Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4836 |
| ensemblid | ENSG00000136448.13 |
| hgncid | 7857 |
| symbol | NMT1 |
| name | N-myristoyltransferase 1 |
| refseq_nuc | NM_021079.5 |
| refseq_prot | NP_066565.1 |
| ensembl_nuc | ENST00000258960.7 |
| ensembl_prot | ENSP00000258960.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 45061317 |
| end | 45109016 |
| strand | + |
| ver | v1.2 |
| region | chr17:45061317-45109016 |
| region5000 | chr17:45056317-45114016 |
| regionname0 | NMT1_chr17_45061317_45109016 |
| regionname5000 | NMT1_chr17_45056317_45114016 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1488 | 161 | 39 | 37 | 63 | 7 | 14 | NMT1_chr17_45056317_45114016 | NMT1 | ATGGC others(1483): Show |
chr17 | 45056317 | 45114016 | ||
| a0001c0002 | 0/1 | 1488 | 84 | 4 | 21 | 41 | 5 | 12 | NMT1_chr17_45056317_45114016 | NMT1 | ATGGC others(1483): Show |
chr17 | 45056317 | 45114016 | ||
| a0001c0003 | 0/0 | 1488 | 71 | 14 | 13 | 35 | 0 | 9 | NMT1_chr17_45056317_45114016 | NMT1 | ATGGC others(1483): Show |
chr17 | 45056317 | 45114016 | ||
| a0001c0004 | 0/0 | 1488 | 67 | 35 | 11 | 6 | 4 | 11 | NMT1_chr17_45056317_45114016 | NMT1 | ATGGC others(1483): Show |
chr17 | 45056317 | 45114016 | ||
| a0001c0005 | 0/0 | 1488 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | ATGGC others(1483): Show |
chr17 | 45056317 | 45114016 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0002 | 0/0 | 4881 | 12 | 11 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0004 | 0/0 | 4881 | 26 | 0 | 0 | 26 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0005 | 0/0 | 4880 | 30 | 3 | 7 | 17 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0006 | 1/0 | 4881 | 21 | 0 | 10 | 2 | 3 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0007 | 0/0 | 4880 | 12 | 0 | 3 | 6 | 0 | 3 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0008 | 0/0 | 4881 | 10 | 8 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0009 | 0/0 | 4881 | 8 | 0 | 6 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0010 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0013 | 0/0 | 4881 | 5 | 0 | 3 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0015 | 0/0 | 4880 | 4 | 1 | 1 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0016 | 0/0 | 4881 | 4 | 4 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0021 | 0/0 | 4880 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0023 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0027 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0028 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0029 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0030 | 0/0 | 4881 | 2 | 1 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0035 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0037 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0039 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0042 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0043 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0045 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0046 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0047 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4875): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0048 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0049 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0050 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0051 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0001t0052 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0001 | 0/1 | 4881 | 63 | 2 | 11 | 38 | 4 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0004 | 0/0 | 4881 | 8 | 1 | 1 | 3 | 1 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0012 | 0/0 | 4881 | 5 | 0 | 5 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0018 | 0/0 | 4881 | 3 | 1 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0024 | 0/0 | 4881 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0025 | 0/0 | 4881 | 2 | 0 | 0 | 0 | 0 | 2 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0002t0034 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0002 | 0/0 | 4881 | 47 | 2 | 8 | 30 | 0 | 7 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0010 | 0/0 | 4881 | 6 | 4 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0011 | 0/0 | 4881 | 6 | 6 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0019 | 0/0 | 4881 | 3 | 0 | 2 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0020 | 0/0 | 4881 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0026 | 0/0 | 4881 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0036 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0038 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0040 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0003t0041 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0003 | 0/0 | 4881 | 46 | 29 | 4 | 6 | 2 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0014 | 0/0 | 4881 | 5 | 0 | 0 | 0 | 0 | 5 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0017 | 0/0 | 4881 | 4 | 1 | 3 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0022 | 0/0 | 4881 | 3 | 1 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0031 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0032 | 0/0 | 4881 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0033 | 0/0 | 4881 | 2 | 0 | 0 | 0 | 2 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0044 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0053 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0004t0054 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| a0001c0005t0002 | 0/0 | 4881 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | CTCGC others(4876): Show |
chr17 | 45056317 | 45114016 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0007g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0013g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0013g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0013g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0013g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0015g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0015g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0015g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0016g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0016g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0021g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0021g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0021g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0023g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0023g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0027g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0028g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0029g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0029g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0030g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0035g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0037g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0039g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0042g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0043g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0045g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0046g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0047g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0048g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0049g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0050g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0051g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0001t0052g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0012g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0012g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0012g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0012g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0018g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0018g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0018g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0024g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0024g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0025g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0025g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0002t0034g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0019g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0019g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0019g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0020g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0020g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0026g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0026g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0036g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0038g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0040g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0003t0041g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0001 | 0/0 | 6 | 0 | 1 | 0 | 2 | 3 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0014g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0014g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0014g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0014g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0014g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0017g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0017g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0022g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0022g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0031g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0032g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0033g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0033g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0044g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0053g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0004t0054g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0005t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0005t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| a0001c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0324 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00099 | hp2 | a0001 | c0004 | t0033 | g0241 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0263 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0233 | EUR | GBR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0194 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00280 | hp2 | a0001 | c0004 | t0033 | g0240 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0019 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00323 | hp2 | a0001 | c0001 | t0050 | g0301 | EUR | FIN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0260 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0182 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0038 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00558 | hp1 | a0001 | c0001 | t0045 | g0008 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00558 | hp2 | a0001 | c0002 | t0004 | g0173 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0333 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00639 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00642 | hp1 | a0001 | c0001 | t0015 | g0264 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0323 | EAS | CHS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00733 | hp1 | a0001 | c0002 | t0012 | g0212 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0332 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00735 | hp1 | a0001 | c0004 | t0022 | g0161 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00735 | hp2 | a0001 | c0001 | t0021 | g0299 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0339 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG00741 | hp2 | a0001 | c0002 | t0024 | g0220 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01069 | hp1 | a0001 | c0004 | t0032 | g0014 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01069 | hp2 | a0001 | c0002 | t0034 | g0211 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01070 | hp1 | a0001 | c0004 | t0017 | g0251 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01071 | hp1 | a0001 | c0004 | t0017 | g0250 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01071 | hp2 | a0001 | c0004 | t0032 | g0014 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0266 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01074 | hp2 | a0001 | c0002 | t0012 | g0200 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01081 | hp1 | a0001 | c0004 | t0003 | g0246 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01081 | hp2 | a0001 | c0002 | t0012 | g0207 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01099 | hp1 | a0001 | c0004 | t0022 | g0145 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01099 | hp2 | a0001 | c0002 | t0012 | g0206 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0274 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01109 | hp1 | a0001 | c0001 | t0035 | g0004 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01109 | hp2 | a0001 | c0003 | t0010 | g0095 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01167 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0291 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01168 | hp1 | a0001 | c0002 | t0012 | g0090 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0325 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0334 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0297 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01175 | hp1 | a0001 | c0003 | t0038 | g0097 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01192 | hp1 | a0001 | c0003 | t0019 | g0056 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0329 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01243 | hp2 | a0001 | c0002 | t0018 | g0205 | AMR | PUR | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0015 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0132 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0267 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0265 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0023 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01261 | hp2 | a0001 | c0003 | t0040 | g0351 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0052 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0300 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0131 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0336 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01361 | hp1 | a0001 | c0001 | t0021 | g0302 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01361 | hp2 | a0001 | c0002 | t0004 | g0231 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01433 | hp1 | a0001 | c0002 | t0024 | g0165 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0273 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01496 | hp1 | a0001 | c0001 | t0030 | g0327 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0118 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0218 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01515 | hp2 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0061 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01517 | hp1 | a0001 | c0001 | t0013 | g0062 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01517 | hp2 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0352 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01891 | hp1 | a0001 | c0003 | t0011 | g0149 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01891 | hp2 | a0001 | c0001 | t0037 | g0313 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0121 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0036 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0331 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0330 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0335 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0035 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0318 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0032 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01993 | hp2 | a0001 | c0004 | t0017 | g0001 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02015 | hp1 | a0001 | c0004 | t0003 | g0237 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0039 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02055 | hp2 | a0001 | c0004 | t0053 | g0071 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0096 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0128 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02129 | hp1 | a0001 | c0004 | t0003 | g0247 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02135 | hp1 | a0001 | c0001 | t0043 | g0345 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | KHV | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02145 | hp2 | a0001 | c0004 | t0003 | g0346 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0102 | EAS | CDX | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CDX | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0184 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0133 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02258 | hp2 | a0001 | c0001 | t0042 | g0018 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02273 | hp1 | a0001 | c0001 | t0013 | g0341 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0159 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0340 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0320 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | PEL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02451 | hp2 | a0001 | c0001 | t0028 | g0189 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02602 | hp2 | a0001 | c0004 | t0003 | g0016 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0295 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02622 | hp1 | a0001 | c0003 | t0011 | g0150 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02622 | hp2 | a0001 | c0004 | t0031 | g0013 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0292 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02630 | hp2 | a0001 | c0004 | t0031 | g0013 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02647 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0293 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0069 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02683 | hp2 | a0001 | c0004 | t0014 | g0252 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02698 | hp1 | a0001 | c0001 | t0052 | g0338 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0262 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02717 | hp1 | a0001 | c0003 | t0011 | g0162 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02717 | hp2 | a0001 | c0004 | t0003 | g0134 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02723 | hp1 | a0001 | c0001 | t0039 | g0314 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02723 | hp2 | a0001 | c0004 | t0003 | g0158 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0280 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02738 | hp1 | a0001 | c0002 | t0025 | g0082 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0344 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0294 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02818 | hp1 | a0001 | c0004 | t0054 | g0138 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02886 | hp1 | a0001 | c0004 | t0003 | g0156 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02886 | hp2 | a0001 | c0003 | t0010 | g0187 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02896 | hp1 | a0001 | c0001 | t0048 | g0193 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02896 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02922 | hp1 | a0001 | c0003 | t0041 | g0054 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02922 | hp2 | a0001 | c0003 | t0011 | g0148 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0142 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02970 | hp2 | a0001 | c0004 | t0003 | g0348 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0238 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03017 | hp1 | a0001 | c0002 | t0018 | g0213 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0019 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0136 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03098 | hp2 | a0001 | c0001 | t0028 | g0188 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03130 | hp1 | a0001 | c0001 | t0049 | g0303 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0140 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03139 | hp2 | a0001 | c0004 | t0017 | g0146 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03195 | hp1 | a0001 | c0004 | t0003 | g0154 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03195 | hp2 | a0001 | c0004 | t0003 | g0139 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0347 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0256 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0160 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03225 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03239 | hp1 | a0001 | c0004 | t0014 | g0249 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03239 | hp2 | a0001 | c0001 | t0021 | g0298 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0258 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03453 | hp2 | a0001 | c0001 | t0029 | g0255 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03486 | hp1 | a0001 | c0003 | t0011 | g0151 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03486 | hp2 | a0001 | c0004 | t0003 | g0157 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03490 | hp2 | a0001 | c0001 | t0015 | g0284 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03491 | hp1 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0316 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0278 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03492 | hp2 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | ESN | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0135 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03540 | hp2 | a0001 | c0003 | t0010 | g0190 | AFR | GWD | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03579 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0055 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03654 | hp1 | a0001 | c0004 | t0014 | g0312 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0045 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0328 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03688 | hp1 | a0001 | c0004 | t0044 | g0001 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03704 | hp1 | a0001 | c0003 | t0019 | g0063 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0342 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03710 | hp2 | a0001 | c0004 | t0003 | g0015 | SAS | PJL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0106 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0319 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03834 | hp1 | a0001 | c0003 | t0010 | g0027 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0232 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03927 | hp1 | a0001 | c0004 | t0003 | g0001 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0059 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03942 | hp1 | a0001 | c0004 | t0014 | g0143 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0343 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0046 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04204 | hp1 | a0001 | c0002 | t0004 | g0185 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0060 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0040 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG04228 | hp2 | a0001 | c0004 | t0014 | g0248 | SAS | STU | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0289 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18747 | hp1 | a0001 | c0001 | t0051 | g0326 | EAS | CHB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0322 | EAS | CHB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0290 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18940 | hp2 | a0001 | c0004 | t0003 | g0245 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18941 | hp2 | a0001 | c0005 | t0002 | g0282 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0195 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18945 | hp2 | a0001 | c0001 | t0027 | g0020 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18951 | hp1 | a0001 | c0005 | t0002 | g0283 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18953 | hp1 | a0001 | c0003 | t0020 | g0105 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18960 | hp1 | a0001 | c0003 | t0002 | g0065 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18962 | hp1 | a0001 | c0004 | t0003 | g0243 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18964 | hp2 | a0001 | c0005 | t0002 | g0022 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18965 | hp1 | a0001 | c0001 | t0027 | g0020 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0317 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18973 | hp1 | a0001 | c0004 | t0003 | g0244 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18973 | hp2 | a0001 | c0003 | t0026 | g0057 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18975 | hp2 | a0001 | c0001 | t0046 | g0286 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18978 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18978 | hp2 | a0001 | c0001 | t0009 | g0126 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0349 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18991 | hp1 | a0001 | c0001 | t0047 | g0235 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18992 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0337 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19002 | hp2 | a0001 | c0003 | t0020 | g0098 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19004 | hp1 | a0001 | c0003 | t0026 | g0058 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19004 | hp2 | a0001 | c0003 | t0020 | g0099 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0104 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19030 | hp1 | a0001 | c0003 | t0010 | g0192 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0257 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19043 | hp1 | a0001 | c0003 | t0036 | g0076 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19043 | hp2 | a0001 | c0002 | t0018 | g0224 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19060 | hp1 | a0001 | c0001 | t0023 | g0124 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19077 | hp2 | a0001 | c0004 | t0003 | g0242 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19090 | hp2 | a0001 | c0001 | t0023 | g0123 | EAS | JPT | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19240 | hp1 | a0001 | c0003 | t0011 | g0152 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | YRI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0031 | AFR | ASW | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20129 | hp2 | a0001 | c0004 | t0003 | g0296 | AFR | ASW | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | TSI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0204 | EUR | TSI | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20905 | hp1 | a0001 | c0002 | t0025 | g0171 | SAS | GIH | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0321 | SAS | GIH | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01123 | hp1 | a0001 | c0003 | t0019 | g0064 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0261 | AMR | CLM | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02109 | hp1 | a0001 | c0004 | t0003 | g0239 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02486 | hp1 | a0001 | c0004 | t0022 | g0144 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02486 | hp2 | a0001 | c0004 | t0003 | g0137 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02559 | hp1 | a0001 | c0004 | t0003 | g0141 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG02559 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | ACB | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03471 | hp1 | a0001 | c0003 | t0010 | g0191 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0155 | AFR | MSL | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0287 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0005 | AFR | USA | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0315 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | LWK | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0091 | REF | REF | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0125 | REF | REF | NMT1_chr17_45056317_45114016 | NMT1 | chr17 | 45056317 | 45114016 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45081713 | A | G | 1 | a0001c0005 | 3 | NA18941.hp2 NA18951.hp1 NA18964.hp2 |
synonymous_variant | LOW | c.201A>G | p.Lys67Lys | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/12 | 214/4881 | 201/1491 | 67/496 | chr17 | 45081713 | |||
| chr17:45093786 | C | T | 1 | a0001c0004 | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
synonymous_variant | LOW | c.487C>T | p.Leu163Leu | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/12 | 500/4881 | 487/1491 | 163/496 | chr17 | 45093786 | |||
| chr17:45098538 | C | T | 2 | a0001c0003 a0001c0005 |
74 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(71): Show |
synonymous_variant | LOW | c.870C>T | p.Pro290Pro | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/12 | 883/4881 | 870/1491 | 290/496 | chr17 | 45098538 | |||
| chr17:45099436 | C | T | 1 | a0001c0002 | 83 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
synonymous_variant | LOW | c.916C>T | p.Leu306Leu | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/12 | 929/4881 | 916/1491 | 306/496 | chr17 | 45099436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45105660 | G | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
212 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 21 | chr17 | 45105660 | ||||||
| chr17:45105681 | G | A | 1 | a0001c0001t0043 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 42 | chr17 | 45105681 | ||||||
| chr17:45105727 | C | T | 1 | a0001c0001t0042 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 88 | chr17 | 45105727 | ||||||
| chr17:45105728 | G | A | 1 | a0001c0001t0027 | 2 | NA18945.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 89 | chr17 | 45105728 | ||||||
| chr17:45105730 | G | A | 1 | a0001c0004t0044 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 91 | chr17 | 45105730 | ||||||
| chr17:45105740 | G | A | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(9): Show |
121 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*101G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 101 | chr17 | 45105740 | ||||||
| chr17:45105832 | G | A | 1 | a0001c0003t0026 | 2 | NA18973.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 193 | chr17 | 45105832 | ||||||
| chr17:45105836 | G | A | 1 | a0001c0002t0034 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 197 | chr17 | 45105836 | ||||||
| chr17:45106035 | T | C | 1 | a0001c0003t0019 | 3 | HG01123.hp1 HG01192.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 396 | chr17 | 45106035 | ||||||
| chr17:45106052 | C | T | 10 | a0001c0004t0003 a0001c0004t0014 a0001c0004t0017 others(7): Show |
67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 413 | chr17 | 45106052 | ||||||
| chr17:45106294 | G | A | 2 | a0001c0001t0007 a0001c0001t0045 |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*655G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 655 | chr17 | 45106294 | ||||||
| chr17:45106486 | G | C | 1 | a0001c0001t0035 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 847 | chr17 | 45106486 | ||||||
| chr17:45106517 | G | C | 1 | a0001c0003t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*878G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 878 | chr17 | 45106517 | ||||||
| chr17:45106577 | A | G | 1 | a0001c0004t0054 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 938 | chr17 | 45106577 | ||||||
| chr17:45106784 | G | T | 1 | a0001c0003t0041 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1145 | chr17 | 45106784 | ||||||
| chr17:45107004 | G | A | 1 | a0001c0001t0028 | 2 | HG02451.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1365 | chr17 | 45107004 | ||||||
| chr17:45107259 | A | G | 1 | a0001c0004t0033 | 2 | HG00099.hp2 HG00280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1620A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 1620 | chr17 | 45107259 | ||||||
| chr17:45107655 | C | A | 4 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0046 others(1): Show |
36 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2016C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2016 | chr17 | 45107655 | ||||||
| chr17:45107874 | G | C | 36 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(33): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2235G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2235 | chr17 | 45107874 | ||||||
| chr17:45107930 | G | C | 6 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0029 others(3): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2291G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2291 | chr17 | 45107930 | ||||||
| chr17:45107931 | GT | G | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0015 others(4): Show |
52 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2295delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2295 | INFO_REALIGN_3_PRIME | chr17 | 45107931 | |||||
| chr17:45108000 | C | G | 5 | a0001c0001t0008 a0001c0001t0016 a0001c0001t0029 others(2): Show |
18 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2361 | chr17 | 45108000 | ||||||
| chr17:45108124 | C | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
224 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2485C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2485 | chr17 | 45108124 | ||||||
| chr17:45108132 | G | A | 16 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0037 others(13): Show |
81 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2493G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2493 | chr17 | 45108132 | ||||||
| chr17:45108132 | G | C | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
221 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*2493G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2493 | chr17 | 45108132 | ||||||
| chr17:45108191 | C | A | 1 | a0001c0001t0049 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2552 | chr17 | 45108191 | ||||||
| chr17:45108313 | C | T | 1 | a0001c0001t0028 | 2 | HG02451.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2674C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2674 | chr17 | 45108313 | ||||||
| chr17:45108314 | G | A | 1 | a0001c0002t0025 | 2 | HG02738.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2675G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2675 | chr17 | 45108314 | ||||||
| chr17:45108452 | T | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(38): Show |
276 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2813T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2813 | chr17 | 45108452 | ||||||
| chr17:45108527 | C | T | 3 | a0001c0003t0020 a0001c0003t0038 a0001c0003t0040 |
5 | HG01175.hp1 HG01261.hp2 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2888C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 2888 | chr17 | 45108527 | ||||||
| chr17:45108744 | C | T | 1 | a0001c0001t0049 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3105C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3105 | chr17 | 45108744 | ||||||
| chr17:45108750 | C | T | 1 | a0001c0001t0023 | 2 | NA19060.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3111C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3111 | chr17 | 45108750 | ||||||
| chr17:45108830 | C | G | 1 | a0001c0003t0011 | 6 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3191C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 12/12 | 3191 | chr17 | 45108830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45061492 | C | T | 1 | a0001c0002t0001g0352 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.131+32C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061492 | |||||||
| chr17:45061644 | A | G | 1 | a0001c0003t0040g0351 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.131+184A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061644 | |||||||
| chr17:45061855 | A | G | 1 | a0001c0003t0002g0350 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.131+395A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45061855 | |||||||
| chr17:45062182 | C | T | 1 | a0001c0001t0007g0349 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.131+722C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062182 | |||||||
| chr17:45062603 | C | T | 3 | a0001c0004t0003g0346 a0001c0004t0003g0347 a0001c0004t0003g0348 |
3 | HG02145.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.131+1143C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062603 | |||||||
| chr17:45062732 | C | T | 41 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(38): Show |
46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+1272C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062732 | |||||||
| chr17:45062775 | A | G | 2 | a0001c0001t0027g0020 a0001c0001t0043g0345 |
3 | HG02135.hp1 NA18945.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.131+1315A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062775 | |||||||
| chr17:45062867 | T | G | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+1407T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062867 | |||||||
