660342 | C | G | 12 | a0001c0001t0002g0019 a0001c0001t0011g0004 a0001c0001t0011g0005 others(9): Show |
12 | HG01496.hp2 HG02040.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-4394C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660342 | |||||||
| chr16:15660544 | G | A | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-4192G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660544 | |||||||
| chr16:15660570 | T | C | 1 | a0001c0001t0004g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-43-4166T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660570 | |||||||
| chr16:15660580 | C | T | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-4156C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660580 | |||||||
| chr16:15660611 | G | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-43-4125G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660611 | |||||||
| chr16:15660696 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43-4040C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660696 | |||||||
| chr16:15660716 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4020C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660716 | |||||||
| chr16:15660788 | G | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-3948G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15660788 | |||||||
| chr16:15661156 | G | GT | 23 | a0001c0001t0002g0269 a0001c0001t0003g0119 a0001c0001t0003g0143 others(20): Show |
23 | HG01106.hp2 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-3564dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661156 | ||||||
| chr16:15661156 | G | T | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-43-3580G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661156 | |||||||
| chr16:15661156 | GT | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(136): Show |
140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-43-3564delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661156 | ||||||
| chr16:15661188 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-43-3548A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661188 | |||||||
| chr16:15661296 | C | T | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-3440C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661296 | |||||||
| chr16:15661360 | GA | G | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-43-3374delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15661360 | ||||||
| chr16:15661399 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-43-3337C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661399 | |||||||
| chr16:15661448 | G | A | 32 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(29): Show |
32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-43-3288G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661448 | |||||||
| chr16:15661557 | C | T | 6 | a0001c0001t0004g0182 a0001c0001t0004g0183 a0001c0001t0004g0184 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-3179C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661557 | |||||||
| chr16:15661800 | A | G | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-2936A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661800 | |||||||
| chr16:15661888 | C | G | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-2848C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661888 | |||||||
| chr16:15661995 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-43-2741G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15661995 | |||||||
| chr16:15662094 | A | G | 1 | a0001c0001t0002g0337 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43-2642A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662094 | |||||||
| chr16:15662095 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-43-2641G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662095 | |||||||
| chr16:15662280 | C | CT | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0087 others(7): Show |
10 | HG00597.hp1 HG01123.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-2436dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15662280 | ||||||
| chr16:15662280 | CT | C | 6 | a0001c0001t0001g0059 a0001c0001t0002g0226 a0001c0001t0002g0270 others(3): Show |
6 | HG00140.hp2 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-2436delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15662280 | ||||||
| chr16:15662356 | C | T | 19 | a0001c0001t0002g0019 a0001c0001t0007g0347 a0001c0001t0007g0348 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-2380C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662356 | |||||||
| chr16:15662630 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0040 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-43-2106G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662630 | |||||||
| chr16:15662678 | G | T | 1 | a0001c0001t0001g0340 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-43-2058G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662678 | |||||||
| chr16:15662790 | G | T | 24 | a0001c0001t0002g0019 a0001c0001t0007g0347 a0001c0001t0007g0348 others(21): Show |
24 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1946G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662790 | |||||||
| chr16:15662807 | A | G | 24 | a0001c0001t0002g0019 a0001c0001t0007g0347 a0001c0001t0007g0348 others(21): Show |
24 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1929A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662807 | |||||||
| chr16:15662817 | G | A | 2 | a0001c0001t0025g0310 a0001c0001t0026g0018 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-1919G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662817 | |||||||
| chr16:15662858 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1878C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662858 | |||||||
| chr16:15662919 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-43-1817C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15662919 | |||||||
| chr16:15663045 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-43-1691G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663045 | |||||||
| chr16:15663052 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-43-1684A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663052 | |||||||
| chr16:15663101 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-43-1635C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663101 | |||||||
| chr16:15663216 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-43-1520C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663216 | |||||||
| chr16:15663241 | CT | C | 16 | a0001c0001t0001g0060 a0001c0001t0001g0195 a0001c0001t0001g0288 others(13): Show |
16 | HG01168.hp1 HG02040.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-1479delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15663241 | ||||||
| chr16:15663266 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-1470G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663266 | |||||||
| chr16:15663396 | C | G | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-1340C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663396 | |||||||
| chr16:15663414 | A | AT | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-43-1313dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15663414 | ||||||
| chr16:15663478 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(200): Show |
204 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-43-1258G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663478 | |||||||
| chr16:15663605 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0328 |
2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-43-1131G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663605 | |||||||
| chr16:15663750 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-986A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663750 | |||||||
| chr16:15663806 | C | CTGGG | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-930_-43-929ins others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663806 | |||||||
| chr16:15663807 | C | T | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-929C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663807 | |||||||
| chr16:15663808 | T | G | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-928T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663808 | |||||||
| chr16:15663811 | A | T | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-925A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663811 | |||||||
| chr16:15663812 | A | C | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-924A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663812 | |||||||
| chr16:15663813 | T | A | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-923T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663813 | |||||||
| chr16:15663814 | A | C | 6 | a0001c0001t0002g0106 a0001c0001t0002g0266 a0001c0001t0002g0280 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-922A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15663814 | |||||||
| chr16:15664120 | C | CT | 5 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0009g0102 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-615dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 15664120 | ||||||
| chr16:15664127 | A | T | 5 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0009g0102 others(2): Show |
5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-609A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664127 | |||||||
| chr16:15664136 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-43-600A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664136 | |||||||
| chr16:15664225 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-511A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664225 | |||||||
| chr16:15664456 | A | G | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-280A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664456 | |||||||
| chr16:15664472 | T | C | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43-264T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664472 | |||||||
| chr16:15664635 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43-101G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 1/8 | chr16 | 15664635 | |||||||
| chr16:15664887 | CT | C | 28 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0286 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.83+42delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 15664887 | ||||||
| chr16:15664986 | C | T | 1 | a0001c0001t0003g0122 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.83+125C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15664986 | |||||||
| chr16:15665049 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.83+188T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665049 | |||||||
| chr16:15665220 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+359A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665220 | |||||||
| chr16:15665262 | A | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.83+401A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665262 | |||||||
| chr16:15665352 | C | A | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+491C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665352 | |||||||
| chr16:15665718 | T | G | 3 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.83+857T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665718 | |||||||
| chr16:15665867 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.83+1006T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665867 | |||||||
| chr16:15665906 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(256): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.83+1045A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665906 | |||||||
| chr16:15665944 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.83+1083C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665944 | |||||||
| chr16:15665956 | A | G | 2 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
2 | HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.83+1095A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15665956 | |||||||
| chr16:15666035 | C | T | 8 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG00597.hp1 HG02083.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+1174C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666035 | |||||||
| chr16:15666051 | C | T | 2 | a0001c0001t0025g0310 a0001c0001t0026g0018 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.83+1190C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666051 | |||||||
| chr16:15666158 | T | C | 31 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(28): Show |
31 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-1128T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666158 | |||||||
| chr16:15666230 | C | T | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-1056C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666230 | |||||||
| chr16:15666553 | G | A | 1 | a0001c0001t0008g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.84-733G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666553 | |||||||
| chr16:15666741 | C | T | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-545C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666741 | |||||||
| chr16:15666851 | T | A | 1 | a0001c0001t0015g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.84-435T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666851 | |||||||
| chr16:15666882 | A | G | 1 | a0001c0001t0002g0265 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.84-404A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666882 | |||||||
| chr16:15666915 | G | T | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-371G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666915 | |||||||
| chr16:15666938 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.84-348A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666938 | |||||||
| chr16:15666945 | T | A | 2 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.84-341T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666945 | |||||||
| chr16:15666983 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84-303C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15666983 | |||||||
| chr16:15667141 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0027g0020 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.84-145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 2/8 | chr16 | 15667141 | |||||||
| chr16:15667520 | C | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.237+81C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667520 | |||||||
| chr16:15667542 | C | G | 19 | a0001c0001t0002g0019 a0001c0001t0007g0347 a0001c0001t0007g0348 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+103C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667542 | |||||||
| chr16:15667574 | T | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.237+135T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667574 | |||||||
| chr16:15667576 | C | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(265): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.237+137C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667576 | |||||||
| chr16:15667627 | G | GT | 79 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0035 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.237+192dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | ||||||
| chr16:15667627 | G | GTT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(68): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.237+191_237+192dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | ||||||
| chr16:15667627 | G | GTTT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0077 others(4): Show |
7 | HG01433.hp2 HG02135.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+190_237+192dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667627 | ||||||
| chr16:15667632 | G | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.237+193G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667632 | |||||||
| chr16:15667633 | T | TTG | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG00735.hp2 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+195_237+196ins others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667633 | ||||||
| chr16:15667634 | T | G | 31 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(28): Show |
31 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.237+195T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667634 | |||||||
| chr16:15667638 | T | G | 3 | a0001c0001t0003g0148 a0001c0001t0003g0309 a0001c0001t0003g0364 |
3 | NA18960.hp1 NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.237+199T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667638 | |||||||
| chr16:15667788 | C | T | 3 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.237+349C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667788 | |||||||
| chr16:15667865 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0027g0020 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+426C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667865 | |||||||
| chr16:15667926 | T | A | 21 | a0001c0001t0002g0223 a0001c0001t0002g0227 a0001c0001t0002g0228 others(18): Show |
21 | HG03834.hp2 NA18940.hp1 NA18946.hp1 others(18): Show |
intron_variant | MODIFIER | c.237+487T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15667926 | |||||||
| chr16:15667968 | C | CT | 12 | a0001c0001t0002g0264 a0001c0001t0002g0283 a0001c0001t0003g0139 others(9): Show |
12 | HG02738.hp1 NA18940.hp1 NA18973.hp2 others(9): Show |
intron_variant | MODIFIER | c.237+543dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667968 | ||||||
| chr16:15667968 | CT | C | 17 | a0001c0001t0001g0051 a0001c0001t0002g0227 a0001c0001t0002g0269 others(14): Show |
17 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.237+543delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15667968 | ||||||
| chr16:15668190 | T | C | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.237+751T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668190 | |||||||
| chr16:15668261 | G | A | 1 | a0001c0001t0018g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.237+822G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668261 | |||||||
| chr16:15668269 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.237+830A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668269 | |||||||
| chr16:15668350 | C | G | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+911C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668350 | |||||||
| chr16:15668418 | C | T | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.237+979C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668418 | |||||||
| chr16:15668454 | A | G | 1 | a0001c0001t0002g0026 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.237+1015A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668454 | |||||||
| chr16:15668497 | G | A | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+1058G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668497 | |||||||
| chr16:15668602 | A | G | 3 | a0001c0001t0002g0263 a0001c0001t0002g0362 a0001c0001t0002g0363 |
3 | HG02622.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.237+1163A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668602 | |||||||
| chr16:15668607 | A | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+1168A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668607 | |||||||
| chr16:15668821 | G | C | 2 | a0001c0001t0002g0019 a0001c0001t0027g0020 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+1382G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668821 | |||||||
| chr16:15668852 | T | A | 1 | a0001c0001t0002g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.237+1413T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668852 | |||||||
| chr16:15668868 | G | A | 1 | a0001c0001t0017g0043 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.237+1429G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668868 | |||||||
| chr16:15668961 | G | A | 1 | a0001c0001t0002g0337 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.237+1522G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668961 | |||||||
| chr16:15668969 | G | A | 1 | a0001c0001t0005g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.237+1530G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668969 | |||||||
| chr16:15668980 | A | C | 2 | a0001c0001t0002g0019 a0001c0001t0027g0020 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.237+1541A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15668980 | |||||||
| chr16:15669044 | C | T | 75 | a0001c0001t0001g0308 a0001c0001t0001g0346 a0001c0001t0002g0013 others(72): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.237+1605C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669044 | |||||||
| chr16:15669142 | C | T | 2 | a0001c0001t0006g0157 a0001c0001t0006g0158 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.237+1703C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669142 | |||||||
| chr16:15669143 | G | A | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1704G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669143 | |||||||
| chr16:15669159 | CA | C | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1723delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15669159 | ||||||
| chr16:15669196 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(128): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.237+1757A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669196 | |||||||
| chr16:15669255 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.237+1816A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669255 | |||||||
| chr16:15669306 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(128): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.237+1867G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669306 | |||||||
| chr16:15669360 | A | AT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0056 others(20): Show |
23 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.237+1941dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15669360 | ||||||
| chr16:15669679 | A | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.237+2240A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669679 | |||||||
| chr16:15669725 | G | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.237+2286G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669725 | |||||||
| chr16:15669781 | C | T | 1 | a0001c0001t0004g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237+2342C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15669781 | |||||||
| chr16:15670184 | A | G | 1 | a0001c0001t0033g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237+2745A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670184 | |||||||
| chr16:15670228 | T | G | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.237+2789T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670228 | |||||||
