Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9397 |
| ensemblid | ENSG00000152465.18 |
| hgncid | 7858 |
| symbol | NMT2 |
| name | N-myristoyltransferase 2 |
| refseq_nuc | NM_004808.3 |
| refseq_prot | NP_004799.1 |
| ensembl_nuc | ENST00000378165.9 |
| ensembl_prot | ENSP00000367407.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 15105770 |
| end | 15168693 |
| strand | - |
| ver | v1.2 |
| region | chr10:15105770-15168693 |
| region5000 | chr10:15100770-15173693 |
| regionname0 | NMT2_chr10_15105770_15168693 |
| regionname5000 | NMT2_chr10_15100770_15173693 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 498 | 275 | 95 | 50 | 94 | 12 | 22 | 60 | NMT2_chr10_15100770_15173693 | NMT2 | MAEDS others(493): Show |
chr10 | 15100770 | 15173693 |
| a0002 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | MAEDS others(493): Show |
chr10 | 15100770 | 15173693 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1494 | 233 | 60 | 48 | 89 | 12 | 22 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0002 | 0/0 | 1494 | 24 | 23 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0003 | 0/0 | 1494 | 5 | 0 | 0 | 5 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0004 | 0/0 | 1494 | 4 | 3 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0005 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0006 | 0/0 | 1494 | 3 | 3 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0007 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0001c0009 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 | ||
| a0002c0008 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | ATGGC others(1489): Show |
chr10 | 15100770 | 15173693 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5002 | 118 | 11 | 28 | 60 | 6 | 13 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0002 | 0/0 | 5001 | 14 | 1 | 2 | 10 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0003 | 0/0 | 5002 | 10 | 0 | 4 | 3 | 2 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0004 | 0/0 | 5002 | 11 | 5 | 1 | 3 | 0 | 2 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0005 | 0/0 | 5003 | 8 | 8 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0006 | 0/0 | 5005 | 9 | 8 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(5000): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0007 | 1/1 | 5003 | 8 | 0 | 3 | 1 | 1 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0008 | 0/0 | 5003 | 4 | 0 | 0 | 4 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0009 | 0/0 | 5001 | 6 | 4 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0011 | 0/0 | 5003 | 5 | 5 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0012 | 0/0 | 5004 | 4 | 1 | 1 | 0 | 2 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0013 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0017 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0020 | 0/0 | 5002 | 2 | 0 | 2 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0021 | 0/0 | 5002 | 2 | 0 | 0 | 2 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0022 | 0/0 | 5002 | 2 | 1 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0023 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0024 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0026 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0028 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(5000): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0029 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0030 | 0/0 | 5004 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0033 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0034 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0035 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0036 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0037 | 0/0 | 5003 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0038 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0039 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0040 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0041 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0042 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0043 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0044 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0045 | 0/0 | 5002 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0046 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0047 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0049 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0050 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0051 | 0/0 | 5001 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0052 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0053 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0001t0054 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4984): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0002 | 0/0 | 5001 | 3 | 3 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0005 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0010 | 0/0 | 4999 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4994): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0012 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0013 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0014 | 0/0 | 5004 | 4 | 4 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0015 | 0/0 | 5003 | 3 | 2 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0018 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0019 | 0/0 | 5005 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(5000): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0031 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(5000): Show |
chr10 | 15100770 | 15173693 |
| a0001c0002t0032 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0003t0001 | 0/0 | 5002 | 2 | 0 | 0 | 2 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0003t0008 | 0/0 | 5003 | 3 | 0 | 0 | 3 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0004t0013 | 0/0 | 5004 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4999): Show |
chr10 | 15100770 | 15173693 |
| a0001c0004t0025 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0004t0048 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0005t0003 | 0/0 | 5002 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0005t0009 | 0/0 | 5001 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4996): Show |
chr10 | 15100770 | 15173693 |
| a0001c0005t0010 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4994): Show |
chr10 | 15100770 | 15173693 |
| a0001c0006t0016 | 0/0 | 5003 | 2 | 2 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0006t0027 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0001c0007t0011 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4998): Show |
chr10 | 15100770 | 15173693 |
| a0001c0009t0055 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4997): Show |
chr10 | 15100770 | 15173693 |
| a0002c0008t0010 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | AGTAC others(4994): Show |
chr10 | 15100770 | 15173693 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0017g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0017g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0020g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0020g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0022g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0023g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0024g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0028g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0029g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0033g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0034g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0035g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0036g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0037g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0038g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0039g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0040g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0041g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0042g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0043g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0044g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0045g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0046g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0047g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0049g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0050g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0051g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0052g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0053g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0001t0054g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0015g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0031g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0002t0032g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0003t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0003t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0003t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0004t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0004t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0004t0025g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0004t0048g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0005t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0005t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0005t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0005t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0006t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0006t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0006t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0007t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0001c0009t0055g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| a0002c0008t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0223 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00140 | hp2 | a0001 | c0001 | t0012 | g0077 | EUR | GBR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00423 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00423 | hp2 | a0001 | c0003 | t0008 | g0146 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0168 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00673 | hp1 | a0001 | c0003 | t0008 | g0248 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0064 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01109 | hp1 | a0001 | c0002 | t0015 | g0123 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01167 | hp2 | a0001 | c0001 | t0020 | g0068 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01175 | hp2 | a0001 | c0001 | t0051 | g0232 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01192 | hp2 | a0001 | c0001 | t0022 | g0080 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0260 | AMR | PUR | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0262 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01261 | hp2 | a0001 | c0001 | t0012 | g0078 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01934 | hp2 | a0001 | c0001 | t0047 | g0200 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01975 | hp2 | a0001 | c0004 | t0025 | g0096 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02027 | hp2 | a0001 | c0001 | t0036 | g0243 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02055 | hp1 | a0001 | c0001 | t0026 | g0100 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02145 | hp1 | a0001 | c0001 | t0028 | g0118 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02145 | hp2 | a0001 | c0002 | t0018 | g0271 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02148 | hp1 | a0001 | c0001 | t0042 | g0225 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02258 | hp2 | a0001 | c0002 | t0010 | g0090 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02280 | hp1 | a0001 | c0002 | t0014 | g0089 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02451 | hp1 | a0001 | c0001 | t0052 | g0067 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02523 | hp1 | a0001 | c0003 | t0008 | g0150 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0246 | EAS | KHV | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0258 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02572 | hp2 | a0001 | c0004 | t0013 | g0113 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02615 | hp1 | a0001 | c0002 | t0031 | g0270 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02622 | hp1 | a0001 | c0007 | t0011 | g0121 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0143 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02630 | hp2 | a0001 | c0001 | t0035 | g0114 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02647 | hp1 | a0001 | c0002 | t0010 | g0012 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02698 | hp2 | a0001 | c0001 | t0046 | g0154 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0275 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02723 | hp2 | a0001 | c0001 | t0023 | g0001 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02735 | hp2 | a0001 | c0001 | t0038 | g0183 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0256 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0228 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02886 | hp1 | a0001 | c0002 | t0013 | g0099 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02896 | hp2 | a0001 | c0004 | t0013 | g0112 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02965 | hp1 | a0001 | c0004 | t0048 | g0016 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02970 | hp1 | a0001 | c0006 | t0016 | g0014 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02976 | hp1 | a0001 | c0002 | t0019 | g0131 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03098 | hp1 | a0001 | c0005 | t0003 | g0129 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03098 | hp2 | a0001 | c0005 | t0009 | g0128 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0126 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03130 | hp2 | a0001 | c0002 | t0014 | g0073 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03139 | hp1 | a0001 | c0002 | t0014 | g0087 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03139 | hp2 | a0001 | c0001 | t0049 | g0203 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03195 | hp2 | a0001 | c0002 | t0032 | g0101 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0111 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03225 | hp1 | a0001 | c0002 | t0019 | g0130 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03225 | hp2 | a0001 | c0002 | t0010 | g0011 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03453 | hp1 | a0001 | c0005 | t0003 | g0125 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0074 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0018 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03516 | hp2 | a0001 | c0002 | t0018 | g0268 | AFR | ESN | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0122 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03540 | hp2 | a0001 | c0001 | t0050 | g0239 | AFR | GWD | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0249 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03688 | hp1 | a0001 | c0001 | t0053 | g0006 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03927 | hp1 | a0001 | c0001 | t0029 | g0224 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | STU | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0098 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18522 | hp2 | a0001 | c0001 | t0043 | g0160 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0097 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18962 | hp2 | a0001 | c0001 | t0045 | g0050 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18972 | hp1 | a0001 | c0001 | t0054 | g0237 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18972 | hp2 | a0001 | c0001 | t0030 | g0082 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18977 | hp2 | a0001 | c0001 | t0021 | g0263 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18980 | hp2 | a0001 | c0001 | t0037 | g0179 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18982 | hp2 | a0001 | c0001 | t0039 | g0021 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19030 | hp2 | a0001 | c0006 | t0016 | g0010 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19043 | hp1 | a0001 | c0002 | t0014 | g0088 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19043 | hp2 | a0001 | c0006 | t0027 | g0015 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA19240 | hp2 | a0001 | c0002 | t0015 | g0102 | AFR | YRI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ASW | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ASW | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0079 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20752 | hp2 | a0001 | c0001 | t0041 | g0044 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | TSI | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02109 | hp1 | a0001 | c0001 | t0033 | g0107 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02486 | hp1 | a0001 | c0001 | t0044 | g0116 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02486 | hp2 | a0001 | c0001 | t0022 | g0086 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02559 | hp1 | a0001 | c0002 | t0015 | g0124 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03471 | hp1 | a0001 | c0005 | t0010 | g0045 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0276 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18955 | hp1 | a0001 | c0001 | t0021 | g0051 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA20300 | hp2 | a0002 | c0008 | t0010 | g0013 | AFR | USA | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA21309 | hp1 | a0001 | c0009 | t0055 | g0022 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0062 | AFR | LWK | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0201 | REF | REF | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0178 | REF | REF | NMT2_chr10_15100770_15173693 | NMT2 | chr10 | 15100770 | 15173693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:15119491 | C | G | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1022G>C | p.Arg341Thr | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/12 | 1103/5003 | 1022/1497 | 341/498 | chr10 | 15119491 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:15112871 | G | C | 1 | a0001c0007 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1263C>G | p.Ala421Ala | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/12 | 1344/5003 | 1263/1497 | 421/498 | chr10 | 15112871 | |||
| chr10:15128427 | A | G | 1 | a0001c0006 | 3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.922T>C | p.Leu308Leu | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/12 | 1003/5003 | 922/1497 | 308/498 | chr10 | 15128427 | |||
| chr10:15130273 | A | G | 1 | a0001c0003 | 5 | HG00423.hp2 HG00673.hp1 HG02083.hp1 others(2): Show |
synonymous_variant | LOW | c.759T>C | p.His253His | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/12 | 840/5003 | 759/1497 | 253/498 | chr10 | 15130273 | |||
| chr10:15133067 | G | A | 1 | a0001c0004 | 4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.588C>T | p.Pro196Pro | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/12 | 669/5003 | 588/1497 | 196/498 | chr10 | 15133067 | |||
| chr10:15135281 | T | C | 4 | a0001c0002 a0001c0005 a0001c0009 others(1): Show |
30 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(27): Show |
synonymous_variant | LOW | c.384A>G | p.Pro128Pro | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/12 | 465/5003 | 384/1497 | 128/498 | chr10 | 15135281 | |||
| chr10:15135340 | T | G | 1 | a0001c0009 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.325A>C | p.Arg109Arg | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/12 | 406/5003 | 325/1497 | 109/498 | chr10 | 15135340 | |||
| chr10:15141464 | C | T | 2 | a0001c0004 a0001c0005 |
8 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
synonymous_variant | LOW | c.204G>A | p.Ser68Ser | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/12 | 285/5003 | 204/1497 | 68/498 | chr10 | 15141464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:15105818 | A | G | 2 | a0001c0002t0014 a0001c0002t0019 |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3377T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3377 | chr10 | 15105818 | ||||||
| chr10:15105869 | GTTA | G | 3 | a0001c0002t0010 a0001c0005t0010 a0002c0008t0010 |
6 | HG02258.hp2 HG02647.hp1 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3323_*3325delTAA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3323 | chr10 | 15105869 | ||||||
| chr10:15105914 | T | C | 3 | a0001c0001t0049 a0001c0002t0015 a0001c0002t0032 |
5 | HG01109.hp1 HG02559.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3281A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3281 | chr10 | 15105914 | ||||||
| chr10:15105966 | T | A | 4 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0033 others(1): Show |
12 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3229A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3229 | chr10 | 15105966 | ||||||
| chr10:15106064 | G | C | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0023 others(6): Show |
21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3131C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3131 | chr10 | 15106064 | ||||||
| chr10:15106080 | G | A | 2 | a0001c0002t0014 a0001c0002t0019 |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3115C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3115 | chr10 | 15106080 | ||||||
| chr10:15106097 | G | A | 1 | a0001c0001t0026 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3098C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3098 | chr10 | 15106097 | ||||||
| chr10:15106116 | C | T | 3 | a0001c0001t0002 a0001c0001t0037 a0001c0002t0002 |
18 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3079G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3079 | chr10 | 15106116 | ||||||
| chr10:15106144 | C | G | 4 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0033 others(1): Show |
12 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3051 | chr10 | 15106144 | ||||||
| chr10:15106149 | A | G | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
126 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*3046T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3046 | chr10 | 15106149 | ||||||
| chr10:15106166 | G | A | 1 | a0001c0001t0041 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3029C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 3029 | chr10 | 15106166 | ||||||
| chr10:15106224 | ACCTCAAG others(6): Show |
A | 1 | a0001c0001t0054 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2958_*2970delAGAT others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2958 | chr10 | 15106224 | ||||||
| chr10:15106239 | C | T | 2 | a0001c0001t0004 a0001c0001t0034 |
12 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2956G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2956 | chr10 | 15106239 | ||||||
| chr10:15106284 | C | T | 4 | a0001c0001t0009 a0001c0001t0051 a0001c0001t0052 others(1): Show |
9 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2911G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2911 | chr10 | 15106284 | ||||||
| chr10:15106327 | T | C | 1 | a0001c0001t0042 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2868 | chr10 | 15106327 | ||||||
| chr10:15106354 | GA | G | 1 | a0001c0002t0015 | 3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2840delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2840 | chr10 | 15106354 | ||||||
| chr10:15106509 | G | A | 1 | a0001c0004t0048 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2686C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2686 | chr10 | 15106509 | ||||||
| chr10:15106548 | G | A | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
125 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2647C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2647 | chr10 | 15106548 | ||||||
| chr10:15106580 | A | T | 15 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(12): Show |
33 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2615T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2615 | chr10 | 15106580 | ||||||
| chr10:15106639 | C | T | 1 | a0001c0001t0039 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2556G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2556 | chr10 | 15106639 | ||||||
| chr10:15106671 | T | A | 1 | a0001c0002t0032 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2524A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2524 | chr10 | 15106671 | ||||||
| chr10:15106673 | C | T | 1 | a0001c0001t0038 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2522 | chr10 | 15106673 | ||||||
| chr10:15106903 | C | A | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0023 others(6): Show |
21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2292G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2292 | chr10 | 15106903 | ||||||
| chr10:15106908 | A | C | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(16): Show |
52 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2287T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2287 | chr10 | 15106908 | ||||||
| chr10:15106961 | C | T | 2 | a0001c0002t0018 a0001c0004t0048 |
3 | HG02145.hp2 HG02965.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2234G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2234 | chr10 | 15106961 | ||||||
| chr10:15107009 | G | A | 1 | a0001c0001t0020 | 2 | HG00741.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2186C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2186 | chr10 | 15107009 | ||||||
| chr10:15107081 | C | T | 1 | a0001c0001t0051 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2114 | chr10 | 15107081 | ||||||
| chr10:15107089 | A | G | 1 | a0001c0001t0045 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2106T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2106 | chr10 | 15107089 | ||||||
| chr10:15107101 | C | G | 3 | a0001c0001t0002 a0001c0001t0037 a0001c0002t0002 |
18 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2094G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2094 | chr10 | 15107101 | ||||||
| chr10:15107108 | TA | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(41): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2086delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2086 | chr10 | 15107108 | ||||||
| chr10:15107108 | TAA | T | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0051 others(3): Show |
26 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2086delTT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2085 | chr10 | 15107108 | ||||||
| chr10:15107166 | C | T | 24 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(21): Show |
63 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2029G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 2029 | chr10 | 15107166 | ||||||
| chr10:15107366 | T | C | 1 | a0001c0001t0044 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1829A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1829 | chr10 | 15107366 | ||||||
| chr10:15107541 | C | T | 1 | a0001c0001t0036 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1654G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1654 | chr10 | 15107541 | ||||||
| chr10:15107607 | A | G | 4 | a0001c0001t0013 a0001c0001t0035 a0001c0002t0013 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1588T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1588 | chr10 | 15107607 | ||||||
| chr10:15107657 | G | A | 7 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0023 others(4): Show |
19 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1538C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1538 | chr10 | 15107657 | ||||||
| chr10:15107710 | C | T | 1 | a0001c0002t0019 | 2 | HG02976.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1485G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1485 | chr10 | 15107710 | ||||||
| chr10:15107714 | C | G | 1 | a0001c0001t0034 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1481 | chr10 | 15107714 | ||||||
| chr10:15107776 | C | CT | 17 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(14): Show |
37 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1418dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1418 | chr10 | 15107776 | ||||||
| chr10:15107978 | C | A | 3 | a0001c0001t0021 a0001c0001t0045 a0001c0001t0047 |
4 | HG01934.hp2 NA18955.hp1 NA18962.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1217G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1217 | chr10 | 15107978 | ||||||
| chr10:15107981 | C | T | 5 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0030 others(2): Show |
16 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1214G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1214 | chr10 | 15107981 | ||||||