| chr17:45062926 | C | T | 1 | a0001c0004t0014g0312 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131+1466C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062926 | |||||||
| chr17:45062937 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+1477G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45062937 | |||||||
| chr17:45063061 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.131+1601C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063061 | |||||||
| chr17:45063063 | G | A | 1 | a0001c0001t0007g0316 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.131+1603G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063063 | |||||||
| chr17:45063064 | G | A | 45 | a0001c0001t0013g0061 a0001c0001t0013g0062 a0001c0002t0001g0049 others(42): Show |
48 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.131+1604G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063064 | |||||||
| chr17:45063066 | G | T | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+1606G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063066 | |||||||
| chr17:45063091 | A | G | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+1631A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063091 | |||||||
| chr17:45063170 | A | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+1710A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063170 | |||||||
| chr17:45063204 | C | CA | 14 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(11): Show |
14 | HG02055.hp2 HG02080.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.131+1768dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | ||||||
| chr17:45063204 | CA | C | 142 | a0001c0001t0002g0021 a0001c0001t0002g0227 a0001c0001t0002g0228 others(139): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.131+1768delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | ||||||
| chr17:45063204 | CAA | C | 74 | a0001c0001t0005g0006 a0001c0001t0005g0259 a0001c0001t0005g0260 others(71): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.131+1767_131+1768d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | ||||||
| chr17:45063204 | CAAA | C | 18 | a0001c0001t0005g0300 a0001c0001t0007g0316 a0001c0001t0008g0017 others(15): Show |
19 | HG00323.hp2 HG00735.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.131+1766_131+1768d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063204 | ||||||
| chr17:45063232 | C | G | 60 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0003t0011g0148 others(57): Show |
71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+1772C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063232 | |||||||
| chr17:45063289 | T | C | 1 | a0001c0001t0004g0072 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.131+1829T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063289 | |||||||
| chr17:45063484 | T | TTTCTTTG others(70): Show |
2 | a0001c0001t0009g0131 a0001c0001t0009g0132 |
2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.131+2039_131+2040i others(79): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45063484 | ||||||
| chr17:45063559 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+2099G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063559 | |||||||
| chr17:45063627 | A | G | 43 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+2167A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063627 | |||||||
| chr17:45063693 | C | T | 3 | a0001c0002t0004g0231 a0001c0002t0004g0232 a0001c0002t0004g0233 |
3 | HG00140.hp2 HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.131+2233C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063693 | |||||||
| chr17:45063759 | G | C | 1 | a0001c0004t0003g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.131+2299G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063759 | |||||||
| chr17:45063783 | C | G | 41 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(38): Show |
46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+2323C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063783 | |||||||
| chr17:45063887 | C | A | 37 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0236 others(34): Show |
39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+2427C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063887 | |||||||
| chr17:45063946 | G | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+2486G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063946 | |||||||
| chr17:45063974 | C | T | 145 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(142): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+2514C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45063974 | |||||||
| chr17:45064215 | G | A | 43 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+2755G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064215 | |||||||
| chr17:45064245 | T | C | 1 | a0001c0003t0002g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.131+2785T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064245 | |||||||
| chr17:45064266 | C | T | 145 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(142): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+2806C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064266 | |||||||
| chr17:45064388 | A | G | 31 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(28): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+2928A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064388 | |||||||
| chr17:45064512 | G | T | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.131+3052G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064512 | |||||||
| chr17:45064513 | A | T | 1 | a0001c0002t0001g0230 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.131+3053A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064513 | |||||||
| chr17:45064583 | G | A | 1 | a0001c0004t0003g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.131+3123G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064583 | |||||||
| chr17:45064598 | A | G | 212 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(209): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.131+3138A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064598 | |||||||
| chr17:45064802 | G | C | 41 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(38): Show |
46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+3342G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064802 | |||||||
| chr17:45064845 | G | A | 5 | a0001c0001t0004g0066 a0001c0001t0004g0072 a0001c0001t0004g0073 others(2): Show |
5 | HG00597.hp1 NA18963.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+3385G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064845 | |||||||
| chr17:45064881 | G | T | 43 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+3421G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45064881 | |||||||
| chr17:45065093 | T | C | 1 | a0001c0003t0010g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+3633T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065093 | |||||||
| chr17:45065296 | A | G | 10 | a0001c0001t0013g0061 a0001c0001t0013g0062 a0001c0003t0002g0055 others(7): Show |
10 | HG01123.hp1 HG01192.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.131+3836A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065296 | |||||||
| chr17:45065358 | T | A | 1 | a0001c0003t0002g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131+3898T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065358 | |||||||
| chr17:45065394 | C | T | 31 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(28): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+3934C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065394 | |||||||
| chr17:45065399 | G | A | 14 | a0001c0004t0003g0134 a0001c0004t0003g0135 a0001c0004t0003g0136 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.131+3939G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065399 | |||||||
| chr17:45065623 | C | CA | 85 | a0001c0001t0004g0067 a0001c0001t0005g0147 a0001c0001t0005g0234 others(82): Show |
99 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.131+4184dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | ||||||
| chr17:45065623 | C | CAA | 30 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(27): Show |
32 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.131+4183_131+4184d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | ||||||
| chr17:45065623 | CA | C | 40 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(37): Show |
43 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.131+4184delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45065623 | ||||||
| chr17:45065965 | G | A | 37 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0236 others(34): Show |
39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+4505G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065965 | |||||||
| chr17:45065973 | A | G | 2 | a0001c0001t0002g0308 a0001c0001t0002g0309 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.131+4513A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45065973 | |||||||
| chr17:45066052 | A | G | 16 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.131+4592A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066052 | |||||||
| chr17:45066117 | G | A | 1 | a0001c0004t0022g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.131+4657G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066117 | |||||||
| chr17:45066294 | A | G | 50 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.131+4834A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066294 | |||||||
| chr17:45066386 | A | G | 1 | a0001c0004t0003g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131+4926A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066386 | |||||||
| chr17:45066672 | T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+5212T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066672 | |||||||
| chr17:45066689 | T | C | 9 | a0001c0001t0013g0061 a0001c0001t0013g0062 a0001c0003t0002g0059 others(6): Show |
9 | HG01123.hp1 HG01192.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.131+5229T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066689 | |||||||
| chr17:45066695 | T | A | 1 | a0001c0002t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.131+5235T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066695 | |||||||
| chr17:45066716 | T | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+5256T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066716 | |||||||
| chr17:45066782 | A | G | 60 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0003t0011g0148 others(57): Show |
71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+5322A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066782 | |||||||
| chr17:45066827 | C | T | 145 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(142): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+5367C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066827 | |||||||
| chr17:45066843 | G | GCTA | 93 | a0001c0001t0005g0186 a0001c0001t0006g0194 a0001c0001t0015g0253 others(90): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.131+5384_131+5386d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45066843 | ||||||
| chr17:45066850 | T | C | 212 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(209): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.131+5390T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066850 | |||||||
| chr17:45066920 | A | G | 61 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0001t0049g0303 others(58): Show |
72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+5460A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066920 | |||||||
| chr17:45066953 | C | T | 1 | a0001c0002t0018g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.131+5493C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45066953 | |||||||
| chr17:45067141 | G | C | 1 | a0001c0003t0036g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.131+5681G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067141 | |||||||
| chr17:45067167 | A | AT | 6 | a0001c0001t0004g0129 a0001c0001t0043g0345 a0001c0003t0010g0027 others(3): Show |
6 | HG02135.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+5722dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45067167 | ||||||
| chr17:45067199 | A | G | 1 | a0001c0001t0005g0285 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.131+5739A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067199 | |||||||
| chr17:45067250 | G | A | 1 | a0001c0003t0010g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+5790G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067250 | |||||||
| chr17:45067445 | T | G | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+5985T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45067445 | |||||||
| chr17:45068433 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131+6973T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068433 | |||||||
| chr17:45068451 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+6991G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068451 | |||||||
| chr17:45068612 | T | G | 33 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0003t0002g0002 others(30): Show |
36 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.131+7152T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068612 | |||||||
| chr17:45068807 | C | T | 1 | a0001c0003t0010g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131+7347C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068807 | |||||||
| chr17:45068808 | G | A | 37 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0236 others(34): Show |
39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.131+7348G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068808 | |||||||
| chr17:45068888 | C | T | 61 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0001t0049g0303 others(58): Show |
72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+7428C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068888 | |||||||
| chr17:45068982 | A | G | 1 | a0001c0001t0021g0302 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131+7522A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45068982 | |||||||
| chr17:45069064 | G | A | 93 | a0001c0001t0005g0186 a0001c0001t0006g0194 a0001c0001t0015g0253 others(90): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.131+7604G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069064 | |||||||
| chr17:45069108 | C | G | 9 | a0001c0002t0001g0094 a0001c0002t0001g0217 a0001c0002t0001g0218 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.131+7648C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069108 | |||||||
| chr17:45069238 | C | T | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | NA18942.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.131+7778C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069238 | |||||||
| chr17:45069269 | TTTTATTA others(4): Show |
T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+7816_131+7826d others(13): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069269 | ||||||
| chr17:45069273 | A | AT | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+7815dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTAT | 6 | a0001c0001t0002g0310 a0001c0001t0004g0072 a0001c0004t0014g0252 others(3): Show |
6 | HG00597.hp1 HG00735.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+7844_131+7847d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTATTTA others(1): Show |
41 | a0001c0001t0021g0298 a0001c0001t0021g0299 a0001c0001t0021g0302 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.131+7840_131+7847d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTATTTA others(5): Show |
38 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0236 others(35): Show |
40 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.131+7836_131+7847d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTATTTA others(9): Show |
4 | a0001c0001t0005g0271 a0001c0001t0005g0273 a0001c0001t0005g0280 others(1): Show |
4 | HG01346.hp2 HG01433.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+7832_131+7847d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTTAT | 23 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0325 others(20): Show |
25 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.131+7815_131+7816i others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | A | ATTTATTT others(2): Show |
3 | a0001c0001t0006g0324 a0001c0001t0006g0331 a0001c0001t0006g0339 |
3 | HG00099.hp1 HG00741.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.131+7815_131+7816i others(11): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069273 | ATTATTTA others(5): Show |
A | 1 | a0001c0004t0003g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.131+7836_131+7847d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069273 | ||||||
| chr17:45069322 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.131+7862C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069322 | |||||||
| chr17:45069360 | T | G | 1 | a0001c0002t0001g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.131+7900T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069360 | |||||||
| chr17:45069362 | G | C | 43 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.131+7902G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069362 | |||||||
| chr17:45069362 | G | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+7902G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069362 | |||||||
| chr17:45069519 | C | G | 14 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(11): Show |
15 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.131+8059C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069519 | |||||||
| chr17:45069649 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8189C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069649 | |||||||
| chr17:45069652 | C | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8192C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069652 | |||||||
| chr17:45069654 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8194C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069654 | |||||||
| chr17:45069839 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+8379C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069839 | |||||||
| chr17:45069879 | C | CA | 38 | a0001c0001t0015g0253 a0001c0001t0047g0235 a0001c0002t0001g0078 others(35): Show |
38 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.131+8435dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069879 | ||||||
| chr17:45069879 | CA | C | 12 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(9): Show |
12 | HG00735.hp1 HG01169.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.131+8435delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45069879 | ||||||