| chr16:15670386 | G | A | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+2947G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670386 | |||||||
| chr16:15670554 | G | A | 7 | a0001c0001t0002g0229 a0001c0001t0002g0240 a0001c0001t0002g0241 others(4): Show |
7 | HG00423.hp1 NA18960.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+3115G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670554 | |||||||
| chr16:15670657 | C | CA | 19 | a0001c0001t0002g0283 a0001c0001t0007g0347 a0001c0001t0007g0348 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+3233dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670657 | ||||||
| chr16:15670657 | CA | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(110): Show |
114 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.237+3233delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670657 | ||||||
| chr16:15670677 | GAAAA | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0288 others(17): Show |
20 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.237+3240_237+3243d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15670677 | ||||||
| chr16:15670940 | T | C | 5 | a0001c0002t0001g0159 a0001c0002t0001g0192 a0001c0002t0001g0193 others(2): Show |
5 | HG00738.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+3501T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15670940 | |||||||
| chr16:15671176 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0277 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.237+3737C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671176 | |||||||
| chr16:15671317 | A | G | 5 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(2): Show |
5 | HG02040.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+3878A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671317 | |||||||
| chr16:15671354 | T | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0062 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.237+3915T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671354 | |||||||
| chr16:15671513 | A | G | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.237+4074A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671513 | |||||||
| chr16:15671546 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(102): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.237+4107T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671546 | |||||||
| chr16:15671838 | C | T | 21 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(18): Show |
21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.237+4399C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671838 | |||||||
| chr16:15671889 | A | C | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237+4450A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15671889 | |||||||
| chr16:15672116 | T | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+4677T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672116 | |||||||
| chr16:15672123 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(125): Show |
129 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.237+4684G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672123 | |||||||
| chr16:15672200 | C | T | 6 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(3): Show |
6 | HG01433.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+4761C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672200 | |||||||
| chr16:15672254 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.237+4815G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672254 | |||||||
| chr16:15672262 | G | A | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+4823G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672262 | |||||||
| chr16:15672533 | G | T | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.237+5094G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672533 | |||||||
| chr16:15672607 | G | A | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.237+5168G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672607 | |||||||
| chr16:15672721 | G | A | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.238-5080G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672721 | |||||||
| chr16:15672746 | C | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0117 |
2 | HG00408.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.238-5055C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672746 | |||||||
| chr16:15672798 | T | C | 1 | a0001c0001t0003g0023 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.238-5003T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672798 | |||||||
| chr16:15672851 | C | T | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-4950C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672851 | |||||||
| chr16:15672969 | G | A | 25 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(22): Show |
25 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.238-4832G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15672969 | |||||||
| chr16:15673152 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0035 |
2 | HG00438.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.238-4649C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673152 | |||||||
| chr16:15673329 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.238-4472G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673329 | |||||||
| chr16:15673392 | C | T | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-4409C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673392 | |||||||
| chr16:15673451 | C | T | 2 | a0001c0001t0010g0311 a0001c0001t0010g0312 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.238-4350C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673451 | |||||||
| chr16:15673488 | C | T | 4 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(1): Show |
4 | HG02040.hp1 HG02818.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-4313C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673488 | |||||||
| chr16:15673547 | AT | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0068 a0001c0001t0001g0212 others(5): Show |
8 | HG01167.hp1 HG02273.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-4238delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15673547 | ||||||
| chr16:15673568 | G | A | 2 | a0001c0001t0013g0343 a0001c0001t0013g0345 |
2 | NA18952.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.238-4233G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673568 | |||||||
| chr16:15673680 | A | G | 8 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(5): Show |
8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-4121A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673680 | |||||||
| chr16:15673995 | A | G | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-3806A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15673995 | |||||||
| chr16:15674002 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.238-3799G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674002 | |||||||
| chr16:15674013 | T | G | 1 | a0001c0001t0002g0271 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.238-3788T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674013 | |||||||
| chr16:15674114 | G | A | 1 | a0001c0001t0033g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.238-3687G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674114 | |||||||
| chr16:15674140 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(227): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.238-3661G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674140 | |||||||
| chr16:15674192 | C | T | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.238-3609C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674192 | |||||||
| chr16:15674324 | AC | A | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3475delC | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15674324 | ||||||
| chr16:15674373 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(239): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.238-3428G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674373 | |||||||
| chr16:15674392 | G | A | 17 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0062 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.238-3409G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674392 | |||||||
| chr16:15674449 | A | G | 1 | a0001c0001t0008g0356 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.238-3352A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674449 | |||||||
| chr16:15674533 | G | A | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-3268G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674533 | |||||||
| chr16:15674564 | A | T | 5 | a0001c0001t0001g0308 a0001c0001t0003g0002 a0001c0001t0003g0127 others(2): Show |
6 | HG00642.hp1 HG02135.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-3237A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674564 | |||||||
| chr16:15674587 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238-3214C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674587 | |||||||
| chr16:15674616 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.238-3185G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674616 | |||||||
| chr16:15674658 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3143C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674658 | |||||||
| chr16:15674728 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.238-3073A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674728 | |||||||
| chr16:15674766 | C | T | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.238-3035C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674766 | |||||||
| chr16:15674771 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238-3030A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674771 | |||||||
| chr16:15674780 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.238-3021C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674780 | |||||||
| chr16:15674845 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238-2956C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674845 | |||||||
| chr16:15674853 | G | A | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-2948G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674853 | |||||||
| chr16:15674855 | C | T | 1 | a0001c0001t0003g0135 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.238-2946C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15674855 | |||||||
| chr16:15675077 | T | C | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-2724T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675077 | |||||||
| chr16:15675284 | C | T | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.238-2517C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675284 | |||||||
| chr16:15675303 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.238-2498A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675303 | |||||||
| chr16:15675352 | C | T | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-2449C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675352 | |||||||
| chr16:15675424 | G | GT | 15 | a0001c0001t0002g0239 a0001c0001t0002g0242 a0001c0001t0002g0260 others(12): Show |
15 | HG00099.hp2 HG00738.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.238-2362dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15675424 | ||||||
| chr16:15675424 | GT | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(201): Show |
206 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.238-2362delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15675424 | ||||||
| chr16:15675444 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.238-2357G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675444 | |||||||
| chr16:15675495 | G | A | 2 | a0001c0001t0005g0165 a0001c0001t0005g0166 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.238-2306G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675495 | |||||||
| chr16:15675508 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0092 |
3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.238-2293C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675508 | |||||||
| chr16:15675510 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(213): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.238-2291C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675510 | |||||||
| chr16:15675536 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.238-2265A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675536 | |||||||
| chr16:15675587 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.238-2214C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675587 | |||||||
| chr16:15675632 | T | G | 1 | a0001c0001t0002g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238-2169T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675632 | |||||||
| chr16:15675687 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238-2114A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675687 | |||||||
| chr16:15675818 | T | A | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-1983T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15675818 | |||||||
| chr16:15676024 | T | C | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1777T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676024 | |||||||
| chr16:15676035 | G | A | 20 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(17): Show |
20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.238-1766G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676035 | |||||||
| chr16:15676086 | CAT | C | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-1713_238-1712d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676086 | ||||||
| chr16:15676089 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.238-1712A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676089 | |||||||
| chr16:15676143 | TTCCTCTC | T | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-1648_238-1642d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676143 | ||||||
| chr16:15676225 | G | GT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(247): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.238-1559dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676225 | ||||||
| chr16:15676225 | G | GTT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0092 a0001c0001t0001g0329 others(6): Show |
9 | HG00642.hp1 HG01515.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-1560_238-1559d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15676225 | ||||||
| chr16:15676226 | T | G | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-1575T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676226 | |||||||
| chr16:15676295 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.238-1506C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676295 | |||||||
| chr16:15676336 | A | C | 2 | a0001c0001t0002g0334 a0001c0001t0002g0339 |
2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.238-1465A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676336 | |||||||
| chr16:15676559 | C | G | 1 | a0001c0001t0002g0276 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.238-1242C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676559 | |||||||
| chr16:15676748 | C | G | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.238-1053C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676748 | |||||||
| chr16:15676786 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(255): Show |
260 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.238-1015C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676786 | |||||||
| chr16:15676940 | G | A | 2 | a0001c0001t0025g0310 a0001c0001t0026g0018 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.238-861G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676940 | |||||||
| chr16:15676957 | G | T | 12 | a0001c0001t0002g0223 a0001c0001t0002g0228 a0001c0001t0002g0231 others(9): Show |
12 | HG03834.hp2 NA18950.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-844G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676957 | |||||||
| chr16:15676998 | G | A | 1 | a0001c0001t0015g0017 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.238-803G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15676998 | |||||||
| chr16:15677001 | T | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-800T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677001 | |||||||
| chr16:15677107 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238-694G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677107 | |||||||
| chr16:15677246 | G | A | 3 | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0003g0143 |
3 | HG01106.hp2 HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.238-555G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677246 | |||||||
| chr16:15677288 | A | G | 1 | a0001c0001t0007g0361 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238-513A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677288 | |||||||
| chr16:15677349 | C | T | 3 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.238-452C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677349 | |||||||
| chr16:15677401 | C | T | 3 | a0001c0001t0013g0343 a0001c0001t0013g0344 a0001c0001t0013g0345 |
3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.238-400C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677401 | |||||||
| chr16:15677422 | C | T | 1 | a0001c0001t0030g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238-379C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677422 | |||||||
| chr16:15677538 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.238-263A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677538 | |||||||
| chr16:15677590 | G | GA | 8 | a0001c0001t0001g0083 a0001c0001t0001g0292 a0001c0001t0002g0274 others(5): Show |
8 | HG02135.hp2 HG02280.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-198dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 15677590 | ||||||
| chr16:15677741 | C | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.238-60C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677741 | |||||||
| chr16:15677744 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.238-57T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677744 | |||||||
| chr16:15677762 | G | A | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-39G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 3/8 | chr16 | 15677762 | |||||||
| chr16:15677990 | C | G | 64 | a0001c0001t0001g0308 a0001c0001t0002g0019 a0001c0001t0002g0103 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.386+41C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15677990 | |||||||
| chr16:15678074 | C | A | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+125C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678074 | |||||||
| chr16:15678094 | G | A | 64 | a0001c0001t0001g0308 a0001c0001t0002g0019 a0001c0001t0002g0103 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.386+145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678094 | |||||||
| chr16:15678101 | A | T | 1 | a0001c0001t0002g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.386+152A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678101 | |||||||
| chr16:15678290 | T | C | 1 | a0001c0001t0002g0314 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.386+341T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678290 | |||||||
| chr16:15678422 | T | C | 1 | a0001c0001t0008g0356 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.386+473T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678422 | |||||||
| chr16:15678467 | C | T | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.386+518C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678467 | |||||||
| chr16:15678555 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.386+606G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678555 | |||||||
| chr16:15678595 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0306 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.386+646G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678595 | |||||||
| chr16:15678632 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+683C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678632 | |||||||
| chr16:15678852 | G | A | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386+903G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678852 | |||||||
| chr16:15678906 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.386+957C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678906 | |||||||
| chr16:15678985 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.386+1036A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15678985 | |||||||
| chr16:15679008 | C | T | 2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.386+1059C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679008 | |||||||
| chr16:15679009 | G | A | 65 | a0001c0001t0001g0308 a0001c0001t0002g0019 a0001c0001t0002g0103 others(62): Show |
66 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.386+1060G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679009 | |||||||
| chr16:15679348 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0285 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.386+1399C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679348 | |||||||
| chr16:15679354 | C | G | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.386+1405C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679354 | |||||||
| chr16:15679529 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.386+1580T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679529 | |||||||
| chr16:15679628 | G | A | 21 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(18): Show |
21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+1679G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679628 | |||||||
| chr16:15679756 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386+1807T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679756 | |||||||
| chr16:15679775 | GTTT | G | 4 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+1830_386+1832d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15679775 | ||||||
| chr16:15679782 | G | GTT | 21 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(18): Show |
21 | HG01109.hp2 HG01891.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.386+1837_386+1838d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15679782 | ||||||
| chr16:15679902 | C | T | 5 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(2): Show |
5 | HG01496.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+1953C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679902 | |||||||
| chr16:15679903 | G | A | 1 | a0001c0001t0002g0338 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.386+1954G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15679903 | |||||||
| chr16:15680030 | C | T | 4 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 others(1): Show |
4 | HG02040.hp1 HG02818.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+2081C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680030 | |||||||