| chr10:15108185 | T | G | 2 | a0001c0006t0016 a0001c0006t0027 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1010A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1010 | chr10 | 15108185 | ||||||
| chr10:15108186 | T | C | 2 | a0001c0006t0016 a0001c0006t0027 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1009A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1009 | chr10 | 15108186 | ||||||
| chr10:15108188 | C | CT | 16 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0012 others(13): Show |
40 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1006dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 1006 | chr10 | 15108188 | ||||||
| chr10:15108269 | C | T | 1 | a0001c0001t0029 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 926 | chr10 | 15108269 | ||||||
| chr10:15108392 | G | A | 3 | a0001c0001t0017 a0001c0001t0046 a0001c0001t0047 |
4 | HG01934.hp2 HG02572.hp1 HG02698.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*803C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 803 | chr10 | 15108392 | ||||||
| chr10:15108440 | C | A | 1 | a0001c0004t0048 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 755 | chr10 | 15108440 | ||||||
| chr10:15108463 | G | A | 1 | a0001c0001t0049 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 732 | chr10 | 15108463 | ||||||
| chr10:15108465 | G | A | 1 | a0001c0001t0050 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 730 | chr10 | 15108465 | ||||||
| chr10:15108495 | T | A | 6 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0028 others(3): Show |
12 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*700A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 700 | chr10 | 15108495 | ||||||
| chr10:15108692 | G | A | 1 | a0001c0002t0018 | 2 | HG02145.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*503C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 503 | chr10 | 15108692 | ||||||
| chr10:15108734 | A | G | 13 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(10): Show |
25 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*461T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 461 | chr10 | 15108734 | ||||||
| chr10:15108859 | G | C | 1 | a0001c0001t0053 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*336C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 336 | chr10 | 15108859 | ||||||
| chr10:15108940 | G | A | 1 | a0001c0001t0054 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 255 | chr10 | 15108940 | ||||||
| chr10:15109036 | G | A | 1 | a0001c0009t0055 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 12/12 | 159 | chr10 | 15109036 | ||||||
| chr10:15168666 | A | T | 1 | a0001c0001t0023 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/12 | 54 | chr10 | 15168666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:15109227 | G | A | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-12C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109227 | |||||||
| chr10:15109229 | A | G | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-14T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109229 | |||||||
| chr10:15109230 | G | A | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1477-15C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109230 | |||||||
| chr10:15109349 | C | A | 9 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(6): Show |
9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1477-134G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109349 | |||||||
| chr10:15109349 | C | T | 1 | a0001c0001t0033g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1477-134G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109349 | |||||||
| chr10:15109536 | A | C | 15 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1476+166T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109536 | |||||||
| chr10:15109574 | A | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0066 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1476+128T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109574 | |||||||
| chr10:15109578 | T | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(21): Show |
24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1476+124A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109578 | |||||||
| chr10:15109582 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1476+120A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109582 | |||||||
| chr10:15109608 | A | C | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1476+94T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 11/11 | chr10 | 15109608 | |||||||
| chr10:15109866 | T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1339-27A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109866 | |||||||
| chr10:15109867 | T | C | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-28A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109867 | |||||||
| chr10:15109868 | A | T | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-29T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109868 | |||||||
| chr10:15109877 | G | A | 9 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(6): Show |
9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1339-38C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109877 | |||||||
| chr10:15109908 | T | G | 91 | a0001c0001t0001g0267 a0001c0001t0003g0049 a0001c0001t0003g0052 others(88): Show |
91 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1339-69A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15109908 | |||||||
| chr10:15110007 | C | T | 1 | a0001c0003t0008g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1339-168G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110007 | |||||||
| chr10:15110141 | C | G | 37 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(34): Show |
37 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1339-302G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110141 | |||||||
| chr10:15110235 | G | T | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-396C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110235 | |||||||
| chr10:15110251 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0161 a0001c0001t0050g0239 |
3 | HG00639.hp2 HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1339-412G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110251 | |||||||
| chr10:15110381 | A | G | 61 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(58): Show |
61 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1339-542T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110381 | |||||||
| chr10:15110496 | C | T | 5 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1339-657G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110496 | |||||||
| chr10:15110534 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1339-695C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110534 | |||||||
| chr10:15110560 | G | C | 140 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(137): Show |
140 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.1339-721C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110560 | |||||||
| chr10:15110606 | A | C | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-767T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110606 | |||||||
| chr10:15110624 | A | C | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-785T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110624 | |||||||
| chr10:15110642 | C | A | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-803G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110642 | |||||||
| chr10:15110643 | A | C | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1339-804T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110643 | |||||||
| chr10:15110646 | C | CAAA | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-810_1339-808d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110646 | |||||||
| chr10:15110662 | C | A | 2 | a0001c0002t0031g0270 a0001c0002t0032g0101 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1339-823G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110662 | |||||||
| chr10:15110690 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1339-851G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110690 | |||||||
| chr10:15110907 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0164 a0001c0001t0001g0254 |
3 | HG00597.hp2 HG01952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1339-1068G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110907 | |||||||
| chr10:15110953 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(21): Show |
24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1339-1114C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110953 | |||||||
| chr10:15110972 | T | C | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1339-1133A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15110972 | |||||||
| chr10:15111279 | A | G | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1339-1440T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111279 | |||||||
| chr10:15111319 | G | A | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1338+1477C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111319 | |||||||
| chr10:15111378 | G | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(22): Show |
25 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1338+1418C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111378 | |||||||
| chr10:15111509 | C | CA | 52 | a0001c0001t0001g0084 a0001c0001t0001g0171 a0001c0001t0001g0210 others(49): Show |
52 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1338+1286dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111509 | |||||||
| chr10:15111509 | CA | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0252 a0001c0001t0001g0259 others(3): Show |
6 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+1286delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111509 | |||||||
| chr10:15111513 | A | G | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1338+1283T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111513 | |||||||
| chr10:15111520 | A | G | 36 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(33): Show |
36 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1338+1276T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111520 | |||||||
| chr10:15111656 | G | A | 37 | a0001c0001t0001g0267 a0001c0001t0003g0049 a0001c0001t0003g0052 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1338+1140C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111656 | |||||||
| chr10:15111686 | G | A | 5 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+1110C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111686 | |||||||
| chr10:15111979 | A | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1338+817T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15111979 | |||||||
| chr10:15112121 | A | G | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+675T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112121 | |||||||
| chr10:15112174 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1338+622A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0135 others(4): Show |
7 | HG01074.hp2 HG01433.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338+620_1338+621d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTATA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0198 others(3): Show |
6 | HG00140.hp1 HG00597.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+618_1338+621d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTATATA | 5 | a0001c0001t0001g0040 a0001c0001t0001g0157 a0001c0001t0001g0190 others(2): Show |
5 | HG01517.hp2 HG01934.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+616_1338+621d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0265 |
2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1338+612_1338+621d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1338+610_1338+621d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1338+608_1338+621d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338+612_1338+621d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112174 | TTATATAT others(5): Show |
T | 1 | a0001c0007t0011g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1338+610_1338+621d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112174 | |||||||
| chr10:15112192 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1338+576_1338+603d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112192 | |||||||
| chr10:15112194 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0012g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1338+575_1338+601d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | |||||||
| chr10:15112194 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0012g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1338+574_1338+601d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | |||||||
| chr10:15112194 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0012g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1338+572_1338+601d others(32): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | |||||||
| chr10:15112194 | ATATATAT others(29): Show |
A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1338+566_1338+601d others(38): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112194 | |||||||
| chr10:15112196 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1338+579_1338+599d others(23): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112196 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0169 |
2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1338+577_1338+599d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112196 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1338+574_1338+599d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112196 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0006g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1338+572_1338+599d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112196 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1338+567_1338+599d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112196 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1338+566_1338+599d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112196 | |||||||
| chr10:15112198 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0267 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1338+579_1338+597d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | |||||||
| chr10:15112198 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0029 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1338+577_1338+597d others(23): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | |||||||
| chr10:15112198 | ATATATAT others(21): Show |
A | 6 | a0001c0001t0006g0048 a0001c0001t0006g0108 a0001c0001t0006g0109 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+570_1338+597d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | |||||||
| chr10:15112198 | ATATATAT others(27): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0002g0065 a0001c0001t0002g0158 others(1): Show |
4 | HG01099.hp1 NA18959.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+564_1338+597d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | |||||||
| chr10:15112198 | ATATATAT others(29): Show |
A | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+562_1338+597d others(38): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112198 | |||||||
| chr10:15112200 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0219 a0001c0001t0001g0266 |
3 | HG02071.hp2 NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1338+576_1338+595d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1338+574_1338+595d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0006g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1338+570_1338+595d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(20): Show |
A | 1 | a0001c0002t0012g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1338+569_1338+595d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0006g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1338+568_1338+595d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0005g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+564_1338+595d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(26): Show |
A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0039g0021 |
3 | HG02071.hp1 HG03927.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1338+563_1338+595d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112200 | ATATATAT others(27): Show |
A | 6 | a0001c0001t0002g0024 a0001c0001t0002g0027 a0001c0001t0002g0041 others(3): Show |
6 | HG01081.hp1 HG02074.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562_1338+595d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112200 | |||||||
| chr10:15112202 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1338+576_1338+593d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(17): Show |
A | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+593d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(18): Show |
A | 1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1338+569_1338+593d others(27): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(19): Show |
A | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1338+568_1338+593d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(25): Show |
A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0037 others(3): Show |
6 | HG00438.hp1 HG02155.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562_1338+593d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1338+560_1338+593d others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112202 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0024g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1338+556_1338+593d others(40): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112202 | |||||||
| chr10:15112204 | ATATATAT others(6): Show |
A | 1 | a0001c0002t0014g0073 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1338+579_1338+591d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1338+578_1338+591d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0047g0200 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1338+576_1338+591d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0009g0168 a0001c0001t0009g0207 |
2 | HG00639.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1338+575_1338+591d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0052g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1338+574_1338+591d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1338+569_1338+591d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(19): Show |
A | 3 | a0001c0001t0013g0111 a0001c0002t0013g0099 a0001c0004t0013g0112 |
3 | HG02886.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1338+566_1338+591d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0005g0255 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1338+563_1338+591d others(31): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112204 | ATATATAT others(25): Show |
A | 2 | a0001c0001t0002g0042 a0001c0002t0002g0142 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1338+560_1338+591d others(34): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112204 | |||||||
| chr10:15112205 | TATATATA others(4): Show |
T | 1 | a0001c0001t0011g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1338+580_1338+590d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112205 | |||||||
| chr10:15112206 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0011g0007 a0001c0001t0011g0122 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1338+579_1338+589d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112206 | ATATATAT others(5): Show |
A | 1 | a0001c0002t0014g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1338+578_1338+589d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112206 | ATATATAT others(6): Show |
A | 2 | a0001c0002t0014g0087 a0001c0002t0014g0089 |
2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1338+577_1338+589d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112206 | ATATATAT others(10): Show |
A | 4 | a0001c0001t0009g0003 a0001c0001t0009g0097 a0001c0001t0022g0086 others(1): Show |
4 | HG00738.hp1 HG02083.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+573_1338+589d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112206 | ATATATAT others(16): Show |
A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1338+567_1338+589d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112206 | ATATATAT others(19): Show |
A | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1338+564_1338+589d others(28): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112206 | |||||||
| chr10:15112208 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0011g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+572_1338+587d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0009g0066 a0001c0001t0022g0080 |
2 | HG01192.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+587d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0033g0107 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1338+566_1338+587d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(16): Show |
A | 3 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0002c0008t0010g0013 |
3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1338+565_1338+587d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1338+564_1338+587d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(20): Show |
A | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1338+561_1338+587d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112208 | ATATATAT others(26): Show |
A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1338+555_1338+587d others(35): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112208 | |||||||
| chr10:15112210 | ATATATAT others(1): Show |
A | 6 | a0001c0001t0004g0002 a0001c0001t0004g0106 a0001c0001t0004g0269 others(3): Show |
6 | HG01243.hp1 HG02922.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+578_1338+585d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(2): Show |
A | 6 | a0001c0001t0001g0171 a0001c0001t0001g0242 a0001c0001t0001g0244 others(3): Show |
6 | HG00735.hp2 HG01975.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1338+577_1338+585d others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1338+576_1338+585d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0051g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1338+573_1338+585d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(8): Show |
A | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1338+571_1338+585d others(17): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0009g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1338+570_1338+585d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112210 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1338+566_1338+585d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112210 | |||||||
| chr10:15112211 | TATATA | T | 3 | a0001c0001t0001g0165 a0001c0001t0003g0071 a0001c0001t0004g0119 |
3 | HG00597.hp1 HG00673.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1338+580_1338+584d others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112211 | |||||||
| chr10:15112214 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1338+570_1338+581d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112214 | |||||||
| chr10:15112214 | ATATTTTT others(12): Show |
A | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1338+563_1338+581d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112214 | |||||||
| chr10:15112216 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1338+579_1338+580i others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | A | T | 1 | a0001c0001t0011g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338+580T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | AT | A | 14 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0137 others(11): Show |
14 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+579delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATT | A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0134 others(7): Show |
10 | HG00621.hp1 HG02027.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+578_1338+579d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTT | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0035 others(9): Show |
12 | HG00558.hp1 HG00738.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1338+577_1338+579d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTTT | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0139 a0001c0001t0001g0191 others(4): Show |
7 | HG00438.hp2 HG00609.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338+576_1338+579d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTTTT | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0162 a0001c0001t0001g0170 others(4): Show |
7 | HG00621.hp2 NA18940.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+575_1338+579d others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTTTTTT | A | 5 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0234 others(2): Show |
5 | HG01071.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+573_1338+579d others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0005g0194 a0001c0001t0005g0195 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1338+570_1338+579d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112216 | ATTTTTTT others(7): Show |
A | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1338+566_1338+579d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112216 | |||||||
| chr10:15112217 | T | TA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0083 others(7): Show |
10 | HG00423.hp1 HG00423.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | |||||||
| chr10:15112217 | T | TATA | 3 | a0001c0001t0001g0197 a0001c0001t0001g0226 a0001c0001t0036g0243 |
3 | HG01074.hp1 HG02027.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1338+578_1338+579i others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | |||||||
| chr10:15112217 | T | TATATATA | 4 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0008g0147 others(1): Show |
4 | HG00558.hp2 HG02129.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(9): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | |||||||
| chr10:15112217 | T | TATATATA others(2): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0001t0001g0247 others(1): Show |
4 | HG01258.hp2 HG02056.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+578_1338+579i others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112217 | |||||||
| chr10:15112218 | T | A | 29 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0033 others(26): Show |
29 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1338+578A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112218 | |||||||
| chr10:15112219 | T | A | 30 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0063 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1338+577A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112219 | |||||||
| chr10:15112220 | T | A | 27 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0039 others(24): Show |
27 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1338+576A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112220 | |||||||
| chr10:15112221 | T | A | 21 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0060 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.1338+575A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112221 | |||||||
| chr10:15112222 | T | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0059 others(11): Show |
14 | HG00597.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+574A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112222 | |||||||
| chr10:15112223 | T | A | 9 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0075 others(6): Show |
9 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1338+573A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112223 | |||||||
| chr10:15112224 | T | A | 4 | a0001c0001t0001g0188 a0001c0001t0053g0006 a0001c0002t0005g0143 others(1): Show |
4 | HG02622.hp2 HG02698.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+572A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112224 | |||||||
| chr10:15112225 | T | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0234 a0001c0001t0026g0100 |
3 | HG01071.hp1 HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1338+571A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112225 | |||||||
| chr10:15112226 | T | A | 5 | a0001c0002t0005g0143 a0001c0002t0005g0276 a0001c0006t0016g0010 others(2): Show |
5 | HG02622.hp2 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+570A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112226 | |||||||