| chr17:45069907 | A | G | 145 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(142): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.131+8447A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069907 | |||||||
| chr17:45069976 | G | T | 1 | a0001c0002t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.131+8516G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069976 | |||||||
| chr17:45069983 | C | T | 41 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(38): Show |
46 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+8523C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45069983 | |||||||
| chr17:45070071 | A | C | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+8611A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070071 | |||||||
| chr17:45070083 | C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+8623C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070083 | |||||||
| chr17:45070175 | G | C | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+8715G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070175 | |||||||
| chr17:45070186 | A | G | 31 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(28): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+8726A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070186 | |||||||
| chr17:45070214 | A | G | 61 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0001t0049g0303 others(58): Show |
72 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.131+8754A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070214 | |||||||
| chr17:45070255 | T | G | 1 | a0001c0004t0022g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.131+8795T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070255 | |||||||
| chr17:45070255 | T | TTG | 31 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(28): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.131+8810_131+8811d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45070255 | ||||||
| chr17:45070399 | C | T | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.131+8939C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070399 | |||||||
| chr17:45070401 | C | T | 2 | a0001c0001t0009g0131 a0001c0001t0009g0132 |
2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.131+8941C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070401 | |||||||
| chr17:45070540 | C | T | 2 | a0001c0003t0002g0051 a0001c0005t0002g0022 |
2 | NA18964.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.131+9080C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070540 | |||||||
| chr17:45070597 | T | C | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+9137T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070597 | |||||||
| chr17:45070657 | T | TTA | 57 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0003t0011g0148 others(54): Show |
68 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.131+9197_131+9198i others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070657 | |||||||
| chr17:45070659 | C | T | 50 | a0001c0001t0002g0130 a0001c0001t0002g0228 a0001c0001t0002g0229 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.131+9199C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070659 | |||||||
| chr17:45070798 | C | T | 60 | a0001c0001t0005g0147 a0001c0001t0030g0153 a0001c0001t0049g0303 others(57): Show |
71 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+9338C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070798 | |||||||
| chr17:45070839 | A | G | 1 | a0001c0002t0001g0214 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.131+9379A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070839 | |||||||
| chr17:45070912 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+9452A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070912 | |||||||
| chr17:45070948 | C | T | 1 | a0001c0003t0002g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131+9488C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45070948 | |||||||
| chr17:45071106 | C | T | 1 | a0001c0003t0010g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131+9646C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071106 | |||||||
| chr17:45071142 | G | A | 34 | a0001c0001t0005g0006 a0001c0001t0005g0234 a0001c0001t0005g0236 others(31): Show |
36 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.131+9682G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071142 | |||||||
| chr17:45071258 | A | C | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+9798A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071258 | |||||||
| chr17:45071276 | C | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.131+9816C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071276 | |||||||
| chr17:45071318 | C | T | 2 | a0001c0004t0003g0134 a0001c0004t0054g0138 |
2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.131+9858C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071318 | |||||||
| chr17:45071389 | G | C | 1 | a0001c0003t0019g0056 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131+9929G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071389 | |||||||
| chr17:45071848 | C | T | 3 | a0001c0003t0019g0056 a0001c0003t0019g0063 a0001c0003t0019g0064 |
3 | HG01123.hp1 HG01192.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.132-9796C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071848 | |||||||
| chr17:45071867 | G | A | 34 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0234 others(31): Show |
36 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.132-9777G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45071867 | |||||||
| chr17:45072066 | A | G | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-9578A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072066 | |||||||
| chr17:45072252 | T | TA | 37 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(34): Show |
39 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.132-9391dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45072252 | ||||||
| chr17:45072254 | C | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-9390C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072254 | |||||||
| chr17:45072404 | C | T | 7 | a0001c0004t0003g0015 a0001c0004t0003g0016 a0001c0004t0014g0248 others(4): Show |
9 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-9240C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072404 | |||||||
| chr17:45072608 | G | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-9036G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072608 | |||||||
| chr17:45072620 | T | C | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-9024T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072620 | |||||||
| chr17:45072672 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.132-8972G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072672 | |||||||
| chr17:45072680 | C | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-8964C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072680 | |||||||
| chr17:45072684 | C | T | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-8960C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072684 | |||||||
| chr17:45072734 | C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.132-8910C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072734 | |||||||
| chr17:45072757 | C | A | 2 | a0001c0003t0026g0057 a0001c0003t0026g0058 |
2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.132-8887C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072757 | |||||||
| chr17:45072825 | C | T | 2 | a0001c0004t0003g0346 a0001c0004t0003g0347 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.132-8819C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072825 | |||||||
| chr17:45072838 | C | T | 2 | a0001c0001t0009g0131 a0001c0001t0009g0132 |
2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.132-8806C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072838 | |||||||
| chr17:45072841 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-8803G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072841 | |||||||
| chr17:45072848 | C | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-8796C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072848 | |||||||
| chr17:45072849 | G | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-8795G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072849 | |||||||
| chr17:45072874 | A | G | 86 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(83): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-8770A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45072874 | |||||||
| chr17:45073045 | G | C | 1 | a0001c0001t0009g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.132-8599G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073045 | |||||||
| chr17:45073206 | G | A | 3 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 |
3 | NA19062.hp1 NA19068.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.132-8438G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073206 | |||||||
| chr17:45073599 | A | G | 2 | a0001c0003t0026g0057 a0001c0003t0026g0058 |
2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.132-8045A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073599 | |||||||
| chr17:45073712 | C | T | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132-7932C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073712 | |||||||
| chr17:45073862 | G | T | 1 | a0001c0003t0011g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132-7782G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073862 | |||||||
| chr17:45073909 | T | C | 353 | a0001c0001t0001g0112 a0001c0001t0002g0021 a0001c0001t0002g0130 others(350): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.132-7735T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45073909 | |||||||
| chr17:45074032 | T | C | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-7612T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074032 | |||||||
| chr17:45074105 | G | T | 86 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(83): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-7539G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074105 | |||||||
| chr17:45074137 | G | T | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.132-7507G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074137 | |||||||
| chr17:45074217 | C | CT | 65 | a0001c0001t0004g0070 a0001c0001t0005g0006 a0001c0001t0005g0147 others(62): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.132-7412dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | ||||||
| chr17:45074217 | C | CTT | 81 | a0001c0001t0002g0021 a0001c0001t0005g0259 a0001c0001t0006g0019 others(78): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.132-7413_132-7412d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | ||||||
| chr17:45074217 | C | CTTT | 6 | a0001c0001t0006g0339 a0001c0001t0006g0342 a0001c0001t0013g0318 others(3): Show |
6 | HG00741.hp1 HG01978.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-7414_132-7412d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45074217 | ||||||
| chr17:45074231 | T | TC | 87 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(84): Show |
90 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.132-7413_132-7412i others(3): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074231 | |||||||
| chr17:45074242 | T | C | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-7402T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074242 | |||||||
| chr17:45074253 | C | T | 1 | a0001c0001t0016g0295 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.132-7391C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074253 | |||||||
| chr17:45074289 | A | G | 1 | a0001c0002t0012g0212 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132-7355A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074289 | |||||||
| chr17:45074317 | C | A | 1 | a0001c0003t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.132-7327C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074317 | |||||||
| chr17:45074942 | G | A | 1 | a0001c0002t0001g0079 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.132-6702G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45074942 | |||||||
| chr17:45075053 | G | A | 1 | a0001c0002t0004g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.132-6591G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075053 | |||||||
| chr17:45075142 | C | G | 1 | a0001c0001t0005g0279 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.132-6502C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075142 | |||||||
| chr17:45075146 | C | T | 1 | a0001c0004t0003g0348 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.132-6498C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075146 | |||||||
| chr17:45075222 | G | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-6422G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075222 | |||||||
| chr17:45075307 | A | G | 86 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(83): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-6337A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075307 | |||||||
| chr17:45075312 | C | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-6332C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075312 | |||||||
| chr17:45075351 | C | G | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-6293C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075351 | |||||||
| chr17:45075434 | G | A | 1 | a0001c0003t0010g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132-6210G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075434 | |||||||
| chr17:45075509 | T | C | 150 | a0001c0001t0002g0021 a0001c0001t0005g0006 a0001c0001t0005g0147 others(147): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.132-6135T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075509 | |||||||
| chr17:45075555 | G | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0320 a0001c0001t0007g0322 others(3): Show |
7 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-6089G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075555 | |||||||
| chr17:45075573 | A | C | 2 | a0001c0001t0015g0278 a0001c0001t0015g0284 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.132-6071A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075573 | |||||||
| chr17:45075580 | G | A | 1 | a0001c0004t0003g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132-6064G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075580 | |||||||
| chr17:45075596 | A | G | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-6048A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075596 | |||||||
| chr17:45075638 | A | G | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-6006A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075638 | |||||||
| chr17:45075732 | T | G | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-5912T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075732 | |||||||
| chr17:45075800 | T | C | 351 | a0001c0001t0001g0112 a0001c0001t0002g0021 a0001c0001t0002g0130 others(348): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.132-5844T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075800 | |||||||
| chr17:45075867 | C | T | 9 | a0001c0002t0001g0094 a0001c0002t0001g0217 a0001c0002t0001g0218 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-5777C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075867 | |||||||
| chr17:45075868 | A | T | 1 | a0001c0001t0052g0338 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.132-5776A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075868 | |||||||
| chr17:45075992 | C | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-5652C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45075992 | |||||||
| chr17:45076021 | G | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-5623G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076021 | |||||||
| chr17:45076196 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.132-5448T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076196 | |||||||
| chr17:45076267 | A | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-5377A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076267 | |||||||
| chr17:45076344 | G | T | 3 | a0001c0004t0022g0144 a0001c0004t0022g0145 a0001c0004t0022g0161 |
3 | HG00735.hp1 HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.132-5300G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076344 | |||||||
| chr17:45076402 | C | T | 1 | a0001c0001t0047g0235 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.132-5242C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076402 | |||||||
| chr17:45076451 | GA | G | 6 | a0001c0001t0008g0287 a0001c0001t0029g0255 a0001c0001t0029g0256 others(3): Show |
6 | HG01069.hp2 HG01361.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-5179delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45076451 | ||||||
| chr17:45076452 | A | C | 36 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(33): Show |
38 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.132-5192A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076452 | |||||||
| chr17:45076477 | C | T | 1 | a0001c0001t0009g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.132-5167C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076477 | |||||||
| chr17:45076890 | T | C | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-4754T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076890 | |||||||
| chr17:45076912 | T | C | 1 | a0001c0003t0002g0029 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.132-4732T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45076912 | |||||||
| chr17:45077004 | T | C | 14 | a0001c0003t0002g0002 a0001c0003t0002g0023 a0001c0003t0002g0024 others(11): Show |
17 | HG01070.hp2 HG01261.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-4640T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077004 | |||||||
| chr17:45077169 | T | C | 16 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-4475T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077169 | |||||||
| chr17:45077225 | T | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-4419T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077225 | |||||||
| chr17:45077789 | A | G | 2 | a0001c0004t0003g0139 a0001c0004t0003g0140 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.132-3855A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077789 | |||||||
| chr17:45077980 | T | A | 1 | a0001c0002t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132-3664T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45077980 | |||||||
| chr17:45078011 | C | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-3633C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078011 | |||||||
| chr17:45078242 | TG | T | 12 | a0001c0002t0001g0068 a0001c0002t0001g0077 a0001c0002t0001g0087 others(9): Show |
12 | HG00597.hp2 NA18940.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.132-3395delG | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45078242 | ||||||