| chr16:15680294 | G | A | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2345G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680294 | |||||||
| chr16:15680456 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.386+2507C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680456 | |||||||
| chr16:15680564 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.386+2615C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680564 | |||||||
| chr16:15680568 | C | T | 30 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(27): Show |
30 | HG01261.hp2 HG01496.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.386+2619C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680568 | |||||||
| chr16:15680820 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.386+2871G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680820 | |||||||
| chr16:15680922 | A | G | 42 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(39): Show |
42 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.386+2973A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680922 | |||||||
| chr16:15680925 | G | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(102): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.386+2976G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15680925 | |||||||
| chr16:15681174 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.386+3225A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681174 | |||||||
| chr16:15681195 | T | G | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+3246T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681195 | |||||||
| chr16:15681224 | C | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18980.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.386+3275C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681224 | |||||||
| chr16:15681253 | C | CT | 35 | a0001c0001t0001g0256 a0001c0001t0002g0218 a0001c0001t0002g0222 others(32): Show |
35 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.386+3334dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTT | 11 | a0001c0001t0004g0163 a0001c0001t0004g0167 a0001c0001t0004g0169 others(8): Show |
11 | HG01261.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.386+3333_386+3334d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTT | 7 | a0001c0001t0004g0104 a0001c0001t0004g0168 a0001c0001t0004g0182 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+3332_386+3334d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTT | 15 | a0001c0001t0001g0346 a0001c0001t0004g0172 a0001c0001t0004g0187 others(12): Show |
15 | HG00140.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.386+3331_386+3334d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(21): Show |
25 | HG00609.hp2 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.386+3330_386+3334d others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTT | 48 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0051 others(45): Show |
49 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.386+3329_386+3334d others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT | 44 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(41): Show |
44 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.386+3328_386+3334d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(1): Show |
40 | a0001c0001t0001g0033 a0001c0001t0001g0090 a0001c0001t0001g0091 others(37): Show |
40 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.386+3327_386+3334d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0073 others(23): Show |
26 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+3326_386+3334d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(3): Show |
26 | a0001c0001t0001g0039 a0001c0001t0001g0070 a0001c0001t0001g0098 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.386+3325_386+3334d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0288 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+3324_386+3334d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+3323_386+3334d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0009g0152 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.386+3322_386+3334d others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681253 | CT | C | 9 | a0001c0001t0002g0099 a0001c0001t0002g0225 a0001c0001t0002g0242 others(6): Show |
9 | HG01891.hp1 HG02040.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+3334delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15681253 | ||||||
| chr16:15681302 | A | G | 13 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(10): Show |
13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+3353A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681302 | |||||||
| chr16:15681322 | A | G | 31 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(28): Show |
31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.386+3373A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681322 | |||||||
| chr16:15681436 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386+3487T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681436 | |||||||
| chr16:15681611 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+3662C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681611 | |||||||
| chr16:15681735 | C | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386+3786C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681735 | |||||||
| chr16:15681781 | C | T | 2 | a0001c0001t0017g0043 a0001c0001t0017g0044 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.386+3832C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15681781 | |||||||
| chr16:15682132 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.386+4183G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682132 | |||||||
| chr16:15682133 | G | A | 21 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(18): Show |
21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+4184G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682133 | |||||||
| chr16:15682230 | C | T | 35 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(32): Show |
35 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.386+4281C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682230 | |||||||
| chr16:15682507 | C | T | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.386+4558C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682507 | |||||||
| chr16:15682655 | G | A | 1 | a0001c0001t0024g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.386+4706G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682655 | |||||||
| chr16:15682658 | A | G | 21 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(18): Show |
21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.386+4709A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682658 | |||||||
| chr16:15682879 | T | C | 8 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(5): Show |
8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-4496T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15682879 | |||||||
| chr16:15683046 | A | G | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.387-4329A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683046 | |||||||
| chr16:15683053 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(205): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.387-4322C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683053 | |||||||
| chr16:15683281 | T | C | 1 | a0001c0001t0028g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.387-4094T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683281 | |||||||
| chr16:15683343 | G | GT | 7 | a0001c0001t0001g0014 a0001c0001t0002g0254 a0001c0001t0002g0260 others(4): Show |
7 | HG00558.hp1 HG00597.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-4024dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15683343 | ||||||
| chr16:15683400 | T | C | 1 | a0001c0001t0014g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.387-3975T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683400 | |||||||
| chr16:15683408 | A | G | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-3967A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683408 | |||||||
| chr16:15683635 | G | A | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387-3740G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683635 | |||||||
| chr16:15683888 | A | G | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387-3487A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683888 | |||||||
| chr16:15683900 | G | C | 2 | a0001c0001t0005g0165 a0001c0001t0005g0166 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.387-3475G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683900 | |||||||
| chr16:15683919 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(205): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.387-3456C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15683919 | |||||||
| chr16:15684023 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.387-3352G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684023 | |||||||
| chr16:15684129 | A | T | 1 | a0001c0001t0003g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.387-3246A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684129 | |||||||
| chr16:15684463 | C | T | 1 | a0001c0001t0031g0047 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.387-2912C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684463 | |||||||
| chr16:15684529 | G | T | 2 | a0001c0001t0006g0157 a0001c0001t0006g0158 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.387-2846G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684529 | |||||||
| chr16:15684556 | G | C | 1 | a0001c0001t0002g0336 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.387-2819G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15684556 | |||||||
| chr16:15684568 | T | TA | 35 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0075 others(32): Show |
35 | HG00408.hp2 HG00639.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.387-2789dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15684568 | ||||||
| chr16:15684568 | TA | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0002g0106 others(7): Show |
10 | HG01256.hp2 HG02897.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-2789delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15684568 | ||||||
| chr16:15685232 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.387-2143C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685232 | |||||||
| chr16:15685350 | G | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.387-2025G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685350 | |||||||
| chr16:15685379 | G | A | 1 | a0001c0001t0002g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387-1996G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685379 | |||||||
| chr16:15685411 | C | T | 9 | a0001c0001t0002g0274 a0001c0001t0005g0176 a0001c0001t0005g0177 others(6): Show |
9 | NA18973.hp2 NA18991.hp2 NA18995.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-1964C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685411 | |||||||
| chr16:15685412 | G | A | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387-1963G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685412 | |||||||
| chr16:15685469 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.387-1906T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685469 | |||||||
| chr16:15685482 | C | T | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.387-1893C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685482 | |||||||
| chr16:15685582 | T | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0040 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.387-1793T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685582 | |||||||
| chr16:15685634 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1741C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685634 | |||||||
| chr16:15685712 | T | C | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1663T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15685712 | |||||||
| chr16:15685953 | A | AT | 10 | a0001c0001t0001g0028 a0001c0001t0002g0264 a0001c0001t0002g0266 others(7): Show |
10 | HG00621.hp2 HG01496.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-1406dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15685953 | ||||||
| chr16:15686032 | A | G | 1 | a0001c0001t0003g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.387-1343A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686032 | |||||||
| chr16:15686054 | C | T | 8 | a0001c0001t0002g0227 a0001c0001t0002g0230 a0001c0001t0002g0233 others(5): Show |
8 | NA18940.hp1 NA18946.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-1321C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686054 | |||||||
| chr16:15686241 | C | T | 1 | a0001c0001t0030g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.387-1134C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686241 | |||||||
| chr16:15686366 | T | TTATAACA others(6062): Show |
1 | a0001c0001t0001g0341 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.387-990_387-989ins others(6069): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15686366 | ||||||
| chr16:15686366 | T | TTATAACA others(6064): Show |
1 | a0001c0001t0001g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.387-990_387-989ins others(6071): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 15686366 | ||||||
| chr16:15686459 | C | A | 4 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-916C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686459 | |||||||
| chr16:15686510 | C | T | 56 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(53): Show |
56 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.387-865C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686510 | |||||||
| chr16:15686553 | C | G | 1 | a0001c0001t0002g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.387-822C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686553 | |||||||
| chr16:15686644 | C | G | 21 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(18): Show |
21 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.387-731C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686644 | |||||||
| chr16:15686841 | A | G | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-534A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686841 | |||||||
| chr16:15686875 | G | C | 1 | a0001c0001t0003g0148 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.387-500G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15686875 | |||||||
| chr16:15687091 | T | G | 1 | a0001c0001t0008g0354 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.387-284T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687091 | |||||||
| chr16:15687197 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.387-178A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687197 | |||||||
| chr16:15687231 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.387-144C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687231 | |||||||
| chr16:15687235 | G | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0200 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.387-140G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687235 | |||||||
| chr16:15687335 | G | C | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-40G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 4/8 | chr16 | 15687335 | |||||||
| chr16:15687612 | A | C | 1 | a0001c0001t0001g0341 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.523+101A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15687612 | |||||||
| chr16:15687647 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.523+136G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15687647 | |||||||
| chr16:15688088 | A | G | 5 | a0001c0001t0002g0229 a0001c0001t0002g0240 a0001c0001t0002g0243 others(2): Show |
5 | HG00423.hp1 NA18975.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+577A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688088 | |||||||
| chr16:15688540 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.523+1029C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688540 | |||||||
| chr16:15688633 | C | CA | 44 | a0001c0001t0001g0045 a0001c0001t0001g0063 a0001c0001t0001g0072 others(41): Show |
44 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.523+1142dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688633 | ||||||
| chr16:15688633 | CA | C | 17 | a0001c0001t0001g0039 a0001c0001t0001g0201 a0001c0001t0002g0041 others(14): Show |
17 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.523+1142delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688633 | ||||||
| chr16:15688689 | C | CT | 35 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0090 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.523+1205dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTT | 6 | a0001c0001t0001g0031 a0001c0001t0002g0226 a0001c0001t0002g0251 others(3): Show |
6 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+1204_523+1205d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTT | 42 | a0001c0001t0002g0111 a0001c0001t0003g0002 a0001c0001t0003g0009 others(39): Show |
43 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.523+1203_523+1205d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTT | 38 | a0001c0001t0001g0305 a0001c0001t0001g0308 a0001c0001t0001g0346 others(35): Show |
38 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.523+1202_523+1205d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0287 others(14): Show |
17 | HG01109.hp2 HG01516.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.523+1201_523+1205d others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTT | 25 | a0001c0001t0001g0060 a0001c0001t0001g0195 a0001c0001t0001g0196 others(22): Show |
25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+1200_523+1205d others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT | 35 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0035 others(32): Show |
35 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.523+1199_523+1205d others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT others(1): Show |
29 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0045 others(26): Show |
29 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.523+1198_523+1205d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT others(2): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0054 others(20): Show |
24 | HG00609.hp2 HG00733.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.523+1197_523+1205d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT others(3): Show |
10 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0071 others(7): Show |
10 | HG00642.hp2 HG01358.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.523+1196_523+1205d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0213 |
2 | HG00741.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.523+1195_523+1205d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0039 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.523+1194_523+1205d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | CT | C | 9 | a0001c0001t0001g0154 a0001c0001t0002g0013 a0001c0001t0002g0106 others(6): Show |
9 | HG02040.hp1 HG02155.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.523+1205delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | CTTTTTTT others(2): Show |
C | 20 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(17): Show |
20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.523+1197_523+1205d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688689 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.523+1196_523+1205d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688689 | ||||||
| chr16:15688843 | G | A | 1 | a0001c0001t0014g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.523+1332G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688843 | |||||||
| chr16:15688885 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(207): Show |
212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.523+1374A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688885 | |||||||
| chr16:15688920 | ACTC | A | 28 | a0001c0001t0002g0106 a0001c0001t0002g0223 a0001c0001t0002g0227 others(25): Show |
28 | HG00438.hp2 HG00621.hp2 HG03834.hp2 others(25): Show |
intron_variant | MODIFIER | c.523+1412_523+1414d others(5): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15688920 | ||||||
| chr16:15688935 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(207): Show |
212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.523+1424C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15688935 | |||||||
| chr16:15689288 | A | G | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523+1777A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689288 | |||||||
| chr16:15689446 | T | A | 1 | a0001c0001t0016g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.524-1698T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689446 | |||||||
| chr16:15689454 | C | T | 3 | a0001c0001t0006g0324 a0001c0001t0006g0325 a0001c0001t0006g0327 |
3 | HG00140.hp2 HG01074.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.524-1690C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689454 | |||||||
| chr16:15689524 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.524-1620G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689524 | |||||||
| chr16:15689617 | C | A | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.524-1527C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689617 | |||||||
| chr16:15689807 | G | A | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.524-1337G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689807 | |||||||
| chr16:15689875 | T | TG | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.524-1269_524-1268i others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689875 | |||||||
| chr16:15689887 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.524-1257C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689887 | |||||||
| chr16:15689936 | CT | C | 28 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(25): Show |
28 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.524-1207delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689936 | |||||||
| chr16:15689937 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0120 a0001c0001t0003g0110 others(1): Show |
4 | HG03209.hp2 NA18522.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1207T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689937 | |||||||
| chr16:15689938 | CA | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(208): Show |
213 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.524-1185delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15689938 | ||||||
| chr16:15689938 | CAA | C | 12 | a0001c0001t0001g0155 a0001c0001t0002g0120 a0001c0001t0003g0110 others(9): Show |
12 | HG01496.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.524-1186_524-1185d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15689938 | ||||||
| chr16:15689939 | A | C | 28 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0111 others(25): Show |