| chr10:15112227 | T | A | 4 | a0001c0001t0005g0204 a0001c0001t0005g0235 a0001c0001t0005g0236 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+569A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112227 | |||||||
| chr10:15112228 | T | A | 7 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0002t0005g0143 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+568A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112228 | |||||||
| chr10:15112229 | T | A | 4 | a0001c0001t0005g0204 a0001c0001t0005g0235 a0001c0001t0005g0236 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+567A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112229 | |||||||
| chr10:15112230 | T | A | 7 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0002t0005g0143 others(4): Show |
7 | HG02622.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1338+566A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112230 | |||||||
| chr10:15112231 | T | A | 4 | a0001c0001t0005g0204 a0001c0001t0005g0235 a0001c0001t0005g0236 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+565A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112231 | |||||||
| chr10:15112232 | T | A | 8 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0002t0005g0143 others(5): Show |
8 | HG01975.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1338+564A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112232 | |||||||
| chr10:15112233 | T | A | 3 | a0001c0001t0005g0204 a0001c0001t0005g0235 a0001c0001t0005g0236 |
3 | HG02055.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1338+563A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112233 | |||||||
| chr10:15112234 | T | A | 6 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0004t0025g0096 others(3): Show |
6 | HG01975.hp2 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+562A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112234 | |||||||
| chr10:15112235 | T | A | 1 | a0001c0001t0005g0235 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1338+561A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112235 | |||||||
| chr10:15112236 | T | A | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1338+560A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112236 | |||||||
| chr10:15112286 | G | A | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1338+510C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112286 | |||||||
| chr10:15112321 | C | G | 14 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+475G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112321 | |||||||
| chr10:15112360 | C | T | 14 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1338+436G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112360 | |||||||
| chr10:15112398 | T | G | 3 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 |
3 | HG01891.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1338+398A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112398 | |||||||
| chr10:15112420 | G | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(20): Show |
23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1338+376C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112420 | |||||||
| chr10:15112502 | T | A | 39 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(36): Show |
39 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1338+294A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 10/11 | chr10 | 15112502 | |||||||
| chr10:15112973 | A | G | 1 | a0001c0001t0007g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1171-10T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15112973 | |||||||
| chr10:15112975 | A | G | 270 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(267): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1171-12T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15112975 | |||||||
| chr10:15113003 | C | T | 8 | a0001c0001t0011g0249 a0001c0001t0023g0001 a0001c0002t0014g0073 others(5): Show |
8 | HG02280.hp1 HG02723.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1171-40G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113003 | |||||||
| chr10:15113087 | G | A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1171-124C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113087 | |||||||
| chr10:15113104 | C | G | 15 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(12): Show |
15 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1171-141G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113104 | |||||||
| chr10:15113296 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(25): Show |
28 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1171-333G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113296 | |||||||
| chr10:15113338 | C | G | 22 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(19): Show |
22 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1171-375G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113338 | |||||||
| chr10:15113463 | C | CA | 51 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0058 others(48): Show |
51 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1171-501dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAA | 33 | a0001c0001t0003g0071 a0001c0001t0003g0233 a0001c0001t0004g0274 others(30): Show |
33 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1171-502_1171-501d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAA | 11 | a0001c0001t0009g0066 a0001c0001t0009g0097 a0001c0001t0009g0207 others(8): Show |
11 | HG01192.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-503_1171-501d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(6): Show |
1 | a0001c0004t0013g0112 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1171-513_1171-501d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0013g0111 a0001c0001t0024g0074 a0001c0002t0018g0271 |
3 | HG02145.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1171-514_1171-501d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0028g0118 a0001c0002t0018g0268 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1171-516_1171-501d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(10): Show |
5 | a0001c0001t0005g0005 a0001c0001t0005g0196 a0001c0001t0005g0255 others(2): Show |
5 | HG02055.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-517_1171-501d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0005g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-518_1171-501d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(13): Show |
1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1171-520_1171-501d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | C | CAAAAAAA others(27): Show |
1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1171-501_1171-500i others(36): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | CA | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0184 a0001c0001t0001g0192 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.1171-501delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | CAAAAAAA others(1): Show |
C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(20): Show |
23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1171-508_1171-501d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113463 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1171-514_1171-501d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113463 | |||||||
| chr10:15113486 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0005g0194 a0001c0001t0005g0195 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1171-524_1171-523i others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113486 | |||||||
| chr10:15113486 | A | G | 1 | a0001c0001t0021g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1171-523T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113486 | |||||||
| chr10:15113549 | G | A | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1171-586C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113549 | |||||||
| chr10:15113567 | G | T | 1 | a0001c0002t0002g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1171-604C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113567 | |||||||
| chr10:15113626 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-663T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113626 | |||||||
| chr10:15113627 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-664C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113627 | |||||||
| chr10:15113630 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-667G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113630 | |||||||
| chr10:15113632 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-669C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113632 | |||||||
| chr10:15113633 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1171-670G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113633 | |||||||
| chr10:15113695 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1171-732A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113695 | |||||||
| chr10:15113748 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1171-785G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113748 | |||||||
| chr10:15113924 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1171-961A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113924 | |||||||
| chr10:15113927 | C | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-964G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15113927 | |||||||
| chr10:15114360 | A | G | 35 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(32): Show |
35 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.1171-1397T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114360 | |||||||
| chr10:15114395 | T | C | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1171-1432A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114395 | |||||||
| chr10:15114457 | C | G | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1494G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114457 | |||||||
| chr10:15114475 | C | A | 71 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(68): Show |
71 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1171-1512G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114475 | |||||||
| chr10:15114510 | C | G | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-1547G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114510 | |||||||
| chr10:15114532 | C | G | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1171-1569G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114532 | |||||||
| chr10:15114570 | A | G | 38 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(35): Show |
38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-1607T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114570 | |||||||
| chr10:15114575 | C | T | 38 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(35): Show |
38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-1612G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114575 | |||||||
| chr10:15114610 | T | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(21): Show |
24 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1171-1647A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114610 | |||||||
| chr10:15114676 | C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1171-1713G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114676 | |||||||
| chr10:15114740 | T | C | 70 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(67): Show |
70 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1171-1777A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114740 | |||||||
| chr10:15114776 | G | C | 41 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1171-1813C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114776 | |||||||
| chr10:15114868 | T | A | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1171-1905A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114868 | |||||||
| chr10:15114934 | G | A | 1 | a0001c0001t0017g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1171-1971C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15114934 | |||||||
| chr10:15115629 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0037g0179 |
2 | NA18980.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1171-2666T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115629 | |||||||
| chr10:15115660 | G | C | 1 | a0001c0001t0036g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1171-2697C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115660 | |||||||
| chr10:15115726 | C | G | 37 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(34): Show |
37 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1171-2763G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115726 | |||||||
| chr10:15115772 | A | G | 57 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(54): Show |
57 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.1171-2809T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115772 | |||||||
| chr10:15115904 | G | A | 6 | a0001c0001t0033g0107 a0001c0002t0010g0011 a0001c0002t0010g0012 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-2941C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115904 | |||||||
| chr10:15115925 | G | A | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1171-2962C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115925 | |||||||
| chr10:15115968 | C | T | 1 | a0001c0001t0044g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1171-3005G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15115968 | |||||||
| chr10:15116051 | G | A | 11 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-3088C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116051 | |||||||
| chr10:15116069 | A | G | 106 | a0001c0001t0001g0063 a0001c0001t0001g0139 a0001c0001t0001g0267 others(103): Show |
106 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1171-3106T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116069 | |||||||
| chr10:15116084 | G | C | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-3121C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116084 | |||||||
| chr10:15116088 | T | C | 38 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(35): Show |
38 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1171-3125A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116088 | |||||||
| chr10:15116123 | G | T | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1171-3160C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116123 | |||||||
| chr10:15116130 | C | T | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1171-3167G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116130 | |||||||
| chr10:15116243 | A | T | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+3100T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116243 | |||||||
| chr10:15116268 | T | C | 53 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(50): Show |
53 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1170+3075A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116268 | |||||||
| chr10:15116271 | G | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0038 others(1): Show |
4 | NA18940.hp2 NA18960.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+3072C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116271 | |||||||
| chr10:15116310 | A | G | 129 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(126): Show |
129 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1170+3033T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116310 | |||||||
| chr10:15116369 | A | G | 80 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(77): Show |
80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1170+2974T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116369 | |||||||
| chr10:15116386 | C | T | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+2957G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116386 | |||||||
| chr10:15116409 | C | T | 63 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(60): Show |
63 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1170+2934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116409 | |||||||
| chr10:15116444 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(25): Show |
28 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1170+2899G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116444 | |||||||
| chr10:15116635 | C | A | 1 | a0001c0001t0003g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1170+2708G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116635 | |||||||
| chr10:15116687 | C | T | 35 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(32): Show |
35 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1170+2656G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116687 | |||||||
| chr10:15116701 | A | G | 2 | a0001c0001t0009g0046 a0001c0001t0009g0066 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1170+2642T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116701 | |||||||
| chr10:15116729 | G | C | 11 | a0001c0001t0026g0100 a0001c0002t0010g0011 a0001c0002t0010g0012 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+2614C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116729 | |||||||
| chr10:15116755 | G | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1170+2588C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116755 | |||||||
| chr10:15116785 | G | GAAC | 95 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(92): Show |
95 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1170+2555_1170+255 others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116785 | |||||||
| chr10:15116826 | T | C | 4 | a0001c0004t0025g0096 a0001c0006t0016g0010 a0001c0006t0016g0014 others(1): Show |
4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+2517A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15116826 | |||||||
| chr10:15117024 | T | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(16): Show |
19 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1170+2319A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117024 | |||||||
| chr10:15117124 | T | C | 29 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(26): Show |
29 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1170+2219A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117124 | |||||||
| chr10:15117219 | T | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(17): Show |
20 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1170+2124A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117219 | |||||||
| chr10:15117246 | G | A | 1 | a0001c0001t0054g0237 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1170+2097C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117246 | |||||||
| chr10:15117303 | T | C | 1 | a0001c0004t0013g0112 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1170+2040A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117303 | |||||||
| chr10:15117497 | A | T | 32 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(29): Show |
32 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1170+1846T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117497 | |||||||
| chr10:15117635 | T | C | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+1708A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117635 | |||||||
| chr10:15117652 | C | G | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1170+1691G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117652 | |||||||
| chr10:15117699 | G | C | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1644C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117699 | |||||||
| chr10:15117706 | AAC | A | 37 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1170+1635_1170+163 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117706 | |||||||
| chr10:15117710 | C | T | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+1633G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117710 | |||||||
| chr10:15117792 | A | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1170+1551T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117792 | |||||||
| chr10:15117884 | C | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0227 a0001c0001t0001g0245 |
3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1170+1459G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15117884 | |||||||
| chr10:15118186 | A | G | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+1157T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118186 | |||||||
| chr10:15118193 | A | G | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1170+1150T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118193 | |||||||
| chr10:15118194 | G | A | 15 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170+1149C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118194 | |||||||
| chr10:15118200 | C | G | 1 | a0001c0001t0012g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1170+1143G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118200 | |||||||
| chr10:15118276 | A | G | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1170+1067T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118276 | |||||||
| chr10:15118319 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1170+1024G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118319 | |||||||
| chr10:15118367 | C | T | 1 | a0001c0001t0005g0194 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1170+976G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118367 | |||||||
| chr10:15118408 | G | A | 15 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170+935C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118408 | |||||||
| chr10:15118412 | G | A | 5 | a0001c0001t0001g0155 a0001c0002t0014g0073 a0001c0002t0014g0087 others(2): Show |
5 | HG01123.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+931C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118412 | |||||||
| chr10:15118484 | A | T | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+859T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118484 | |||||||
| chr10:15118504 | A | G | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+839T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118504 | |||||||
| chr10:15118589 | C | CA | 45 | a0001c0001t0001g0063 a0001c0001t0001g0226 a0001c0001t0001g0267 others(42): Show |
45 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1170+753dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118589 | |||||||
| chr10:15118758 | C | G | 6 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0079 others(3): Show |
6 | HG00140.hp2 HG01261.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+585G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118758 | |||||||
| chr10:15118786 | G | C | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1170+557C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118786 | |||||||
| chr10:15118960 | G | T | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1170+383C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15118960 | |||||||
| chr10:15119030 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0049g0203 |
2 | HG03139.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1170+313G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119030 | |||||||
| chr10:15119063 | G | C | 10 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+280C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119063 | |||||||
| chr10:15119125 | C | T | 6 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(3): Show |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+218G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119125 | |||||||
| chr10:15119263 | T | C | 2 | a0001c0001t0005g0194 a0001c0001t0005g0195 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1170+80A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119263 | |||||||
| chr10:15119275 | A | C | 81 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(78): Show |
81 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1170+68T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119275 | |||||||
| chr10:15119335 | G | T | 22 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(19): Show |
22 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.1170+8C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 9/11 | chr10 | 15119335 | |||||||
| chr10:15119518 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | splice_region_variant&intron_variant | LOW | c.1000-5A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119518 | |||||||
| chr10:15119672 | G | A | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-159C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119672 | |||||||
| chr10:15119697 | T | G | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(4): Show |
7 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000-184A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119697 | |||||||
| chr10:15119855 | C | T | 14 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-342G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119855 | |||||||
| chr10:15119879 | G | A | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1000-366C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119879 | |||||||
| chr10:15119884 | T | C | 4 | a0001c0001t0013g0111 a0001c0002t0013g0099 a0001c0004t0013g0112 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-371A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119884 | |||||||
| chr10:15119959 | C | G | 1 | a0001c0001t0006g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1000-446G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119959 | |||||||
| chr10:15119964 | C | T | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-451G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119964 | |||||||
| chr10:15119965 | G | A | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-452C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15119965 | |||||||
| chr10:15120062 | G | A | 17 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(14): Show |
17 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000-549C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120062 | |||||||
| chr10:15120106 | A | G | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-593T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120106 | |||||||
| chr10:15120127 | T | C | 9 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(6): Show |
9 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000-614A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120127 | |||||||
| chr10:15120230 | G | A | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1000-717C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120230 | |||||||
| chr10:15120273 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1000-760G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120273 | |||||||
| chr10:15120294 | C | T | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000-781G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120294 | |||||||
| chr10:15120295 | G | A | 6 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(3): Show |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-782C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120295 | |||||||
| chr10:15120306 | A | G | 1 | a0001c0001t0024g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1000-793T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120306 | |||||||
| chr10:15120319 | G | A | 14 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-806C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120319 | |||||||
| chr10:15120384 | G | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-871C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120384 | |||||||
| chr10:15120720 | T | G | 1 | a0001c0002t0012g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1000-1207A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120720 | |||||||
| chr10:15120739 | G | A | 19 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(16): Show |
19 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1000-1226C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120739 | |||||||
| chr10:15120756 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1000-1243C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120756 | |||||||
| chr10:15120835 | C | T | 18 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(15): Show |
18 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000-1322G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120835 | |||||||
| chr10:15120856 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1000-1343C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120856 | |||||||
| chr10:15120928 | C | T | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-1415G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120928 | |||||||
| chr10:15120970 | A | C | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1000-1457T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120970 | |||||||
| chr10:15120978 | G | C | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-1465C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15120978 | |||||||