| chr17:45078245 | G | A | 2 | a0001c0004t0033g0240 a0001c0004t0033g0241 |
2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.132-3399G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078245 | |||||||
| chr17:45078483 | C | T | 5 | a0001c0002t0004g0184 a0001c0002t0004g0185 a0001c0002t0004g0231 others(2): Show |
5 | HG00140.hp2 HG01361.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-3161C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078483 | |||||||
| chr17:45078486 | G | GTA | 6 | a0001c0001t0005g0277 a0001c0001t0010g0018 a0001c0001t0010g0315 others(3): Show |
6 | HG01891.hp2 HG02132.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-3145_132-3144d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45078486 | ||||||
| chr17:45078546 | G | A | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.132-3098G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078546 | |||||||
| chr17:45078579 | T | C | 4 | a0001c0001t0005g0259 a0001c0001t0005g0261 a0001c0001t0005g0262 others(1): Show |
4 | HG00140.hp1 HG01123.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-3065T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078579 | |||||||
| chr17:45078612 | A | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-3032A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078612 | |||||||
| chr17:45078655 | T | C | 82 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0002t0001g0050 others(79): Show |
83 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.132-2989T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078655 | |||||||
| chr17:45078708 | C | T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.132-2936C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078708 | |||||||
| chr17:45078767 | A | T | 81 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0002t0001g0050 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.132-2877A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078767 | |||||||
| chr17:45078836 | G | A | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-2808G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078836 | |||||||
| chr17:45078907 | C | T | 1 | a0001c0003t0041g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.132-2737C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45078907 | |||||||
| chr17:45079077 | T | C | 1 | a0001c0004t0003g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.132-2567T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079077 | |||||||
| chr17:45079085 | T | C | 16 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-2559T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079085 | |||||||
| chr17:45079117 | T | TC | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-2523dupC | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45079117 | ||||||
| chr17:45079190 | A | C | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-2454A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079190 | |||||||
| chr17:45079348 | T | C | 151 | a0001c0001t0002g0021 a0001c0001t0005g0006 a0001c0001t0005g0147 others(148): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.132-2296T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079348 | |||||||
| chr17:45079351 | C | T | 42 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(39): Show |
55 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.132-2293C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079351 | |||||||
| chr17:45079449 | A | G | 1 | a0001c0001t0010g0315 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132-2195A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079449 | |||||||
| chr17:45079450 | C | T | 9 | a0001c0004t0003g0134 a0001c0004t0003g0136 a0001c0004t0003g0137 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.132-2194C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079450 | |||||||
| chr17:45079478 | A | G | 1 | a0001c0001t0006g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.132-2166A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079478 | |||||||
| chr17:45079494 | C | G | 1 | a0001c0003t0002g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132-2150C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079494 | |||||||
| chr17:45079547 | T | C | 16 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-2097T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079547 | |||||||
| chr17:45079591 | C | T | 1 | a0001c0003t0002g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.132-2053C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079591 | |||||||
| chr17:45079615 | A | G | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.132-2029A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079615 | |||||||
| chr17:45079724 | G | A | 86 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(83): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-1920G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079724 | |||||||
| chr17:45079756 | G | A | 1 | a0001c0002t0012g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.132-1888G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079756 | |||||||
| chr17:45079840 | T | C | 4 | a0001c0001t0015g0253 a0001c0001t0015g0264 a0001c0001t0015g0278 others(1): Show |
4 | HG00642.hp1 HG02109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-1804T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079840 | |||||||
| chr17:45079866 | AT | A | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132-1772delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45079866 | ||||||
| chr17:45079890 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132-1754G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079890 | |||||||
| chr17:45079961 | A | G | 148 | a0001c0001t0002g0021 a0001c0001t0005g0006 a0001c0001t0005g0147 others(145): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.132-1683A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45079961 | |||||||
| chr17:45080167 | CT | C | 88 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(85): Show |
91 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.132-1467delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080167 | ||||||
| chr17:45080279 | G | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.132-1365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080279 | |||||||
| chr17:45080288 | G | C | 31 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(28): Show |
33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.132-1356G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080288 | |||||||
| chr17:45080322 | G | A | 5 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(2): Show |
6 | HG02451.hp1 HG03516.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-1322G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080322 | |||||||
| chr17:45080341 | G | A | 148 | a0001c0001t0002g0021 a0001c0001t0005g0006 a0001c0001t0005g0147 others(145): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.132-1303G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080341 | |||||||
| chr17:45080465 | C | CT | 23 | a0001c0001t0004g0067 a0001c0001t0004g0072 a0001c0001t0007g0007 others(20): Show |
27 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.132-1158dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | ||||||
| chr17:45080465 | CT | C | 201 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(198): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.132-1158delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | ||||||
| chr17:45080465 | CTT | C | 76 | a0001c0001t0013g0061 a0001c0001t0028g0188 a0001c0001t0028g0189 others(73): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.132-1159_132-1158d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080465 | ||||||
| chr17:45080534 | TCTCGGCT others(87): Show |
T | 1 | a0001c0004t0003g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.132-1108_132-1015d others(96): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 45080534 | ||||||
| chr17:45080535 | C | G | 8 | a0001c0001t0028g0188 a0001c0001t0028g0189 a0001c0003t0010g0095 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.132-1109C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080535 | |||||||
| chr17:45080614 | G | A | 76 | a0001c0001t0008g0287 a0001c0001t0028g0188 a0001c0001t0028g0189 others(73): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.132-1030G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080614 | |||||||
| chr17:45080623 | C | T | 1 | a0001c0004t0031g0013 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.132-1021C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080623 | |||||||
| chr17:45080688 | C | G | 1 | a0001c0003t0002g0036 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.132-956C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080688 | |||||||
| chr17:45080847 | A | G | 1 | a0001c0001t0005g0281 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.132-797A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45080847 | |||||||
| chr17:45081268 | T | C | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.132-376T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081268 | |||||||
| chr17:45081306 | G | A | 86 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(83): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-338G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081306 | |||||||
| chr17:45081454 | C | T | 1 | a0001c0003t0019g0064 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.132-190C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081454 | |||||||
| chr17:45081534 | G | A | 31 | a0001c0001t0002g0021 a0001c0001t0006g0019 a0001c0001t0006g0194 others(28): Show |
33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.132-110G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 1/11 | chr17 | 45081534 | |||||||
| chr17:45081782 | C | T | 1 | a0001c0001t0004g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.240+30C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45081782 | |||||||
| chr17:45081951 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240+199G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45081951 | |||||||
| chr17:45082057 | G | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+305G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082057 | |||||||
| chr17:45082091 | C | T | 5 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0215 others(2): Show |
5 | NA18942.hp2 NA18986.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+339C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082091 | |||||||
| chr17:45082272 | G | GT | 7 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+535dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45082272 | ||||||
| chr17:45082375 | C | G | 9 | a0001c0001t0028g0188 a0001c0001t0028g0189 a0001c0003t0010g0027 others(6): Show |
9 | HG01109.hp2 HG02451.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+623C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082375 | |||||||
| chr17:45082465 | C | T | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+713C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082465 | |||||||
| chr17:45082517 | A | G | 3 | a0001c0003t0010g0095 a0001c0003t0010g0191 a0001c0003t0010g0192 |
3 | HG01109.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.240+765A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082517 | |||||||
| chr17:45082565 | A | G | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.240+813A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082565 | |||||||
| chr17:45082605 | T | A | 1 | a0001c0004t0003g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240+853T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082605 | |||||||
| chr17:45082705 | C | T | 1 | a0001c0001t0004g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.240+953C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082705 | |||||||
| chr17:45082786 | C | T | 1 | a0001c0001t0008g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.240+1034C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082786 | |||||||
| chr17:45082788 | G | T | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1036G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082788 | |||||||
| chr17:45082974 | G | A | 3 | a0001c0001t0008g0287 a0001c0001t0029g0255 a0001c0001t0029g0256 |
3 | HG03209.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.240+1222G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45082974 | |||||||
| chr17:45083131 | A | G | 73 | a0001c0001t0028g0188 a0001c0001t0028g0189 a0001c0003t0002g0002 others(70): Show |
76 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.240+1379A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083131 | |||||||
| chr17:45083171 | T | C | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1419T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083171 | |||||||
| chr17:45083180 | G | T | 81 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0002t0001g0050 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.240+1428G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083180 | |||||||
| chr17:45083182 | G | C | 1 | a0001c0002t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.240+1430G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083182 | |||||||
| chr17:45083190 | G | A | 76 | a0001c0001t0008g0287 a0001c0001t0028g0188 a0001c0001t0028g0189 others(73): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.240+1438G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083190 | |||||||
| chr17:45083203 | C | T | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1451C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083203 | |||||||
| chr17:45083271 | A | G | 1 | a0001c0002t0004g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.240+1519A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083271 | |||||||
| chr17:45083297 | C | T | 1 | a0001c0003t0011g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.240+1545C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083297 | |||||||
| chr17:45083318 | C | CA | 12 | a0001c0001t0002g0310 a0001c0001t0006g0339 a0001c0001t0043g0345 others(9): Show |
12 | HG00423.hp2 HG00741.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+1581dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45083318 | ||||||
| chr17:45083334 | T | A | 1 | a0001c0002t0001g0093 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.240+1582T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083334 | |||||||
| chr17:45083335 | TA | T | 80 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0002t0001g0050 others(77): Show |
81 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.240+1592delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45083335 | ||||||
| chr17:45083336 | A | T | 40 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(37): Show |
42 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.240+1584A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083336 | |||||||
| chr17:45083360 | A | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.240+1608A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083360 | |||||||
| chr17:45083395 | C | G | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+1643C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083395 | |||||||
| chr17:45083442 | A | G | 3 | a0001c0003t0010g0095 a0001c0003t0010g0191 a0001c0003t0010g0192 |
3 | HG01109.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.240+1690A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083442 | |||||||
| chr17:45083468 | A | G | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1716A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083468 | |||||||
| chr17:45083471 | G | A | 3 | a0001c0001t0005g0265 a0001c0001t0005g0266 a0001c0001t0005g0267 |
3 | HG01074.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.240+1719G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083471 | |||||||
| chr17:45083647 | C | G | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.240+1895C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083647 | |||||||
| chr17:45083737 | C | T | 84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.240+1985C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083737 | |||||||
| chr17:45083746 | A | G | 148 | a0001c0001t0002g0310 a0001c0001t0005g0006 a0001c0001t0005g0147 others(145): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.240+1994A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083746 | |||||||
| chr17:45083787 | A | G | 2 | a0001c0001t0005g0275 a0001c0001t0005g0276 |
2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.240+2035A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083787 | |||||||
| chr17:45083807 | C | A | 1 | a0001c0002t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.240+2055C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083807 | |||||||
| chr17:45083952 | T | C | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.240+2200T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083952 | |||||||
| chr17:45083985 | C | T | 240 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(237): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.240+2233C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45083985 | |||||||
| chr17:45084046 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.240+2294A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084046 | |||||||
| chr17:45084336 | C | CT | 334 | a0001c0001t0001g0112 a0001c0001t0002g0130 a0001c0001t0002g0227 others(331): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.241-2158dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45084336 | ||||||
| chr17:45084336 | C | CTT | 20 | a0001c0001t0002g0021 a0001c0001t0002g0229 a0001c0001t0004g0127 others(17): Show |
20 | HG00438.hp1 HG01109.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.241-2159_241-2158d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45084336 | ||||||
| chr17:45084352 | C | T | 1 | a0001c0001t0047g0235 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.241-2156C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084352 | |||||||
| chr17:45084456 | T | C | 1 | a0001c0001t0006g0324 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.241-2052T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084456 | |||||||
| chr17:45084475 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.241-2033C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084475 | |||||||
| chr17:45084483 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.241-2025C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084483 | |||||||
| chr17:45084494 | T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.241-2014T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084494 | |||||||
| chr17:45084572 | A | G | 1 | a0001c0001t0039g0314 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241-1936A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084572 | |||||||