28 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.524-1205A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15689939 | |||||||
| chr16:15690035 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1109C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690035 | |||||||
| chr16:15690068 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.524-1076T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690068 | |||||||
| chr16:15690133 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(207): Show |
212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.524-1011C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690133 | |||||||
| chr16:15690185 | C | T | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-959C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690185 | |||||||
| chr16:15690190 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-954G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690190 | |||||||
| chr16:15690191 | C | G | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-953C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690191 | |||||||
| chr16:15690200 | A | G | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-944A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690200 | |||||||
| chr16:15690201 | C | A | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-943C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690201 | |||||||
| chr16:15690202 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-942G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690202 | |||||||
| chr16:15690235 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.524-909G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690235 | |||||||
| chr16:15690336 | C | CCTTTTTT others(8): Show |
3 | a0001c0001t0007g0359 a0001c0001t0014g0160 a0001c0001t0014g0161 |
3 | HG02970.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.524-807_524-793dup others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690336 | ||||||
| chr16:15690337 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0007g0351 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.524-793_524-792ins others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690337 | ||||||
| chr16:15690337 | CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0002g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.524-791_524-764del others(28): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690337 | ||||||
| chr16:15690338 | T | TTTTTTTT others(7): Show |
3 | a0001c0001t0007g0350 a0001c0001t0007g0352 a0001c0001t0007g0361 |
3 | HG01109.hp2 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.524-793_524-792ins others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690338 | ||||||
| chr16:15690339 | T | TTTTTTTT others(6): Show |
5 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-793_524-792ins others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690339 | ||||||
| chr16:15690340 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0006g0323 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.524-794_524-793ins others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690340 | ||||||
| chr16:15690340 | TTTTTTTT others(6): Show |
T | 14 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(11): Show |
14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-791_524-779del others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690340 | ||||||
| chr16:15690341 | T | TTTTTTTT others(3): Show |
2 | a0001c0001t0006g0322 a0001c0001t0006g0325 |
2 | HG01074.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.524-794_524-793ins others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690341 | ||||||
| chr16:15690342 | TTTTTTTT others(4): Show |
T | 2 | a0001c0001t0004g0170 a0001c0001t0004g0174 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.524-791_524-781del others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690342 | ||||||
| chr16:15690343 | TTTTTTTT others(3): Show |
T | 18 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(15): Show |
18 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.524-791_524-782del others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690343 | ||||||
| chr16:15690344 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.524-800T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690344 | |||||||
| chr16:15690353 | C | CT | 81 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.524-763dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | ||||||
| chr16:15690353 | C | CTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
24 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.524-764_524-763dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | ||||||
| chr16:15690353 | C | CTTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0086 others(3): Show |
6 | HG00609.hp2 HG00735.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-765_524-763dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | ||||||
| chr16:15690353 | C | T | 33 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0155 others(30): Show |
33 | HG00140.hp2 HG00597.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.524-791C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690353 | |||||||
| chr16:15690353 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0030g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.524-774_524-763del others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | ||||||
| chr16:15690353 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0005g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.524-775_524-763del others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690353 | ||||||
| chr16:15690354 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690354 | |||||||
| chr16:15690355 | T | C | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.524-789T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690355 | |||||||
| chr16:15690356 | T | C | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-788T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690356 | |||||||
| chr16:15690357 | T | TC | 80 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0287 others(77): Show |
81 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.524-787_524-786ins others(1): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690357 | |||||||
| chr16:15690358 | T | C | 1 | a0001c0001t0028g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524-786T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690358 | |||||||
| chr16:15690359 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-785T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690359 | |||||||
| chr16:15690360 | T | C | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-784T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690360 | |||||||
| chr16:15690362 | T | C | 18 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(15): Show |
18 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.524-782T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690362 | |||||||
| chr16:15690363 | T | C | 2 | a0001c0001t0004g0170 a0001c0001t0004g0174 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.524-781T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690363 | |||||||
| chr16:15690365 | T | C | 14 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(11): Show |
14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-779T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690365 | |||||||
| chr16:15690433 | C | CTG | 3 | a0001c0001t0002g0099 a0001c0001t0002g0277 a0001c0001t0002g0284 |
3 | HG03942.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.524-710_524-709dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 15690433 | ||||||
| chr16:15690446 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.524-698T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690446 | |||||||
| chr16:15690505 | G | A | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.524-639G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690505 | |||||||
| chr16:15690518 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.524-626C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690518 | |||||||
| chr16:15690526 | T | A | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-618T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690526 | |||||||
| chr16:15690617 | A | C | 1 | a0001c0001t0003g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.524-527A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690617 | |||||||
| chr16:15690672 | A | G | 64 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(61): Show |
64 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.524-472A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690672 | |||||||
| chr16:15690829 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0040 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.524-315C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15690829 | |||||||
| chr16:15691046 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0288 others(18): Show |
21 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.524-98G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691046 | |||||||
| chr16:15691099 | C | T | 3 | a0001c0001t0013g0343 a0001c0001t0013g0344 a0001c0001t0013g0345 |
3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.524-45C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691099 | |||||||
| chr16:15691100 | G | A | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-44G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 5/8 | chr16 | 15691100 | |||||||
| chr16:15691348 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.703+25T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691348 | |||||||
| chr16:15691504 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+181T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691504 | |||||||
| chr16:15691647 | G | GT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(213): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.703+335dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | ||||||
| chr16:15691647 | G | GTT | 30 | a0001c0001t0001g0090 a0001c0001t0003g0138 a0001c0001t0004g0104 others(27): Show |
30 | HG00423.hp2 HG01106.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.703+334_703+335dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | ||||||
| chr16:15691647 | G | GTTT | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+333_703+335dup others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15691647 | ||||||
| chr16:15691787 | C | T | 17 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0062 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.703+464C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691787 | |||||||
| chr16:15691818 | A | G | 13 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(10): Show |
13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.703+495A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691818 | |||||||
| chr16:15691889 | C | A | 1 | a0001c0001t0007g0360 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+566C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691889 | |||||||
| chr16:15691892 | A | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(125): Show |
129 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.703+569A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691892 | |||||||
| chr16:15691922 | C | T | 1 | a0001c0001t0007g0361 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+599C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15691922 | |||||||
| chr16:15692031 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+708C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692031 | |||||||
| chr16:15692032 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.703+709G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692032 | |||||||
| chr16:15692047 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0040 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.703+724C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692047 | |||||||
| chr16:15692204 | C | A | 1 | a0001c0001t0007g0361 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+881C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692204 | |||||||
| chr16:15692441 | G | T | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703+1118G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692441 | |||||||
| chr16:15692517 | C | G | 4 | a0001c0001t0002g0245 a0001c0001t0002g0257 a0001c0001t0002g0258 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+1194C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692517 | |||||||
| chr16:15692554 | G | A | 1 | a0001c0001t0021g0015 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+1231G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692554 | |||||||
| chr16:15692611 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.703+1288T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692611 | |||||||
| chr16:15692862 | G | C | 64 | a0001c0001t0001g0308 a0001c0001t0002g0019 a0001c0001t0002g0103 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.704-1303G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692862 | |||||||
| chr16:15692939 | G | A | 12 | a0001c0001t0002g0219 a0001c0001t0002g0269 a0001c0001t0002g0313 others(9): Show |
12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-1226G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15692939 | |||||||
| chr16:15693003 | C | CT | 18 | a0001c0001t0002g0229 a0001c0001t0002g0240 a0001c0001t0002g0241 others(15): Show |
18 | HG00423.hp1 HG01074.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.704-1147dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 15693003 | ||||||
| chr16:15693127 | G | A | 3 | a0001c0001t0002g0260 a0001c0001t0002g0268 a0001c0001t0002g0278 |
3 | HG02083.hp2 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.704-1038G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693127 | |||||||
| chr16:15693134 | T | A | 1 | a0001c0001t0024g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704-1031T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693134 | |||||||
| chr16:15693180 | T | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(190): Show |
195 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.704-985T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693180 | |||||||
| chr16:15693256 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.704-909C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693256 | |||||||
| chr16:15693302 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.704-863G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693302 | |||||||
| chr16:15693617 | A | G | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-548A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693617 | |||||||
| chr16:15693677 | C | T | 3 | a0001c0001t0007g0358 a0001c0001t0007g0359 a0001c0001t0007g0360 |
3 | HG02622.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.704-488C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693677 | |||||||
| chr16:15693678 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0105 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.704-487G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693678 | |||||||
| chr16:15693738 | G | A | 1 | a0001c0001t0024g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704-427G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693738 | |||||||
| chr16:15693762 | G | A | 19 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.704-403G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693762 | |||||||
| chr16:15693854 | C | T | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.704-311C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693854 | |||||||
| chr16:15693994 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.704-171C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15693994 | |||||||
| chr16:15694084 | G | A | 1 | a0001c0001t0009g0102 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.704-81G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 6/8 | chr16 | 15694084 | |||||||
| chr16:15694369 | A | C | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+113A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694369 | |||||||
| chr16:15694623 | C | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.795+367C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694623 | |||||||
| chr16:15694838 | G | C | 37 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(34): Show |
37 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.795+582G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694838 | |||||||
| chr16:15694980 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(124): Show |
128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.795+724G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15694980 | |||||||
| chr16:15695078 | G | A | 19 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.795+822G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695078 | |||||||
| chr16:15695173 | C | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.795+917C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695173 | |||||||
| chr16:15695203 | C | CT | 24 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0045 others(21): Show |
24 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.795+971dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | C | CTT | 10 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0006g0322 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+970_795+971dup others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+963_795+971dup others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0007g0350 a0001c0001t0007g0358 a0001c0001t0007g0359 others(2): Show |
5 | HG01109.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.795+962_795+971dup others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0007g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795+961_795+971dup others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | CT | C | 70 | a0001c0001t0001g0027 a0001c0001t0001g0346 a0001c0001t0002g0019 others(67): Show |
70 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.795+971delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | CTT | C | 7 | a0001c0001t0003g0002 a0001c0001t0003g0127 a0001c0001t0003g0140 others(4): Show |
8 | HG00544.hp1 HG00642.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+970_795+971del others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0015g0017 a0001c0001t0021g0015 |
2 | HG02040.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.795+962_795+971del others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695203 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0015g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.795+961_795+971del others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695203 | ||||||
| chr16:15695263 | T | G | 1 | a0001c0001t0003g0122 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.795+1007T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695263 | |||||||
| chr16:15695274 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.795+1018G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695274 | |||||||
| chr16:15695432 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+1176C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695432 | |||||||
| chr16:15695433 | G | C | 63 | a0001c0001t0002g0019 a0001c0001t0002g0103 a0001c0001t0002g0105 others(60): Show |
64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.795+1177G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695433 | |||||||
| chr16:15695495 | C | CA | 10 | a0001c0001t0002g0233 a0001c0001t0002g0236 a0001c0001t0002g0237 others(7): Show |
10 | HG01255.hp2 HG03942.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.796-1194dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | ||||||
| chr16:15695495 | CA | C | 72 | a0001c0001t0001g0095 a0001c0001t0001g0346 a0001c0001t0002g0013 others(69): Show |
72 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.796-1194delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | ||||||
| chr16:15695495 | CAA | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(183): Show |
188 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.796-1195_796-1194d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15695495 | ||||||
| chr16:15695626 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0289 others(8): Show |
11 | HG00639.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-1083A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695626 | |||||||
| chr16:15695855 | A | G | 1 | a0001c0001t0002g0337 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.796-854A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695855 | |||||||
| chr16:15695891 | T | G | 63 | a0001c0001t0002g0019 a0001c0001t0002g0103 a0001c0001t0002g0105 others(60): Show |
64 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.796-818T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695891 | |||||||
| chr16:15695950 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.796-759G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15695950 | |||||||
| chr16:15696027 | AT | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.796-676delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696027 | ||||||
| chr16:15696048 | AT | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0022 others(173): Show |
177 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.796-645delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696048 | ||||||
| chr16:15696048 | ATT | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0062 others(22): Show |
25 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.796-646_796-645del others(2): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696048 | ||||||
| chr16:15696121 | T | TGCTTGAG others(7): Show |
267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.796-587_796-586ins others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696121 | ||||||
| chr16:15696152 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.796-557T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696152 | |||||||
| chr16:15696174 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.796-535T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696174 | |||||||
| chr16:15696192 | TAAAA | T | 13 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(10): Show |
13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.796-512_796-509del others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696192 | ||||||
| chr16:15696252 | A | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0288 others(17): Show |
20 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.796-457A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696252 | |||||||
| chr16:15696289 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0092 |
3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.796-420T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696289 | |||||||
| chr16:15696386 | C | CA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(100): Show |