| chr10:15121027 | T | G | 6 | a0001c0001t0013g0111 a0001c0001t0024g0074 a0001c0001t0028g0118 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-1514A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121027 | |||||||
| chr10:15121055 | C | G | 3 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 |
3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1000-1542G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121055 | |||||||
| chr10:15121056 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1000-1543T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121056 | |||||||
| chr10:15121076 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0220 |
2 | HG01433.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1000-1563G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121076 | |||||||
| chr10:15121154 | T | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0164 a0001c0001t0001g0254 others(1): Show |
4 | HG00597.hp2 HG01952.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-1641A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121154 | |||||||
| chr10:15121199 | T | A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1000-1686A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121199 | |||||||
| chr10:15121228 | T | C | 6 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1715A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121228 | |||||||
| chr10:15121292 | T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1000-1779A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121292 | |||||||
| chr10:15121301 | G | T | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1788C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121301 | |||||||
| chr10:15121363 | G | C | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-1850C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121363 | |||||||
| chr10:15121510 | G | A | 14 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-1997C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121510 | |||||||
| chr10:15121613 | C | T | 6 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(3): Show |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-2100G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15121613 | |||||||
| chr10:15122042 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000-2529C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122042 | |||||||
| chr10:15122080 | T | A | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-2567A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122080 | |||||||
| chr10:15122127 | A | C | 6 | a0001c0001t0033g0107 a0001c0002t0010g0011 a0001c0002t0010g0012 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000-2614T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122127 | |||||||
| chr10:15122134 | C | T | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1000-2621G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122134 | |||||||
| chr10:15122458 | C | T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0001g0171 others(10): Show |
13 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000-2945G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122458 | |||||||
| chr10:15122464 | C | T | 1 | a0001c0001t0046g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1000-2951G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122464 | |||||||
| chr10:15122493 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000-2980G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122493 | |||||||
| chr10:15122511 | G | A | 2 | a0001c0001t0024g0074 a0001c0001t0028g0118 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1000-2998C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122511 | |||||||
| chr10:15122678 | C | T | 5 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-3165G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122678 | |||||||
| chr10:15122689 | G | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(20): Show |
23 | HG00438.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1000-3176C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122689 | |||||||
| chr10:15122884 | C | A | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1000-3371G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122884 | |||||||
| chr10:15122933 | T | TAA | 16 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(13): Show |
16 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1000-3422_1000-342 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122933 | |||||||
| chr10:15122933 | TA | T | 6 | a0001c0001t0001g0091 a0001c0002t0010g0011 a0001c0002t0010g0012 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-3421delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15122933 | |||||||
| chr10:15123161 | C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000-3648G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123161 | |||||||
| chr10:15123186 | A | C | 4 | a0001c0004t0025g0096 a0001c0006t0016g0010 a0001c0006t0016g0014 others(1): Show |
4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-3673T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123186 | |||||||
| chr10:15123473 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1000-3960C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123473 | |||||||
| chr10:15123502 | C | T | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-3989G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123502 | |||||||
| chr10:15123514 | C | T | 4 | a0001c0004t0025g0096 a0001c0006t0016g0010 a0001c0006t0016g0014 others(1): Show |
4 | HG01975.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-4001G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123514 | |||||||
| chr10:15123531 | G | GA | 15 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0084 others(12): Show |
15 | HG01261.hp1 HG01361.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1000-4019dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | |||||||
| chr10:15123531 | GA | G | 30 | a0001c0001t0001g0141 a0001c0001t0003g0049 a0001c0001t0003g0072 others(27): Show |
30 | HG00140.hp2 HG00621.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000-4019delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | |||||||
| chr10:15123531 | GAA | G | 33 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0052 others(30): Show |
33 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1000-4020_1000-401 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123531 | |||||||
| chr10:15123616 | C | G | 134 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1000-4103G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123616 | |||||||
| chr10:15123705 | T | C | 51 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(48): Show |
51 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1000-4192A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123705 | |||||||
| chr10:15123800 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000-4287A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123800 | |||||||
| chr10:15123850 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0240 |
2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1000-4337A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15123850 | |||||||
| chr10:15124034 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.999+4316T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124034 | |||||||
| chr10:15124177 | C | A | 10 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(7): Show |
10 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.999+4173G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124177 | |||||||
| chr10:15124179 | C | A | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999+4171G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124179 | |||||||
| chr10:15124556 | C | T | 106 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(103): Show |
106 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.999+3794G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124556 | |||||||
| chr10:15124564 | A | G | 7 | a0001c0001t0005g0196 a0001c0001t0005g0204 a0001c0001t0005g0235 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+3786T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124564 | |||||||
| chr10:15124568 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.999+3782C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124568 | |||||||
| chr10:15124635 | C | T | 1 | a0001c0002t0010g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999+3715G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124635 | |||||||
| chr10:15124722 | C | A | 4 | a0001c0001t0009g0003 a0001c0001t0009g0168 a0001c0001t0009g0207 others(1): Show |
4 | HG00639.hp1 HG00738.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+3628G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124722 | |||||||
| chr10:15124726 | G | A | 104 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(101): Show |
104 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.999+3624C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124726 | |||||||
| chr10:15124906 | A | G | 132 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(129): Show |
132 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.999+3444T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124906 | |||||||
| chr10:15124923 | A | G | 11 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0108 others(8): Show |
11 | HG00642.hp1 HG01109.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+3427T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15124923 | |||||||
| chr10:15125001 | TG | T | 4 | a0001c0001t0004g0119 a0001c0002t0013g0099 a0001c0004t0013g0112 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+3348delC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125001 | |||||||
| chr10:15125107 | C | T | 10 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.999+3243G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125107 | |||||||
| chr10:15125278 | G | C | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+3072C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125278 | |||||||
| chr10:15125294 | A | G | 5 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+3056T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125294 | |||||||
| chr10:15125308 | A | C | 41 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0003g0049 others(38): Show |
41 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.999+3042T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125308 | |||||||
| chr10:15125452 | A | G | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.999+2898T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125452 | |||||||
| chr10:15125512 | G | C | 6 | a0001c0001t0049g0203 a0001c0002t0010g0011 a0001c0002t0010g0012 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+2838C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125512 | |||||||
| chr10:15125628 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.999+2722A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125628 | |||||||
| chr10:15125628 | T | TTGTA | 7 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0242 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+2718_999+2721d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125628 | |||||||
| chr10:15125658 | GTATTTAG others(5): Show |
G | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+2680_999+2691d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125658 | |||||||
| chr10:15125698 | C | T | 6 | a0001c0002t0005g0276 a0001c0002t0014g0073 a0001c0002t0014g0087 others(3): Show |
6 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+2652G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125698 | |||||||
| chr10:15125801 | G | A | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.999+2549C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125801 | |||||||
| chr10:15125911 | C | T | 3 | a0001c0001t0049g0203 a0001c0002t0031g0270 a0001c0002t0032g0101 |
3 | HG02615.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.999+2439G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125911 | |||||||
| chr10:15125916 | T | C | 11 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.999+2434A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125916 | |||||||
| chr10:15125944 | T | C | 92 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(89): Show |
92 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.999+2406A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125944 | |||||||
| chr10:15125955 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.999+2395C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125955 | |||||||
| chr10:15125955 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.999+2395C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125955 | |||||||
| chr10:15125960 | T | C | 1 | a0001c0002t0019g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.999+2390A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125960 | |||||||
| chr10:15125964 | C | T | 1 | a0001c0002t0018g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.999+2386G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15125964 | |||||||
| chr10:15126008 | A | G | 2 | a0001c0002t0010g0090 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.999+2342T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126008 | |||||||
| chr10:15126024 | A | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(14): Show |
17 | HG00438.hp1 HG00609.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.999+2326T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126024 | |||||||
| chr10:15126041 | GC | G | 7 | a0001c0001t0005g0194 a0001c0001t0005g0195 a0001c0002t0010g0090 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.999+2308delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126041 | |||||||
| chr10:15126154 | C | T | 1 | a0001c0001t0009g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.999+2196G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126154 | |||||||
| chr10:15126155 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0151 |
2 | HG01258.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.999+2195C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126155 | |||||||
| chr10:15126244 | T | C | 29 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(26): Show |
29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+2106A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126244 | |||||||
| chr10:15126325 | A | G | 2 | a0001c0001t0009g0003 a0001c0001t0009g0168 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.999+2025T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126325 | |||||||
| chr10:15126338 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.999+2012T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126338 | |||||||
| chr10:15126428 | T | TA | 53 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0031 others(50): Show |
53 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.999+1921dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126428 | |||||||
| chr10:15126428 | TA | T | 20 | a0001c0001t0001g0025 a0001c0001t0001g0149 a0001c0001t0001g0191 others(17): Show |
20 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+1921delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126428 | |||||||
| chr10:15126460 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0138 |
2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.999+1890C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126460 | |||||||
| chr10:15126494 | G | C | 2 | a0001c0002t0002g0017 a0001c0002t0012g0018 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.999+1856C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126494 | |||||||
| chr10:15126560 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(91): Show |
94 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.999+1790A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126560 | |||||||
| chr10:15126711 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.999+1639A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126711 | |||||||
| chr10:15126821 | A | G | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.999+1529T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126821 | |||||||
| chr10:15126957 | G | A | 29 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(26): Show |
29 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.999+1393C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15126957 | |||||||
| chr10:15127007 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0242 others(1): Show |
4 | HG00735.hp2 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+1343G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127007 | |||||||
| chr10:15127048 | T | C | 63 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(60): Show |
63 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.999+1302A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127048 | |||||||
| chr10:15127164 | G | A | 5 | a0001c0002t0013g0099 a0001c0004t0013g0112 a0001c0004t0013g0113 others(2): Show |
5 | HG01975.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+1186C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127164 | |||||||
| chr10:15127241 | T | A | 4 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0079 others(1): Show |
4 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+1109A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127241 | |||||||
| chr10:15127246 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.999+1104T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127246 | |||||||
| chr10:15127249 | T | TA | 6 | a0001c0001t0001g0020 a0001c0002t0010g0011 a0001c0002t0010g0012 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+1100dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127249 | |||||||
| chr10:15127314 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999+1036C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127314 | |||||||
| chr10:15127375 | G | A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.999+975C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127375 | |||||||
| chr10:15127416 | G | A | 1 | a0001c0001t0004g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.999+934C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127416 | |||||||
| chr10:15127427 | G | C | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.999+923C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127427 | |||||||
| chr10:15127482 | G | A | 28 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(25): Show |
28 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.999+868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127482 | |||||||
| chr10:15127493 | G | A | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+857C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127493 | |||||||
| chr10:15127502 | C | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(17): Show |
20 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+848G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127502 | |||||||
| chr10:15127502 | C | G | 44 | a0001c0001t0004g0119 a0001c0001t0009g0003 a0001c0001t0009g0046 others(41): Show |
44 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.999+848G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127502 | |||||||
| chr10:15127503 | C | T | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.999+847G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127503 | |||||||
| chr10:15127508 | C | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(17): Show |
20 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+842G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127508 | |||||||
| chr10:15127525 | C | T | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+825G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127525 | |||||||
| chr10:15127530 | G | C | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+820C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127530 | |||||||
| chr10:15127533 | T | C | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+817A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127533 | |||||||
| chr10:15127538 | C | T | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+812G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127538 | |||||||
| chr10:15127542 | G | A | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+808C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127542 | |||||||
| chr10:15127546 | C | CA | 54 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0032 others(51): Show |
54 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.999+803dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127546 | |||||||
| chr10:15127546 | C | CAA | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0093 others(10): Show |
13 | HG00673.hp2 HG00735.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.999+802_999+803dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127546 | |||||||
| chr10:15127548 | A | G | 1 | a0001c0003t0008g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.999+802T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127548 | |||||||
| chr10:15127556 | A | T | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+794T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127556 | |||||||
| chr10:15127557 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.999+779_999+792del others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127557 | |||||||
| chr10:15127557 | AAAAAAAA others(23): Show |
A | 65 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(62): Show |
65 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.999+763_999+792del others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127557 | |||||||
| chr10:15127560 | A | AT | 29 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(26): Show |
29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+789_999+790ins others(1): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127560 | |||||||
| chr10:15127562 | A | T | 6 | a0001c0001t0001g0191 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG01433.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+788T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127562 | |||||||
| chr10:15127563 | A | AAT | 7 | a0001c0001t0006g0108 a0001c0001t0006g0110 a0001c0001t0006g0115 others(4): Show |
7 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+786_999+787ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127563 | |||||||
| chr10:15127563 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0007g0156 |
2 | HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.999+787T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127563 | |||||||
| chr10:15127565 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999+785T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127565 | |||||||
| chr10:15127567 | A | T | 1 | a0001c0001t0007g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.999+783T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127567 | |||||||
| chr10:15127570 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0006g0109 |
2 | HG02083.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.999+780T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127570 | |||||||
| chr10:15127570 | AT | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0140 a0001c0001t0001g0184 others(3): Show |
6 | HG00597.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+779delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127570 | |||||||
| chr10:15127571 | T | A | 184 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0030 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.999+779A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127571 | |||||||
| chr10:15127575 | T | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0032 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.999+775A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127575 | |||||||
| chr10:15127578 | A | AAAAAATA others(4): Show |
4 | a0001c0001t0005g0194 a0001c0001t0011g0007 a0001c0001t0011g0009 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | |||||||
| chr10:15127578 | A | AAT | 8 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0006g0109 others(5): Show |
8 | HG01975.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | |||||||
| chr10:15127578 | A | AATAAAAT | 7 | a0001c0001t0006g0108 a0001c0001t0006g0110 a0001c0001t0006g0115 others(4): Show |
7 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+771_999+772ins others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | |||||||
| chr10:15127578 | A | T | 3 | a0001c0001t0011g0122 a0001c0001t0011g0249 a0001c0001t0044g0116 |
3 | HG02486.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.999+772T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127578 | |||||||
| chr10:15127579 | T | A | 50 | a0001c0001t0001g0033 a0001c0001t0001g0141 a0001c0001t0001g0144 others(47): Show |
50 | HG00642.hp1 HG00735.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.999+771A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127579 | |||||||
| chr10:15127582 | A | T | 6 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0235 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+768T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127582 | |||||||
| chr10:15127582 | AT | A | 29 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(26): Show |
29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+767delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127582 | |||||||
| chr10:15127583 | T | A | 7 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0235 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+767A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127583 | |||||||
| chr10:15127586 | A | AAT | 20 | a0001c0001t0005g0194 a0001c0001t0006g0048 a0001c0001t0006g0081 others(17): Show |
20 | HG00642.hp1 HG01975.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.999+763_999+764ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | |||||||
| chr10:15127586 | A | AATAAAAT others(5): Show |
8 | a0001c0001t0005g0005 a0001c0001t0005g0204 a0001c0001t0005g0255 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+763_999+764ins others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | |||||||
| chr10:15127586 | A | T | 29 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(26): Show |
29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.999+764T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127586 | |||||||
| chr10:15127587 | T | A | 57 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(54): Show |
57 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.999+763A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127587 | |||||||
| chr10:15127587 | T | TAAAATAA others(4): Show |
6 | a0001c0001t0005g0195 a0001c0001t0005g0196 a0001c0001t0005g0235 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.999+762_999+763ins others(11): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127587 | |||||||
| chr10:15127591 | T | TA | 3 | a0001c0001t0001g0140 a0001c0001t0001g0164 a0001c0001t0001g0254 |
3 | HG00597.hp2 HG01952.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.999+758dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127591 | |||||||
| chr10:15127760 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.999+590C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127760 | |||||||
| chr10:15127788 | AGCTACTT others(22): Show |
A | 1 | a0001c0001t0035g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.999+533_999+561del others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127788 | |||||||
| chr10:15127794 | T | A | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+556A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127794 | |||||||
| chr10:15127867 | C | T | 5 | a0001c0002t0013g0099 a0001c0004t0013g0112 a0001c0004t0013g0113 others(2): Show |
5 | HG01975.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+483G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127867 | |||||||
| chr10:15127896 | TC | T | 53 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(50): Show |
53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.999+453delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127896 | |||||||
| chr10:15127898 | CA | C | 44 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(41): Show |
44 | HG00140.hp2 HG00642.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.999+451delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127898 | |||||||
| chr10:15127898 | CAA | C | 6 | a0001c0002t0005g0143 a0001c0002t0015g0102 a0001c0002t0015g0123 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.999+450_999+451del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127898 | |||||||
| chr10:15127899 | A | T | 53 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(50): Show |
53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.999+451T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15127899 | |||||||