| chr17:45084584 | C | T | 54 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(51): Show |
67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-1924C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084584 | |||||||
| chr17:45084622 | C | T | 73 | a0001c0001t0028g0188 a0001c0001t0028g0189 a0001c0003t0002g0002 others(70): Show |
76 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.241-1886C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084622 | |||||||
| chr17:45084641 | T | C | 4 | a0001c0001t0015g0253 a0001c0001t0015g0264 a0001c0001t0015g0278 others(1): Show |
4 | HG00642.hp1 HG02109.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1867T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084641 | |||||||
| chr17:45084756 | C | T | 1 | a0001c0002t0004g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.241-1752C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084756 | |||||||
| chr17:45084772 | C | T | 6 | a0001c0001t0007g0008 a0001c0001t0007g0320 a0001c0001t0007g0322 others(3): Show |
7 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-1736C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084772 | |||||||
| chr17:45084797 | A | G | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.241-1711A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084797 | |||||||
| chr17:45084899 | A | G | 1 | a0001c0003t0019g0064 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.241-1609A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45084899 | |||||||
| chr17:45085017 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.241-1491T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085017 | |||||||
| chr17:45085018 | T | TGGGCACA others(11): Show |
1 | a0001c0002t0001g0167 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.241-1485_241-1484i others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085018 | ||||||
| chr17:45085027 | C | G | 1 | a0001c0001t0006g0335 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.241-1481C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085027 | |||||||
| chr17:45085408 | C | G | 85 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(82): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.241-1100C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085408 | |||||||
| chr17:45085470 | T | C | 1 | a0001c0004t0003g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.241-1038T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085470 | |||||||
| chr17:45085520 | T | C | 2 | a0001c0002t0025g0082 a0001c0002t0025g0171 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.241-988T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085520 | |||||||
| chr17:45085554 | A | G | 14 | a0001c0003t0002g0055 a0001c0003t0002g0059 a0001c0003t0002g0060 others(11): Show |
14 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-954A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085554 | |||||||
| chr17:45085651 | T | C | 54 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(51): Show |
67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-857T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085651 | |||||||
| chr17:45085704 | G | A | 2 | a0001c0001t0008g0287 a0001c0001t0029g0255 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.241-804G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085704 | |||||||
| chr17:45085709 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.241-799G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085709 | |||||||
| chr17:45085819 | C | CT | 39 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(36): Show |
41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.241-676dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | ||||||
| chr17:45085819 | C | CTT | 12 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(9): Show |
13 | HG01169.hp2 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-677_241-676dup others(2): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | ||||||
| chr17:45085819 | CT | C | 13 | a0001c0001t0006g0325 a0001c0001t0007g0007 a0001c0001t0007g0008 others(10): Show |
16 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.241-676delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45085819 | ||||||
| chr17:45085870 | G | A | 19 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0080 others(16): Show |
19 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.241-638G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085870 | |||||||
| chr17:45085957 | G | C | 93 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(90): Show |
96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.241-551G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085957 | |||||||
| chr17:45085965 | G | T | 2 | a0001c0004t0003g0160 a0001c0004t0031g0013 |
3 | HG02622.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.241-543G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085965 | |||||||
| chr17:45085970 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-538C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085970 | |||||||
| chr17:45085974 | G | A | 1 | a0001c0003t0041g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.241-534G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085974 | |||||||
| chr17:45085987 | A | T | 2 | a0001c0001t0009g0131 a0001c0001t0009g0132 |
2 | HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.241-521A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45085987 | |||||||
| chr17:45086124 | C | CT | 12 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(9): Show |
12 | HG00735.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.241-367dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | ||||||
| chr17:45086124 | C | CTTT | 28 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(25): Show |
30 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.241-369_241-367dup others(3): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | ||||||
| chr17:45086124 | C | CTTTT | 10 | a0001c0001t0005g0259 a0001c0001t0005g0262 a0001c0001t0005g0263 others(7): Show |
10 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-370_241-367dup others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 45086124 | ||||||
| chr17:45086185 | G | A | 2 | a0001c0004t0022g0145 a0001c0004t0022g0161 |
2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.241-323G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086185 | |||||||
| chr17:45086322 | A | G | 1 | a0001c0001t0006g0339 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241-186A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086322 | |||||||
| chr17:45086325 | A | T | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-183A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086325 | |||||||
| chr17:45086373 | C | T | 1 | a0001c0004t0003g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.241-135C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086373 | |||||||
| chr17:45086385 | A | G | 1 | a0001c0003t0010g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241-123A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086385 | |||||||
| chr17:45086388 | A | G | 240 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(237): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.241-120A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086388 | |||||||
| chr17:45086483 | T | C | 150 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(147): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.241-25T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 2/11 | chr17 | 45086483 | |||||||
| chr17:45086799 | A | T | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+147A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45086799 | |||||||
| chr17:45086878 | G | T | 84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.385+226G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45086878 | |||||||
| chr17:45086998 | T | TA | 152 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.385+360dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45086998 | ||||||
| chr17:45087187 | CA | C | 5 | a0001c0002t0012g0090 a0001c0002t0012g0200 a0001c0002t0012g0206 others(2): Show |
5 | HG00733.hp1 HG01074.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+545delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45087187 | ||||||
| chr17:45087774 | G | A | 1 | a0001c0001t0006g0339 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.385+1122G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087774 | |||||||
| chr17:45087774 | G | C | 15 | a0001c0003t0002g0055 a0001c0003t0002g0059 a0001c0003t0002g0060 others(12): Show |
15 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.385+1122G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087774 | |||||||
| chr17:45087817 | T | C | 150 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(147): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.385+1165T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087817 | |||||||
| chr17:45087891 | C | A | 1 | a0001c0001t0005g0261 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.385+1239C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45087891 | |||||||
| chr17:45088016 | T | A | 84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.385+1364T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088016 | |||||||
| chr17:45088180 | G | A | 7 | a0001c0004t0003g0134 a0001c0004t0003g0136 a0001c0004t0003g0137 others(4): Show |
7 | HG02486.hp2 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+1528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088180 | |||||||
| chr17:45088470 | T | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1818T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088470 | |||||||
| chr17:45088519 | T | C | 150 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(147): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.385+1867T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088519 | |||||||
| chr17:45088556 | A | G | 2 | a0001c0001t0005g0275 a0001c0001t0005g0276 |
2 | NA19002.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.385+1904A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088556 | |||||||
| chr17:45088584 | G | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+1932G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088584 | |||||||
| chr17:45088689 | G | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2037G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088689 | |||||||
| chr17:45088764 | T | TAAA | 36 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(33): Show |
38 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.385+2112_385+2113i others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088764 | |||||||
| chr17:45088765 | T | A | 39 | a0001c0001t0004g0107 a0001c0001t0005g0006 a0001c0001t0005g0147 others(36): Show |
41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.385+2113T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088765 | |||||||
| chr17:45088765 | TA | T | 12 | a0001c0001t0028g0188 a0001c0001t0028g0189 a0001c0002t0001g0223 others(9): Show |
12 | HG01109.hp2 HG01516.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.385+2128delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45088765 | ||||||
| chr17:45088766 | A | T | 1 | a0001c0003t0020g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.385+2114A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088766 | |||||||
| chr17:45088792 | G | A | 10 | a0001c0004t0003g0134 a0001c0004t0003g0136 a0001c0004t0003g0137 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+2140G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088792 | |||||||
| chr17:45088845 | C | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2193C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45088845 | |||||||
| chr17:45089019 | C | T | 4 | a0001c0003t0020g0098 a0001c0003t0020g0099 a0001c0003t0038g0097 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+2367C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089019 | |||||||
| chr17:45089082 | G | T | 240 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(237): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.385+2430G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089082 | |||||||
| chr17:45089172 | G | A | 1 | a0001c0004t0003g0242 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.385+2520G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089172 | |||||||
| chr17:45089342 | G | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2690G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089342 | |||||||
| chr17:45089454 | G | A | 7 | a0001c0003t0002g0055 a0001c0003t0011g0148 a0001c0003t0011g0149 others(4): Show |
7 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+2802G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089454 | |||||||
| chr17:45089486 | T | C | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.385+2834T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089486 | |||||||
| chr17:45089502 | C | T | 1 | a0001c0004t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+2850C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089502 | |||||||
| chr17:45089528 | G | T | 2 | a0001c0003t0002g0045 a0001c0003t0002g0046 |
2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.385+2876G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089528 | |||||||
| chr17:45089789 | C | T | 112 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(109): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.385+3137C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089789 | |||||||
| chr17:45089918 | G | T | 16 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0287 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.385+3266G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089918 | |||||||
| chr17:45089925 | A | G | 1 | a0001c0001t0007g0319 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385+3273A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45089925 | |||||||
| chr17:45090106 | G | C | 1 | a0001c0002t0001g0223 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.385+3454G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090106 | |||||||
| chr17:45090112 | G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+3460G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090112 | |||||||
| chr17:45090189 | T | G | 1 | a0001c0003t0026g0057 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.386-3496T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090189 | |||||||
| chr17:45090398 | G | GTCGTTCT others(3): Show |
84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.386-3285_386-3276d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45090398 | ||||||
| chr17:45090401 | GTTC | G | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3278_386-3276d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45090401 | ||||||
| chr17:45090495 | G | C | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.386-3190G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090495 | |||||||
| chr17:45090584 | C | T | 49 | a0001c0003t0002g0002 a0001c0003t0002g0023 a0001c0003t0002g0024 others(46): Show |
52 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.386-3101C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090584 | |||||||
| chr17:45090906 | A | G | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.386-2779A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45090906 | |||||||
| chr17:45091152 | T | C | 1 | a0001c0004t0022g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.386-2533T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091152 | |||||||
| chr17:45091157 | G | A | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.386-2528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091157 | |||||||
| chr17:45091160 | A | G | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2525A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091160 | |||||||
| chr17:45091161 | G | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2524G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091161 | |||||||
| chr17:45091162 | A | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2523A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091162 | |||||||
| chr17:45091164 | A | G | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2521A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091164 | |||||||
| chr17:45091165 | T | G | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2520T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091165 | |||||||
| chr17:45091166 | T | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2519T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091166 | |||||||
| chr17:45091167 | T | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2518T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091167 | |||||||
| chr17:45091168 | C | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2517C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091168 | |||||||
| chr17:45091170 | T | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2515T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091170 | |||||||
| chr17:45091171 | C | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2514C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091171 | |||||||
| chr17:45091172 | T | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2513T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091172 | |||||||
| chr17:45091174 | A | T | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2511A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091174 | |||||||
| chr17:45091178 | G | A | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2507G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091178 | |||||||
| chr17:45091179 | T | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2506T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091179 | |||||||
| chr17:45091181 | T | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2504T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091181 | |||||||
| chr17:45091183 | T | G | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2502T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091183 | |||||||
| chr17:45091184 | C | T | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2501C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091184 | |||||||
| chr17:45091187 | G | C | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2498G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091187 | |||||||
| chr17:45091187 | G | GAC | 21 | a0001c0001t0004g0111 a0001c0001t0006g0019 a0001c0001t0006g0328 others(18): Show |
22 | HG00323.hp1 HG00609.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.386-2449_386-2448d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACAC | 28 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0013g0341 others(25): Show |