104 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.796-312dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 15696386 | ||||||
| chr16:15696390 | A | AC | 23 | a0001c0001t0001g0014 a0001c0001t0001g0197 a0001c0001t0001g0286 others(20): Show |
23 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.796-319_796-318ins others(1): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696390 | |||||||
| chr16:15696391 | A | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0040 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.796-318A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696391 | |||||||
| chr16:15696471 | C | T | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.796-238C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696471 | |||||||
| chr16:15696602 | C | T | 1 | a0001c0001t0002g0337 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.796-107C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696602 | |||||||
| chr16:15696632 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-77G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696632 | |||||||
| chr16:15696686 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18980.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.796-23G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 7/8 | chr16 | 15696686 | |||||||
| chr16:15697105 | A | G | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+245A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697105 | |||||||
| chr16:15697134 | C | G | 1 | a0001c0001t0002g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.947+274C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697134 | |||||||
| chr16:15697189 | C | T | 3 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.947+329C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697189 | |||||||
| chr16:15697280 | T | C | 52 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(49): Show |
52 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.947+420T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697280 | |||||||
| chr16:15697312 | C | T | 1 | a0001c0002t0001g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.947+452C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697312 | |||||||
| chr16:15697380 | A | G | 1 | a0001c0001t0005g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.947+520A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697380 | |||||||
| chr16:15697386 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.947+526G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697386 | |||||||
| chr16:15697442 | C | T | 1 | a0001c0001t0002g0342 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.947+582C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697442 | |||||||
| chr16:15697451 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0298 a0001c0001t0025g0310 |
3 | HG02055.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.947+591G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697451 | |||||||
| chr16:15697504 | T | C | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.947+644T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697504 | |||||||
| chr16:15697706 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0072 others(1): Show |
4 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+846C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697706 | |||||||
| chr16:15697710 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0298 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.947+850A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697710 | |||||||
| chr16:15697743 | A | G | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.947+883A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697743 | |||||||
| chr16:15697767 | C | T | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+907C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697767 | |||||||
| chr16:15697795 | GT | G | 6 | a0001c0001t0004g0104 a0001c0001t0004g0168 a0001c0001t0004g0171 others(3): Show |
6 | HG01261.hp2 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+946delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15697795 | ||||||
| chr16:15697802 | T | G | 9 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(6): Show |
9 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+942T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697802 | |||||||
| chr16:15697881 | A | G | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+1021A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697881 | |||||||
| chr16:15697904 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+1044C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15697904 | |||||||
| chr16:15698030 | G | A | 38 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(35): Show |
38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+1170G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698030 | |||||||
| chr16:15698121 | C | G | 6 | a0001c0001t0001g0292 a0001c0001t0006g0108 a0001c0001t0006g0156 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+1261C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698121 | |||||||
| chr16:15698198 | G | A | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+1338G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698198 | |||||||
| chr16:15698247 | CAG | C | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+1388_947+1389d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698247 | |||||||
| chr16:15698307 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+1447G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698307 | |||||||
| chr16:15698376 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.947+1516T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698376 | |||||||
| chr16:15698534 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.947+1674A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698534 | |||||||
| chr16:15698677 | A | G | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+1817A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698677 | |||||||
| chr16:15698729 | C | T | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.947+1869C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698729 | |||||||
| chr16:15698779 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.947+1919T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698779 | |||||||
| chr16:15698784 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.947+1924C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698784 | |||||||
| chr16:15698863 | GA | G | 7 | a0001c0001t0003g0307 a0001c0001t0006g0322 a0001c0001t0006g0323 others(4): Show |
7 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.947+2016delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15698863 | ||||||
| chr16:15698878 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0201 |
2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.947+2018T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698878 | |||||||
| chr16:15698880 | AT | A | 38 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(35): Show |
38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+2025delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15698880 | ||||||
| chr16:15698915 | T | C | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2055T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15698915 | |||||||
| chr16:15699067 | A | T | 3 | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0003g0143 |
3 | HG01106.hp2 HG01167.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.947+2207A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699067 | |||||||
| chr16:15699235 | G | C | 52 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(49): Show |
52 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.947+2375G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699235 | |||||||
| chr16:15699263 | C | CT | 6 | a0001c0001t0001g0302 a0001c0001t0003g0024 a0001c0001t0011g0004 others(3): Show |
6 | HG01496.hp2 HG02056.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+2416dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | ||||||
| chr16:15699263 | C | CTT | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2415_947+2416d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | ||||||
| chr16:15699263 | CT | C | 51 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(48): Show |
51 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.947+2416delT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699263 | ||||||
| chr16:15699294 | C | G | 4 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+2434C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699294 | |||||||
| chr16:15699309 | G | A | 13 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(10): Show |
13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.947+2449G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699309 | |||||||
| chr16:15699316 | G | A | 1 | a0001c0001t0015g0017 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.947+2456G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699316 | |||||||
| chr16:15699363 | G | A | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+2503G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699363 | |||||||
| chr16:15699432 | G | T | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947+2572G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699432 | |||||||
| chr16:15699480 | AAAAC | A | 32 | a0001c0001t0002g0019 a0001c0001t0002g0103 a0001c0001t0002g0105 others(29): Show |
32 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.947+2631_947+2634d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15699480 | ||||||
| chr16:15699650 | T | C | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+2790T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699650 | |||||||
| chr16:15699653 | T | C | 1 | a0001c0001t0013g0343 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.947+2793T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699653 | |||||||
| chr16:15699697 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.947+2837T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699697 | |||||||
| chr16:15699758 | C | T | 38 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(35): Show |
38 | HG01109.hp2 HG01261.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.947+2898C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699758 | |||||||
| chr16:15699780 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.947+2920G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699780 | |||||||
| chr16:15699782 | C | T | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+2922C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699782 | |||||||
| chr16:15699938 | G | A | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+3078G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699938 | |||||||
| chr16:15699970 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.947+3110G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15699970 | |||||||
| chr16:15700012 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.947+3152C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700012 | |||||||
| chr16:15700017 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+3157C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700017 | |||||||
| chr16:15700088 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.947+3228C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700088 | |||||||
| chr16:15700157 | C | T | 1 | a0001c0001t0006g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.947+3297C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700157 | |||||||
| chr16:15700398 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0212 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.947+3538C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700398 | |||||||
| chr16:15700437 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.947+3577G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700437 | |||||||
| chr16:15700440 | C | CT | 43 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(40): Show |
43 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.947+3594dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15700440 | ||||||
| chr16:15700440 | C | CTT | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+3593_947+3594d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15700440 | ||||||
| chr16:15700528 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(228): Show |
233 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.947+3668C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700528 | |||||||
| chr16:15700578 | A | G | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+3718A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700578 | |||||||
| chr16:15700588 | A | G | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+3728A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700588 | |||||||
| chr16:15700671 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.947+3811G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700671 | |||||||
| chr16:15700697 | C | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+3837C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700697 | |||||||
| chr16:15700740 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.947+3880C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700740 | |||||||
| chr16:15700963 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0341 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.947+4103C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15700963 | |||||||
| chr16:15701191 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(267): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.947+4331T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701191 | |||||||
| chr16:15701200 | G | C | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.947+4340G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701200 | |||||||
| chr16:15701218 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.947+4358C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701218 | |||||||
| chr16:15701237 | CA | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(235): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.947+4392delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15701237 | ||||||
| chr16:15701256 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+4396G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701256 | |||||||
| chr16:15701316 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+4456C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701316 | |||||||
| chr16:15701388 | C | T | 1 | a0001c0001t0003g0023 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.947+4528C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701388 | |||||||
| chr16:15701407 | G | T | 1 | a0001c0001t0015g0017 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.947+4547G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701407 | |||||||
| chr16:15701598 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.947+4738G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701598 | |||||||
| chr16:15701615 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(260): Show |
265 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.947+4755T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701615 | |||||||
| chr16:15701666 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.947+4806C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701666 | |||||||
| chr16:15701800 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.947+4940C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701800 | |||||||
| chr16:15701802 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.947+4942G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701802 | |||||||
| chr16:15701819 | G | A | 20 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(17): Show |
20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.947+4959G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15701819 | |||||||
| chr16:15702087 | G | A | 2 | a0001c0001t0005g0165 a0001c0001t0005g0166 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.947+5227G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702087 | |||||||
| chr16:15702094 | A | G | 1 | a0001c0001t0003g0125 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.947+5234A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702094 | |||||||
| chr16:15702119 | G | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+5259G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702119 | |||||||
| chr16:15702266 | A | T | 82 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0287 others(79): Show |
83 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.947+5406A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702266 | |||||||
| chr16:15702282 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+5422C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702282 | |||||||
| chr16:15702400 | T | C | 1 | a0001c0001t0006g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.947+5540T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702400 | |||||||
| chr16:15702462 | C | G | 83 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0287 others(80): Show |
84 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.947+5602C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702462 | |||||||
| chr16:15702567 | C | CA | 21 | a0001c0001t0001g0063 a0001c0001t0001g0095 a0001c0001t0002g0013 others(18): Show |
21 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.947+5709dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702567 | ||||||
| chr16:15702581 | C | CT | 152 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0039 others(149): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.947+5729dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702581 | ||||||
| chr16:15702581 | C | CTT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.947+5728_947+5729d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15702581 | ||||||
| chr16:15702590 | A | T | 1 | a0001c0001t0029g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.947+5730A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702590 | |||||||
| chr16:15702711 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
111 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.947+5851C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702711 | |||||||
| chr16:15702759 | G | A | 1 | a0001c0001t0022g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.947+5899G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15702759 | |||||||
| chr16:15703103 | T | C | 12 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(9): Show |
12 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+6243T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703103 | |||||||
| chr16:15703129 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0285 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.947+6269A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703129 | |||||||
| chr16:15703355 | T | C | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+6495T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703355 | |||||||
| chr16:15703360 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0328 |
2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.947+6500G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703360 | |||||||
| chr16:15703447 | C | T | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+6587C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703447 | |||||||
| chr16:15703480 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.947+6620C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703480 | |||||||
| chr16:15703571 | G | C | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+6711G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703571 | |||||||
| chr16:15703633 | G | C | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+6773G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703633 | |||||||
| chr16:15703835 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.947+6975G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703835 | |||||||
| chr16:15703925 | G | GT | 18 | a0001c0001t0002g0338 a0001c0001t0007g0347 a0001c0001t0007g0348 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+7073dupT | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15703925 | ||||||
| chr16:15703954 | G | T | 3 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0132 |
3 | NA18945.hp2 NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.947+7094G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703954 | |||||||
| chr16:15703986 | G | C | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+7126G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15703986 | |||||||
| chr16:15704114 | G | A | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.947+7254G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704114 | |||||||
| chr16:15704158 | G | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0285 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.947+7298G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704158 | |||||||
| chr16:15704238 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+7378T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704238 | |||||||
| chr16:15704353 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(190): Show |
195 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.947+7493G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704353 | |||||||
| chr16:15704401 | AAT | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0092 |
3 | HG01884.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.947+7544_947+7545d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15704401 | ||||||
| chr16:15704608 | G | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01934.hp2 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+7748G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704608 | |||||||
| chr16:15704614 | A | T | 1 | a0001c0001t0003g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.947+7754A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704614 | |||||||
| chr16:15704619 | G | A | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+7759G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704619 | |||||||
| chr16:15704633 | G | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0091 others(2): Show |
5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+7773G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704633 | |||||||
| chr16:15704665 | G | A | 3 | a0001c0001t0015g0016 a0001c0001t0015g0017 a0001c0001t0021g0015 |
3 | HG02040.hp1 HG03491.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.947+7805G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704665 | |||||||
| chr16:15704764 | T | A | 1 | a0001c0001t0015g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.947+7904T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704764 | |||||||
| chr16:15704765 | C | A | 2 | a0001c0001t0008g0357 a0001c0001t0015g0016 |
2 | HG02572.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.947+7905C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704765 | |||||||