| chr10:15128162 | G | A | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+188C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128162 | |||||||
| chr10:15128163 | G | A | 6 | a0001c0002t0005g0143 a0001c0002t0015g0102 a0001c0002t0015g0123 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.999+187C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128163 | |||||||
| chr10:15128209 | G | A | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+141C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128209 | |||||||
| chr10:15128243 | T | C | 5 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.999+107A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 8/11 | chr10 | 15128243 | |||||||
| chr10:15129059 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.891-601C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129059 | |||||||
| chr10:15129154 | C | A | 2 | a0001c0001t0024g0074 a0001c0001t0028g0118 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.891-696G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129154 | |||||||
| chr10:15129269 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.891-811C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129269 | |||||||
| chr10:15129721 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0155 |
2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.890+421G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129721 | |||||||
| chr10:15129841 | G | A | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.890+301C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129841 | |||||||
| chr10:15129894 | T | C | 41 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(38): Show |
41 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.890+248A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129894 | |||||||
| chr10:15129907 | C | CA | 64 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0031 others(61): Show |
64 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.890+234dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | |||||||
| chr10:15129907 | C | CAA | 9 | a0001c0001t0001g0029 a0001c0001t0005g0196 a0001c0001t0005g0204 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.890+233_890+234dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | |||||||
| chr10:15129907 | CA | C | 15 | a0001c0001t0001g0141 a0001c0001t0001g0157 a0001c0001t0001g0221 others(12): Show |
15 | HG00673.hp1 HG01081.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.890+234delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129907 | |||||||
| chr10:15129908 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.890+234T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129908 | |||||||
| chr10:15129933 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.890+209A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15129933 | |||||||
| chr10:15130094 | A | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0053 others(5): Show |
8 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.890+48T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 7/11 | chr10 | 15130094 | |||||||
| chr10:15130445 | G | A | 42 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(39): Show |
42 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.720-133C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130445 | |||||||
| chr10:15130549 | C | CAG | 66 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(63): Show |
66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.720-238_720-237ins others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130549 | |||||||
| chr10:15130679 | G | C | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.720-367C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130679 | |||||||
| chr10:15130703 | C | CA | 67 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0069 others(64): Show |
67 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.720-392dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | |||||||
| chr10:15130703 | C | CAA | 24 | a0001c0001t0001g0026 a0001c0001t0002g0023 a0001c0001t0002g0027 others(21): Show |
24 | HG01099.hp1 HG01192.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.720-393_720-392dup others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | |||||||
| chr10:15130703 | C | CAAA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0031 others(10): Show |
13 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.720-394_720-392dup others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | |||||||
| chr10:15130703 | CA | C | 9 | a0001c0001t0008g0092 a0001c0001t0012g0077 a0001c0001t0012g0079 others(6): Show |
9 | HG00140.hp2 HG00438.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-392delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130703 | |||||||
| chr10:15130756 | A | G | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.720-444T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130756 | |||||||
| chr10:15130786 | C | CT | 19 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0059 others(16): Show |
19 | HG01074.hp2 HG02027.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.720-475dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | |||||||
| chr10:15130786 | CT | C | 13 | a0001c0001t0009g0168 a0001c0001t0022g0080 a0001c0001t0035g0114 others(10): Show |
13 | HG00639.hp1 HG01192.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.720-475delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | |||||||
| chr10:15130786 | CTT | C | 7 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(4): Show |
7 | HG00738.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-476_720-475del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130786 | |||||||
| chr10:15130790 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720-478A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130790 | |||||||
| chr10:15130876 | T | G | 66 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(63): Show |
66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.720-564A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130876 | |||||||
| chr10:15130879 | T | C | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720-567A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130879 | |||||||
| chr10:15130892 | C | T | 2 | a0001c0001t0020g0064 a0001c0001t0020g0068 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.720-580G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130892 | |||||||
| chr10:15130983 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0138 |
2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.720-671A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15130983 | |||||||
| chr10:15131000 | C | T | 5 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0079 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.720-688G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131000 | |||||||
| chr10:15131009 | C | T | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.720-697G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131009 | |||||||
| chr10:15131067 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG00099.hp1 HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.720-755G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131067 | |||||||
| chr10:15131157 | A | C | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.720-845T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131157 | |||||||
| chr10:15131209 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0227 a0001c0001t0001g0245 others(1): Show |
4 | HG01175.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-897G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131209 | |||||||
| chr10:15131257 | A | G | 36 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(33): Show |
36 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.720-945T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131257 | |||||||
| chr10:15131287 | A | G | 4 | a0001c0001t0001g0221 a0001c0001t0001g0227 a0001c0001t0001g0245 others(1): Show |
4 | HG01175.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-975T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131287 | |||||||
| chr10:15131312 | C | CT | 6 | a0001c0001t0001g0135 a0001c0001t0001g0153 a0001c0001t0001g0175 others(3): Show |
6 | HG01109.hp2 HG02970.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.720-1001dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131312 | |||||||
| chr10:15131348 | G | A | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720-1036C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131348 | |||||||
| chr10:15131440 | C | T | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.720-1128G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131440 | |||||||
| chr10:15131450 | G | A | 1 | a0001c0002t0014g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.720-1138C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131450 | |||||||
| chr10:15131506 | G | C | 2 | a0001c0001t0017g0228 a0001c0001t0017g0258 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.720-1194C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131506 | |||||||
| chr10:15131560 | C | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0038g0183 |
3 | HG01123.hp1 HG02735.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.720-1248G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131560 | |||||||
| chr10:15131742 | G | T | 7 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.719+1075C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131742 | |||||||
| chr10:15131832 | G | A | 3 | a0001c0005t0003g0125 a0001c0005t0003g0129 a0001c0005t0009g0128 |
3 | HG03098.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.719+985C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131832 | |||||||
| chr10:15131876 | T | G | 2 | a0001c0001t0011g0249 a0001c0001t0044g0116 |
2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.719+941A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131876 | |||||||
| chr10:15131976 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.719+841C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15131976 | |||||||
| chr10:15132170 | G | T | 27 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(24): Show |
27 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.719+647C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132170 | |||||||
| chr10:15132231 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.719+586T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132231 | |||||||
| chr10:15132276 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.719+541C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132276 | |||||||
| chr10:15132276 | GT | G | 21 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.719+540delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132276 | |||||||
| chr10:15132489 | G | A | 27 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(24): Show |
27 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.719+328C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132489 | |||||||
| chr10:15132633 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.719+184C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132633 | |||||||
| chr10:15132720 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.719+97C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132720 | |||||||
| chr10:15132780 | A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.719+37T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132780 | |||||||
| chr10:15132793 | G | A | 2 | a0001c0001t0009g0097 a0001c0001t0052g0067 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.719+24C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132793 | |||||||
| chr10:15132810 | C | T | 2 | a0001c0001t0006g0120 a0001c0001t0033g0107 |
2 | HG00642.hp1 HG02109.hp1 |
splice_region_variant&intron_variant | LOW | c.719+7G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 6/11 | chr10 | 15132810 | |||||||
| chr10:15133008 | A | G | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.602+45T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/11 | chr10 | 15133008 | |||||||
| chr10:15133013 | G | A | 7 | a0001c0002t0005g0143 a0001c0002t0013g0099 a0001c0002t0015g0102 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602+40C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 5/11 | chr10 | 15133013 | |||||||
| chr10:15133206 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.510+39T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 4/11 | chr10 | 15133206 | |||||||
| chr10:15133435 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.392-72A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133435 | |||||||
| chr10:15133459 | A | C | 7 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-96T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133459 | |||||||
| chr10:15133579 | A | G | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.392-216T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133579 | |||||||
| chr10:15133609 | C | T | 23 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(20): Show |
23 | HG00642.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.392-246G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133609 | |||||||
| chr10:15133622 | T | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0205 others(3): Show |
6 | HG01943.hp1 HG01952.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-259A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133622 | |||||||
| chr10:15133627 | C | T | 5 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-264G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133627 | |||||||
| chr10:15133671 | T | C | 66 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(63): Show |
66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.392-308A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133671 | |||||||
| chr10:15133782 | C | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0241 a0001c0001t0036g0243 |
3 | HG02027.hp2 HG02135.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.392-419G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133782 | |||||||
| chr10:15133837 | C | G | 4 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0079 others(1): Show |
4 | HG00140.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-474G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133837 | |||||||
| chr10:15133857 | G | C | 7 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-494C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15133857 | |||||||
| chr10:15134158 | A | G | 128 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(125): Show |
128 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.392-795T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134158 | |||||||
| chr10:15134297 | C | T | 6 | a0001c0002t0005g0143 a0001c0002t0015g0102 a0001c0002t0015g0123 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134297 | |||||||
| chr10:15134324 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.391+950G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134324 | |||||||
| chr10:15134354 | G | A | 1 | a0001c0001t0006g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.391+920C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134354 | |||||||
| chr10:15134442 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.391+832C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134442 | |||||||
| chr10:15134454 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0219 a0001c0001t0001g0266 |
3 | HG02071.hp2 NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.391+820G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134454 | |||||||
| chr10:15134564 | A | T | 3 | a0001c0002t0005g0143 a0001c0002t0031g0270 a0001c0002t0032g0101 |
3 | HG02615.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.391+710T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134564 | |||||||
| chr10:15134572 | C | T | 14 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(11): Show |
14 | HG01109.hp1 HG01891.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+702G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134572 | |||||||
| chr10:15134599 | C | T | 3 | a0001c0004t0013g0112 a0001c0004t0013g0113 a0001c0004t0025g0096 |
3 | HG01975.hp2 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.391+675G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134599 | |||||||
| chr10:15134791 | A | G | 66 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(63): Show |
66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.391+483T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134791 | |||||||
| chr10:15134814 | T | C | 66 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(63): Show |
66 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.391+460A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134814 | |||||||
| chr10:15134947 | C | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.391+327G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15134947 | |||||||
| chr10:15135049 | G | A | 10 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.391+225C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135049 | |||||||
| chr10:15135125 | G | C | 7 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+149C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135125 | |||||||
| chr10:15135190 | G | GGT | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+83_391+84insAC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135190 | |||||||
| chr10:15135190 | GT | G | 36 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+83delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135190 | |||||||
| chr10:15135192 | T | G | 41 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(38): Show |
41 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.391+82A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135192 | |||||||
| chr10:15135192 | T | TTTG | 34 | a0001c0001t0001g0063 a0001c0001t0001g0171 a0001c0001t0001g0205 others(31): Show |
34 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.391+79_391+81dupCA others(1): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135192 | |||||||
| chr10:15135200 | T | G | 36 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+74A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135200 | |||||||
| chr10:15135238 | T | C | 36 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
36 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.391+36A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 3/11 | chr10 | 15135238 | |||||||
| chr10:15135542 | C | T | 1 | a0001c0001t0009g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.247-124G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135542 | |||||||
| chr10:15135731 | G | A | 53 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(50): Show |
53 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.247-313C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135731 | |||||||
| chr10:15135775 | T | TG | 24 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0031 others(21): Show |
24 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.247-358dupC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135775 | |||||||
| chr10:15135779 | T | G | 50 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(47): Show |
50 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.247-361A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135779 | |||||||
| chr10:15135780 | G | A | 13 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.247-362C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135780 | |||||||
| chr10:15135780 | G | T | 1 | a0001c0002t0010g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247-362C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135780 | |||||||
| chr10:15135828 | A | G | 67 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(64): Show |
67 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.247-410T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135828 | |||||||
| chr10:15135908 | CAAAG | C | 3 | a0001c0001t0001g0267 a0001c0001t0004g0002 a0001c0001t0004g0095 |
3 | HG02615.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.247-494_247-491del others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135908 | |||||||
| chr10:15135969 | A | AT | 3 | a0001c0002t0005g0143 a0001c0002t0031g0270 a0001c0002t0032g0101 |
3 | HG02615.hp1 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.247-552dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135969 | |||||||
| chr10:15135997 | T | C | 95 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(92): Show |
95 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.247-579A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15135997 | |||||||
| chr10:15136046 | G | A | 11 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(8): Show |
11 | HG01975.hp2 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-628C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136046 | |||||||
| chr10:15136175 | C | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0066 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.247-757G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136175 | |||||||
| chr10:15136176 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247-758C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136176 | |||||||
| chr10:15136177 | C | T | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.247-759G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136177 | |||||||
| chr10:15136212 | ACT | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0168 a0001c0001t0009g0207 |
3 | HG00639.hp1 HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.247-796_247-795del others(2): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136212 | |||||||
| chr10:15136223 | A | AAAGGGAA others(20): Show |
5 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-832_247-806dup others(27): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136223 | |||||||
| chr10:15136232 | G | A | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.247-814C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136232 | |||||||
| chr10:15136253 | G | A | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247-835C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136253 | |||||||
| chr10:15136395 | AG | A | 5 | a0001c0002t0005g0143 a0001c0002t0019g0130 a0001c0002t0019g0131 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-978delC | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136395 | |||||||
| chr10:15136397 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.247-979C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136397 | |||||||
| chr10:15136398 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.247-980C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136398 | |||||||
| chr10:15136400 | G | A | 37 | a0001c0001t0001g0063 a0001c0001t0001g0267 a0001c0001t0002g0047 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.247-982C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136400 | |||||||
| chr10:15136460 | G | C | 34 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0155 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.247-1042C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136460 | |||||||
| chr10:15136677 | C | G | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-1259G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136677 | |||||||
| chr10:15136679 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.247-1261C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136679 | |||||||
| chr10:15136694 | G | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.247-1276C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136694 | |||||||
| chr10:15136727 | T | C | 49 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(46): Show |
49 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.247-1309A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136727 | |||||||
| chr10:15136743 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.247-1325A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136743 | |||||||
| chr10:15136827 | CT | C | 110 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.247-1410delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136827 | |||||||
| chr10:15136827 | CTTT | C | 10 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(7): Show |
10 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-1412_247-1410d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136827 | |||||||
| chr10:15136903 | C | T | 32 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(29): Show |
32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-1485G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136903 | |||||||
| chr10:15136962 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.247-1544A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15136962 | |||||||
| chr10:15137082 | A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.247-1664T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137082 | |||||||
| chr10:15137096 | G | A | 1 | a0001c0001t0028g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.247-1678C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137096 | |||||||
| chr10:15137191 | G | T | 128 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(125): Show |
128 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.247-1773C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137191 | |||||||
| chr10:15137378 | A | T | 69 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0093 others(66): Show |
69 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.247-1960T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137378 | |||||||
| chr10:15137736 | C | A | 32 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0093 others(29): Show |
32 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-2318G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137736 | |||||||
| chr10:15137740 | G | T | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247-2322C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15137740 | |||||||
| chr10:15138004 | C | CT | 54 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0031 others(51): Show |
54 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2587dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138004 | |||||||
| chr10:15138109 | C | A | 34 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0085 others(31): Show |
34 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.247-2691G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138109 | |||||||
| chr10:15138257 | C | T | 8 | a0001c0004t0013g0112 a0001c0004t0013g0113 a0001c0004t0025g0096 others(5): Show |
8 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.247-2839G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138257 | |||||||
| chr10:15138358 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0008g0092 |
3 | HG00438.hp2 HG02074.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.247-2940T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138358 | |||||||
| chr10:15138452 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0252 |
2 | HG00621.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.246+2970C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138452 | |||||||
| chr10:15138504 | C | T | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+2918G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138504 | |||||||
| chr10:15138554 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.246+2868T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138554 | |||||||
| chr10:15138647 | A | C | 1 | a0001c0001t0022g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.246+2775T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138647 | |||||||
| chr10:15138709 | A | G | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.246+2713T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138709 | |||||||
| chr10:15138731 | T | C | 2 | a0001c0004t0013g0112 a0001c0004t0025g0096 |
2 | HG01975.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.246+2691A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138731 | |||||||
| chr10:15138994 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.246+2428G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15138994 | |||||||
| chr10:15139130 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0069 |
3 | HG00099.hp1 HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.246+2292C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139130 | |||||||
| chr10:15139250 | C | CTCTA | 62 | a0001c0001t0001g0019 a0001c0001t0001g0136 a0001c0001t0001g0138 others(59): Show |
62 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.246+2168_246+2171d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | |||||||
| chr10:15139250 | CTCTA | C | 60 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0059 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.246+2168_246+2171d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | |||||||
| chr10:15139250 | CTCTATCT others(1): Show |