29 | HG00544.hp1 HG01081.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.386-2451_386-2448d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACAC | 11 | a0001c0001t0004g0119 a0001c0001t0006g0343 a0001c0001t0013g0318 others(8): Show |
11 | HG01123.hp1 HG01516.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.386-2453_386-2448d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(1): Show |
15 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0004g0108 others(12): Show |
15 | HG00408.hp1 HG00735.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-2455_386-2448d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(3): Show |
16 | a0001c0001t0002g0309 a0001c0002t0001g0083 a0001c0002t0001g0167 others(13): Show |
16 | HG00140.hp2 HG01069.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.386-2457_386-2448d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(5): Show |
21 | a0001c0001t0002g0308 a0001c0001t0006g0317 a0001c0001t0049g0303 others(18): Show |
22 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.386-2459_386-2448d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(7): Show |
12 | a0001c0002t0001g0168 a0001c0002t0001g0170 a0001c0002t0001g0174 others(9): Show |
12 | HG00438.hp2 HG00609.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-2461_386-2448d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(9): Show |
12 | a0001c0001t0006g0337 a0001c0002t0001g0080 a0001c0002t0001g0093 others(9): Show |
12 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-2463_386-2448d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(11): Show |
5 | a0001c0001t0002g0305 a0001c0002t0001g0079 a0001c0002t0001g0216 others(2): Show |
5 | HG03098.hp1 NA18986.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-2465_386-2448d others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(13): Show |
3 | a0001c0002t0001g0163 a0001c0002t0001g0181 a0001c0002t0024g0165 |
3 | HG01433.hp1 NA19054.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.386-2467_386-2448d others(22): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(15): Show |
1 | a0001c0002t0001g0172 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.386-2469_386-2448d others(24): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | G | GACACACA others(17): Show |
2 | a0001c0002t0001g0087 a0001c0002t0001g0088 |
2 | NA18947.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.386-2471_386-2448d others(26): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GAC | G | 72 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0070 others(69): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.386-2449_386-2448d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACAC | G | 29 | a0001c0001t0004g0072 a0001c0001t0005g0259 a0001c0001t0005g0261 others(26): Show |
32 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.386-2451_386-2448d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACAC | G | 6 | a0001c0001t0008g0291 a0001c0001t0008g0297 a0001c0001t0010g0018 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-2453_386-2448d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACACA others(3): Show |
G | 3 | a0001c0001t0002g0021 a0001c0001t0007g0322 a0001c0003t0002g0053 |
3 | HG03516.hp1 NA18747.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.386-2457_386-2448d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACACA others(5): Show |
G | 17 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(14): Show |
20 | HG00558.hp1 HG00673.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2459_386-2448d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACACA others(7): Show |
G | 2 | a0001c0001t0004g0074 a0001c0001t0004g0075 |
2 | NA18966.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.386-2461_386-2448d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACACA others(9): Show |
G | 1 | a0001c0004t0053g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.386-2463_386-2448d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091187 | GACACACA others(11): Show |
G | 1 | a0001c0004t0003g0005 | 3 | HG02257.hp2 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.386-2465_386-2448d others(20): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091187 | ||||||
| chr17:45091188 | A | T | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2497A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091188 | |||||||
| chr17:45091190 | A | T | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2495A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091190 | |||||||
| chr17:45091192 | A | T | 1 | a0001c0001t0005g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-2493A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091192 | |||||||
| chr17:45091236 | A | G | 30 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(27): Show |
32 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.386-2449A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091236 | |||||||
| chr17:45091237 | C | CGT | 7 | a0001c0001t0005g0260 a0001c0001t0005g0268 a0001c0001t0005g0269 others(4): Show |
7 | HG00423.hp1 HG01361.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-2447_386-2446d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45091237 | ||||||
| chr17:45091237 | C | T | 30 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(27): Show |
32 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.386-2448C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091237 | |||||||
| chr17:45091358 | C | A | 1 | a0001c0004t0017g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.386-2327C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091358 | |||||||
| chr17:45091388 | T | G | 9 | a0001c0004t0003g0133 a0001c0004t0003g0142 a0001c0004t0003g0154 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-2297T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091388 | |||||||
| chr17:45091597 | G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-2088G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091597 | |||||||
| chr17:45091680 | C | G | 1 | a0001c0004t0003g0348 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-2005C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091680 | |||||||
| chr17:45091694 | T | C | 1 | a0001c0001t0004g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.386-1991T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091694 | |||||||
| chr17:45091698 | C | G | 1 | a0001c0003t0041g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.386-1987C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091698 | |||||||
| chr17:45091741 | T | A | 112 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(109): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.386-1944T>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091741 | |||||||
| chr17:45091913 | C | G | 54 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(51): Show |
67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.386-1772C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45091913 | |||||||
| chr17:45092024 | A | G | 240 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(237): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.386-1661A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092024 | |||||||
| chr17:45092186 | A | G | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1499A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092186 | |||||||
| chr17:45092219 | AGGGACTT | A | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(8): Show |
14 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.386-1463_386-1457d others(9): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092219 | ||||||
| chr17:45092316 | G | A | 1 | a0001c0003t0040g0351 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.386-1369G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092316 | |||||||
| chr17:45092336 | G | A | 1 | a0001c0003t0002g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.386-1349G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092336 | |||||||
| chr17:45092346 | C | T | 1 | a0001c0001t0004g0070 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.386-1339C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092346 | |||||||
| chr17:45092347 | G | A | 9 | a0001c0002t0001g0094 a0001c0002t0001g0217 a0001c0002t0001g0218 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-1338G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092347 | |||||||
| chr17:45092397 | AT | A | 98 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(95): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.386-1287delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092397 | |||||||
| chr17:45092536 | G | GA | 43 | a0001c0001t0004g0109 a0001c0001t0005g0006 a0001c0001t0005g0147 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.386-1137dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092536 | ||||||
| chr17:45092544 | A | C | 2 | a0001c0002t0025g0082 a0001c0002t0025g0171 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.386-1141A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092544 | |||||||
| chr17:45092548 | A | C | 1 | a0001c0001t0030g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.386-1137A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092548 | |||||||
| chr17:45092571 | G | A | 47 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(44): Show |
49 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-1114G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092571 | |||||||
| chr17:45092602 | C | A | 1 | a0001c0002t0004g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-1083C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092602 | |||||||
| chr17:45092602 | C | T | 6 | a0001c0003t0011g0148 a0001c0003t0011g0149 a0001c0003t0011g0150 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1083C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45092602 | |||||||
| chr17:45092707 | CA | C | 215 | a0001c0001t0001g0112 a0001c0001t0004g0003 a0001c0001t0004g0004 others(212): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.386-964delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092707 | ||||||
| chr17:45092716 | AAAAAAG | A | 94 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(91): Show |
97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.386-964_386-959del others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 45092716 | ||||||
| chr17:45093054 | G | A | 84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.386-631G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093054 | |||||||
| chr17:45093099 | A | G | 351 | a0001c0001t0001g0112 a0001c0001t0002g0021 a0001c0001t0002g0130 others(348): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.386-586A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093099 | |||||||
| chr17:45093301 | G | A | 1 | a0001c0004t0053g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.386-384G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093301 | |||||||
| chr17:45093539 | C | T | 320 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(317): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.386-146C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093539 | |||||||
| chr17:45093673 | C | G | 1 | a0001c0004t0003g0348 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-12C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 3/11 | chr17 | 45093673 | |||||||
| chr17:45093866 | G | C | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+63G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093866 | |||||||
| chr17:45093881 | C | T | 2 | a0001c0004t0003g0244 a0001c0004t0003g0245 |
2 | NA18940.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.504+78C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093881 | |||||||
| chr17:45093936 | G | A | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+133G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45093936 | |||||||
| chr17:45094153 | C | G | 93 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(90): Show |
96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.504+350C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094153 | |||||||
| chr17:45094270 | G | A | 1 | a0001c0004t0003g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.504+467G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094270 | |||||||
| chr17:45094366 | C | T | 93 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(90): Show |
96 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.504+563C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094366 | |||||||
| chr17:45094466 | C | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+663C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094466 | |||||||
| chr17:45094494 | C | CA | 6 | a0001c0001t0010g0315 a0001c0001t0021g0298 a0001c0001t0037g0313 others(3): Show |
6 | HG00735.hp1 HG01099.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+705dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094494 | ||||||
| chr17:45094518 | A | AT | 9 | a0001c0001t0005g0272 a0001c0001t0010g0018 a0001c0001t0010g0315 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+729dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094518 | ||||||
| chr17:45094518 | A | T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+715A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094518 | |||||||
| chr17:45094814 | C | CT | 107 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(104): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.504+1027dupT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45094814 | ||||||
| chr17:45094839 | G | A | 1 | a0001c0001t0006g0324 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.504+1036G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094839 | |||||||
| chr17:45094999 | G | T | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.505-1195G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45094999 | |||||||
| chr17:45095110 | CT | C | 107 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(104): Show |
111 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.505-1070delT | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45095110 | ||||||
| chr17:45095110 | CTT | C | 133 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(130): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.505-1071_505-1070d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 45095110 | ||||||
| chr17:45095263 | C | T | 1 | a0001c0001t0005g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-931C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095263 | |||||||
| chr17:45095393 | C | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-801C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095393 | |||||||
| chr17:45095481 | T | C | 148 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(145): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.505-713T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095481 | |||||||
| chr17:45095512 | A | G | 1 | a0001c0001t0004g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.505-682A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095512 | |||||||
| chr17:45095538 | A | G | 49 | a0001c0003t0002g0002 a0001c0003t0002g0023 a0001c0003t0002g0024 others(46): Show |
52 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.505-656A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095538 | |||||||
| chr17:45095566 | A | G | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-628A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095566 | |||||||
| chr17:45095763 | C | G | 147 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(144): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.505-431C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095763 | |||||||
| chr17:45095849 | C | T | 1 | a0001c0001t0021g0298 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.505-345C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095849 | |||||||
| chr17:45095850 | G | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-344G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095850 | |||||||
| chr17:45095905 | T | C | 122 | a0001c0001t0005g0006 a0001c0001t0005g0186 a0001c0001t0005g0234 others(119): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.505-289T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45095905 | |||||||
| chr17:45096148 | A | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-46A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096148 | |||||||
| chr17:45096154 | T | C | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505-40T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096154 | |||||||
| chr17:45096182 | A | C | 1 | a0001c0002t0004g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.505-12A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 4/11 | chr17 | 45096182 | |||||||
| chr17:45096459 | C | T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+174C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096459 | |||||||
| chr17:45096534 | TCTGGTGA | T | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+252_596+258del others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 45096534 | ||||||
| chr17:45096673 | C | T | 1 | a0001c0003t0011g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.596+388C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096673 | |||||||
| chr17:45096705 | C | G | 1 | a0001c0002t0001g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.596+420C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096705 | |||||||
| chr17:45096739 | G | A | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.597-389G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096739 | |||||||
| chr17:45096848 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.597-280G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096848 | |||||||
| chr17:45096853 | A | C | 7 | a0001c0003t0010g0027 a0001c0003t0010g0095 a0001c0003t0010g0187 others(4): Show |
7 | HG01109.hp2 HG02886.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.597-275A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 5/11 | chr17 | 45096853 | |||||||
| chr17:45097436 | C | A | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.713+192C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097436 | |||||||
| chr17:45097567 | G | A | 1 | a0001c0002t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.713+323G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097567 | |||||||
| chr17:45097687 | C | T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.713+443C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097687 | |||||||
| chr17:45097733 | C | G | 1 | a0001c0002t0001g0176 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.713+489C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097733 | |||||||
| chr17:45097794 | G | A | 84 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(81): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.713+550G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097794 | |||||||