| chr16:15704943 | C | T | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG00673.hp2 HG02056.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.947+8083C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704943 | |||||||
| chr16:15704999 | G | C | 2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.947+8139G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15704999 | |||||||
| chr16:15705106 | TAGCTGGG others(4): Show |
T | 1 | a0001c0001t0001g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.947+8247_947+8257d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705106 | |||||||
| chr16:15705125 | G | A | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8265G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705125 | |||||||
| chr16:15705444 | A | G | 13 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(10): Show |
13 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.947+8584A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705444 | |||||||
| chr16:15705518 | G | A | 1 | a0001c0001t0004g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.947+8658G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705518 | |||||||
| chr16:15705545 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.947+8685C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705545 | |||||||
| chr16:15705663 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.947+8803A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705663 | |||||||
| chr16:15705670 | G | A | 4 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+8810G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705670 | |||||||
| chr16:15705700 | G | A | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8840G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705700 | |||||||
| chr16:15705728 | T | A | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+8868T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705728 | |||||||
| chr16:15705772 | G | C | 67 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(64): Show |
67 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.947+8912G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705772 | |||||||
| chr16:15705898 | T | A | 1 | a0001c0001t0004g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.947+9038T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705898 | |||||||
| chr16:15705971 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(264): Show |
269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.947+9111T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15705971 | |||||||
| chr16:15705984 | C | CA | 12 | a0001c0001t0001g0213 a0001c0001t0002g0216 a0001c0001t0002g0229 others(9): Show |
12 | HG00597.hp2 HG00741.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9145dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(1): Show |
67 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0203 others(64): Show |
68 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.947+9138_947+9145d others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(2): Show |
80 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(77): Show |
81 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.947+9137_947+9145d others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(3): Show |
37 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0033 others(34): Show |
37 | HG00408.hp1 HG00544.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.947+9136_947+9145d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0080 others(13): Show |
16 | HG00099.hp1 HG00597.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.947+9135_947+9145d others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0039 a0001c0001t0007g0360 a0001c0001t0027g0020 |
3 | HG02818.hp1 HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.947+9134_947+9145d others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0008g0356 a0001c0001t0011g0004 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+9133_947+9145d others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0004g0167 a0001c0001t0008g0353 a0001c0001t0008g0357 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+9132_947+9145d others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(8): Show |
9 | a0001c0001t0004g0104 a0001c0001t0004g0168 a0001c0001t0004g0173 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+9131_947+9145d others(17): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(9): Show |
18 | a0001c0001t0004g0163 a0001c0001t0004g0169 a0001c0001t0004g0170 others(15): Show |
18 | HG01261.hp2 HG01891.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.947+9130_947+9145d others(18): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0004g0175 a0001c0001t0004g0303 a0001c0001t0005g0164 others(3): Show |
6 | HG01255.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+9129_947+9145d others(19): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0004g0174 a0001c0001t0005g0181 a0001c0001t0006g0108 |
3 | HG02486.hp2 NA19043.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.947+9128_947+9145d others(20): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0165 a0001c0001t0005g0166 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.947+9127_947+9145d others(21): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15705984 | CA | C | 13 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0065 others(10): Show |
13 | HG00558.hp1 HG00639.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.947+9145delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15705984 | ||||||
| chr16:15706039 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.947+9179G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706039 | |||||||
| chr16:15706046 | G | C | 69 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(66): Show |
69 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.947+9186G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706046 | |||||||
| chr16:15706170 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.947+9310T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706170 | |||||||
| chr16:15706257 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0065 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+9397A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706257 | |||||||
| chr16:15706287 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.947+9427C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706287 | |||||||
| chr16:15706331 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(189): Show |
194 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.947+9471C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706331 | |||||||
| chr16:15706340 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.947+9480G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706340 | |||||||
| chr16:15706404 | GGT | G | 12 | a0001c0001t0002g0219 a0001c0001t0002g0269 a0001c0001t0002g0313 others(9): Show |
12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9545_947+9546d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706404 | |||||||
| chr16:15706408 | C | A | 12 | a0001c0001t0002g0219 a0001c0001t0002g0269 a0001c0001t0002g0313 others(9): Show |
12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9548C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706408 | |||||||
| chr16:15706412 | CCCTG | C | 12 | a0001c0001t0002g0219 a0001c0001t0002g0269 a0001c0001t0002g0313 others(9): Show |
12 | HG01109.hp1 HG01255.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+9553_947+9556d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706412 | |||||||
| chr16:15706563 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.947+9703C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706563 | |||||||
| chr16:15706564 | G | T | 2 | a0001c0001t0010g0311 a0001c0001t0010g0312 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.947+9704G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706564 | |||||||
| chr16:15706587 | A | C | 9 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(6): Show |
9 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.947+9727A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706587 | |||||||
| chr16:15706709 | A | C | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+9849A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706709 | |||||||
| chr16:15706943 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.947+10083G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15706943 | |||||||
| chr16:15707069 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.947+10209C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707069 | |||||||
| chr16:15707098 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.947+10238G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707098 | |||||||
| chr16:15707247 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.947+10387G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707247 | |||||||
| chr16:15707348 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.947+10488G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707348 | |||||||
| chr16:15707568 | T | G | 1 | a0001c0001t0002g0338 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.947+10708T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707568 | |||||||
| chr16:15707573 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.947+10713T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707573 | |||||||
| chr16:15707625 | G | T | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+10765G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707625 | |||||||
| chr16:15707729 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0212 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.947+10869G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707729 | |||||||
| chr16:15707745 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.947+10885G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707745 | |||||||
| chr16:15707756 | G | T | 1 | a0001c0001t0003g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.947+10896G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707756 | |||||||
| chr16:15707827 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.947+10967C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707827 | |||||||
| chr16:15707832 | C | T | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+10972C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707832 | |||||||
| chr16:15707841 | G | C | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+10981G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707841 | |||||||
| chr16:15707937 | A | G | 15 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(12): Show |
15 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.947+11077A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707937 | |||||||
| chr16:15707959 | CA | C | 87 | a0001c0001t0001g0256 a0001c0001t0002g0013 a0001c0001t0002g0040 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.947+11119delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | ||||||
| chr16:15707959 | CAA | C | 52 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0059 others(49): Show |
52 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.947+11118_947+1111 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | ||||||
| chr16:15707959 | CAAA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(170): Show |
174 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.947+11117_947+1111 others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15707959 | ||||||
| chr16:15707978 | A | C | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947+11118A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707978 | |||||||
| chr16:15707978 | AAG | A | 12 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(9): Show |
12 | HG01261.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.947+11119_947+1112 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707978 | |||||||
| chr16:15707979 | AG | A | 6 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0182 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+11120delG | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15707979 | |||||||
| chr16:15708006 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+11146C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708006 | |||||||
| chr16:15708153 | C | T | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.947+11293C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708153 | |||||||
| chr16:15708225 | C | T | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947+11365C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708225 | |||||||
| chr16:15708292 | G | A | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.947+11432G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708292 | |||||||
| chr16:15708351 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0091 others(2): Show |
5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+11491G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708351 | |||||||
| chr16:15708423 | G | T | 1 | a0001c0003t0002g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.947+11563G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708423 | |||||||
| chr16:15708477 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(198): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.947+11617C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15708477 | |||||||
| chr16:15708747 | CAGAAA | C | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+11893_947+1189 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15708747 | ||||||
| chr16:15709089 | G | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(233): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.947+12229G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709089 | |||||||
| chr16:15709121 | T | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.947+12261T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709121 | |||||||
| chr16:15709414 | A | C | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+12554A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709414 | |||||||
| chr16:15709503 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.947+12643C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709503 | |||||||
| chr16:15709606 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0330 |
2 | HG00735.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.947+12746C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709606 | |||||||
| chr16:15709610 | C | T | 19 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0062 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.947+12750C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709610 | |||||||
| chr16:15709807 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.947+12947A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709807 | |||||||
| chr16:15709831 | G | C | 1 | a0001c0001t0007g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.947+12971G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709831 | |||||||
| chr16:15709877 | C | G | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+13017C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15709877 | |||||||
| chr16:15710108 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.947+13248T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710108 | |||||||
| chr16:15710123 | C | T | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+13263C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710123 | |||||||
| chr16:15710179 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.947+13319C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710179 | |||||||
| chr16:15710311 | A | G | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+13451A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710311 | |||||||
| chr16:15710319 | G | A | 14 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0005g0164 others(11): Show |
14 | HG01255.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.947+13459G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710319 | |||||||
| chr16:15710391 | C | T | 3 | a0001c0001t0013g0343 a0001c0001t0013g0344 a0001c0001t0013g0345 |
3 | NA18952.hp2 NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.947+13531C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710391 | |||||||
| chr16:15710427 | A | G | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+13567A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710427 | |||||||
| chr16:15710469 | C | T | 4 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(1): Show |
4 | NA18998.hp2 NA19009.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.947+13609C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710469 | |||||||
| chr16:15710503 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0091 others(2): Show |
5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+13643G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710503 | |||||||
| chr16:15710531 | TAAAAA | T | 7 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0293 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-13659_948-1365 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710531 | |||||||
| chr16:15710669 | C | G | 1 | a0001c0001t0004g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.948-13522C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710669 | |||||||
| chr16:15710695 | T | G | 22 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(19): Show |
22 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-13496T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710695 | |||||||
| chr16:15710699 | G | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(230): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.948-13492G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710699 | |||||||
| chr16:15710834 | C | T | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-13357C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710834 | |||||||
| chr16:15710873 | T | C | 11 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(8): Show |
11 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.948-13318T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710873 | |||||||
| chr16:15710967 | C | T | 27 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(24): Show |
27 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-13224C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15710967 | |||||||
| chr16:15711008 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.948-13183C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711008 | |||||||
| chr16:15711107 | G | A | 5 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(2): Show |
5 | HG02155.hp1 NA18998.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-13084G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711107 | |||||||
| chr16:15711108 | C | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-13083C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711108 | |||||||
| chr16:15711120 | C | T | 1 | a0001c0001t0032g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.948-13071C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711120 | |||||||
| chr16:15711155 | C | T | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-13036C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711155 | |||||||
| chr16:15711199 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0285 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.948-12992C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711199 | |||||||
| chr16:15711381 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-12810G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711381 | |||||||
| chr16:15711411 | C | G | 1 | a0001c0001t0003g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.948-12780C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711411 | |||||||
| chr16:15711716 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.948-12475C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711716 | |||||||
| chr16:15711722 | T | G | 48 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(45): Show |
48 | HG00140.hp2 HG00733.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.948-12469T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711722 | |||||||
| chr16:15711725 | G | C | 1 | a0001c0001t0002g0270 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.948-12466G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711725 | |||||||
| chr16:15711786 | A | T | 3 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 |
3 | HG01496.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.948-12405A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711786 | |||||||
| chr16:15711795 | C | T | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-12396C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711795 | |||||||
| chr16:15711816 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.948-12375C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711816 | |||||||
| chr16:15711941 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.948-12250C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15711941 | |||||||
| chr16:15712066 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.948-12125G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712066 | |||||||
| chr16:15712289 | A | T | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-11902A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712289 | |||||||
| chr16:15712323 | T | G | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11868T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712323 | |||||||
| chr16:15712344 | C | T | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-11847C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712344 | |||||||
| chr16:15712346 | C | T | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-11845C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712346 | |||||||
| chr16:15712373 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0032g0089 |
2 | NA18945.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.948-11818C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712373 | |||||||
| chr16:15712421 | G | A | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11770G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712421 | |||||||
| chr16:15712477 | A | G | 33 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(30): Show |
33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.948-11714A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712477 | |||||||
| chr16:15712505 | A | C | 1 | a0001c0001t0003g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.948-11686A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712505 | |||||||
| chr16:15712593 | C | T | 193 | a0001c0001t0001g0256 a0001c0001t0002g0013 a0001c0001t0002g0019 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.948-11598C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712593 | |||||||
| chr16:15712609 | T | C | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11582T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712609 | |||||||