C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG00423.hp1 HG00558.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+2164_246+2171d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | |||||||
| chr10:15139250 | CTCTATCT others(5): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.246+2160_246+2171d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139250 | |||||||
| chr10:15139277 | TATCTATC others(13): Show |
T | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2125_246+2144d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139277 | |||||||
| chr10:15139293 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0028g0118 |
2 | HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.246+2129A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | |||||||
| chr10:15139293 | T | TATCC | 3 | a0001c0001t0009g0207 a0001c0006t0016g0010 a0001c0006t0027g0015 |
3 | HG02257.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+2125_246+2128d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | |||||||
| chr10:15139293 | T | TATCTATC others(1): Show |
22 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(19): Show |
22 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.246+2128_246+2129i others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | |||||||
| chr10:15139293 | T | TATCTATC others(5): Show |
1 | a0001c0001t0002g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+2128_246+2129i others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139293 | |||||||
| chr10:15139398 | C | T | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.246+2024G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139398 | |||||||
| chr10:15139510 | G | A | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246+1912C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139510 | |||||||
| chr10:15139570 | T | G | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1852A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139570 | |||||||
| chr10:15139606 | G | C | 1 | a0001c0001t0011g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.246+1816C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139606 | |||||||
| chr10:15139737 | C | G | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+1685G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139737 | |||||||
| chr10:15139863 | C | CCATATA | 5 | a0001c0004t0013g0112 a0001c0004t0013g0113 a0001c0004t0025g0096 others(2): Show |
5 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1558_246+1559i others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | C | CTA | 10 | a0001c0001t0001g0139 a0001c0001t0001g0174 a0001c0001t0001g0199 others(7): Show |
10 | HG00423.hp2 HG00735.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.246+1557_246+1558d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | C | CTATA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0181 others(4): Show |
7 | HG00140.hp1 HG01071.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+1555_246+1558d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | C | CTATATA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0057 others(5): Show |
8 | HG00280.hp1 HG01109.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+1553_246+1558d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | C | CTATATAT others(1): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0009g0097 |
3 | HG02155.hp1 NA18906.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.246+1551_246+1558d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0242 |
2 | HG01975.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.246+1549_246+1558d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTA | C | 48 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0034 others(45): Show |
48 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.246+1557_246+1558d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATA | C | 63 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.246+1555_246+1558d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATA | C | 13 | a0001c0001t0001g0136 a0001c0001t0001g0144 a0001c0001t0001g0151 others(10): Show |
13 | HG01099.hp2 HG01243.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.246+1553_246+1558d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(1): Show |
C | 6 | a0001c0001t0001g0253 a0001c0001t0012g0077 a0001c0001t0024g0074 others(3): Show |
6 | HG00140.hp2 HG01109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+1551_246+1558d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(3): Show |
C | 2 | a0001c0001t0001g0197 a0001c0002t0010g0126 |
2 | HG01074.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.246+1549_246+1558d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(5): Show |
C | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.246+1547_246+1558d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(7): Show |
C | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246+1545_246+1558d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(11): Show |
C | 4 | a0001c0001t0003g0052 a0001c0001t0003g0070 a0001c0001t0021g0263 others(1): Show |
4 | HG00642.hp2 HG01081.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1541_246+1558d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(13): Show |
C | 25 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0093 others(22): Show |
25 | HG00438.hp2 HG00735.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.246+1539_246+1558d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(15): Show |
C | 50 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0001t0001g0155 others(47): Show |
50 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.246+1537_246+1558d others(24): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(17): Show |
C | 2 | a0001c0001t0001g0075 a0001c0002t0010g0090 |
2 | HG00738.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.246+1535_246+1558d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139863 | CTATATAT others(21): Show |
C | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1531_246+1558d others(30): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139863 | |||||||
| chr10:15139864 | TATATATA others(6): Show |
T | 1 | a0001c0001t0007g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.246+1545_246+1557d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139864 | |||||||
| chr10:15139866 | T | C | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.246+1556A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139866 | |||||||
| chr10:15139868 | T | C | 1 | a0001c0005t0003g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246+1554A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139868 | |||||||
| chr10:15139870 | T | C | 1 | a0001c0005t0003g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.246+1552A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139870 | |||||||
| chr10:15139872 | T | C | 3 | a0001c0002t0015g0102 a0001c0002t0015g0123 a0001c0002t0015g0124 |
3 | HG01109.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.246+1550A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139872 | |||||||
| chr10:15139874 | T | C | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.246+1548A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139874 | |||||||
| chr10:15139878 | T | C | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246+1544A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139878 | |||||||
| chr10:15139882 | T | C | 3 | a0001c0001t0003g0052 a0001c0001t0003g0070 a0001c0001t0042g0225 |
3 | HG00642.hp2 HG01081.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.246+1540A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139882 | |||||||
| chr10:15139883 | A | T | 1 | a0001c0004t0013g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.246+1539T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139883 | |||||||
| chr10:15139884 | T | C | 24 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0094 others(21): Show |
24 | HG00438.hp2 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.246+1538A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139884 | |||||||
| chr10:15139886 | T | C | 47 | a0001c0001t0001g0035 a0001c0001t0001g0155 a0001c0001t0001g0267 others(44): Show |
47 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.246+1536A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139886 | |||||||
| chr10:15139888 | T | C | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+1534A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15139888 | |||||||
| chr10:15140014 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.246+1408C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140014 | |||||||
| chr10:15140103 | C | T | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.246+1319G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140103 | |||||||
| chr10:15140130 | T | C | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.246+1292A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140130 | |||||||
| chr10:15140183 | C | T | 3 | a0001c0001t0006g0108 a0001c0001t0006g0110 a0001c0001t0006g0115 |
3 | HG02280.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.246+1239G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140183 | |||||||
| chr10:15140277 | C | T | 2 | a0001c0001t0009g0003 a0001c0001t0009g0168 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.246+1145G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140277 | |||||||
| chr10:15140299 | T | A | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+1123A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140299 | |||||||
| chr10:15140525 | T | C | 4 | a0001c0004t0013g0112 a0001c0004t0013g0113 a0001c0004t0025g0096 others(1): Show |
4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+897A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140525 | |||||||
| chr10:15140573 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246+849T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140573 | |||||||
| chr10:15140591 | C | T | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.246+831G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140591 | |||||||
| chr10:15140619 | T | G | 81 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0063 others(78): Show |
81 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.246+803A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140619 | |||||||
| chr10:15140632 | C | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(12): Show |
15 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+790G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140632 | |||||||
| chr10:15140894 | A | G | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+528T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15140894 | |||||||
| chr10:15141160 | G | A | 32 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(29): Show |
32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.246+262C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141160 | |||||||
| chr10:15141354 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246+68C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141354 | |||||||
| chr10:15141364 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.246+58C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 2/11 | chr10 | 15141364 | |||||||
| chr10:15141748 | GC | G | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(4): Show |
7 | HG01243.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-192delG | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141748 | |||||||
| chr10:15141771 | G | A | 2 | a0001c0005t0003g0125 a0001c0005t0003g0129 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.111-214C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141771 | |||||||
| chr10:15141859 | T | A | 71 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0063 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.111-302A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141859 | |||||||
| chr10:15141927 | T | C | 3 | a0001c0005t0003g0125 a0001c0005t0003g0129 a0001c0005t0009g0128 |
3 | HG03098.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.111-370A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141927 | |||||||
| chr10:15141969 | T | G | 4 | a0001c0002t0014g0073 a0001c0002t0014g0087 a0001c0002t0014g0088 others(1): Show |
4 | HG02280.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-412A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141969 | |||||||
| chr10:15141998 | A | G | 5 | a0001c0001t0001g0019 a0001c0002t0002g0017 a0001c0002t0002g0142 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-441T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15141998 | |||||||
| chr10:15142051 | G | A | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-494C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142051 | |||||||
| chr10:15142273 | C | T | 1 | a0001c0001t0006g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.111-716G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142273 | |||||||
| chr10:15142401 | GA | G | 32 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(29): Show |
32 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.111-845delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142401 | |||||||
| chr10:15142421 | G | C | 9 | a0001c0001t0009g0003 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-864C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142421 | |||||||
| chr10:15142506 | G | A | 71 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0063 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.111-949C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142506 | |||||||
| chr10:15142519 | G | A | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-962C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142519 | |||||||
| chr10:15142528 | C | T | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-971G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142528 | |||||||
| chr10:15142585 | T | C | 2 | a0001c0002t0018g0268 a0001c0002t0018g0271 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111-1028A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142585 | |||||||
| chr10:15142625 | T | C | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.111-1068A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142625 | |||||||
| chr10:15142744 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.111-1187G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142744 | |||||||
| chr10:15142881 | A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111-1324T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15142881 | |||||||
| chr10:15143033 | G | T | 4 | a0001c0002t0002g0017 a0001c0002t0002g0142 a0001c0002t0002g0238 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-1476C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143033 | |||||||
| chr10:15143110 | T | C | 5 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-1553A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143110 | |||||||
| chr10:15143213 | A | G | 33 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0031 others(30): Show |
33 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.111-1656T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143213 | |||||||
| chr10:15143295 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.111-1738G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143295 | |||||||
| chr10:15143331 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.111-1774G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143331 | |||||||
| chr10:15143502 | G | C | 9 | a0001c0001t0009g0097 a0001c0001t0011g0007 a0001c0001t0011g0008 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-1945C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143502 | |||||||
| chr10:15143504 | C | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0026 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.111-1947G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143504 | |||||||
| chr10:15143542 | T | C | 25 | a0001c0001t0001g0091 a0001c0001t0001g0231 a0001c0001t0006g0081 others(22): Show |
25 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.111-1985A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143542 | |||||||
| chr10:15143581 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2024C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143581 | |||||||
| chr10:15143582 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2025G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143582 | |||||||
| chr10:15143588 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.111-2031C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143588 | |||||||
| chr10:15143602 | A | C | 1 | a0001c0001t0036g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111-2045T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143602 | |||||||
| chr10:15143636 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111-2079G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143636 | |||||||
| chr10:15143747 | G | A | 22 | a0001c0001t0001g0221 a0001c0001t0001g0227 a0001c0001t0001g0245 others(19): Show |
22 | HG01109.hp1 HG01175.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.111-2190C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143747 | |||||||
| chr10:15143842 | G | T | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-2285C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143842 | |||||||
| chr10:15143978 | A | G | 5 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-2421T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15143978 | |||||||
| chr10:15144041 | CA | C | 16 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(13): Show |
16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-2485delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144041 | |||||||
| chr10:15144209 | T | C | 1 | a0001c0001t0008g0189 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.111-2652A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144209 | |||||||
| chr10:15144263 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.111-2706G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144263 | |||||||
| chr10:15144372 | C | T | 2 | a0001c0001t0033g0107 a0001c0001t0045g0050 |
2 | HG02109.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.111-2815G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144372 | |||||||
| chr10:15144405 | C | T | 8 | a0001c0001t0009g0046 a0001c0001t0009g0066 a0001c0001t0022g0080 others(5): Show |
8 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-2848G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144405 | |||||||
| chr10:15144457 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.111-2900A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144457 | |||||||
| chr10:15144478 | T | C | 8 | a0001c0001t0001g0019 a0001c0004t0013g0112 a0001c0004t0025g0096 others(5): Show |
8 | HG01975.hp2 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-2921A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144478 | |||||||
| chr10:15144526 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.111-2969A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144526 | |||||||
| chr10:15144527 | C | G | 6 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(3): Show |
6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-2970G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144527 | |||||||
| chr10:15144594 | G | A | 17 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(14): Show |
17 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.111-3037C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144594 | |||||||
| chr10:15144598 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(3): Show |
6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-3041C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144598 | |||||||
| chr10:15144678 | C | T | 104 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(101): Show |
104 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-3121G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144678 | |||||||
| chr10:15144679 | C | G | 104 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(101): Show |
104 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.111-3122G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144679 | |||||||
| chr10:15144706 | G | C | 109 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(106): Show |
109 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.111-3149C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144706 | |||||||
| chr10:15144718 | G | A | 5 | a0001c0001t0012g0077 a0001c0001t0012g0078 a0001c0001t0012g0079 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-3161C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144718 | |||||||
| chr10:15144725 | C | T | 8 | a0001c0001t0006g0048 a0001c0001t0009g0046 a0001c0001t0009g0066 others(5): Show |
8 | HG01192.hp2 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-3168G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144725 | |||||||
| chr10:15144821 | G | T | 112 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(109): Show |
112 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.111-3264C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15144821 | |||||||
| chr10:15145337 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.111-3780G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145337 | |||||||
| chr10:15145382 | T | C | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111-3825A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145382 | |||||||
| chr10:15145582 | G | A | 1 | a0001c0001t0009g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.111-4025C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145582 | |||||||
| chr10:15145722 | T | G | 9 | a0001c0001t0006g0048 a0001c0001t0009g0046 a0001c0001t0009g0066 others(6): Show |
9 | HG01192.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-4165A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145722 | |||||||
| chr10:15145757 | A | T | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.111-4200T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145757 | |||||||
| chr10:15145799 | C | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(13): Show |
16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-4242G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145799 | |||||||
| chr10:15145834 | G | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(13): Show |
16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-4277C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145834 | |||||||
| chr10:15145839 | C | T | 33 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(30): Show |
33 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.111-4282G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145839 | |||||||
| chr10:15145840 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.111-4283C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145840 | |||||||
| chr10:15145907 | G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-4350C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145907 | |||||||
| chr10:15145929 | C | T | 2 | a0001c0001t0003g0152 a0001c0001t0003g0233 |
2 | HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-4372G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145929 | |||||||
| chr10:15145951 | G | T | 107 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(104): Show |
107 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.111-4394C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15145951 | |||||||
| chr10:15146596 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.111-5039T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146596 | |||||||
| chr10:15146612 | G | A | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-5055C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146612 | |||||||
| chr10:15146627 | G | A | 5 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-5070C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146627 | |||||||
| chr10:15146738 | C | T | 6 | a0001c0002t0010g0126 a0001c0002t0015g0102 a0001c0002t0015g0123 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-5181G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146738 | |||||||
| chr10:15146756 | G | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(14): Show |
17 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.111-5199C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146756 | |||||||
| chr10:15146785 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.111-5228T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146785 | |||||||
| chr10:15146830 | C | T | 1 | a0001c0004t0048g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111-5273G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15146830 | |||||||
| chr10:15147069 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.111-5512C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147069 | |||||||
| chr10:15147095 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0059 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.111-5539dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-5550_111-5539d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0134 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.111-5551_111-5539d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CA | C | 30 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0151 others(27): Show |
30 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.111-5539delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111-5548_111-5539d others(12): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.111-5549_111-5539d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(5): Show |
C | 3 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0002c0008t0010g0013 |
3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.111-5550_111-5539d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0065 a0001c0001t0003g0061 a0001c0001t0003g0072 others(2): Show |
5 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-5551_111-5539d others(15): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(7): Show |
C | 12 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(9): Show |
12 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-5552_111-5539d others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0035g0114 a0001c0004t0013g0113 a0001c0004t0025g0096 others(4): Show |
7 | HG01975.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-5554_111-5539d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(10): Show |
C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0006g0108 others(12): Show |
15 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.111-5555_111-5539d others(19): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(11): Show |
C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(26): Show |
29 | HG00438.hp1 HG00609.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.111-5556_111-5539d others(20): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0002g0027 a0001c0001t0004g0273 a0001c0004t0048g0016 |
3 | HG02965.hp1 NA18984.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.111-5557_111-5539d others(21): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(13): Show |
C | 20 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(17): Show |
20 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-5558_111-5539d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(16): Show |
C | 9 | a0001c0001t0004g0269 a0001c0002t0010g0126 a0001c0002t0015g0102 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5561_111-5539d others(25): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147095 | CAAAAAAA others(20): Show |
C | 1 | a0001c0003t0008g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.111-5565_111-5539d others(29): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147095 | |||||||
| chr10:15147411 | A | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0151 a0001c0001t0001g0174 others(3): Show |
6 | HG01109.hp2 HG01258.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-5854T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147411 | |||||||
| chr10:15147436 | G | A | 9 | a0001c0001t0004g0269 a0001c0002t0010g0126 a0001c0002t0015g0102 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-5879C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147436 | |||||||
| chr10:15147519 | T | C | 1 | a0001c0004t0025g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.111-5962A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147519 | |||||||
| chr10:15147625 | C | T | 1 | a0001c0001t0013g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.111-6068G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147625 | |||||||
| chr10:15147635 | G | GA | 13 | a0001c0001t0001g0019 a0001c0001t0002g0024 a0001c0001t0004g0095 others(10): Show |
13 | HG02258.hp2 HG02647.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-6079dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147635 | |||||||