| chr17:45097796 | C | T | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.713+552C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45097796 | |||||||
| chr17:45098301 | G | A | 1 | a0001c0003t0019g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714-81G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 6/11 | chr17 | 45098301 | |||||||
| chr17:45098954 | T | C | 2 | a0001c0001t0016g0258 a0001c0001t0016g0292 |
2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.884+402T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45098954 | |||||||
| chr17:45098955 | C | G | 3 | a0001c0001t0008g0287 a0001c0001t0029g0255 a0001c0001t0029g0256 |
3 | HG03209.hp2 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.884+403C>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45098955 | |||||||
| chr17:45099040 | G | A | 1 | a0001c0003t0002g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.885-365G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099040 | |||||||
| chr17:45099160 | C | T | 5 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(2): Show |
5 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.885-245C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099160 | |||||||
| chr17:45099241 | C | T | 1 | a0001c0003t0002g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.885-164C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099241 | |||||||
| chr17:45099254 | G | A | 51 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(48): Show |
64 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.885-151G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099254 | |||||||
| chr17:45099264 | A | C | 87 | a0001c0001t0006g0019 a0001c0001t0006g0194 a0001c0001t0006g0317 others(84): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.885-141A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099264 | |||||||
| chr17:45099288 | C | T | 1 | a0001c0001t0008g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.885-117C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099288 | |||||||
| chr17:45099385 | G | A | 1 | a0001c0002t0001g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.885-20G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 7/11 | chr17 | 45099385 | |||||||
| chr17:45099894 | C | T | 2 | a0001c0002t0001g0203 a0001c0002t0018g0213 |
2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.993+381C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45099894 | |||||||
| chr17:45099945 | C | T | 1 | a0001c0001t0006g0333 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.993+432C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45099945 | |||||||
| chr17:45100110 | A | G | 1 | a0001c0004t0003g0247 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.993+597A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100110 | |||||||
| chr17:45100352 | A | G | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.993+839A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100352 | |||||||
| chr17:45100527 | C | T | 1 | a0001c0004t0003g0245 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.993+1014C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100527 | |||||||
| chr17:45100583 | T | C | 239 | a0001c0001t0002g0021 a0001c0001t0002g0130 a0001c0001t0002g0227 others(236): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.993+1070T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100583 | |||||||
| chr17:45100626 | C | T | 51 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(48): Show |
54 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.993+1113C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100626 | |||||||
| chr17:45100659 | A | C | 1 | a0001c0002t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.993+1146A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100659 | |||||||
| chr17:45100678 | G | A | 2 | a0001c0003t0002g0225 a0001c0003t0002g0350 |
2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.993+1165G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100678 | |||||||
| chr17:45100721 | C | T | 1 | a0001c0004t0032g0014 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.993+1208C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100721 | |||||||
| chr17:45100862 | C | CA | 36 | a0001c0001t0004g0003 a0001c0001t0004g0073 a0001c0001t0004g0075 others(33): Show |
38 | HG00544.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.993+1383dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | C | CAA | 30 | a0001c0001t0004g0066 a0001c0001t0004g0074 a0001c0001t0004g0108 others(27): Show |
33 | HG00408.hp1 HG01070.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.993+1382_993+1383d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | C | CAAA | 16 | a0001c0001t0004g0072 a0001c0003t0002g0023 a0001c0003t0002g0024 others(13): Show |
16 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.993+1381_993+1383d others(5): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | C | CAAAA | 10 | a0001c0003t0002g0031 a0001c0003t0002g0032 a0001c0003t0002g0037 others(7): Show |
10 | HG00423.hp2 HG00609.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.993+1380_993+1383d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CA | C | 38 | a0001c0001t0001g0112 a0001c0001t0004g0120 a0001c0001t0009g0132 others(35): Show |
39 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.993+1383delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAA | C | 10 | a0001c0002t0001g0086 a0001c0002t0001g0092 a0001c0002t0001g0215 others(7): Show |
10 | HG01243.hp2 HG01943.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.993+1382_993+1383d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAA | C | 15 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(12): Show |
15 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.993+1380_993+1383d others(6): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAA | C | 15 | a0001c0001t0005g0236 a0001c0001t0005g0261 a0001c0001t0005g0270 others(12): Show |
16 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.993+1379_993+1383d others(7): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAA | C | 31 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(28): Show |
33 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.993+1378_993+1383d others(8): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA | C | 9 | a0001c0001t0005g0280 a0001c0001t0007g0007 a0001c0001t0007g0008 others(6): Show |
12 | HG00558.hp1 HG01255.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.993+1377_993+1383d others(9): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0006g0329 a0001c0001t0006g0337 a0001c0001t0007g0316 others(6): Show |
9 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+1376_993+1383d others(10): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(2): Show |
C | 70 | a0001c0001t0006g0019 a0001c0001t0006g0317 a0001c0001t0006g0324 others(67): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.993+1375_993+1383d others(11): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0006g0194 a0001c0001t0051g0326 a0001c0004t0003g0012 others(4): Show |
9 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+1374_993+1383d others(12): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0019g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.993+1373_993+1383d others(13): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0028g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.993+1372_993+1383d others(14): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0028g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.993+1371_993+1383d others(15): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(7): Show |
C | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+1370_993+1383d others(16): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(8): Show |
C | 8 | a0001c0001t0004g0004 a0001c0001t0004g0070 a0001c0001t0004g0107 others(5): Show |
10 | HG01109.hp1 HG01928.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.993+1369_993+1383d others(17): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0009g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.993+1368_993+1383d others(18): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100862 | CAAAAAAA others(15): Show |
C | 4 | a0001c0001t0005g0265 a0001c0001t0005g0266 a0001c0001t0005g0267 others(1): Show |
4 | HG01074.hp1 HG01106.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+1362_993+1383d others(24): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45100862 | ||||||
| chr17:45100896 | A | G | 1 | a0001c0001t0004g0067 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1383A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100896 | |||||||
| chr17:45100897 | G | A | 1 | a0001c0001t0004g0067 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1384G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100897 | |||||||
| chr17:45100899 | A | G | 1 | a0001c0001t0004g0067 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993+1386A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45100899 | |||||||
| chr17:45101041 | G | A | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.993+1528G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101041 | |||||||
| chr17:45101076 | C | T | 1 | a0001c0001t0049g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.993+1563C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101076 | |||||||
| chr17:45101109 | G | A | 2 | a0001c0001t0028g0188 a0001c0001t0028g0189 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.993+1596G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101109 | |||||||
| chr17:45101140 | C | A | 1 | a0001c0003t0010g0027 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.993+1627C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101140 | |||||||
| chr17:45101216 | G | A | 1 | a0001c0001t0050g0301 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.993+1703G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101216 | |||||||
| chr17:45101226 | C | T | 1 | a0001c0004t0014g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.993+1713C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101226 | |||||||
| chr17:45101298 | A | G | 16 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(13): Show |
19 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.994-1653A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101298 | |||||||
| chr17:45101341 | T | C | 2 | a0001c0001t0008g0291 a0001c0001t0008g0297 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.994-1610T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101341 | |||||||
| chr17:45101362 | C | T | 1 | a0001c0003t0002g0025 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.994-1589C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101362 | |||||||
| chr17:45101363 | G | T | 1 | a0001c0003t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.994-1588G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101363 | |||||||
| chr17:45101461 | A | G | 6 | a0001c0002t0001g0080 a0001c0002t0001g0163 a0001c0002t0001g0170 others(3): Show |
6 | HG02083.hp1 HG02155.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-1490A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101461 | |||||||
| chr17:45101496 | G | A | 7 | a0001c0003t0010g0027 a0001c0003t0010g0095 a0001c0003t0010g0187 others(4): Show |
7 | HG01109.hp2 HG02886.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1455G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101496 | |||||||
| chr17:45101547 | A | AG | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.994-1402dupG | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101547 | ||||||
| chr17:45101563 | G | A | 1 | a0001c0003t0002g0025 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.994-1388G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101563 | |||||||
| chr17:45101574 | G | A | 1 | a0001c0003t0002g0350 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.994-1377G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101574 | |||||||
| chr17:45101617 | C | CA | 85 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(82): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.994-1312dupA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | ||||||
| chr17:45101617 | C | CAA | 12 | a0001c0001t0002g0021 a0001c0001t0002g0305 a0001c0001t0002g0309 others(9): Show |
12 | HG00423.hp1 HG01361.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.994-1313_994-1312d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | ||||||
| chr17:45101617 | CA | C | 71 | a0001c0002t0001g0009 a0001c0002t0001g0050 a0001c0002t0001g0068 others(68): Show |
72 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.994-1312delA | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 45101617 | ||||||
| chr17:45101678 | C | A | 1 | a0001c0003t0041g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.994-1273C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101678 | |||||||
| chr17:45101687 | A | G | 2 | a0001c0001t0010g0315 a0001c0001t0037g0313 |
2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.994-1264A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101687 | |||||||
| chr17:45101700 | G | A | 1 | a0001c0001t0005g0280 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.994-1251G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101700 | |||||||
| chr17:45101938 | G | T | 10 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0316 others(7): Show |
13 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.994-1013G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45101938 | |||||||
| chr17:45102149 | C | T | 1 | a0001c0003t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.994-802C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102149 | |||||||
| chr17:45102166 | A | G | 1 | a0001c0001t0005g0234 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.994-785A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102166 | |||||||
| chr17:45102294 | G | A | 10 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.994-657G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102294 | |||||||
| chr17:45102306 | A | G | 75 | a0001c0001t0002g0021 a0001c0001t0008g0017 a0001c0001t0008g0257 others(72): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.994-645A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102306 | |||||||
| chr17:45102816 | G | C | 1 | a0001c0001t0005g0268 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.994-135G>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102816 | |||||||
| chr17:45102834 | G | A | 1 | a0001c0001t0030g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.994-117G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 8/11 | chr17 | 45102834 | |||||||
| chr17:45103203 | A | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1164+82A>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103203 | |||||||
| chr17:45103249 | C | T | 54 | a0001c0004t0003g0001 a0001c0004t0003g0005 a0001c0004t0003g0011 others(51): Show |
67 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1164+128C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103249 | |||||||
| chr17:45103479 | G | A | 4 | a0001c0001t0002g0310 a0001c0005t0002g0022 a0001c0005t0002g0282 others(1): Show |
4 | HG02145.hp1 NA18941.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-230G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103479 | |||||||
| chr17:45103610 | G | T | 3 | a0001c0002t0004g0231 a0001c0002t0004g0232 a0001c0002t0004g0233 |
3 | HG00140.hp2 HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1165-99G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 9/11 | chr17 | 45103610 | |||||||
| chr17:45103890 | G | A | 1 | a0001c0001t0016g0295 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1332+14G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103890 | |||||||
| chr17:45103895 | G | T | 16 | a0001c0001t0002g0130 a0001c0001t0002g0227 a0001c0001t0002g0228 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+19G>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103895 | |||||||
| chr17:45103919 | A | G | 352 | a0001c0001t0001g0112 a0001c0001t0002g0021 a0001c0001t0002g0130 others(349): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.1332+43A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103919 | |||||||
| chr17:45103957 | A | G | 38 | a0001c0001t0005g0006 a0001c0001t0005g0147 a0001c0001t0005g0186 others(35): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1332+81A>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45103957 | |||||||
| chr17:45104256 | C | T | 2 | a0001c0003t0002g0034 a0001c0003t0002g0065 |
2 | NA18960.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1332+380C>T | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104256 | |||||||
| chr17:45104264 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1332+388G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104264 | |||||||
| chr17:45104569 | TAG | T | 34 | a0001c0001t0001g0112 a0001c0001t0004g0003 a0001c0001t0004g0004 others(31): Show |
38 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1333-287_1333-286d others(4): Show |
NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 45104569 | ||||||
| chr17:45104634 | G | A | 1 | a0001c0001t0009g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1333-225G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104634 | |||||||
| chr17:45104650 | A | C | 1 | a0001c0004t0003g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1333-209A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104650 | |||||||
| chr17:45104697 | C | A | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1333-162C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104697 | |||||||
| chr17:45104747 | C | A | 5 | a0001c0001t0010g0018 a0001c0001t0010g0315 a0001c0001t0037g0313 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-112C>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 10/11 | chr17 | 45104747 | |||||||
| chr17:45105112 | T | C | 1 | a0001c0001t0037g0313 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1470+116T>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105112 | |||||||
| chr17:45105238 | A | C | 1 | a0001c0004t0003g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1470+242A>C | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105238 | |||||||
| chr17:45105261 | G | A | 1 | a0001c0001t0004g0115 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1470+265G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105261 | |||||||
| chr17:45105442 | T | G | 75 | a0001c0001t0002g0021 a0001c0001t0008g0287 a0001c0001t0029g0255 others(72): Show |
78 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1471-177T>G | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105442 | |||||||
| chr17:45105524 | G | A | 13 | a0001c0001t0008g0017 a0001c0001t0008g0257 a0001c0001t0008g0288 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1471-95G>A | NMT1 | ENSG00000136448.13 | transcript | ENST00000258960.7 | protein_coding | 11/11 | chr17 | 45105524 |