| chr16:15712655 | G | T | 1 | a0002c0004t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.948-11536G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712655 | |||||||
| chr16:15712801 | C | CTGGCCAT | 119 | a0001c0001t0001g0256 a0001c0001t0002g0019 a0001c0001t0002g0079 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.948-11388_948-1138 others(11): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712801 | ||||||
| chr16:15712872 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.948-11319T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712872 | |||||||
| chr16:15712878 | TAC | T | 7 | a0001c0001t0002g0099 a0001c0001t0002g0251 a0001c0001t0002g0253 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11311_948-1131 others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712878 | ||||||
| chr16:15712881 | A | AGTTTTTT others(2): Show |
10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.948-11309_948-1130 others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712881 | ||||||
| chr16:15712882 | G | GTTTT | 11 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0289 others(8): Show |
11 | HG00639.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.948-11299_948-1129 others(8): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTT | 45 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0090 others(42): Show |
46 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.948-11300_948-1129 others(9): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTT | 7 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0302 others(4): Show |
7 | HG00544.hp2 HG02055.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11301_948-1129 others(10): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0008g0353 a0001c0001t0008g0355 a0001c0001t0008g0356 others(5): Show |
8 | HG02040.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.948-11304_948-1129 others(13): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(3): Show |
19 | a0001c0001t0004g0104 a0001c0001t0004g0168 a0001c0001t0004g0171 others(16): Show |
19 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-11305_948-1129 others(14): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0007g0358 a0001c0001t0007g0361 |
2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.948-11306_948-1129 others(15): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.948-11307_948-1129 others(16): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0009g0102 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.948-11296_948-1129 others(18): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(8): Show |
23 | a0001c0001t0002g0019 a0001c0001t0002g0103 a0001c0001t0002g0111 others(20): Show |
23 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(19): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(9): Show |
5 | a0001c0001t0002g0105 a0001c0001t0002g0285 a0001c0001t0003g0118 others(2): Show |
5 | HG00609.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(20): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(11): Show |
5 | a0001c0001t0002g0232 a0001c0001t0011g0004 a0001c0001t0011g0005 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(22): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0346 a0001c0001t0004g0167 |
2 | HG02615.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(25): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(18): Show |
5 | a0001c0001t0004g0170 a0001c0001t0004g0184 a0001c0001t0004g0185 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(29): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(19): Show |
6 | a0001c0001t0004g0163 a0001c0001t0004g0174 a0001c0001t0004g0182 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(30): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(20): Show |
3 | a0001c0001t0002g0106 a0001c0001t0002g0342 a0001c0001t0004g0172 |
3 | HG02280.hp2 NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(31): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(21): Show |
27 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0216 others(24): Show |
27 | HG00597.hp2 HG00621.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(32): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(22): Show |
23 | a0001c0001t0002g0153 a0001c0001t0002g0225 a0001c0001t0002g0226 others(20): Show |
23 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(33): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(23): Show |
17 | a0001c0001t0002g0223 a0001c0001t0002g0259 a0001c0001t0002g0271 others(14): Show |
17 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(34): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(24): Show |
13 | a0001c0001t0002g0219 a0001c0001t0002g0228 a0001c0001t0002g0230 others(10): Show |
13 | HG01175.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(35): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(25): Show |
6 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0272 others(3): Show |
6 | HG02004.hp2 NA18979.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(36): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(26): Show |
4 | a0001c0001t0001g0256 a0001c0001t0002g0227 a0001c0001t0002g0264 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(37): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(27): Show |
1 | a0001c0001t0002g0339 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.948-11296_948-1129 others(38): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(28): Show |
1 | a0001c0001t0002g0276 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.948-11296_948-1129 others(39): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(29): Show |
4 | a0001c0001t0002g0237 a0001c0001t0002g0239 a0001c0001t0002g0314 others(1): Show |
4 | HG01934.hp1 NA18965.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-11296_948-1129 others(40): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712882 | G | GTTTTTTT others(32): Show |
2 | a0001c0001t0002g0331 a0001c0001t0002g0332 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.948-11296_948-1129 others(43): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15712882 | ||||||
| chr16:15712989 | A | G | 193 | a0001c0001t0001g0256 a0001c0001t0002g0013 a0001c0001t0002g0019 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.948-11202A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15712989 | |||||||
| chr16:15713061 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-11130A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713061 | |||||||
| chr16:15713220 | C | T | 8 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(5): Show |
8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.948-10971C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713220 | |||||||
| chr16:15713280 | A | C | 33 | a0001c0001t0002g0276 a0001c0001t0004g0104 a0001c0001t0004g0163 others(30): Show |
33 | HG00733.hp1 HG01255.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.948-10911A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713280 | |||||||
| chr16:15713291 | A | G | 52 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(49): Show |
52 | HG00140.hp2 HG00733.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.948-10900A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713291 | |||||||
| chr16:15713295 | TGAG | T | 27 | a0001c0001t0002g0019 a0001c0001t0002g0103 a0001c0001t0002g0105 others(24): Show |
27 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.948-10894_948-1089 others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15713295 | ||||||
| chr16:15713318 | G | A | 20 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(17): Show |
20 | HG01261.hp2 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-10873G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713318 | |||||||
| chr16:15713409 | A | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0293 a0001c0001t0001g0297 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-10782A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713409 | |||||||
| chr16:15713597 | C | A | 17 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.948-10594C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713597 | |||||||
| chr16:15713601 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01168.hp2 HG01261.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.948-10590T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713601 | |||||||
| chr16:15713614 | G | C | 5 | a0001c0001t0008g0353 a0001c0001t0008g0354 a0001c0001t0008g0355 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-10577G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713614 | |||||||
| chr16:15713684 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0065 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-10507G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713684 | |||||||
| chr16:15713820 | T | C | 118 | a0001c0001t0002g0019 a0001c0001t0002g0079 a0001c0001t0002g0099 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.948-10371T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713820 | |||||||
| chr16:15713863 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.948-10328G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15713863 | |||||||
| chr16:15714027 | C | T | 4 | a0001c0001t0003g0134 a0001c0001t0003g0136 a0001c0001t0003g0138 others(1): Show |
4 | HG02129.hp2 NA18949.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-10164C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714027 | |||||||
| chr16:15714078 | C | T | 31 | a0001c0001t0003g0002 a0001c0001t0003g0125 a0001c0001t0003g0126 others(28): Show |
32 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-10113C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714078 | |||||||
| chr16:15714166 | C | T | 27 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0034 others(24): Show |
27 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.948-10025C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714166 | |||||||
| chr16:15714201 | G | A | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-9990G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714201 | |||||||
| chr16:15714218 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0340 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.948-9973C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714218 | |||||||
| chr16:15714294 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0212 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.948-9897G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714294 | |||||||
| chr16:15714470 | G | A | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-9721G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714470 | |||||||
| chr16:15714582 | G | C | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.948-9609G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714582 | |||||||
| chr16:15714689 | G | T | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-9502G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714689 | |||||||
| chr16:15714727 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.948-9464C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714727 | |||||||
| chr16:15714774 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.948-9417A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714774 | |||||||
| chr16:15714849 | G | A | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-9342G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714849 | |||||||
| chr16:15714999 | T | C | 2 | a0001c0001t0003g0002 a0001c0001t0003g0147 |
3 | HG02135.hp1 NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.948-9192T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15714999 | |||||||
| chr16:15715115 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-9076G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715115 | |||||||
| chr16:15715119 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-9072G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715119 | |||||||
| chr16:15715260 | C | T | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-8931C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715260 | |||||||
| chr16:15715320 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.948-8871C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715320 | |||||||
| chr16:15715426 | T | C | 1 | a0001c0001t0002g0285 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.948-8765T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715426 | |||||||
| chr16:15715497 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-8694C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715497 | |||||||
| chr16:15715550 | G | A | 2 | a0001c0001t0007g0349 a0001c0001t0007g0350 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.948-8641G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715550 | |||||||
| chr16:15715562 | G | C | 1 | a0001c0001t0003g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.948-8629G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715562 | |||||||
| chr16:15715684 | G | T | 1 | a0001c0001t0008g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.948-8507G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715684 | |||||||
| chr16:15715692 | A | G | 2 | a0001c0001t0015g0016 a0001c0001t0021g0015 |
2 | HG02040.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.948-8499A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715692 | |||||||
| chr16:15715697 | T | G | 1 | a0002c0004t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.948-8494T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715697 | |||||||
| chr16:15715972 | C | T | 1 | a0001c0001t0002g0320 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.948-8219C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15715972 | |||||||
| chr16:15716013 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.948-8178G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716013 | |||||||
| chr16:15716014 | C | T | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.948-8177C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716014 | |||||||
| chr16:15716081 | A | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-8110A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716081 | |||||||
| chr16:15716124 | T | G | 22 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(19): Show |
22 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-8067T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716124 | |||||||
| chr16:15716201 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0257 |
2 | HG03225.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.948-7990G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716201 | |||||||
| chr16:15716354 | G | A | 88 | a0001c0001t0002g0079 a0001c0001t0002g0099 a0001c0001t0002g0106 others(85): Show |
88 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.948-7837G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716354 | |||||||
| chr16:15716410 | A | G | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-7781A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716410 | |||||||
| chr16:15716445 | C | G | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-7746C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716445 | |||||||
| chr16:15716445 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0091 others(2): Show |
5 | HG00733.hp2 HG02602.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-7746C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716445 | |||||||
| chr16:15716524 | G | T | 136 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0091 others(133): Show |
136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.948-7667G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716524 | |||||||
| chr16:15716524 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-7658_948-7649d others(12): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15716524 | ||||||
| chr16:15716616 | C | T | 1 | a0001c0001t0006g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.948-7575C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716616 | |||||||
| chr16:15716617 | G | A | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-7574G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716617 | |||||||
| chr16:15716662 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-7529T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716662 | |||||||
| chr16:15716742 | G | C | 5 | a0001c0001t0006g0108 a0001c0001t0006g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-7449G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716742 | |||||||
| chr16:15716793 | C | T | 1 | a0001c0001t0004g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.948-7398C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716793 | |||||||
| chr16:15716827 | G | T | 6 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948-7364G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716827 | |||||||
| chr16:15716872 | G | C | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-7319G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716872 | |||||||
| chr16:15716915 | T | G | 1 | a0001c0001t0003g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.948-7276T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716915 | |||||||
| chr16:15716957 | G | C | 2 | a0001c0001t0002g0216 a0001c0001t0002g0255 |
2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.948-7234G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15716957 | |||||||
| chr16:15717025 | G | C | 19 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(16): Show |
19 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-7166G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717025 | |||||||
| chr16:15717043 | C | G | 1 | a0001c0002t0001g0328 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.948-7148C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717043 | |||||||
| chr16:15717166 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(123): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.948-7025C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717166 | |||||||
| chr16:15717205 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(123): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.948-6986C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717205 | |||||||
| chr16:15717274 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0287 others(19): Show |
22 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.948-6917G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717274 | |||||||
| chr16:15717314 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-6877C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717314 | |||||||
| chr16:15717351 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.948-6840G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717351 | |||||||
| chr16:15717397 | G | C | 15 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(12): Show |
15 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.948-6794G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717397 | |||||||
| chr16:15717401 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.948-6790G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717401 | |||||||
| chr16:15717546 | G | A | 2 | a0001c0001t0002g0226 a0001c0001t0002g0270 |
2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.948-6645G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717546 | |||||||
| chr16:15717571 | A | G | 51 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(48): Show |
51 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.948-6620A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717571 | |||||||
| chr16:15717620 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-6571C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717620 | |||||||
| chr16:15717652 | G | A | 2 | a0001c0002t0001g0192 a0001c0002t0001g0193 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.948-6539G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717652 | |||||||
| chr16:15717805 | G | A | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-6386G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717805 | |||||||
| chr16:15717833 | A | C | 1 | a0001c0001t0002g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.948-6358A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717833 | |||||||
| chr16:15717965 | C | T | 1 | a0001c0001t0005g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.948-6226C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15717965 | |||||||
| chr16:15718046 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.948-6145G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718046 | |||||||
| chr16:15718072 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.948-6119G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718072 | |||||||
| chr16:15718239 | G | A | 19 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(16): Show |
19 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-5952G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718239 | |||||||
| chr16:15718333 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-5858G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718333 | |||||||
| chr16:15718334 | A | C | 1 | a0001c0001t0002g0227 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948-5857A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718334 | |||||||
| chr16:15718452 | G | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-5739G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718452 | |||||||
| chr16:15718497 | C | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0333 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.948-5694C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718497 | |||||||
| chr16:15718693 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-5498C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718693 | |||||||
| chr16:15718761 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.948-5430C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718761 | |||||||
| chr16:15718768 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.948-5423G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718768 | |||||||
| chr16:15718799 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | NA18959.hp2 NA19004.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-5392A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718799 | |||||||
| chr16:15718899 | A | G | 18 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-5292A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718899 | |||||||
| chr16:15718925 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.948-5266C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15718925 | |||||||
| chr16:15719116 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.948-5075A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719116 | |||||||
| chr16:15719134 | A | C | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-5057A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719134 | |||||||
| chr16:15719138 | A | T | 1 | a0001c0001t0030g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.948-5053A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719138 | |||||||