| chr10:15147697 | T | G | 28 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(25): Show |
28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.111-6140A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147697 | |||||||
| chr10:15147850 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.111-6293G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15147850 | |||||||
| chr10:15148103 | C | T | 1 | a0001c0001t0009g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111-6546G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148103 | |||||||
| chr10:15148320 | A | G | 7 | a0001c0001t0001g0134 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-6763T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148320 | |||||||
| chr10:15148580 | G | A | 24 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(21): Show |
24 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.111-7023C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148580 | |||||||
| chr10:15148600 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.111-7043T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148600 | |||||||
| chr10:15148604 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111-7047C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148604 | |||||||
| chr10:15148612 | C | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0186 a0001c0001t0002g0047 others(13): Show |
16 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.111-7055G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148612 | |||||||
| chr10:15148683 | C | T | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7126G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148683 | |||||||
| chr10:15148808 | A | AC | 18 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(15): Show |
18 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-7252_111-7251i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148808 | |||||||
| chr10:15148877 | A | C | 18 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(15): Show |
18 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-7320T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148877 | |||||||
| chr10:15148888 | A | T | 62 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.111-7331T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148888 | |||||||
| chr10:15148931 | C | A | 1 | a0001c0001t0005g0236 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.111-7374G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15148931 | |||||||
| chr10:15149133 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.111-7576C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149133 | |||||||
| chr10:15149148 | C | T | 116 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(113): Show |
116 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.111-7591G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149148 | |||||||
| chr10:15149149 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.111-7592C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149149 | |||||||
| chr10:15149192 | C | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-7635G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149192 | |||||||
| chr10:15149198 | TCAC | T | 7 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0001t0008g0147 others(4): Show |
7 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-7644_111-7642d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149198 | |||||||
| chr10:15149314 | CCAT | C | 4 | a0001c0001t0013g0111 a0001c0004t0013g0112 a0001c0004t0013g0113 others(1): Show |
4 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7760_111-7758d others(5): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149314 | |||||||
| chr10:15149442 | C | CCACCATC others(539): Show |
6 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(3): Show |
6 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(548): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
3 | a0001c0001t0004g0269 a0001c0002t0018g0268 a0001c0002t0018g0271 |
3 | HG01243.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(539): Show |
4 | a0001c0002t0010g0126 a0001c0002t0015g0102 a0001c0002t0015g0123 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(548): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(533): Show |
4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(542): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(521): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(530): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(526): Show |
2 | a0001c0001t0009g0003 a0001c0001t0009g0168 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(535): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(518): Show |
1 | a0001c0001t0001g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0138 |
2 | HG00140.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
1 | a0001c0001t0001g0215 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
1 | a0001c0001t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(530): Show |
149 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0032 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
1 | a0001c0001t0007g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(527): Show |
3 | a0001c0001t0022g0080 a0001c0001t0041g0044 a0001c0001t0049g0203 |
3 | HG01192.hp2 HG03139.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(536): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(518): Show |
5 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(530): Show |
2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(518): Show |
4 | a0001c0001t0009g0097 a0001c0001t0024g0074 a0001c0001t0052g0067 others(1): Show |
4 | HG02451.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(530): Show |
63 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(530): Show |
1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(512): Show |
15 | a0001c0001t0001g0063 a0001c0001t0002g0047 a0001c0001t0002g0065 others(12): Show |
15 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.111-7886_111-7885i others(521): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149442 | C | CCACCATC others(518): Show |
1 | a0001c0001t0006g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111-7886_111-7885i others(527): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149442 | |||||||
| chr10:15149446 | C | CATCACAT others(530): Show |
1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.111-7890_111-7889i others(539): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149446 | |||||||
| chr10:15149466 | T | C | 3 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.111-7909A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149466 | |||||||
| chr10:15149562 | ACATCATC others(5): Show |
A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0002g0065 others(14): Show |
17 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.111-8017_111-8006d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149562 | |||||||
| chr10:15149604 | T | A | 98 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(95): Show |
98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.111-8047A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149604 | |||||||
| chr10:15149817 | CAG | C | 13 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(10): Show |
13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8262_111-8261d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149817 | |||||||
| chr10:15149820 | G | C | 13 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(10): Show |
13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8263C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149820 | |||||||
| chr10:15149822 | C | T | 13 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(10): Show |
13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-8265G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149822 | |||||||
| chr10:15149958 | T | G | 1 | a0001c0001t0021g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.111-8401A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15149958 | |||||||
| chr10:15150229 | C | T | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.111-8672G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150229 | |||||||
| chr10:15150538 | G | A | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-8981C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150538 | |||||||
| chr10:15150609 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0250 |
2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.111-9052A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150609 | |||||||
| chr10:15150765 | C | T | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-9208G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150765 | |||||||
| chr10:15150786 | G | A | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-9229C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150786 | |||||||
| chr10:15150828 | A | C | 13 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(10): Show |
13 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.111-9271T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150828 | |||||||
| chr10:15150852 | A | G | 12 | a0001c0001t0009g0097 a0001c0001t0011g0007 a0001c0001t0011g0008 others(9): Show |
12 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.111-9295T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150852 | |||||||
| chr10:15150884 | C | A | 1 | a0001c0001t0005g0235 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111-9327G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15150884 | |||||||
| chr10:15151059 | C | CTTTTTT | 11 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(8): Show |
11 | HG00140.hp2 HG01109.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.111-9508_111-9503d others(8): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151059 | |||||||
| chr10:15151059 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-9503_111-9502i others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151059 | |||||||
| chr10:15151061 | T | C | 2 | a0001c0002t0002g0017 a0001c0002t0012g0018 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.111-9504A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151061 | |||||||
| chr10:15151075 | G | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-9518C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151075 | |||||||
| chr10:15151127 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.111-9570G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151127 | |||||||
| chr10:15151128 | G | A | 4 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0002t0010g0090 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-9571C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151128 | |||||||
| chr10:15151243 | G | A | 1 | a0001c0001t0051g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.111-9686C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151243 | |||||||
| chr10:15151245 | C | T | 1 | a0001c0001t0022g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.111-9688G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151245 | |||||||
| chr10:15151290 | C | T | 26 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(23): Show |
26 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-9733G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151290 | |||||||
| chr10:15151425 | G | A | 24 | a0001c0001t0001g0063 a0001c0001t0002g0047 a0001c0001t0002g0065 others(21): Show |
24 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.111-9868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151425 | |||||||
| chr10:15151471 | C | T | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111-9914G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151471 | |||||||
| chr10:15151479 | C | T | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.111-9922G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151479 | |||||||
| chr10:15151490 | A | C | 3 | a0001c0001t0006g0048 a0001c0001t0009g0046 a0001c0001t0009g0066 |
3 | HG01884.hp2 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.111-9933T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151490 | |||||||
| chr10:15151514 | T | C | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0105 others(2): Show |
5 | HG02723.hp1 HG02922.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-9957A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151514 | |||||||
| chr10:15151842 | T | C | 4 | a0001c0001t0001g0134 a0001c0001t0012g0077 a0001c0001t0012g0078 others(1): Show |
4 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-10285A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151842 | |||||||
| chr10:15151898 | C | T | 26 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(23): Show |
26 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.111-10341G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15151898 | |||||||
| chr10:15152032 | A | C | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-10475T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152032 | |||||||
| chr10:15152049 | G | A | 14 | a0001c0001t0001g0134 a0001c0001t0004g0269 a0001c0001t0012g0077 others(11): Show |
14 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.111-10492C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152049 | |||||||
| chr10:15152058 | A | C | 10 | a0001c0001t0001g0019 a0001c0001t0013g0111 a0001c0004t0013g0112 others(7): Show |
10 | HG01975.hp2 HG02572.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-10501T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152058 | |||||||
| chr10:15152268 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.111-10711T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152268 | |||||||
| chr10:15152295 | C | A | 33 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(30): Show |
33 | HG00438.hp2 HG00642.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.111-10738G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152295 | |||||||
| chr10:15152362 | A | G | 5 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG00280.hp2 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-10805T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152362 | |||||||
| chr10:15152577 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.111-11020C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152577 | |||||||
| chr10:15152845 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.111-11288C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15152845 | |||||||
| chr10:15153004 | T | C | 10 | a0001c0001t0006g0108 a0001c0001t0006g0109 a0001c0001t0006g0110 others(7): Show |
10 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-11447A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153004 | |||||||
| chr10:15153009 | C | T | 1 | a0001c0001t0040g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-11452G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153009 | |||||||
| chr10:15153028 | T | C | 3 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0002c0008t0010g0013 |
3 | HG02647.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.111-11471A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153028 | |||||||
| chr10:15153089 | T | C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0134 others(9): Show |
12 | HG00140.hp2 HG01243.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-11532A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153089 | |||||||
| chr10:15153104 | C | T | 1 | a0001c0001t0023g0001 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.111-11547G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153104 | |||||||
| chr10:15153121 | C | A | 2 | a0001c0001t0009g0003 a0001c0001t0009g0168 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.111-11564G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153121 | |||||||
| chr10:15153333 | G | A | 3 | a0001c0001t0009g0097 a0001c0001t0052g0067 a0001c0005t0003g0125 |
3 | HG02451.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.111-11776C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153333 | |||||||
| chr10:15153373 | T | G | 11 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0001t0001g0134 others(8): Show |
11 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-11816A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153373 | |||||||
| chr10:15153406 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.111-11849A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153406 | |||||||
| chr10:15153432 | C | T | 2 | a0001c0002t0002g0142 a0001c0002t0002g0238 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.111-11875G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153432 | |||||||
| chr10:15153657 | T | A | 2 | a0001c0001t0024g0074 a0001c0002t0014g0073 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.111-12100A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153657 | |||||||
| chr10:15153658 | A | T | 18 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0091 others(15): Show |
18 | HG00597.hp1 HG00621.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-12101T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153658 | |||||||
| chr10:15153663 | T | A | 1 | a0001c0001t0049g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.111-12106A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153663 | |||||||
| chr10:15153670 | A | T | 1 | a0001c0001t0040g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111-12113T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153670 | |||||||
| chr10:15153806 | C | T | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111-12249G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153806 | |||||||
| chr10:15153810 | C | T | 1 | a0001c0001t0041g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111-12253G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153810 | |||||||
| chr10:15153816 | A | AT | 6 | a0001c0001t0001g0155 a0001c0001t0007g0156 a0001c0001t0011g0007 others(3): Show |
6 | HG01123.hp2 HG01167.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-12260dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153816 | |||||||
| chr10:15153843 | C | T | 9 | a0001c0001t0001g0076 a0001c0001t0001g0134 a0001c0001t0012g0077 others(6): Show |
9 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-12286G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153843 | |||||||
| chr10:15153864 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.111-12307T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153864 | |||||||
| chr10:15153899 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.111-12342G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153899 | |||||||
| chr10:15153900 | G | A | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-12343C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153900 | |||||||
| chr10:15153910 | C | A | 5 | a0001c0001t0001g0091 a0001c0002t0005g0276 a0001c0002t0010g0126 others(2): Show |
5 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-12353G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15153910 | |||||||
| chr10:15154070 | T | C | 1 | a0001c0002t0032g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.111-12513A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154070 | |||||||
| chr10:15154232 | G | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(28): Show |
31 | HG00438.hp1 HG00609.hp2 HG01975.hp2 others(28): Show |
intron_variant | MODIFIER | c.111-12675C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154232 | |||||||
| chr10:15154346 | G | T | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(22): Show |
25 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.111-12789C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154346 | |||||||
| chr10:15154368 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.111-12811G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154368 | |||||||
| chr10:15154373 | G | A | 5 | a0001c0002t0010g0012 a0001c0006t0016g0010 a0001c0006t0016g0014 others(2): Show |
5 | HG02647.hp1 HG02970.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-12816C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154373 | |||||||
| chr10:15154384 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.111-12827C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154384 | |||||||
| chr10:15154475 | G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-12918C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154475 | |||||||
| chr10:15154587 | A | G | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-13030T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154587 | |||||||
| chr10:15154631 | T | C | 27 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(24): Show |
27 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-13074A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154631 | |||||||
| chr10:15154665 | A | C | 4 | a0001c0001t0001g0019 a0001c0001t0034g0098 a0001c0002t0002g0017 others(1): Show |
4 | HG02809.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-13108T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154665 | |||||||
| chr10:15154992 | G | T | 2 | a0001c0001t0021g0051 a0001c0001t0045g0050 |
2 | NA18955.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.111-13435C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15154992 | |||||||
| chr10:15155077 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110+13426T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155077 | |||||||
| chr10:15155462 | G | A | 1 | a0001c0001t0052g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110+13041C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155462 | |||||||
| chr10:15155472 | G | A | 9 | a0001c0001t0001g0076 a0001c0001t0001g0134 a0001c0001t0012g0077 others(6): Show |
9 | HG00140.hp2 HG01261.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.110+13031C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155472 | |||||||
| chr10:15155529 | G | A | 1 | a0001c0001t0050g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110+12974C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155529 | |||||||
| chr10:15155535 | G | GT | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0003g0049 others(2): Show |
5 | HG01243.hp2 HG01978.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+12967dupA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155535 | GT | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0035 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.110+12967delA | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155535 | GTT | G | 66 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0026 others(63): Show |
66 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.110+12966_110+1296 others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155535 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | NA18940.hp2 NA19012.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.110+12956_110+1296 others(16): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155535 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+12955_110+1296 others(17): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155535 | GTTTTTTT others(7): Show |
G | 2 | a0001c0002t0002g0017 a0001c0002t0012g0018 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.110+12954_110+1296 others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155535 | |||||||
| chr10:15155634 | T | C | 61 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0093 others(58): Show |
61 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.110+12869A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155634 | |||||||
| chr10:15155635 | G | A | 1 | a0001c0001t0035g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.110+12868C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155635 | |||||||
| chr10:15155668 | C | T | 43 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0093 others(40): Show |
43 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+12835G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155668 | |||||||
| chr10:15155677 | C | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(14): Show |
17 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.110+12826G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155677 | |||||||
| chr10:15155715 | ATCT | A | 3 | a0001c0006t0016g0010 a0001c0006t0016g0014 a0001c0006t0027g0015 |
3 | HG02970.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.110+12785_110+1278 others(7): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155715 | |||||||
| chr10:15155740 | C | T | 2 | a0001c0002t0002g0017 a0001c0002t0012g0018 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.110+12763G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155740 | |||||||
| chr10:15155777 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+12726T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155777 | |||||||
| chr10:15155819 | G | A | 1 | a0001c0001t0009g0168 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.110+12684C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15155819 | |||||||
| chr10:15156061 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.110+12442C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156061 | |||||||
| chr10:15156124 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.110+12379C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156124 | |||||||
| chr10:15156250 | G | T | 10 | a0001c0001t0001g0144 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
10 | HG01934.hp1 NA18940.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+12253C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156250 | |||||||
| chr10:15156414 | A | G | 1 | a0001c0002t0013g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110+12089T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156414 | |||||||
| chr10:15156442 | G | A | 6 | a0001c0001t0001g0091 a0001c0002t0005g0276 a0001c0002t0010g0126 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+12061C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156442 | |||||||
| chr10:15156470 | G | A | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+12033C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156470 | |||||||
| chr10:15156577 | G | C | 4 | a0001c0001t0004g0269 a0001c0002t0018g0268 a0001c0002t0018g0271 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+11926C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156577 | |||||||
| chr10:15156585 | T | C | 29 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(26): Show |
29 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+11918A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156585 | |||||||
| chr10:15156625 | G | A | 6 | a0001c0001t0001g0091 a0001c0002t0005g0276 a0001c0002t0010g0126 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+11878C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156625 | |||||||
| chr10:15156626 | C | T | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.110+11877G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156626 | |||||||
| chr10:15156636 | C | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+11867G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156636 | |||||||
| chr10:15156783 | C | A | 3 | a0001c0001t0005g0204 a0001c0001t0005g0235 a0001c0001t0005g0236 |
3 | HG02055.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.110+11720G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156783 | |||||||
| chr10:15156844 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0043 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.110+11659G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156844 | |||||||
| chr10:15156901 | A | C | 4 | a0001c0001t0004g0269 a0001c0002t0018g0268 a0001c0002t0018g0271 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+11602T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15156901 | |||||||
| chr10:15157082 | T | C | 10 | a0001c0001t0009g0097 a0001c0001t0011g0007 a0001c0001t0011g0008 others(7): Show |
10 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+11421A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157082 | |||||||
| chr10:15157164 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.110+11339G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157164 | |||||||
| chr10:15157223 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.110+11280G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157223 | |||||||
| chr10:15157348 | C | A | 18 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(15): Show |
18 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.110+11155G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157348 | |||||||
| chr10:15157433 | C | T | 2 | a0001c0002t0010g0090 a0001c0005t0009g0128 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+11070G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157433 | |||||||
| chr10:15157569 | A | G | 5 | a0001c0001t0004g0269 a0001c0001t0034g0098 a0001c0002t0018g0268 others(2): Show |
5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+10934T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157569 | |||||||
| chr10:15157686 | A | G | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+10817T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157686 | |||||||
| chr10:15157718 | T | A | 7 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0205 others(4): Show |
7 | HG01943.hp1 HG01952.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+10785A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157718 | |||||||
| chr10:15157739 | T | C | 1 | a0001c0001t0009g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.110+10764A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157739 | |||||||
| chr10:15157754 | T | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+10749A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157754 | |||||||
| chr10:15157778 | T | C | 2 | a0001c0002t0002g0142 a0001c0002t0002g0238 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.110+10725A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157778 | |||||||
| chr10:15157823 | C | G | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.110+10680G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157823 | |||||||
| chr10:15157827 | T | C | 5 | a0001c0001t0004g0269 a0001c0001t0034g0098 a0001c0002t0018g0268 others(2): Show |
5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+10676A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15157827 | |||||||
| chr10:15158133 | T | C | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+10370A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158133 | |||||||
| chr10:15158152 | C | T | 1 | a0001c0001t0009g0168 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.110+10351G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158152 | |||||||
| chr10:15158173 | G | A | 10 | a0001c0001t0005g0005 a0001c0001t0005g0194 a0001c0001t0005g0195 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+10330C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158173 | |||||||
| chr10:15158315 | CA | C | 40 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(37): Show |
40 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.110+10187delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158315 | |||||||
| chr10:15158438 | C | G | 22 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(19): Show |
22 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.110+10065G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158438 | |||||||
| chr10:15158561 | A | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+9942T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158561 | |||||||
| chr10:15158608 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.110+9895A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158608 | |||||||
| chr10:15158783 | C | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+9720G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158783 | |||||||
| chr10:15158885 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18999.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.110+9618G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15158885 | |||||||
| chr10:15159396 | A | ATATT | 14 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0135 others(11): Show |
14 | HG00597.hp2 HG00673.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.110+9103_110+9106d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | A | ATATTTAT others(1): Show |
21 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(18): Show |
21 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.110+9099_110+9106d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | A | ATATTTAT others(5): Show |
10 | a0001c0001t0001g0040 a0001c0001t0002g0041 a0001c0001t0002g0047 others(7): Show |
10 | HG00735.hp1 HG01081.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+9095_110+9106d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | A | ATATTTAT others(9): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0032 others(4): Show |
7 | HG02258.hp2 HG03098.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+9091_110+9106d others(18): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | A | ATATTTAT others(13): Show |
16 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0031 others(13): Show |
16 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.110+9087_110+9106d others(22): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | A | ATATTTAT others(17): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0247 a0001c0001t0002g0036 |
3 | HG00558.hp1 HG02155.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.110+9083_110+9106d others(26): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | ATATTTAT others(1): Show |
A | 17 | a0001c0001t0001g0076 a0001c0001t0001g0134 a0001c0001t0006g0081 others(14): Show |
17 | HG00140.hp2 HG01192.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.110+9099_110+9106d others(10): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159396 | ATATTTAT others(5): Show |
A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(30): Show |
33 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+9095_110+9106d others(14): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159396 | |||||||
| chr10:15159429 | G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+9074C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159429 | |||||||
| chr10:15159553 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110+8950C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159553 | |||||||
| chr10:15159639 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.110+8864C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159639 | |||||||
| chr10:15159852 | G | A | 1 | a0001c0002t0002g0238 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110+8651C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159852 | |||||||
| chr10:15159875 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.110+8628G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159875 | |||||||
| chr10:15159887 | T | G | 31 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
31 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.110+8616A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159887 | |||||||
| chr10:15159925 | G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+8578C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159925 | |||||||
| chr10:15159994 | C | T | 26 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
26 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+8509G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15159994 | |||||||
| chr10:15160215 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.110+8288G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160215 | |||||||
| chr10:15160254 | T | C | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8249A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160254 | |||||||
| chr10:15160338 | A | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+8165T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160338 | |||||||
| chr10:15160448 | A | ACATG | 4 | a0001c0001t0004g0269 a0001c0002t0018g0268 a0001c0002t0018g0271 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+8051_110+8054d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160448 | |||||||
| chr10:15160507 | G | C | 2 | a0001c0002t0010g0090 a0001c0005t0009g0128 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+7996C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160507 | |||||||
| chr10:15160534 | G | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0134 others(3): Show |
6 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7969C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160534 | |||||||
| chr10:15160554 | T | G | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+7949A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160554 | |||||||
| chr10:15160573 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.110+7930C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160573 | |||||||
| chr10:15160582 | C | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(25): Show |
28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+7921G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160582 | |||||||
| chr10:15160583 | G | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0134 others(7): Show |
10 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+7920C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160583 | |||||||
| chr10:15160727 | T | A | 1 | a0001c0001t0026g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110+7776A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160727 | |||||||
| chr10:15160817 | G | C | 1 | a0001c0001t0050g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110+7686C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160817 | |||||||
| chr10:15160874 | C | T | 2 | a0001c0001t0034g0098 a0001c0002t0014g0073 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.110+7629G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15160874 | |||||||
| chr10:15161061 | C | G | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.110+7442G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161061 | |||||||
| chr10:15161081 | C | CA | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(75): Show |
78 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.110+7421dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | |||||||
| chr10:15161081 | C | CAA | 25 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(22): Show |
25 | HG00140.hp2 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.110+7420_110+7421d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | |||||||
| chr10:15161081 | CA | C | 33 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0093 others(30): Show |
33 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.110+7421delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | |||||||
| chr10:15161081 | CAA | C | 21 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.110+7420_110+7421d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161081 | |||||||
| chr10:15161102 | A | C | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7401T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161102 | |||||||
| chr10:15161276 | C | T | 85 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(82): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.110+7227G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161276 | |||||||
| chr10:15161311 | A | C | 28 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(25): Show |
28 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+7192T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161311 | |||||||
| chr10:15161391 | G | A | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+7112C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161391 | |||||||
| chr10:15161548 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.110+6955A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161548 | |||||||
| chr10:15161602 | C | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+6901G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161602 | |||||||
| chr10:15161683 | C | T | 1 | a0001c0001t0043g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.110+6820G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161683 | |||||||
| chr10:15161948 | A | G | 7 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0002g0158 others(4): Show |
7 | HG01099.hp1 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+6555T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15161948 | |||||||
| chr10:15162251 | C | CA | 13 | a0001c0001t0001g0069 a0001c0001t0001g0240 a0001c0001t0001g0241 others(10): Show |
13 | HG00673.hp1 HG00735.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.110+6251dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | |||||||
| chr10:15162251 | CA | C | 18 | a0001c0001t0001g0033 a0001c0001t0001g0075 a0001c0001t0001g0076 others(15): Show |
18 | HG00140.hp2 HG00738.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.110+6251delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | |||||||
| chr10:15162251 | CAA | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
26 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+6250_110+6251d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162251 | |||||||
| chr10:15162370 | G | T | 1 | a0001c0002t0010g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.110+6133C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162370 | |||||||
| chr10:15162437 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.110+6066C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162437 | |||||||
| chr10:15162464 | A | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+6039T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162464 | |||||||
| chr10:15162567 | C | A | 1 | a0001c0001t0006g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.110+5936G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162567 | |||||||
| chr10:15162569 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.110+5934G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162569 | |||||||
| chr10:15162653 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.110+5850T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162653 | |||||||
| chr10:15162747 | G | GAT | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0134 others(10): Show |
13 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+5754_110+5755d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162747 | |||||||
| chr10:15162928 | G | T | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+5575C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162928 | |||||||
| chr10:15162930 | T | G | 1 | a0001c0001t0008g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.110+5573A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162930 | |||||||
| chr10:15162973 | C | T | 1 | a0001c0001t0030g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.110+5530G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15162973 | |||||||
| chr10:15163058 | C | T | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+5445G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163058 | |||||||
| chr10:15163096 | C | T | 33 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0267 others(30): Show |
33 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.110+5407G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163096 | |||||||
| chr10:15163322 | A | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0008g0147 others(4): Show |
7 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+5181T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163322 | |||||||
| chr10:15163353 | G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+5150C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163353 | |||||||
| chr10:15163473 | C | T | 54 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(51): Show |
54 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+5030G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163473 | |||||||
| chr10:15163478 | G | C | 2 | a0001c0002t0010g0090 a0001c0005t0009g0128 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+5025C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163478 | |||||||
| chr10:15163656 | A | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.110+4847T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163656 | |||||||
| chr10:15163721 | T | G | 132 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(129): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.110+4782A>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163721 | |||||||
| chr10:15163724 | G | A | 72 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(69): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.110+4779C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163724 | |||||||
| chr10:15163743 | T | C | 62 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.110+4760A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163743 | |||||||
| chr10:15163772 | A | T | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+4731T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163772 | |||||||
| chr10:15163773 | C | A | 4 | a0001c0001t0004g0269 a0001c0002t0018g0268 a0001c0002t0018g0271 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+4730G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163773 | |||||||
| chr10:15163813 | T | C | 2 | a0001c0001t0003g0071 a0001c0001t0003g0072 |
2 | HG00597.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.110+4690A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163813 | |||||||
| chr10:15163824 | T | C | 1 | a0001c0002t0032g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.110+4679A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163824 | |||||||
| chr10:15163826 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0134 others(7): Show |
10 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.110+4677G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163826 | |||||||
| chr10:15163827 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.110+4676G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163827 | |||||||
| chr10:15163909 | G | A | 1 | a0001c0005t0010g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110+4594C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163909 | |||||||
| chr10:15163950 | C | T | 5 | a0001c0001t0004g0269 a0001c0001t0034g0098 a0001c0002t0018g0268 others(2): Show |
5 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.110+4553G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163950 | |||||||
| chr10:15163975 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.110+4528C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163975 | |||||||
| chr10:15163995 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4508A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163995 | |||||||
| chr10:15163996 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4507C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15163996 | |||||||
| chr10:15164003 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.110+4500G>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164003 | |||||||
| chr10:15164049 | G | A | 35 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.110+4454C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164049 | |||||||
| chr10:15164132 | G | A | 1 | a0001c0002t0010g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110+4371C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164132 | |||||||
| chr10:15164182 | C | CA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0132 a0001c0001t0001g0135 others(18): Show |
21 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.110+4320dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | |||||||
| chr10:15164182 | CA | C | 54 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(51): Show |
54 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.110+4320delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | |||||||
| chr10:15164182 | CAA | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(67): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.110+4319_110+4320d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164182 | |||||||
| chr10:15164269 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.110+4234T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164269 | |||||||
| chr10:15164271 | A | G | 1 | a0001c0001t0004g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+4232T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164271 | |||||||
| chr10:15164461 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.110+4042G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164461 | |||||||
| chr10:15164516 | G | A | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3987C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164516 | |||||||
| chr10:15164518 | T | A | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3985A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164518 | |||||||
| chr10:15164726 | G | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0076 others(21): Show |
24 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.110+3777C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164726 | |||||||
| chr10:15164760 | G | A | 1 | a0001c0001t0034g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+3743C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164760 | |||||||
| chr10:15164804 | A | G | 108 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(105): Show |
108 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.110+3699T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164804 | |||||||
| chr10:15164849 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0006g0127 a0001c0002t0005g0276 others(4): Show |
7 | HG01109.hp1 HG01975.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+3654A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164849 | |||||||
| chr10:15164865 | C | CTACTAAA others(4): Show |
30 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0076 others(27): Show |
30 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.110+3627_110+3637d others(13): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164865 | |||||||
| chr10:15164903 | C | T | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+3600G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164903 | |||||||
| chr10:15164992 | T | C | 132 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(129): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.110+3511A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15164992 | |||||||
| chr10:15165024 | G | A | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3479C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165024 | |||||||
| chr10:15165035 | C | T | 57 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(54): Show |
57 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.110+3468G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165035 | |||||||
| chr10:15165094 | T | C | 66 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(63): Show |
66 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.110+3409A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165094 | |||||||
| chr10:15165098 | G | A | 2 | a0001c0002t0010g0090 a0001c0005t0009g0128 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.110+3405C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165098 | |||||||
| chr10:15165109 | G | A | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3394C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165109 | |||||||
| chr10:15165163 | C | CA | 33 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0091 others(30): Show |
33 | HG00140.hp2 HG01192.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.110+3339dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165163 | |||||||
| chr10:15165163 | CA | C | 59 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(56): Show |
59 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.110+3339delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165163 | |||||||
| chr10:15165178 | A | T | 1 | a0001c0009t0055g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+3325T>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165178 | |||||||
| chr10:15165197 | T | TC | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3305_110+3306i others(3): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165197 | |||||||
| chr10:15165370 | G | T | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3133C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165370 | |||||||
| chr10:15165395 | G | C | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3108C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165395 | |||||||
| chr10:15165435 | A | C | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(57): Show |
60 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.110+3068T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165435 | |||||||
| chr10:15165455 | A | G | 1 | a0001c0002t0015g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.110+3048T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165455 | |||||||
| chr10:15165875 | C | CA | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0091 others(10): Show |
13 | HG00140.hp2 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+2627dupT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | |||||||
| chr10:15165875 | C | CAA | 75 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(72): Show |
75 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.110+2626_110+2627d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | |||||||
| chr10:15165875 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0135 a0001c0001t0006g0081 others(7): Show |
10 | HG01192.hp2 HG01884.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+2627delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | |||||||
| chr10:15165875 | CAA | C | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2626_110+2627d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15165875 | |||||||
| chr10:15166012 | A | G | 43 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(40): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.110+2491T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166012 | |||||||
| chr10:15166025 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
28 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.110+2478G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166025 | |||||||
| chr10:15166079 | TA | T | 4 | a0001c0001t0001g0019 a0001c0002t0002g0017 a0001c0002t0012g0018 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+2423delT | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166079 | |||||||
| chr10:15166132 | A | G | 9 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(6): Show |
9 | HG00438.hp2 HG01975.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+2371T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166132 | |||||||
| chr10:15166232 | T | A | 48 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(45): Show |
48 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.110+2271A>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166232 | |||||||
| chr10:15166284 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.110+2219G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166284 | |||||||
| chr10:15166395 | G | C | 1 | a0001c0005t0009g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110+2108C>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166395 | |||||||
| chr10:15166442 | C | CTACT | 6 | a0001c0002t0010g0011 a0001c0002t0010g0012 a0001c0006t0016g0010 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2057_110+2060d others(6): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166442 | |||||||
| chr10:15166471 | C | T | 1 | a0001c0001t0004g0002 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110+2032G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166471 | |||||||
| chr10:15166473 | A | G | 3 | a0001c0001t0011g0007 a0001c0001t0011g0008 a0001c0001t0011g0009 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110+2030T>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166473 | |||||||
| chr10:15166617 | T | C | 1 | a0001c0005t0003g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110+1886A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166617 | |||||||
| chr10:15166637 | T | C | 2 | a0001c0002t0019g0130 a0001c0002t0019g0131 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+1866A>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15166637 | |||||||
| chr10:15167181 | TAA | T | 127 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(124): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.110+1320_110+1321d others(4): Show |
NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167181 | |||||||
| chr10:15167431 | C | T | 127 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(124): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.110+1072G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167431 | |||||||
| chr10:15167571 | A | C | 1 | a0001c0001t0053g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.110+932T>G | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167571 | |||||||
| chr10:15167959 | C | G | 1 | a0001c0001t0005g0005 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.110+544G>C | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167959 | |||||||
| chr10:15167991 | G | A | 1 | a0001c0002t0005g0276 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.110+512C>T | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15167991 | |||||||
| chr10:15168101 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0009g0003 |
2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.110+402G>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15168101 | |||||||
| chr10:15168244 | G | T | 1 | a0001c0001t0004g0002 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110+259C>A | NMT2 | ENSG00000152465.18 | transcript | ENST00000378165.9 | protein_coding | 1/11 | chr10 | 15168244 |