| chr16:15719156 | C | T | 1 | a0001c0001t0026g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.948-5035C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719156 | |||||||
| chr16:15719159 | G | A | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-5032G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719159 | |||||||
| chr16:15719233 | T | G | 1 | a0001c0001t0003g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.948-4958T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719233 | |||||||
| chr16:15719354 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(97): Show |
101 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.948-4837G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719354 | |||||||
| chr16:15719541 | G | A | 13 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(10): Show |
13 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.948-4650G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719541 | |||||||
| chr16:15719600 | G | T | 1 | a0001c0001t0002g0243 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.948-4591G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719600 | |||||||
| chr16:15719776 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(188): Show |
193 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.948-4415G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719776 | |||||||
| chr16:15719860 | A | T | 1 | a0001c0001t0003g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.948-4331A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719860 | |||||||
| chr16:15719874 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0010g0279 |
2 | HG00733.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.948-4317G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719874 | |||||||
| chr16:15719909 | C | A | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-4282C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719909 | |||||||
| chr16:15719947 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.948-4244C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15719947 | |||||||
| chr16:15720071 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.948-4120G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720071 | |||||||
| chr16:15720088 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(234): Show |
239 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.948-4103C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720088 | |||||||
| chr16:15720265 | G | T | 1 | a0001c0001t0001g0341 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.948-3926G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720265 | |||||||
| chr16:15720420 | A | G | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-3771A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720420 | |||||||
| chr16:15720587 | G | GA | 40 | a0001c0001t0002g0227 a0001c0001t0002g0233 a0001c0001t0002g0235 others(37): Show |
41 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.948-3589dupA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720587 | ||||||
| chr16:15720587 | GA | G | 16 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(13): Show |
16 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.948-3589delA | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720587 | ||||||
| chr16:15720613 | A | G | 32 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(29): Show |
32 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.948-3578A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720613 | |||||||
| chr16:15720625 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0004g0184 |
2 | HG00733.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.948-3566G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720625 | |||||||
| chr16:15720723 | ACT | A | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-3465_948-3464d others(4): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720723 | ||||||
| chr16:15720738 | A | G | 3 | a0001c0001t0004g0163 a0001c0001t0004g0169 a0001c0001t0004g0175 |
3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.948-3453A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720738 | |||||||
| chr16:15720742 | T | TAAAAA | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3446_948-3445i others(7): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720742 | ||||||
| chr16:15720742 | TAAAG | T | 38 | a0001c0001t0003g0002 a0001c0001t0003g0023 a0001c0001t0003g0024 others(35): Show |
39 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.948-3445_948-3442d others(6): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15720742 | ||||||
| chr16:15720770 | A | G | 1 | a0001c0001t0033g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.948-3421A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720770 | |||||||
| chr16:15720825 | C | G | 1 | a0001c0001t0003g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.948-3366C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720825 | |||||||
| chr16:15720835 | G | A | 1 | a0001c0001t0025g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.948-3356G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15720835 | |||||||
| chr16:15721027 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.948-3164G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721027 | |||||||
| chr16:15721064 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.948-3127C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721064 | |||||||
| chr16:15721080 | A | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3111A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721080 | |||||||
| chr16:15721191 | A | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-3000A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721191 | |||||||
| chr16:15721214 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.948-2977C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721214 | |||||||
| chr16:15721320 | C | T | 1 | a0001c0001t0024g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.948-2871C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721320 | |||||||
| chr16:15721403 | A | G | 8 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(5): Show |
8 | NA18973.hp2 NA18995.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.948-2788A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721403 | |||||||
| chr16:15721478 | T | C | 1 | a0001c0001t0027g0020 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.948-2713T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721478 | |||||||
| chr16:15721494 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0072 others(1): Show |
4 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-2697G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721494 | |||||||
| chr16:15721762 | G | GCTATGGG others(26): Show |
1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-2426_948-2394d others(35): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15721762 | ||||||
| chr16:15721765 | A | G | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-2426A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721765 | |||||||
| chr16:15721921 | A | G | 7 | a0001c0001t0002g0120 a0001c0001t0002g0285 a0001c0001t0006g0108 others(4): Show |
7 | HG01891.hp1 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-2270A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15721921 | |||||||
| chr16:15722090 | C | G | 5 | a0001c0001t0001g0346 a0001c0001t0011g0004 a0001c0001t0011g0005 others(2): Show |
5 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-2101C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722090 | |||||||
| chr16:15722254 | G | C | 14 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(11): Show |
14 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-1937G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722254 | |||||||
| chr16:15722289 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(268): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.948-1902T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722289 | |||||||
| chr16:15722520 | G | A | 39 | a0001c0001t0002g0251 a0001c0001t0003g0002 a0001c0001t0003g0023 others(36): Show |
40 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.948-1671G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722520 | |||||||
| chr16:15722801 | C | T | 4 | a0001c0001t0011g0004 a0001c0001t0011g0005 a0001c0001t0011g0006 others(1): Show |
4 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.948-1390C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722801 | |||||||
| chr16:15722831 | C | A | 1 | a0001c0001t0002g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.948-1360C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15722831 | |||||||
| chr16:15723024 | G | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0200 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.948-1167G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723024 | |||||||
| chr16:15723067 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.948-1124C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723067 | |||||||
| chr16:15723089 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.948-1102A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723089 | |||||||
| chr16:15723175 | A | C | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-1016A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723175 | |||||||
| chr16:15723192 | C | A | 3 | a0001c0001t0003g0110 a0001c0001t0003g0117 a0001c0001t0003g0119 |
3 | HG00408.hp2 NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.948-999C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723192 | |||||||
| chr16:15723315 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-876C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723315 | |||||||
| chr16:15723316 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-875A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723316 | |||||||
| chr16:15723333 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-858A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723333 | |||||||
| chr16:15723338 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(81): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.948-853G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723338 | |||||||
| chr16:15723356 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-835A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723356 | |||||||
| chr16:15723367 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-824C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723367 | |||||||
| chr16:15723368 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-823C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723368 | |||||||
| chr16:15723389 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.948-802A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723389 | |||||||
| chr16:15723401 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-790C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723401 | |||||||
| chr16:15723414 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-777A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723414 | |||||||
| chr16:15723417 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-774C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723417 | |||||||
| chr16:15723421 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-770C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723421 | |||||||
| chr16:15723422 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-769A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723422 | |||||||
| chr16:15723426 | C | A | 1 | a0001c0001t0002g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.948-765C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723426 | |||||||
| chr16:15723426 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.948-765C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723426 | |||||||
| chr16:15723436 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-755C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723436 | |||||||
| chr16:15723443 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-748T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723443 | |||||||
| chr16:15723454 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-737C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723454 | |||||||
| chr16:15723470 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-721A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723470 | |||||||
| chr16:15723471 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-720A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723471 | |||||||
| chr16:15723472 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-719C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723472 | |||||||
| chr16:15723473 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-718C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723473 | |||||||
| chr16:15723480 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-711C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723480 | |||||||
| chr16:15723493 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-698A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723493 | |||||||
| chr16:15723508 | ATAG | A | 12 | a0001c0001t0007g0347 a0001c0001t0007g0348 a0001c0001t0007g0349 others(9): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-681_948-679del others(3): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 15723508 | ||||||
| chr16:15723522 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-669C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723522 | |||||||
| chr16:15723534 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-657C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723534 | |||||||
| chr16:15723539 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-652T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723539 | |||||||
| chr16:15723543 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-648A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723543 | |||||||
| chr16:15723556 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-635A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723556 | |||||||
| chr16:15723561 | C | T | 2 | a0001c0001t0002g0331 a0001c0001t0002g0332 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.948-630C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723561 | |||||||
| chr16:15723563 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-628C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723563 | |||||||
| chr16:15723565 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-626T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723565 | |||||||
| chr16:15723584 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-607T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723584 | |||||||
| chr16:15723585 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-606G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723585 | |||||||
| chr16:15723586 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-605C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723586 | |||||||
| chr16:15723589 | G | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-602G>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723589 | |||||||
| chr16:15723607 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-584C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723607 | |||||||
| chr16:15723619 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-572C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723619 | |||||||
| chr16:15723620 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-571T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723620 | |||||||
| chr16:15723621 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-570G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723621 | |||||||
| chr16:15723630 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-561A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723630 | |||||||
| chr16:15723631 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-560G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723631 | |||||||
| chr16:15723632 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-559C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723632 | |||||||
| chr16:15723633 | T | C | 52 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0041 others(49): Show |
52 | HG00140.hp2 HG01074.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.948-558T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723633 | |||||||
| chr16:15723663 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-528A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723663 | |||||||
| chr16:15723664 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-527A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723664 | |||||||
| chr16:15723673 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-518A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723673 | |||||||
| chr16:15723750 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-441C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723750 | |||||||
| chr16:15723755 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-436A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723755 | |||||||
| chr16:15723772 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0340 |
2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.948-419T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723772 | |||||||
| chr16:15723795 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-396A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723795 | |||||||
| chr16:15723805 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-386C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723805 | |||||||
| chr16:15723806 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-385T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723806 | |||||||
| chr16:15723808 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-383A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723808 | |||||||
| chr16:15723839 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-352A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723839 | |||||||
| chr16:15723851 | T | C | 38 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(35): Show |
38 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.948-340T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723851 | |||||||
| chr16:15723864 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-327A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723864 | |||||||
| chr16:15723865 | G | C | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-326G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723865 | |||||||
| chr16:15723867 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-324A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723867 | |||||||
| chr16:15723873 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-318T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723873 | |||||||
| chr16:15723875 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-316C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723875 | |||||||
| chr16:15723876 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-315C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723876 | |||||||
| chr16:15723878 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-313T>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723878 | |||||||
| chr16:15723879 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-312C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723879 | |||||||
| chr16:15723880 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-311T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723880 | |||||||
| chr16:15723881 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-310T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723881 | |||||||
| chr16:15723885 | G | C | 1 | a0001c0001t0004g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.948-306G>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723885 | |||||||
| chr16:15723890 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-301A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723890 | |||||||
| chr16:15723892 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-299A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723892 | |||||||
| chr16:15723893 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-298C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723893 | |||||||
| chr16:15723894 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-297T>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723894 | |||||||
| chr16:15723931 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-260C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723931 | |||||||
| chr16:15723936 | A | C | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-255A>C | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723936 | |||||||
| chr16:15723937 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-254C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723937 | |||||||
| chr16:15723938 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-253C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723938 | |||||||
| chr16:15723939 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-252C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723939 | |||||||
| chr16:15723940 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-251A>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723940 | |||||||
| chr16:15723942 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-249A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723942 | |||||||
| chr16:15723963 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-228T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723963 | |||||||
| chr16:15723966 | T | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-225T>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723966 | |||||||
| chr16:15723985 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-206C>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15723985 | |||||||
| chr16:15724004 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-187C>G | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724004 | |||||||
| chr16:15724021 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-170A>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724021 | |||||||
| chr16:15724035 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948-156C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724035 | |||||||
| chr16:15724138 | G | A | 33 | a0001c0001t0004g0104 a0001c0001t0004g0163 a0001c0001t0004g0167 others(30): Show |
33 | HG01255.hp1 HG01261.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.948-53G>A | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724138 | |||||||
| chr16:15724151 | C | T | 1 | a0001c0001t0023g0007 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948-40C>T | NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | chr16 | 15724151 |